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              <text>Rabari, Mahima; Hegde, Vasundhara; Hegde, Gurumurthy; Prajapati, A.K.</text>
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              <text>Systematic investigation on unsymmetrical mesogenic cyanobiphenyl dimers towards optical storage devices: synthesis, mesomorphic, photo switching and DFT studies</text>
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              <text>01-01-2025</text>
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              <text>Journal of Materials Chemistry C;Volume;13;Issue;21;pp.10700-10713</text>
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              <text>&lt;a href="https://doi.org/10.1039/d5tc00421g" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1039/d5tc00421g&lt;/a&gt; &lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/pages/publications/105003871846?origin=resultslist" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/pages/publications/105003871846?origin=resultslist&lt;/a&gt;</text>
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              <text>Rabari M., Department of Chemistry, Faculty of Science, The Maharaja Sayajirao University of Baroda, Vadodara, 390002, India; Hegde V., Department of Chemistry, Christ University, Hosur Road, Bengaluru, 560029, India; Hegde G., Department of Chemistry, Christ University, Hosur Road, Bengaluru, 560029, India, Centre for Advanced Research and Development, Christ University, Hosur Road, Bengaluru, 560029, India; Prajapati A.K., Department of Chemistry, Faculty of Science, The Maharaja Sayajirao University of Baroda, Vadodara, 390002, India</text>
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              <text>This research presents the synthesis and analysis of a novel series of mesogenic dimers comprising cyanobiphenyl and azonaphthyl units. Structural validation was performed using FT-IR, 1H-NMR, 13C-NMR, elemental analysis, mass spectrometry, etc. The dimers thermotropic behaviours were studied through POM and DSC, revealing enantiotropic nematic phases in all cases, with some also showing monotropic smectic C phases. The study explores the relationship between the chemical structure of the dimers and the length of the flexible spacer, the odd-even effect, and their phase transition temperatures. Longer chains tended to form smectic phases, while shorter chains primarily exhibited nematic phases. Computational analysis using B3LYP/6-31g(d,p) and evaluations of electrostatic potential (ESP) and optical properties provided further insight into the electronic structures. Photoisomerization studies demonstrated consistent photochromic responses, with all dimers showing high conversion efficiency (88-95%) under UV light along with similar back relaxation times (?10-12 hours). Optical storage devices prepared by these materials showed excellent contrast between dark and bright states elucidating the importance of such materials for the future.  2025 The Royal Society of Chemistry.</text>
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              <text>Royal Society of Chemistry</text>
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              <text>ISSN: 20507526; CODEN: JMCCC</text>
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              <text>All Open Access; Hybrid Gold Open Access</text>
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              <text>online</text>
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