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Two dimensional inorganic electride-promoted electron transfer efficiency in transfer hydrogenation of alkynes and alkenes

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dc.contributor.authorKim, Ye Ji-
dc.contributor.authorKim, Sun Min-
dc.contributor.authorCho, Eun Jin-
dc.contributor.authorHosono, Hideo-
dc.contributor.authorYang, Jung Woon-
dc.contributor.authorKim, Sung Wng-
dc.date.available2019-03-08T20:38:11Z-
dc.date.issued2015-06-
dc.identifier.issn2041-6520-
dc.identifier.issn2041-6539-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/11383-
dc.description.abstractA simple and highly efficient transfer hydrogenation of alkynes and alkenes by using a two-dimensional electride, dicalcium nitride ([Ca2N](+).e(-)), as an electron transfer agent is disclosed. Excellent yields in the transformation are attributed to the remarkable electron transfer efficiency in the electride-mediated reactions. It is clarified that an effective discharge of electrons from the [Ca2N](+).e(-) electride in alcoholic solvents is achieved by the decomposition of the electride via alcoholysis and the generation of ammonia and Ca((OPr)-Pr-i)(2). We found that the choice of solvent was crucial for enhancing the electron transfer efficiency, and a maximum efficiency of 80% was achieved by using a DMF mixed isopropanol co-solvent system. This is the highest value reported to date among single electron transfer agents in the reduction of C-C multiple bonds. The observed reactivity and efficiency establish that electrides with a high density of anionic electrons can readily participate in the reduction of organic functional groups.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleTwo dimensional inorganic electride-promoted electron transfer efficiency in transfer hydrogenation of alkynes and alkenes-
dc.typeArticle-
dc.identifier.doi10.1039/c5sc00933b-
dc.identifier.bibliographicCitationCHEMICAL SCIENCE, v.6, no.6, pp 3577 - 3581-
dc.description.isOpenAccessN-
dc.identifier.wosid000354815600041-
dc.identifier.scopusid2-s2.0-84929589672-
dc.citation.endPage3581-
dc.citation.number6-
dc.citation.startPage3577-
dc.citation.titleCHEMICAL SCIENCE-
dc.citation.volume6-
dc.type.docTypeArticle-
dc.publisher.location영국-
dc.subject.keywordPlusCATALYTIC TRANSFER HYDROGENATION-
dc.subject.keywordPlusSTABLE ELECTRIDE-
dc.subject.keywordPlusMULTIPLE BONDS-
dc.subject.keywordPlusREDUCTION-
dc.subject.keywordPlusDONOR-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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