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    <name>Article</name>
    <description>Faculty Publications -Articles</description>
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          <name>Title</name>
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              <text>Size Tuning, Phase Stabilization, and Anticancer Efficacy of Amorphous Selenium Nanoparticles: Effect of Ion-Pair Interaction, ?OH Functionalization, and Reuse of RTILs as Host Matrix</text>
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              <text>Se nanoparticles (NPs) of predominantly amorphous phase (?-Se) have been prepared in room-temperature ionic liquids (RTILs). The effects of ion-pair combination and ?OH functionalization of RTILs on the size and phase stability of Se NPs were investigated. The RTILs used were 1-ethyl-3-methyl imidazolium boron tetrafluoride ([EMIM][BF4]), 1-(2-hydroxyethyl)-3-methyl imidazolium boron tetrafluoride ([EOHMIM][BF4]), and 1-ethyl-3-methyl imidazolium methane sulfonate ([EMIM][MS]). The size of Se NPs@[EOHMIM][BF4] was found to be the smallest (?32 nm), followed by Se NPs@[EMIM][BF4] (?57 nm) and Se NPs@[EMIM][MS] (?60 nm), respectively. Interestingly, the stability studies revealed minimal size variations for Se NPs@[EMIM][MS], followed by Se NPs@[EOHMIM][BF4] and Se NPs@[EMIM][BF4], respectively. The observed trends could be correlated with the strength of interionic interactions in the respective RTILs, as well as their packing order (density). Importantly, the RTILs played the role of a solvent, a stabilizer, and an in situ source of reducing species. Pulse radiolysis study revealed imidazolium-originated radical species-driven formation of Se NPs. Further, anticancer efficacy studies demonstrated the role of NP size, wherein Se NPs@[EOHMIM][BF4] exhibited the highest cancer cell killing, followed by Se NPs@[EMIM][BF4] and Se NPs@[EMIM][MS]. Another significant highlight of this work is the reuse of the spent RTILs for the synthesis of the next batch of Se NPs.  2021 American Chemical Society</text>
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          <name>Creator</name>
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              <text>Guleria A.; Baby C.M.; Tomy A.; Maurya D.K.; Neogy S.; Debnath A.K.; Adhikari S.</text>
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              <text>Journal of Physical Chemistry C, Vol-125, No. 25, pp. 13933-13945.</text>
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              <text>American Chemical Society</text>
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          <name>Date</name>
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              <text>2021-01-01</text>
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          <name>Identifier</name>
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              <text>&lt;a href="https://doi.org/10.1021/acs.jpcc.1c02894" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1021/acs.jpcc.1c02894&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85110419962&amp;amp;doi=10.1021%2Facs.jpcc.1c02894&amp;amp;partnerID=40&amp;amp;md5=e1a3bf8e940c74c31eb99f65f8e8f498" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-85110419962&amp;amp;doi=10.1021%2facs.jpcc.1c02894&amp;amp;partnerID=40&amp;amp;md5=e1a3bf8e940c74c31eb99f65f8e8f498&lt;/a&gt;</text>
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              <text>Restricted Access</text>
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          <description>A related resource</description>
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              <text>ISSN: 19327447</text>
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              <text>Online</text>
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              <text>English</text>
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              <text>Article</text>
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              <text>Guleria A., Radiation &amp;amp; Photochemistry Division, Bhabha Atomic Research Centre, Mumbai, 400085, India; Baby C.M., Christ University, Bengaluru, 560029, India; Tomy A., Christ University, Bengaluru, 560029, India; Maurya D.K., Radiation Biology &amp;amp; Health Sciences Division, Bhabha Atomic Research Centre, Mumbai, 400085, India; Neogy S., Materials Science Division, Bhabha Atomic Research Centre, Mumbai, 400085, India; Debnath A.K., Technical Physics Division, Bhabha Atomic Research Centre, Mumbai, 400085, India; Adhikari S., Radiation &amp;amp; Photochemistry Division, Bhabha Atomic Research Centre, Mumbai, 400085, India</text>
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