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DC Field | Value | Language |
---|---|---|
dc.citation.endPage | 49 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 43 | - |
dc.citation.title | JOURNAL OF MOLECULAR CATALYSIS | - |
dc.citation.volume | 73 | - |
dc.contributor.author | LEE, Sang Moo | - |
dc.contributor.author | CHO, Nag Sug | - |
dc.contributor.author | KIM, Kye Duck | - |
dc.contributor.author | OH, Jae Seung | - |
dc.contributor.author | LEE, Chul Woo | - |
dc.contributor.author | Lee, Jae Sung | - |
dc.date.accessioned | 2023-12-22T13:07:31Z | - |
dc.date.available | 2023-12-22T13:07:31Z | - |
dc.date.created | 2015-07-27 | - |
dc.date.issued | 1992-04 | - |
dc.description.abstract | By using deuterated nitrobenzene as a reactant, it was found that Pd-catalyzed synthesis of N,N'-diphenylurea from nitrobenzene, aniline and CO proceeded via two parallel routes: (i) PhNO2+PhNH2+3CO-->PhNHCONHPh+2CO2, and (ii) PhNO2+5PhNH2+3CO -->3PhNHCONHPh+2H2O. The relative importance of these two routes depended strongly on the ratio of aniline to nitrobenzene initially fed to the reactor. Mechanisms are proposed that account for these reaction stoichiometries | - |
dc.identifier.bibliographicCitation | JOURNAL OF MOLECULAR CATALYSIS, v.73, no.1, pp.43 - 49 | - |
dc.identifier.doi | 10.1016/0304-5102(92)80060-T | - |
dc.identifier.issn | 0304-5102 | - |
dc.identifier.scopusid | 2-s2.0-44049121308 | - |
dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/13023 | - |
dc.identifier.url | http://www.sciencedirect.com/science/article/pii/030451029280060T# | - |
dc.identifier.wosid | A1992HZ17000007 | - |
dc.language | 영어 | - |
dc.publisher | Elsevier BV | - |
dc.title.alternative | STOICHIOMETRY OF PALLADIUM-CATALYZED N,N'-DIPHENYLUREA SYNTHESIS FROM NITROBENZENE, ANILINE AND CARBON-MONOXIDE | - |
dc.title | STOICHIOMETRY OF PALLADIUM-CATALYZED N,N'-DIPHENYLUREA SYNTHESIS FROM NITROBENZENE, ANILINE AND CARBON-MONOXIDE | - |
dc.type | Article | - |
dc.description.journalRegisteredClass | scopus | - |
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