Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/94943
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dc.titleSubstituted metal carbonyls XIII. Fe(CO)4(η1-dppf) [where dppf = (Ph2PC5H4)2Fe]: a convenient building block for heterometallic complexes
dc.contributor.authorAndy Hor, T.S.
dc.contributor.authorPhang, L.-T.
dc.date.accessioned2014-10-16T08:41:58Z
dc.date.available2014-10-16T08:41:58Z
dc.date.issued1990-07-10
dc.identifier.citationAndy Hor, T.S.,Phang, L.-T. (1990-07-10). Substituted metal carbonyls XIII. Fe(CO)4(η1-dppf) [where dppf = (Ph2PC5H4)2Fe]: a convenient building block for heterometallic complexes. Journal of Organometallic Chemistry 390 (3) : 345-350. ScholarBank@NUS Repository.
dc.identifier.issn0022328X
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/94943
dc.description.abstractThe potential of Fe(CO)4(η1-dppf) (dppf = 1,1′-bis(diphenylphosphino)ferrocene) as a precursor for heterometallic species is fully expanded in the synthesis of (OC)4Fe(μ-dppf)Cr(CO)5, (OC)4Fe(μ-dppf)W(CO)5, and (OC)4Fe(μ-dppf)Mn2(CO)9, all of which have been characterized by IR, NMR (1H and 31P) and elemental analyses. The low energy requirement of TMNO (Me3NO · 2H2O)decarbonylation allows the formation of monosubstituted Mn2(CO)10 as the major product. This aspect is further substantiated by the isolation of Mn4(CO)18(μ-dppf) in which the single bridging of a diphosphine group between two Mn2(CO)9 moieties is unprecedented. © 1990.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleJournal of Organometallic Chemistry
dc.description.volume390
dc.description.issue3
dc.description.page345-350
dc.description.codenJORCA
dc.identifier.isiutNOT_IN_WOS
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