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  3. SYNTHESIS AND REACTIVITY OF THE IRIDIUM VINYLIDENE IR=C=CH2[N(SIME2CH2PPH2)2] - FORMATION OF CARBON-CARBON BONDS VIA MIGRATORY INSERTION OF A VINYLIDENE UNIT

SYNTHESIS AND REACTIVITY OF THE IRIDIUM VINYLIDENE IR=C=CH2[N(SIME2CH2PPH2)2] - FORMATION OF CARBON-CARBON BONDS VIA MIGRATORY INSERTION OF A VINYLIDENE UNIT

TitleSYNTHESIS AND REACTIVITY OF THE IRIDIUM VINYLIDENE IR=C=CH2[N(SIME2CH2PPH2)2] - FORMATION OF CARBON-CARBON BONDS VIA MIGRATORY INSERTION OF A VINYLIDENE UNIT
Publication TypeJournal Article
Year of Publication1992
AuthorsFryzuk, MD, Huang, L, McManus, NT, Paglia, P, Rettig, SJ, White, GS
JournalOrganometallics
Volume11
Pagination2979-2990
Date PublishedSep
Type of ArticleArticle
ISBN Number0276-7333
KeywordsACETYLIDE COMPLEXES, ALKYNE, CARBENE, COMPLEX, FISCHER-TROPSCH REACTION, LIGAND, MECHANISM, PHOTOINDUCED RING EXPANSION, REARRANGEMENT, SATURATED CARBON, TRANSITION-METAL
Abstract

{The synthesis of the 16-electron iridium vinylidene complex Ir=C=CH2[N(SiMe2CH2PPh2)2] is described by starting from the cyclooctene derivative Ir(eta-2-C8H14)[N(SiMe2CH2PPh2)2] with addition of acetylene. This vinylidene complex reacts with a variety of electrophiles; thus, reaction with AlR3 (R = Me, Et) or GaMe3 leads to the formation of the new derivatives Ir(ER2)CR=CH2[N(SiMe2CH2PPh2)2] (E = Al
URL<Go to ISI>://A1992JN06600009