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indranil,sinha
분자활성촉매반응연구단
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Computer-aided rational design of Fe(iii)-catalysts for the selective formation of cyclic carbonates from CO2 and internal epoxides

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dc.contributor.authorIndranil Sinha-
dc.contributor.authorYuseop Lee-
dc.contributor.authorChoongman Bae-
dc.contributor.authorSamat Tussupbayev-
dc.contributor.authorYujin Lee-
dc.contributor.authorMin-Seob Seo-
dc.contributor.authorJin Kim-
dc.contributor.authorMu-Hyun Baik-
dc.contributor.authorYunho Lee-
dc.contributor.authorHyunwoo Kim-
dc.date.available2017-10-31T05:34:31Z-
dc.date.created2017-10-19-
dc.date.issued2017-10-
dc.identifier.issn2044-4753-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/3960-
dc.description.abstractThe catalytic mechanism of the cyclic carbonate formation reaction between CO2 and internal epoxides promoted by Fe-salen and the Kleij catalyst was examined in detail to better understand how the catalytic efficiency can be increased. Specifically, we aimed to make the catalyst more chemoselective towards forming cyclic carbonates and preventing the competing side reaction leading to polycarbonates via ring-opening polymerization. A few rational design principles were derived and first tested using computer models based on density functional theory. The most promising candidate that was identified in the computer model was then prepared and found to display significantly enhanced reactivity towards forming the cyclic carbonates, supporting the validity of the mechanistic insights deduced from the computer simulations. We propose that a cyclic carbonate is formed most efficiently via an inner-sphere mechanism where both the CO2 and epoxide substrates utilize the metal center for the key bond forming events. In contrast, the ring-opening polymerization uses an outer-sphere mechanism, where a carbonate attacks and ring-opens the epoxide bound to the metal without engaging the metal directly. These mechanistic differences are exploited to implement a chemoselective catalyst by enhancing the rate of the cyclic carbonate formation reaction while leaving the polymerization pathway largely unaffected. © 2017 The Royal Society of Chemistry-
dc.description.uri1-
dc.language영어-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleComputer-aided rational design of Fe(iii)-catalysts for the selective formation of cyclic carbonates from CO2 and internal epoxides-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000413190800014-
dc.identifier.scopusid2-s2.0-85030661700-
dc.identifier.rimsid60750ko
dc.date.tcdate2018-10-01-
dc.contributor.affiliatedAuthorIndranil Sinha-
dc.contributor.affiliatedAuthorSamat Tussupbayev-
dc.contributor.affiliatedAuthorYujin Lee-
dc.contributor.affiliatedAuthorMu-Hyun Baik-
dc.contributor.affiliatedAuthorYunho Lee-
dc.identifier.doi10.1039/c7cy01435j-
dc.identifier.bibliographicCitationCATALYSIS SCIENCE & TECHNOLOGY, v.7, no.19, pp.4375 - 4387-
dc.citation.titleCATALYSIS SCIENCE & TECHNOLOGY-
dc.citation.volume7-
dc.citation.number19-
dc.citation.startPage4375-
dc.citation.endPage4387-
dc.date.scptcdate2018-10-01-
dc.description.wostc2-
dc.description.scptc3-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
Appears in Collections:
Center for Catalytic Hydrocarbon Functionalizations(분자활성 촉매반응 연구단) > 1. Journal Papers (저널논문)
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