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Cited 106 time in webofscience Cited 107 time in scopus
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dc.contributor.authorMina Jeon-
dc.contributor.authorJunghoon Han-
dc.contributor.authorPark, J-
dc.date.accessioned2016-03-31T08:45:34Z-
dc.date.available2016-03-31T08:45:34Z-
dc.date.created2013-03-05-
dc.date.issued2012-08-
dc.identifier.issn2155-5435-
dc.identifier.other2012-OAK-0000026663-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/15985-
dc.description.abstractIn recent years reusable and highly active metal-nanoparticle catalysts were developed for the selective transformation of hydrosilanes into the corresponding silanols using water as the oxidant. The catalysts are much more active catalyst than conventional homogeneous ones under ambient conditions. In this perspective, we summarize known catalyst systems as well as stoichiometric methods for the synthesis of silanols from hydrosilanes. Plausible pathways for the hydrolytic oxidation of hydrosilanes on metal nanoparticles are described on the basis of the observations of mechanistic studies, including Si-H bond activation, nucleophilic attack of water (or silanol) at the silicon bonded to metal, and the liberation of silanol (or disiloxane) products. The applications of silanols are classified into usages in organic synthesis and silicon-based materials. Silanols were employed as nucleophilic partners in transition-metal catalyzed carbon-carbon cross-coupling reactions, organocatalysts for activating carbonyl compounds, intramolecular guiding groups for C-H bond activation reactions, inhibitors of enzymes, and isosteres of bioactive compounds. Various polymeric silicon-based materials were synthesized by the activation of Si-H bonds in bis-trihydrosilanes, bis-hydrosilanes, and polyhedral oligomeric silsesquioxanes (POSS).-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherAmerican Chemical Society-
dc.relation.isPartOfACS CATALYSIS-
dc.subjectsilanol-
dc.subjectheterogeneous catalysis-
dc.subjecthomogeneous catalysis-
dc.subjectsilane-
dc.subjectoxidation-
dc.subjectCROSS-COUPLING REACTIONS-
dc.subjectORGANOBORON COMPOUNDS-
dc.subjectHYDROLYTIC OXIDATION-
dc.subjectSELECTIVE OXIDATION-
dc.subjectAROMATIC BROMIDES-
dc.subjectHETEROGENEOUS OXIDATION-
dc.subjectORGANIC ELECTROPHILES-
dc.subjectDIRECTING GROUP-
dc.subjectARYL HALIDES-
dc.subjectTI-BETA-
dc.titleCatalytic Synthesis of Silanols from Hydrosilanes and Applications-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1021/CS300296X-
dc.author.googleJeon, M-
dc.author.googleHan, J-
dc.author.googlePark, J-
dc.relation.volume2-
dc.relation.issue8-
dc.relation.startpage1539-
dc.relation.lastpage1549-
dc.contributor.id10075891-
dc.relation.journalACS CATALYSIS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationACS CATALYSIS, v.2, no.8, pp.1539 - 1549-
dc.identifier.wosid000307257800003-
dc.date.tcdate2019-01-01-
dc.citation.endPage1549-
dc.citation.number8-
dc.citation.startPage1539-
dc.citation.titleACS CATALYSIS-
dc.citation.volume2-
dc.contributor.affiliatedAuthorPark, J-
dc.identifier.scopusid2-s2.0-84864604541-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc41-
dc.description.scptc37*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusCROSS-COUPLING REACTIONS-
dc.subject.keywordPlusHYDROLYTIC OXIDATION-
dc.subject.keywordPlusSELECTIVE OXIDATION-
dc.subject.keywordPlusHETEROGENEOUS OXIDATION-
dc.subject.keywordPlusAROMATIC BROMIDES-
dc.subject.keywordPlusDIRECTING GROUP-
dc.subject.keywordPlusTI-BETA-
dc.subject.keywordPlusORGANOSILANES-
dc.subject.keywordPlusSILICON-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordAuthorsilanol-
dc.subject.keywordAuthorheterogeneous catalysis-
dc.subject.keywordAuthorhomogeneous catalysis-
dc.subject.keywordAuthorsilane-
dc.subject.keywordAuthoroxidation-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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