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                <text>Modified Genesio-Tesi systems with trigonometric functions and the Caputo fractional derivative</text>
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                <text>Caputo fractional derivative; fractional order; Genesio-Tesi system; Lyapunov stability; numerical method</text>
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                <text>The new fractional-order Genesio-Tesi system is introduced, and its boundedness, stability of the equilibrium points, Lyapunov stability, uniqueness of the solution, and bifurcation are all discussed in this paper. Using the efficient predictor-corrector approach, we statistically analyze the Genesio-Tesi system in fractional order. The results effectively conceptualize and visualize the novel fractional order Genesio-Tesi systems that are suggested. When the systems order shifts from integer to fractional, the revolution around the fixed point increases. The chaotic character of the modified Genesio-Tesi system is comparable to that of the original Genesio system. The major changes were made to the Geensio-Tesi system by including the trigonometric functions, keeping the initial conditions and parameter values intact. The system is fractionalised with the help of Caputo fractional operator. In particular, the modified systems nature is more complex, which may aid in signal processing and secure communication. Future research on the modified Genesio-Tesi system can now proceed in light of this finding. This article offers a fresh approach to utilizing and thoroughly researching the Genesio-Tesi systems that have been provided.  CSP - Cambridge, UK; I&amp;amp;S - Florida, USA, 2024</text>
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                <text>Deepika S.; Veeresha P.</text>
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                <text>Mathematics in Engineering, Science and Aerospace, Vol-15, No. 1, pp. 115-129.</text>
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                <text>Deepika S., CHRIST (Deemed to be University), Department of Mathematics, Bengaluru, 560029, India; Veeresha P., CHRIST (Deemed to be University), Department of Mathematics, Bengaluru, 560029, India</text>
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                <text>Modified Metal Organic Frameworks for Electrocatalytic Water Splitting and Energy Storage Applications   </text>
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                <text>Metal-organic frameworks (MOFs) are a class of crystalline material formed by the newlinecombination of metal ions/clusters along with organic linkers. This work is mainly based on newlinesynthesizing MOFs and their application in electrocatalytic water splitting and newlinesupercapacitors. The MOFs synthesized in the present work are Ni-Cu, {Mn-NiNH2(h2fipbb)}, Mn-MOF/rGO, and Sm-MOF/rGO/PANI using different ditopic and tritopic linkers. Using various characterization techniques, the formation of the synthesized MOFs is confirmed. The increasing use of fossil fuels now contributes to a number of environmental problems, including climate change and global warming. High-performance electrochemical energy storage devices are essential for portable electronics, electric cars, newlineand renewable energy storage medium, driving demand. MOFs are emerged as a promising newlinecontender for energy storage applications owing to their novel microstructures, atomically dispersed metal centers, and earth-abundant metal components. Electrochemical water splitting is a crucial approach in the pursuit of producing environmentally friendly fuels such newlineas H2 and O2, reducing our dependence on traditional fossil fuels while promoting newlinesustainable and clean energy sources. In order to produce hydrogen with the best efficiency and lowest cost, these MOFs are used. Electrochemical studies like cyclic voltammetry, galvanostatic charge discharge, and electrochemical impedance spectroscopy reveal that the prepared MOFs can be used as supercapacitors. Linear sweep voltammetry and Tafel plot determine the performance of these MOFs towards water splitting studies. Supercapacitors, which are electrochemical capacitors, are popular energy storage devices with quick charge rate, high power density, excellent rate capability, and outstanding life expectancy.</text>
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                <text>Rajasekaran, Sruthi</text>
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                <text>K R, Sunaja Devi.</text>
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                <text>Modified Montmorillonite Catalysed Ultrasonic Assisted one-pot Synthesis of Novel 2,3-dihydroisoxazolo[5,4-d] pyrimidin-4(7H)-ones as Potential Anticancer Agents</text>
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                <text>2,3-dihydroisoxazolo[5,4-d] pyrimidin-4(7H)-ones; Al&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt;; Anticancer Activity; CeO&lt;sub&gt;2&lt;/sub&gt;; Montmorillonite</text>
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                <text>The development of novel compounds with potential anticancer activity is imperative for combating the challenges posed by cancer. In this study, a modified montmorillonite based catalyst is employed for the synthesis of 2,3-dihydroisoxazolo[5,4-d] pyrimidin-4(7H)-ones, which are promising candidates for anticancer agents. Montmorillonite is modified using mixed metal oxides, typically Al2O3 and CeO2, by a facile approach followed by standard spectroscopic and electron microscopic characterizations. It is then employed for the one-pot synthesis of a series of 2,3-dihydroisoxazolo[5,4-d] pyrimidin-4(7H)-ones. The synthesis protocol, mediated by ultrasound, is simple, efficient, and environment friendly. The mixed metal oxide pillared montmorillonite catalyst exhibits high catalytic activity and selectivity, facilitating the formation of the desired compounds in good to excellent yields. The synthesized compounds are characterized using various spectroscopic techniques such as 1H NMR, 13C NMR and mass spectrometry. Furthermore, the anticancer activity of the synthesized compounds is evaluated against a series of cancer cell lines, revealing promising cytotoxic effects. The findings of this study highlight the potential of novel 2,3-dihydroisoxazolo[5,4-d] pyrimidin-4(7H)-ones as promising anticancer agent, warranting further investigation for their therapeutic potential.  The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2024.</text>
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                <text>Anand S.; Devi K. R S.; Govindaraju S.; Tabassum S.</text>
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                <text>Catalysis Surveys from Asia, Vol-28, No. 4, pp. 435-451.</text>
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                <text>Anand S., Department of Chemistry, CHRIST (Deemed to be University), Bengaluru, 560029, India; Devi K. R S., Department of Chemistry, CHRIST (Deemed to be University), Bengaluru, 560029, India; Govindaraju S., Department of Sciences and Humanities, CHRIST (Deemed to be University), School of Engineering and Technology, Kumbalagodu, Mysore Road, Bengaluru, 560074, India; Tabassum S., Department of Chemistry, Surana College - Autonomous, South End Road, Basavanagudi, Bengaluru, 560004, India</text>
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                <text>Modified Non-local Means Model for Speckle Noise Reduction in Ultrasound Images</text>
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            <name>Subject</name>
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                <text>Alpha position; Grey wolf optimization; Non-local means filter; Speckle noise; Ultrasound image</text>
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                <text>In the modern health care field, various medical imaging modalities play a vital role in diagnosis. Among the modalities, Medical Ultrasound Imaging is the most popular and economic modality. But its vulnerability to multiplicative speckle noise is challenging, which obscure accurate diagnosis. To reduce the influence of the speckle noise, various noise filtering models have been proposed. But while filtering the noise, these filters exhibit limitations like high computational complexity and loss of detailed structures and edges of organs. In this article, a novel Non-local means (NLM)-based model is proposed for the speckle reduction of Ultrasound images. The design parameters of the NLM filter are obtained by applying the Grey Wolf Optimization (GWO) to the input image. The optimized parameters and the noisy image are passed to the NLM filter to get the denoised image. The efficiency of this proposed method is evaluated with standard performance metrics. A comparative analysis with existing methods highlights the merit of the proposal.  2022, The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd.</text>
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                <text>Shereena V.B.; Raju G.</text>
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                <text>Lecture Notes on Data Engineering and Communications Technologies, Vol-111, pp. 691-707.</text>
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                <text>Springer Science and Business Media Deutschland GmbH</text>
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            <description>Information about rights held in and over the resource</description>
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              <elementText elementTextId="156921">
                <text>Restricted Access</text>
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              <elementText elementTextId="156922">
                <text>ISSN: 23674512</text>
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                <text>Shereena V.B., School of Computer Sciences, Mahatma Gandhi University, Kerala, India; Raju G., Christ University, Bengaluru, India</text>
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          <element elementId="50">
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              <elementText elementTextId="109496">
                <text>Modified PredictorCorrector Method for the Numerical Solution of a Fractional-Order SIR Model with 2019-nCoV</text>
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            <elementTextContainer>
              <elementText elementTextId="109497">
                <text>Caputo derivative; Coronavirus; Epidemic mathematical model; Fractional predictorcorrector method</text>
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          <element elementId="41">
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            <description>An account of the resource</description>
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                <text>In this paper, we analyzed and found the solution for a suitable nonlinear fractional dynamical system that describes coronavirus (2019-nCoV) using a novel computational method. A compartmental model with four compartments, namely, susceptible, infected, reported and unreported, was adopted and modified to a new model incorporating fractional operators. In particular, by using a modified predictorcorrector method, we captured the nature of the obtained solution for different arbitrary orders. We investigated the influence of the fractional operator to present and discuss some interesting properties of the novel coronavirus infection.  2022 by the authors. Licensee MDPI, Basel, Switzerland.</text>
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            <elementTextContainer>
              <elementText elementTextId="109499">
                <text>Gao W.; Veeresha P.; Cattani C.; Baishya C.; Baskonus H.M.</text>
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              <elementText elementTextId="109500">
                <text>Fractal and Fractional, Vol-6, No. 2</text>
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              <elementText elementTextId="109501">
                <text>MDPI</text>
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                <text>&lt;a href="https://doi.org/10.3390/fractalfract6020092" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.3390/fractalfract6020092&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85124195730&amp;amp;doi=10.3390%2Ffractalfract6020092&amp;amp;partnerID=40&amp;amp;md5=4480fd30c6d91ad9973ace43009998ba" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-85124195730&amp;amp;doi=10.3390%2ffractalfract6020092&amp;amp;partnerID=40&amp;amp;md5=4480fd30c6d91ad9973ace43009998ba&lt;/a&gt;</text>
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          <element elementId="47">
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            <description>Information about rights held in and over the resource</description>
            <elementTextContainer>
              <elementText elementTextId="109504">
                <text>All Open Access; Gold Open Access</text>
              </elementText>
            </elementTextContainer>
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          <element elementId="46">
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            <description>A related resource</description>
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              <elementText elementTextId="109505">
                <text>ISSN: 25043110</text>
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            <description>The file format, physical medium, or dimensions of the resource</description>
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            <description>A language of the resource</description>
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            <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
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              <elementText elementTextId="109509">
                <text>Gao W., School of Information Science and Technology, Yunnan Normal University, Kunming, 650092, China; Veeresha P., Center for Mathematical Needs, Department of Mathematics, CHRIST (Deemed to be University), Bengaluru, 560029, India; Cattani C., Engineering School (DEIM), Tuscia University, Viterbo, 01100, Italy; Baishya C., Department of Studies and Research in Mathematics, Tumkur University, Tumkur, 572103, India; Baskonus H.M., Department of Mathematics and Science Education, Faculty of Education, Harran University, Sanliurfa, 63100, Turkey</text>
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            <element elementId="50">
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    <itemType itemTypeId="19">
      <name>Article</name>
      <description>Faculty Publications -Articles</description>
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          <element elementId="50">
            <name>Title</name>
            <description>A name given to the resource</description>
            <elementTextContainer>
              <elementText elementTextId="123442">
                <text>Modified Rice Husk Silica from Biowaste: An Efficient Catalyst for Transesterification of Diethyl Malonate and Benzyl Alcohol</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="49">
            <name>Subject</name>
            <description>The topic of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="123443">
                <text>Benzyl alcohol; Biomass; Diethyl malonate; Modified silica; Transesterification</text>
              </elementText>
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          </element>
          <element elementId="41">
            <name>Description</name>
            <description>An account of the resource</description>
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              <elementText elementTextId="123444">
                <text>Abstract: Molybdenum and lanthanum oxide modified silica-based catalysts were prepared from the agricultural waste rice husk. These synthesized catalysts were characterized by various spectroscopic and non-spectroscopic techniques. The catalytic performance was investigated by transesterification reaction between diethyl malonate and benzyl alcohol in the liquid phase using modified silica as a heterogeneous catalyst. Molybdenum modified silica-based catalyst showed the highest conversion efficiency of 95.6% and selectivity of 96.8% for dibenzyl malonate. The reaction conditions were optimized to give maximum efficiency with the highest selectivity in a solvent-free green method. Graphic Abstract: [Figure not available: see fulltext.].  2019, Springer Nature B.V.</text>
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              <elementText elementTextId="123445">
                <text>Priya A.S.; Devi K.R.S.; Karthik K.; Sugunan S.</text>
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              <elementText elementTextId="123446">
                <text>Waste and Biomass Valorization, Vol-11, No. 9, pp. 4809-4819.</text>
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                <text>&lt;a href="https://doi.org/10.1007/s12649-019-00808-5" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1007/s12649-019-00808-5&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85073794117&amp;amp;doi=10.1007%2Fs12649-019-00808-5&amp;amp;partnerID=40&amp;amp;md5=7ea60929258ee40f543d7cf22c9c83de" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-85073794117&amp;amp;doi=10.1007%2fs12649-019-00808-5&amp;amp;partnerID=40&amp;amp;md5=7ea60929258ee40f543d7cf22c9c83de&lt;/a&gt;</text>
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            <name>Rights</name>
            <description>Information about rights held in and over the resource</description>
            <elementTextContainer>
              <elementText elementTextId="123450">
                <text>Restricted Access</text>
              </elementText>
            </elementTextContainer>
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              <elementText elementTextId="123451">
                <text>ISSN: 18772641</text>
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            <description>The file format, physical medium, or dimensions of the resource</description>
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            <description>A language of the resource</description>
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              <elementText elementTextId="123453">
                <text>English</text>
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                <text>Priya A.S., Department of Chemistry, CHRIST (Deemed To Be University), Bangalore, 560029, Karnataka, India; Devi K.R.S., Department of Chemistry, CHRIST (Deemed To Be University), Bangalore, 560029, Karnataka, India; Karthik K., Department of Chemistry, CHRIST (Deemed To Be University), Bangalore, 560029, Karnataka, India; Sugunan S., Department of Applied Chemistry, Cochin University of Science and Technology, Kochi, 682022, Kerala, India</text>
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            <element elementId="50">
              <name>Title</name>
              <description>A name given to the resource</description>
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                <elementText elementTextId="18692">
                  <text>Thesis</text>
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      <name>PhD</name>
      <description>PhD Thesis</description>
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          <element elementId="50">
            <name>Title</name>
            <description>A name given to the resource</description>
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              <elementText elementTextId="8616">
                <text>Modulated Rayleigh-benard ferroconvection in couple stress fluid</text>
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          <element elementId="49">
            <name>Subject</name>
            <description>The topic of the resource</description>
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              <elementText elementTextId="8617">
                <text>Mathematics</text>
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                <text>Ferromagnetic fluid with couple-stress confined between two stress-free, isothermal horizontal plates is considered in this study. The effect of different types of modulation on Rayleigh-Bénard convection in a ferromagnetic fluid with couple-stress is examined by considering sinusoidal (sine) and non-sinusoidal (square, triangular, and sawtooth) wave type of modulation. Rayleigh-Bénard convection in a ferromagnetic fluid with couple-stress subjected to gravity, rotation, temperature, and internal heat modulation is discussed by performing linear and non-linear analyses. The effect of various parameters on the onset of convection and heat transport is studied. The ferromagnetic parameters hasten the convection onset and enhance the heat transfer under various modulations. The results of a Newtonian fluid, ferromagnetic fluid, and couple-stress fluid are obtained as the limiting cases of this study.</text>
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                <text>J, Meghana - 1881511</text>
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                <text>Modulated rayleigh-benard ferroconvection in couple stress fluid  </text>
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                <text>Ferromagnetic fluid with couple stress confined between two stress-free, isothermal horizontal plates is considered in this study. The effect of different types of modulation on Rayleigh-Bard convection in a ferromagnetic fluid with couple stress is examined by considering sinusoidal (sine) and non-sinusoidal (square, triangular, and sawtooth) wave types of modulation. Rayleigh- Bard convection in a ferromagnetic fluid with couple stress subjected to gravity, rotation, temperature, and internal heat modulation is discussed by performing linear and non-linear analyses. The expression for the critical Rayleigh number and the correction Rayleigh number are deduced using the Venezian approach. The effect of gravity, rotation, temperature and internal heat modulation on heat transport is studied using the generalized Lorenz model. The effect of various parameters on the onset of convection and heat transport is studied. The ferromagnetic parameters hasten the convection onset and enhance the heat transfer under various modulations. The results of a Newtonian fluid, ferromagnetic fluid, and couple stress fluid is obtained as the limiting cases of this study.</text>
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                <text>J, Meghana.</text>
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                <text>Christ(Deemed to be University)</text>
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              <elementText elementTextId="67482">
                <text>Pranesh, S.</text>
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            <description>Information about rights held in and over the resource</description>
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                <text>Open Access</text>
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                <text>&lt;a href="http://hdl.handle.net/10603/394298" target="_blank" rel="noreferrer noopener"&gt;http://hdl.handle.net/10603/394298&lt;/a&gt;</text>
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              <elementText elementTextId="199517">
                <text>George, Jelby; Balachandran, Manoj</text>
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            <description>A name given to the resource</description>
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              <elementText elementTextId="199518">
                <text>Modulating Electrochemical Energy Storage Properties of Cassava Peel-Derived Carbon Dots Via Solvent Engineering</text>
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            <name>Date</name>
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            <description>A related resource from which the described resource is derived</description>
            <elementTextContainer>
              <elementText elementTextId="199520">
                <text>Advanced Sustainable Systems;Volume;9;Issue;10;Article No.;e00325;</text>
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            <name>Identifier</name>
            <description>An unambiguous reference to the resource within a given context</description>
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                <text>&lt;a href="https://doi.org/10.1002/adsu.202500325" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1002/adsu.202500325&lt;/a&gt; &lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/pages/publications/105011838992?origin=resultslist" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/pages/publications/105011838992?origin=resultslist&lt;/a&gt;</text>
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              <elementText elementTextId="199522">
                <text>George J., Department ofPhysics andElectronics, Christ (Deemed To Be University), Bangalore, 560029, India; Balachandran M., Department ofPhysics andElectronics, Christ (Deemed To Be University), Bangalore, 560029, India</text>
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            <description>An account of the resource</description>
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              <elementText elementTextId="199523">
                <text>Despite their small size, constrained within a few nanometers, Carbon dots, the tiny 0D materials, have the potential to revolutionize the realm of materials, design, and technology. The elemental composition of carbon dots, more specifically, the non-carbon elements forming functional groups, has crucial roles in determining the structure and properties, opening a wide scope for tailoring through compositional engineering. In this work, tuned carbon dots derived from waste Cassava peel, synthesized by applying solvent engineering strategy in facile single-step microwave-assisted solvothermal treatment, are reported. The proportion of charge accumulation mechanisms is found to be highly dependent on the elemental composition of oxygen and nitrogen in the carbon dots, evidencing the pivotal role of functional groups. Among the carbon dots synthesized using three different solvents. Ethylenediamine based ones show highest energy storage capability (114.57Fg?1 at 0.1Ag?1) owing to nitrogen-oxygen co-functionalization. Though these carbon dots have low storage capabilities as such, they have potential prospects to be incorporated into electrode materials to tune charge storage mechanisms desirably, often with the added advantage of enhanced stability and performance. Additionally, the redox properties exhibited by the tuned samples give promising prospects toward applications like electrochemical sensing and electrolyte engineering for energy storage.  2025 Wiley-VCH GmbH.</text>
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          <element elementId="49">
            <name>Subject</name>
            <description>The topic of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="199524">
                <text>carbon dots; compositional engineering; electrochemical properties; energy storage mechanism; solvent engineering</text>
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            </elementTextContainer>
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          <element elementId="45">
            <name>Publisher</name>
            <description>An entity responsible for making the resource available</description>
            <elementTextContainer>
              <elementText elementTextId="199525">
                <text>John Wiley and Sons Inc</text>
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                <text>ISSN: 23667486;</text>
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            <description>A language of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="199527">
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              <elementText elementTextId="199528">
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            <description>Information about rights held in and over the resource</description>
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              <elementText elementTextId="199529">
                <text>Restricted Access; Hardcopy may be available in the library</text>
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          <element elementId="50">
            <name>Title</name>
            <description>A name given to the resource</description>
            <elementTextContainer>
              <elementText elementTextId="78191">
                <text>MOF derived cobalt-phospho-boride for rapid hydrogen generation via NaBH4 hydrolysis</text>
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          </element>
          <element elementId="49">
            <name>Subject</name>
            <description>The topic of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="78192">
                <text>Hydrogen generation; Hydrolysis of NaBH&lt;sub&gt;4&lt;/sub&gt;; Metal-organic framework; Transition metal phospho-borides</text>
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            </elementTextContainer>
          </element>
          <element elementId="41">
            <name>Description</name>
            <description>An account of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="78193">
                <text>Developing effective transition metal catalysts that can replace precious metal-based catalysts for hydrogen generation from the hydrolysis of chemical hydride has attracted extensive interest. This study focuses on synthesizing cobalt phospho-boride (CoPB) within a metal-organic framework (MOF) framework using hydrothermal and chemical reduction methodologies. Incorporating boron and phosphorous into Co-MOF enhances the hydrogen generation rate, reaching 1.8 L/min/g and 3.6 L/min/g for CoB-MOF and CoPB-MOF, respectively, during NaBH4 hydrolysis. Along with the nanostructured morphology of MOF, the electron modulation around Co-sites due to the presence of P and B creates a synergic effect to produce this high H2 generation rate and very low activation energy of 20.7 kJ/mol. The kinetic studies on NaBH4 hydrolysis reaction revealed zero-order kinetics with respect to NaBH4 concentration for CoPB-MOF, where porous morphology renders facile movement of BH4? ions to the active sites. The heat treatment at 773 K in the N2 atmosphere did not show any significant fall in the activity of CoPB-MOF, thus showcasing its robust nature. Moreover, the present catalyst also displayed recycling behavior with no signs of deactivation.  2024 Hydrogen Energy Publications LLC</text>
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          <element elementId="39">
            <name>Creator</name>
            <description>An entity primarily responsible for making the resource</description>
            <elementTextContainer>
              <elementText elementTextId="78194">
                <text>Abraham A.; Silviya R.; Patel R.; Patel N.; Fernandes R.</text>
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            </elementTextContainer>
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          <element elementId="48">
            <name>Source</name>
            <description>A related resource from which the described resource is derived</description>
            <elementTextContainer>
              <elementText elementTextId="78195">
                <text>International Journal of Hydrogen Energy, Vol-77, pp. 1245-1253.</text>
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            <name>Publisher</name>
            <description>An entity responsible for making the resource available</description>
            <elementTextContainer>
              <elementText elementTextId="78196">
                <text>Elsevier Ltd</text>
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          <element elementId="40">
            <name>Date</name>
            <description>A point or period of time associated with an event in the lifecycle of the resource</description>
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              <elementText elementTextId="78197">
                <text>2024-01-01</text>
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              <elementText elementTextId="78198">
                <text>&lt;a href="https://doi.org/10.1016/j.ijhydene.2024.06.247" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1016/j.ijhydene.2024.06.247&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85196516475&amp;amp;doi=10.1016%2Fj.ijhydene.2024.06.247&amp;amp;partnerID=40&amp;amp;md5=5050b01c79dc3666d3de39dba2a80760" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-85196516475&amp;amp;doi=10.1016%2fj.ijhydene.2024.06.247&amp;amp;partnerID=40&amp;amp;md5=5050b01c79dc3666d3de39dba2a80760&lt;/a&gt;</text>
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          <element elementId="47">
            <name>Rights</name>
            <description>Information about rights held in and over the resource</description>
            <elementTextContainer>
              <elementText elementTextId="78199">
                <text>Restricted Access</text>
              </elementText>
            </elementTextContainer>
          </element>
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            <description>A related resource</description>
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              <elementText elementTextId="78200">
                <text>ISSN: 3603199; CODEN: IJHED</text>
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            <description>The file format, physical medium, or dimensions of the resource</description>
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              <elementText elementTextId="78201">
                <text>Online</text>
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            <name>Language</name>
            <description>A language of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="78202">
                <text>English</text>
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          <element elementId="51">
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              <elementText elementTextId="78203">
                <text>Article</text>
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            <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
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              <elementText elementTextId="78204">
                <text>Abraham A., Department of Physics and Electronics, CHRIST University, Bengaluru, 560029, India; Silviya R., Department of Physics and Electronics, CHRIST University, Bengaluru, 560029, India; Patel R., Department of Physics and Electronics, CHRIST University, Bengaluru, 560029, India; Patel N., Department of Physics and Electronics, CHRIST University, Bengaluru, 560029, India; Fernandes R., Department of Physics and Electronics, CHRIST University, Bengaluru, 560029, India</text>
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  <item itemId="12866" public="1" featured="0">
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          <description>The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.</description>
          <elementContainer>
            <element elementId="50">
              <name>Title</name>
              <description>A name given to the resource</description>
              <elementTextContainer>
                <elementText elementTextId="64">
                  <text>Articles</text>
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    <itemType itemTypeId="19">
      <name>Article</name>
      <description>Faculty Publications -Articles</description>
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    <elementSetContainer>
      <elementSet elementSetId="1">
        <name>Dublin Core</name>
        <description>The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.</description>
        <elementContainer>
          <element elementId="50">
            <name>Title</name>
            <description>A name given to the resource</description>
            <elementTextContainer>
              <elementText elementTextId="77078">
                <text>Moisture-Sensitive Fe2O3 Nanoparticle-Based Magnetic Soft Actuators</text>
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            </elementTextContainer>
          </element>
          <element elementId="49">
            <name>Subject</name>
            <description>The topic of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="77079">
                <text>DFT; flexible actuator; moisture; soft magnetic actuators; soft robotics</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="41">
            <name>Description</name>
            <description>An account of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="77080">
                <text>Multifunctional soft robots are emerging as a new-generation intelligent device for challenging environments. To meet the requirements of smart applications and soft robotics, developing a soft actuator capable of multiple functions and mechanical deformation is essential. In this study, we designed a free-standing magnetic soft actuator constructed from iron oxide (Fe2O3) nanoparticles and poly(vinyl alcohol) (PVA), that responds to both moisture and magnetic fields. We used computational modeling (density functional theory and ab initio molecular dynamics) to explain the experimental findings demonstrating the deformation and high-bending angle (?150), which is about twice as large under combined moisture and magnetic field exposure compared to their individual effect. Additionally, a flower-shaped soft robot was designed by using the continuous bending deformation of the actuator in response to moisture changes, performing directional bending in an ambient environment. These findings demonstrate the materials sensitivity to moisture and magnetic fields, opening up new possibilities for designing responsive structures in the smart device industry.  2024 American Chemical Society.</text>
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            <name>Creator</name>
            <description>An entity primarily responsible for making the resource</description>
            <elementTextContainer>
              <elementText elementTextId="77081">
                <text>Narendhiran S.; Meher S.; Midya S.; Mishra S.; Prusti S.P.; Balachandran M.; Singh A.K.; Kumbhakar P.</text>
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          </element>
          <element elementId="48">
            <name>Source</name>
            <description>A related resource from which the described resource is derived</description>
            <elementTextContainer>
              <elementText elementTextId="77082">
                <text>ACS Applied Nano Materials, Vol-7, No. 17, pp. 21200-21208.</text>
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                <text>&lt;a href="https://doi.org/10.1021/acsanm.4c04627" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1021/acsanm.4c04627&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85202751803&amp;amp;doi=10.1021%2Facsanm.4c04627&amp;amp;partnerID=40&amp;amp;md5=e2c5de6cc7174167224d32a6959f98d0" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-85202751803&amp;amp;doi=10.1021%2facsanm.4c04627&amp;amp;partnerID=40&amp;amp;md5=e2c5de6cc7174167224d32a6959f98d0&lt;/a&gt;</text>
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                <text>Narendhiran S., Department of Physics and Electronics, CHRIST (Deemed to be University), Bangalore, 560029, India; Meher S., Materials Research Centre, Indian Institute of Science, Karnataka, Bangalore, 560012, India; Midya S., Materials Research Centre, Indian Institute of Science, Karnataka, Bangalore, 560012, India; Mishra S., Materials Research Centre, Indian Institute of Science, Karnataka, Bangalore, 560012, India; Prusti S.P., Department of Physics and Electronics, CHRIST (Deemed to be University), Bangalore, 560029, India; Balachandran M., Department of Physics and Electronics, CHRIST (Deemed to be University), Bangalore, 560029, India; Singh A.K., Materials Research Centre, Indian Institute of Science, Karnataka, Bangalore, 560012, India; Kumbhakar P., Department of Physics and Electronics, CHRIST (Deemed to be University), Bangalore, 560029, India</text>
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                <text>Vishwanath, Murugiah; Rajaram, Rajendran; Thomas, Jisha Mary; Nandhakumar, Velankanni; Christopher Jeyakumar, Thayalaraj</text>
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                <text>Molecular and electronic structure of 5-coordinated [Fe(CO)?(X?)] complexes: A quantum chemical study</text>
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                <text>Inorganica Chimica Acta;Volume;588;Issue;;Article No.;122879;</text>
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                <text>&lt;a href="https://doi.org/10.1016/j.ica.2025.122879" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1016/j.ica.2025.122879&lt;/a&gt; &lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/pages/publications/105014164812?origin=resultslist" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/pages/publications/105014164812?origin=resultslist&lt;/a&gt;</text>
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                <text>Vishwanath M., PG and Research Department of Chemistry, The American College (Autonomous), Tamil Nadu, Madurai, 625002, India; Rajaram R., Department of Chemistry, Madanapalle Institute of Technology &amp;amp; Science, Angallu (V), Andhra Pradesh, Madanapalle, 517325, India; Thomas J.M., Department of Chemistry, CHRIST University, Karnataka, Bengaluru, 560029, India; Nandhakumar V., Department of Biomaterials (Prosthodontics), Saveetha Dental College and Hospitals, Tamil Nadu, Chennai, 600077, India; Christopher Jeyakumar T., PG and Research Department of Chemistry, The American College (Autonomous), Tamil Nadu, Madurai, 625002, India</text>
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                <text>Quantum mechanical DFT calculations were performed on Fe(CO)5 and for the axial and equatorial isomers of 5-coordinated [Fe(CO)4(X2)] (where X = N, P, As, and Sb) complexes. The equatorially substituted complexes of 5-coordinated [Fe(CO)4(X2)] are more stable than the axially substituted complexes, as seen from their energy values. These complexes were further studied to understand their bonding nature using results from Natural population analysis (NPA) and energy decomposition analysis (EDA) calculations. The Wiberg bond indices (WBI) analysis provides the bond index of the bond between Fe and X2. The Frontier molecular orbital (FMO) studies show these complexes have a HOMO-LUMO energy gap in the values ranging from 1.99 to 5.04 eV, which is less than that of [Fe(CO)5]. From the Natural bond order (NBO) analysis, the contribution of the X?-atom is smaller in the ? bond formation compared to X? in P2, As2, and Sb2. Similar contributions are seen with the carbonyl group (in the Fe[sbnd]C bond), although the contribution of the carbon atom is larger than that of the X atom.  2025 Elsevier B.V.</text>
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                <text>Carbonyl; Di-pnictogens; EDA; FMO; WBI</text>
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              <elementText elementTextId="207048">
                <text>Elsevier B.V.</text>
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                <text>ISSN: 201693; CODEN: ICHAA</text>
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                <text>Restricted Access; Hardcopy may be available in the library</text>
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                <text>Molecular architecture of PANI/V2O5/MnO2 composite designed for hydrogen evolution reaction</text>
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              <elementText elementTextId="93244">
                <text>Energy production; HER; PANI/V&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;/MnO&lt;sub&gt;2&lt;/sub&gt; ; Polyaniline composites; Water splitting</text>
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          <element elementId="41">
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            <description>An account of the resource</description>
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                <text>An ever increasing demand for energy has mandated scientists towards exploring innovative and environmentally friendly energy production techniques that can meet the needs of human beings and the world at large. Among the various techniques, hydrogen evolution reaction (HER) is a cost-effective and efficient method that produces hydrogen, a better fuel, for meeting our energy requirements. The large surface area, good redox capacity, high electroactivity, and tunable bandgap of polyaniline (PANI) makes it a preferred candidate for various energy-related applications. Incorporating mixed metal oxides into a polymer enhances its catalytic activities and can be used as an electrocatalyst for HER. In situ chemical oxidative polymerization method has been carried out to synthesize PANI/V2O5/MnO2 composite. The characterization studies of PANI/V2O5/MnO2 composite are done using XRD, FT-IR, BET, XPS, and FE-SEM analysis. The PANI/V2O5/MnO2 composite is used for linear sweep voltammetry studies and shows that it acts as an efficient electrocatalyst which gives an overpotential of 130 mV at 10 mA/cm2. The high electrocatalytic activity of the composite is due to the better surface phenomenon that is enhanced by the high porosity and surface area. The electrochemical impedance spectroscopy also shows lower charge transfer resistance for the PANI/V2O5/MnO2, confirming its excellent electroactivity. 90% of the current density is retained even after 7200 seconds, validating its stability.  2023 Elsevier B.V.</text>
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            <name>Creator</name>
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            <elementTextContainer>
              <elementText elementTextId="93246">
                <text>Varghese A.; Devi K R S.; Pinheiro D.; Mohan M.K.</text>
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          <element elementId="48">
            <name>Source</name>
            <description>A related resource from which the described resource is derived</description>
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              <elementText elementTextId="93247">
                <text>Surfaces and Interfaces, Vol-41</text>
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            <description>An entity responsible for making the resource available</description>
            <elementTextContainer>
              <elementText elementTextId="93248">
                <text>Elsevier B.V.</text>
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                <text>2023-01-01</text>
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                <text>&lt;a href="https://doi.org/10.1016/j.surfin.2023.103221" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1016/j.surfin.2023.103221&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85166288515&amp;amp;doi=10.1016%2Fj.surfin.2023.103221&amp;amp;partnerID=40&amp;amp;md5=58b25b10df81f15822d96a2d277c0d54" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-85166288515&amp;amp;doi=10.1016%2fj.surfin.2023.103221&amp;amp;partnerID=40&amp;amp;md5=58b25b10df81f15822d96a2d277c0d54&lt;/a&gt;</text>
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            <name>Rights</name>
            <description>Information about rights held in and over the resource</description>
            <elementTextContainer>
              <elementText elementTextId="93251">
                <text>Restricted Access</text>
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                <text>ISSN: 24680230</text>
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                <text>Varghese A., Department of Chemistry, CHRIST (Deemed to be University), Karnataka, Bengaluru, 560029, India; Devi K R S., Department of Chemistry, CHRIST (Deemed to be University), Karnataka, Bengaluru, 560029, India; Pinheiro D., Department of Chemistry, CHRIST (Deemed to be University), Karnataka, Bengaluru, 560029, India; Mohan M.K., Department of Sciences and Humanities, School of Engineering and Technology, CHRIST (Deemed to be University), Kumbalagodu, Mysore Road, Bangalore, 560074, India</text>
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  <item itemId="17070" public="1" featured="0">
    <collection collectionId="5">
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          <description>The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.</description>
          <elementContainer>
            <element elementId="50">
              <name>Title</name>
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      <name>Article</name>
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      <elementSet elementSetId="1">
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        <description>The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.</description>
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          <element elementId="50">
            <name>Title</name>
            <description>A name given to the resource</description>
            <elementTextContainer>
              <elementText elementTextId="135607">
                <text>Molecular detection of Kudoa septempunctata (Myxozoa: Multivalvulida) in sea water and marine invertebrates</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="49">
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            <description>The topic of the resource</description>
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              <elementText elementTextId="135608">
                <text>Kudoa septempunctata; Myxozoa; Naineris laevigata; Olive flounder; Paralichthys olivaceus</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="41">
            <name>Description</name>
            <description>An account of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="135609">
                <text>The exportation of cultured olive flounder (Paralichthys olivaceus) in Korea has been recently decreasing due to the infections with a myxozoan parasite Kudoa septempunctata, and there is a strong demand for strict food safety management because the food poisoning associated with consumption of raw olive flounder harbouring K. septempunctata has been frequently reported in Japan. The life cycle and infection dynamics of K. septempunctata in aquatic environment are currently unknown, which hamper establishment of effective control methods. We investigated sea water and marine invertebrates collected from olive flounder farms for detecting K. septempunctata by DNA-based analysis, to elucidate infection dynamics of K. septempunctata in aquaculture farms. In addition, live marine polychaetes were collected and maintained in well plates to find any possible actinosporean state of K. septempunctata. The level of K. septempunctata DNA in rearing water fluctuated during the sampling period but the DNA was not detected in summer (June-July in farm A and August in farm B). K. septempunctata DNA was also detected in the polychaetes Naineris laevigata intestinal samples, showing decreased pattern of 40 to 0%. No actinosporean stage of K. septempunctata was observed in the polychaetes by microscopy. The absence of K. septempunctata DNA in rearing water of fish farm and the polychaetes N. laevigata intestinal samples during late spring and early summer indicate that the infection may not occur during this period. N. laevigata was suspected as the possible alternate invertebrate host of K. septempunctata, but the actinosporean stage was not found by well plate method and further studies will be necessary. This research provides important baseline information for understanding the infection dynamics of K. septempunctata in olive flounder farms and further establishment of control strategies.  2017 The Author(s).</text>
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            <description>An entity primarily responsible for making the resource</description>
            <elementTextContainer>
              <elementText elementTextId="135610">
                <text>Paari A.; Jeon C.-H.; Choi H.-S.; Jung S.-H.; Kim J.-H.</text>
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            <name>Source</name>
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            <elementTextContainer>
              <elementText elementTextId="135611">
                <text>Fisheries and Aquatic Sciences, Vol-20, No. 1</text>
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            <name>Publisher</name>
            <description>An entity responsible for making the resource available</description>
            <elementTextContainer>
              <elementText elementTextId="135612">
                <text>BioMed Central Ltd.</text>
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            <name>Date</name>
            <description>A point or period of time associated with an event in the lifecycle of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="135613">
                <text>2017-01-01</text>
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                <text>&lt;a href="https://doi.org/10.1186/s41240-017-0062-z" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1186/s41240-017-0062-z&lt;/a&gt;
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                <text>Paari A., Gangneung-Wonju National University, Department of Marine Bioscience, Gangneung, Gangwon, 25457, South Korea, Gangneung-Wonju National University, East Coast Life Science Institute, Gangneung, Gangwon, 25457, South Korea, Christ University, Department of Life science, Bengaluru, Karnataka, India; Jeon C.-H., Gangneung-Wonju National University, Department of Marine Bioscience, Gangneung, Gangwon, 25457, South Korea, Gangneung-Wonju National University, East Coast Life Science Institute, Gangneung, Gangwon, 25457, South Korea, Korea Fisheries Resources Agency, East Sea Life Resources Center, Uljin, 36340, South Korea; Choi H.-S., National Institute of Fisheries Science (NIFS), Pathology Division, Busan, 46041, South Korea, NIFS, Inland Aquaculture Research Center, Changwon, 51688, South Korea; Jung S.-H., National Institute of Fisheries Science (NIFS), Pathology Division, Busan, 46041, South Korea; Kim J.-H., Gangneung-Wonju National University, Department of Marine Bioscience, Gangneung, Gangwon, 25457, South Korea, Gangneung-Wonju National University, Department of Marine Bioscience, Gangneung, Gangwon, 210-702, South Korea</text>
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                <text>Molecular docking study, and ADMET analysis for the synthesized novel Zn(II) complexes as potential SARS-CoV-2 inhibitors</text>
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                <text>A new SARS-CoV-2 virus and its variants including omicron created a pandemic situation and caused more deaths in worldwide prompted many researchers to explore potential drug candidates. In this connection, we explored the first-of-its-kind report on computational studies such as molecular docking, and ADMET properties of Zn(II) complexes. The studies revealed the novel zinc complexes have high binding affinities with the SARS-CoV-2 spike glycoprotein (6vxx) alpha variant (7EKF), beta variant (7ekg), gamma variant (7EKC), delta variant (7V8B), and the omicron variant (7T9J). Molecular docking results of RMSD for SARS-CoV-2 beta variant (7ekg) and gamma variant (7EKC) are within excellent chemical stability in their protein-ligand complex state and should be effective in the biological system. ADME studies provided the better results with no adverse effect of toxicity related AMES along with absence of hepatotoxicity and skin sensitization when compared to Molnupiravir drug and it has a greater hepatotoxicity. This study could open further exploration of these novel zinc complexes for SARS-CoV-2 inhibition.  (2024) DergiPark.</text>
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                <text>Turkish Computational and Theoretical Chemistry, Vol-8, No. 3, pp. 122-128.</text>
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                <text>&lt;a href="https://doi.org/10.33435/tcandtc.1385998" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.33435/tcandtc.1385998&lt;/a&gt;
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                <text>All Open Access; Gold Open Access</text>
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                <text>ISSN: 25871722</text>
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                <text>Manjunatha M.N., Department of Chemistry, M. S. Ramaiah Institute of Technology (Affiliated to Visvesvaraya Technological University Belgaum), Karnataka, Bengaluru, 560054, India; Chinnam S., Department of Chemistry, M. S. Ramaiah Institute of Technology (Affiliated to Visvesvaraya Technological University Belgaum), Karnataka, Bengaluru, 560054, India; Challa M., Department of Chemistry, M. S. Ramaiah Institute of Technology (Affiliated to Visvesvaraya Technological University Belgaum), Karnataka, Bengaluru, 560054, India; Sushmitha N., Department of Chemistry, M. S. Ramaiah Institute of Technology (Affiliated to Visvesvaraya Technological University Belgaum), Karnataka, Bengaluru, 560054, India; Chigurupati S., Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Qassim University, Buraydah, 52571, Saudi Arabia, Department of Biotechnology, Saveetha School of Engineering, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Saveetha Nagar Thandalam, Chennai, 602105, India; Bobbala P., R.K. College of Engineering, Kethanakonda, Ibrahimpatnam, Andhra Pradesh, Vijayawada, 521456, India; Patnala H., Department of Science &amp;amp; Humanities, MLR Institute of Technology, Telangana, Hyderabad, 500043, India; Madamala S., Department of Chemistry, MVJ College of Engineering, Near ITBP, Whitefield, Karnataka, Bengaluru, 560067, India; Fernandes V.T., CHRIST (Deemed to be University), Hosur Road, Karnataka, Bengaluru, 560029, India</text>
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                <text>Venkatesan, Aakash; Nizam, Aatika; Cherian, Anila Rose; Patel, Rupali; Xavier, Jobi; Pooja, K.R.; Harini, R.; Nagaraju, G.</text>
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                <text>Molecular energy transfer: utilizing biogenically-synthesized ZnMn2O4 nanoparticles from Arachis hypogaea seeds for photoluminescence, adsorption, and photocatalytic applications</text>
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                <text>RSC Advances;Volume;15;Issue;39;pp.32638-32653</text>
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                <text>&lt;a href="https://doi.org/10.1039/d5ra05696a" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1039/d5ra05696a&lt;/a&gt; &lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/pages/publications/105015812073?origin=resultslist" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/pages/publications/105015812073?origin=resultslist&lt;/a&gt;</text>
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                <text>Venkatesan A., Department of Chemistry, Christ University, Bangalore, 560029, India; Nizam A., Department of Chemistry, Christ University, Bangalore, 560029, India; Cherian A.R., Department of Chemistry, Christ University, Bangalore, 560029, India; Patel R., Department of Physics, Christ University, Bangalore, 560029, India; Xavier J., Department of Life Sciences, Christ University, Bangalore, 560029, India; Pooja K.R., Department of Chemistry, Rani Channamma University, Belagavi, 591156, India; Harini R., Department of Electronics and Communication Engineering, Govt. Polytechnic, Hiriyur, 577599, India; Nagaraju G., Energy Materials Research Laboratory, Department of Chemistry, Siddaganga Institute of Technology, Tumakuru, 572103, India</text>
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                <text>The green synthesis of nanoparticles (NPs) has emerged as a sustainable alternative to conventional chemical approaches, primarily due to the use of phytochemicals as reducing and stabilizing agents. In the present study, bimetallic ZnMn2O4 nanoparticles were synthesized via a green combustion method employing Arachis hypogaea (peanut) seed powder as a natural fuel source. The synthesized ZnMn2O4 NPs were systematically characterized using XRD, FTIR, SEM, BET, UV-Vis, and PL spectroscopy to elucidate their structural, morphological, and optical properties. Distinct bluish-green fluorescence was observed under short-wave UV irradiation (254 nm), enabling their application in latent fingerprint visualization. The multifunctional performance of the ZnMn2O4 NPs was further demonstrated in environmental applications. The materials exhibited enhanced adsorption (63%  0.2%) and photocatalytic degradation (79%  0.3%) efficiencies against Methylene Blue (MB) dye under UV irradiation, with results statistically significant (p &amp;lt; 0.05). In addition, the NPs effectively reduced toxic Cr(vi) ions in aqueous media, highlighting their potential as efficient detoxification agents. Overall, this work demonstrates a novel, green synthesis route for ZnMn2O4 nanoparticles that uniquely integrates environmental remediation and forensic applications. The dual functionality addressing both pollutant degradation/detoxification and forensic fingerprint visualization positions this study as a rare and innovative contribution to the field of nanotechnology.  2025 The Royal Society of Chemistry.</text>
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                <text>Molecular level investigation on the impact of geometric isomers as fluorinated ligands in SIFSIX MOF for natural gas sweetening</text>
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                <text>In natural gas (NG), significant amounts of hydrogen sulfide (H2S) and carbon dioxide (CO2) are the most menacing contaminants that cause degradation of the purity of fuel. We considered fluorine-functionalized MOFs and employed cheaper and faster computational simulation techniques to understand the adsorption process. Hence, this includes structural optimization of newly designed fluorine-functionalized MOF with Density Functional Theory (DFT) and further Grand Canonical Monte Carlo (GCMC) simulation at room temperature on those MOFs for understanding in detail the adsorptive separation process on sour gases. However, the main emphasis has been made on the adsorptive separation of H2S gas from sour gas. Eventually, the fluorination of organic ligand in [(SiF6)Ni(1,2-di(pyridin-4-yl)ethyne)2] MOF has resulted in an excellent H2S/CO2 separation performance from NG because of the different geometrical isomers. The cis isomer of 1,2-di(pyridin-4-yl)ethyne as ligand in MOF, i.e., SIFSIX-Ni-dpe-3-cis, shows a high CO2 affinity than H2S; on the contrary, the trans isomer of 1,2-di(pyridin-4-yl)ethyne as ligand in MOF, i.e., SIFSIX-Ni-dpe-3-trans, has H2S selective over CO2 and CH4. So, the resulting affinity variation indicates that structural variation by the stereochemistry of ligands in MOF plays a significant role in NG purification, which is further validated through detailed molecular simulation analysis.  2022 Taylor &amp;amp; Francis Group, LLC.</text>
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                <text>Palakkal A.S.; Prabhakar S.; Pillai R.S.</text>
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                <text>Separation Science and Technology (Philadelphia), Vol-57, No. 16, pp. 2554-2565.</text>
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                <text>&lt;a href="https://doi.org/10.1080/01496395.2022.2083639" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1080/01496395.2022.2083639&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85131596625&amp;amp;doi=10.1080%2F01496395.2022.2083639&amp;amp;partnerID=40&amp;amp;md5=c201eded8f3719623d3fb7daa53c5bc0" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-85131596625&amp;amp;doi=10.1080%2f01496395.2022.2083639&amp;amp;partnerID=40&amp;amp;md5=c201eded8f3719623d3fb7daa53c5bc0&lt;/a&gt;</text>
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            <description>Information about rights held in and over the resource</description>
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                <text>Restricted Access</text>
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                <text>ISSN: 1496395; CODEN: SSTED</text>
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            <name>Format</name>
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                <text>Palakkal A.S., Department of Chemistry, School of Basic Sciences, SRM Institute of Science and Technology, Kattankulathur, India; Prabhakar S., Department of Chemistry, School of Basic Sciences, SRM Institute of Science and Technology, Kattankulathur, India; Pillai R.S., Department of Chemistry, Christ University, Bengaluru, India</text>
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          <element elementId="50">
            <name>Title</name>
            <description>A name given to the resource</description>
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                <text>Molecular phylogenetics and character evolution in Haplanthodes (Acanthaceae), an endemic genus from peninsular India</text>
              </elementText>
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          </element>
          <element elementId="49">
            <name>Subject</name>
            <description>The topic of the resource</description>
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              <elementText elementTextId="108814">
                <text>Acanthaceae; Andrographis; cladode; endemic genus; Haplanthodes</text>
              </elementText>
            </elementTextContainer>
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          <element elementId="41">
            <name>Description</name>
            <description>An account of the resource</description>
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              <elementText elementTextId="108815">
                <text>Haplanthodes (Acanthaceae) is an Indian endemic genus with four species. It is closely related to Andrographis which is also mainly distributed in India. Haplanthodes differs from Andrographis by the presence of cladodes in the inflorescences, subactinomorphic flowers, stamens included within the corolla tube, pouched stamens and oblate pollen grains. To understand the phylogenetic relationship of Haplanthodes, Andrographis and Haplanthus, which are putatively closely related taxa, we used four plastid markers, matK, rbcL, psbA-trnH and trnGRto construct a molecular phylogeny. Our results established the monophyly of Haplanthodes and revealed a sister relationship to Andrographis and Haplanthus. Further, to understand the historical biogeography of the genus, we inferred the divergence time and performed an ancestral area reconstruction. Our analyses suggest that Haplanthodes evolved during Late Miocene 5.85 Ma (95%HPD: 2.1810.34 Ma) in peninsular India where it might have shared a common ancestor with Andrographis. To understand character evolution, the ancestral states of important morphological characters were inferred and discussed based on the equal rate model. The generic status of Haplanthus was not resolved due to incomplete sampling.  2022 Nordic Society Oikos. Published by John Wiley &amp;amp; Sons Ltd.</text>
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              <elementText elementTextId="108816">
                <text>Surveswaran S.; Tiwari N.; Karanth P.K.; Deshmukh P.V.; Lekhak M.M.</text>
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            <name>Source</name>
            <description>A related resource from which the described resource is derived</description>
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              <elementText elementTextId="108817">
                <text>Nordic Journal of Botany, Vol-2022, No. 4</text>
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          <element elementId="45">
            <name>Publisher</name>
            <description>An entity responsible for making the resource available</description>
            <elementTextContainer>
              <elementText elementTextId="108818">
                <text>John Wiley and Sons Inc</text>
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            </elementTextContainer>
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            <name>Date</name>
            <description>A point or period of time associated with an event in the lifecycle of the resource</description>
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              <elementText elementTextId="108819">
                <text>2022-01-01</text>
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            <name>Identifier</name>
            <description>An unambiguous reference to the resource within a given context</description>
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              <elementText elementTextId="108820">
                <text>&lt;a href="https://doi.org/10.1111/njb.03238" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1111/njb.03238&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85125049893&amp;amp;doi=10.1111%2Fnjb.03238&amp;amp;partnerID=40&amp;amp;md5=ff47c7b106bd07a515c7cddc72f32bf4" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-85125049893&amp;amp;doi=10.1111%2fnjb.03238&amp;amp;partnerID=40&amp;amp;md5=ff47c7b106bd07a515c7cddc72f32bf4&lt;/a&gt;</text>
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          <element elementId="47">
            <name>Rights</name>
            <description>Information about rights held in and over the resource</description>
            <elementTextContainer>
              <elementText elementTextId="108821">
                <text>All Open Access; Green Open Access</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="46">
            <name>Relation</name>
            <description>A related resource</description>
            <elementTextContainer>
              <elementText elementTextId="108822">
                <text>ISSN: 0107055X; CODEN: NJBOD</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="42">
            <name>Format</name>
            <description>The file format, physical medium, or dimensions of the resource</description>
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              <elementText elementTextId="108823">
                <text>Online</text>
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            </elementTextContainer>
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          <element elementId="44">
            <name>Language</name>
            <description>A language of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="108824">
                <text>English</text>
              </elementText>
            </elementTextContainer>
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            <name>Type</name>
            <description>The nature or genre of the resource</description>
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              <elementText elementTextId="108825">
                <text>Article</text>
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            <name>Coverage</name>
            <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
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              <elementText elementTextId="108826">
                <text>Surveswaran S., Dept of Life Sciences, CHRIST (Deemed to be Univ.), Karnataka, Bangalore, India; Tiwari N., Centre for Ecological Sciences, Indian Inst. of Science, Karnataka, Bangalore, India, Suri Sehgal Centre for Biodiversity and Conservation, Ashoka Trust for Research in Ecology and the Environment, Royal Enclave, Shrirampura, Jakkur, Karnataka, Bangalore, India; Karanth P.K., Centre for Ecological Sciences, Indian Inst. of Science, Karnataka, Bangalore, India; Deshmukh P.V., Angiosperm Taxonomy Laboratory, Dept of Botany, Shivaji Univ., Maharashtra, Kolhapur, India; Lekhak M.M., Angiosperm Taxonomy Laboratory, Dept of Botany, Shivaji Univ., Maharashtra, Kolhapur, India</text>
              </elementText>
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    </elementSetContainer>
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  <item itemId="13005" public="1" featured="0">
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      <elementSetContainer>
        <elementSet elementSetId="1">
          <name>Dublin Core</name>
          <description>The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.</description>
          <elementContainer>
            <element elementId="50">
              <name>Title</name>
              <description>A name given to the resource</description>
              <elementTextContainer>
                <elementText elementTextId="64">
                  <text>Articles</text>
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    <itemType itemTypeId="19">
      <name>Article</name>
      <description>Faculty Publications -Articles</description>
    </itemType>
    <elementSetContainer>
      <elementSet elementSetId="1">
        <name>Dublin Core</name>
        <description>The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.</description>
        <elementContainer>
          <element elementId="50">
            <name>Title</name>
            <description>A name given to the resource</description>
            <elementTextContainer>
              <elementText elementTextId="79012">
                <text>Molecular Simulation Prediction on SO2 Gas Adsorption in Bipyridine Ligand-Based Square-Pillared MOFs</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="49">
            <name>Subject</name>
            <description>The topic of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="79013">
                <text>adsorption; DFT; flue gas; GCMC; SO&lt;sub&gt;2&lt;/sub&gt;; square-pillared fluorinated MOFs, bipyridine ligand</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="41">
            <name>Description</name>
            <description>An account of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="79014">
                <text>Increasing concentrations of toxic gases caused by the burning of fossil fuels necessitates the development of efficient porous materials for gas capture. Metal-organic frameworks (MOFs) have attracted a lot of attention as potential porous materials due to their effectiveness in adsorption of toxic gases. In particular, square-pillared metal-organic frameworks stand out for their exceptional potential toward gas adsorption, attributed to their remarkable surface area, thermal and chemical stabilities, and tunable properties. In this context, molecular simulations have been executed to observe and analyze the adsorption process of toxic flue gases such as SO2 and CO2 on MOFs. The present work deals with two different stable fluorinated MOFs named [Ni(4,4?-bipyridine)2(AlF5)]n (ALFFIVE-Ni-bipy) and [Ni(4,4?-bipyridine)2(NbOF5)]n, (NBOFFIVE-Ni-bipy) featuring AlF52- and NbOF52- anion pillars, respectively, comprising 4,4?-bipyridine as organic ligand and nickel as the central metal. The significance of utilizing the 4,4?-bipyridine ligands in these fluorinated MOFs enhances the SO2 gas adsorption and selectivity in the framework. Density functional theory has been implemented for geometry optimization, and Grand Canonical Monte Carlo simulations have been performed to forecast the adsorption isotherms. Both ALFFIVE-Ni-bipy (11.4 mmol/g) and NBOFFIVE-Ni-bipy (8.7 mmol/g) showed high SO2 adsorption capacity at 1 bar pressure, but ALFFIVE-Ni-bipy showed very good adsorption than other square-pillared MOFs and also unveiled good selectivity of SO2 gas. The coadsorption of binary SO2/CO2 and ternary SO2/CO2/N2 gas mixtures at ambient conditions indicated that the cost-effective aluminum (Al)-based square-pillared ALFFIVE-Ni-bipy is particularly suitable for acid gas adsorption.  2024 American Chemical Society</text>
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            <name>Creator</name>
            <description>An entity primarily responsible for making the resource</description>
            <elementTextContainer>
              <elementText elementTextId="79015">
                <text>Devaraj M.; Devi Kalathiparambil Rajendra Pai S.; Badawi M.; Pillai R.S.</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="48">
            <name>Source</name>
            <description>A related resource from which the described resource is derived</description>
            <elementTextContainer>
              <elementText elementTextId="79016">
                <text>ACS Applied Nano Materials, Vol-7, No. 14, pp. 16630-16638.</text>
              </elementText>
            </elementTextContainer>
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          <element elementId="45">
            <name>Publisher</name>
            <description>An entity responsible for making the resource available</description>
            <elementTextContainer>
              <elementText elementTextId="79017">
                <text>American Chemical Society</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="40">
            <name>Date</name>
            <description>A point or period of time associated with an event in the lifecycle of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="79018">
                <text>2024-01-01</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="43">
            <name>Identifier</name>
            <description>An unambiguous reference to the resource within a given context</description>
            <elementTextContainer>
              <elementText elementTextId="79019">
                <text>&lt;a href="https://doi.org/10.1021/acsanm.4c02680" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1021/acsanm.4c02680&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85199181616&amp;amp;doi=10.1021%2Facsanm.4c02680&amp;amp;partnerID=40&amp;amp;md5=05ac5bce989cafb76df2a89bb159c78f" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-85199181616&amp;amp;doi=10.1021%2facsanm.4c02680&amp;amp;partnerID=40&amp;amp;md5=05ac5bce989cafb76df2a89bb159c78f&lt;/a&gt;</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="47">
            <name>Rights</name>
            <description>Information about rights held in and over the resource</description>
            <elementTextContainer>
              <elementText elementTextId="79020">
                <text>Restricted Access</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="46">
            <name>Relation</name>
            <description>A related resource</description>
            <elementTextContainer>
              <elementText elementTextId="79021">
                <text>ISSN: 25740970</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="42">
            <name>Format</name>
            <description>The file format, physical medium, or dimensions of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="79022">
                <text>Online</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="44">
            <name>Language</name>
            <description>A language of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="79023">
                <text>English</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="51">
            <name>Type</name>
            <description>The nature or genre of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="79024">
                <text>Article</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="38">
            <name>Coverage</name>
            <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
            <elementTextContainer>
              <elementText elementTextId="79025">
                <text>Devaraj M., Department of Chemistry, Christ University, Karnataka, Bengaluru, 560029, India; Devi Kalathiparambil Rajendra Pai S., Department of Chemistry, Christ University, Karnataka, Bengaluru, 560029, India; Badawi M., Laboratoire Lorrain de Chimie Molulaire, UMR CNRS 7053, Universitde Lorraine, Nancy, 54000, France; Pillai R.S., Analytical and Spectroscopy Division, Vikram Sarabhai Space Center, Indian Space Research Organisation, Kerala, Thiruvananthapuram, 695022, India</text>
              </elementText>
            </elementTextContainer>
          </element>
        </elementContainer>
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</itemContainer>
