Nitrile exchange reactions of [WI(CO)(NCMe){P(OiPr)3}2(η2-MeC2Me)][BPh4]; X-ray crystal structures of [WI(CO)(L){P(OiPr)3}2(η2-MeC2Me)][BPh4] {L=NCiPr, NCtBu, NCCH2Ph, 1,2-C6H4(NCCH2)2}
Autor: | Deborah S Moore, Michael G. B. Drew, Paul K. Baker |
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Rok vydání: | 2002 |
Předmět: |
chemistry.chemical_classification
Tetraphenylborate Nitrile Ligand Stereochemistry Organic Chemistry Cationic polymerization X-ray Alkyne Crystal structure Biochemistry Medicinal chemistry Inorganic Chemistry chemistry.chemical_compound chemistry Materials Chemistry 2-Butyne Physical and Theoretical Chemistry |
Zdroj: | Journal of Organometallic Chemistry. 664:37-44 |
ISSN: | 0022-328X |
DOI: | 10.1016/s0022-328x(02)01893-4 |
Popis: | Equimolar quantities of [WI(CO)(NCMe){P(OiPr)3}2(η2-MeC2Me)][BPh4] and L {L=NCEt, NCiPr, NCtBu, NCPh, NCCH2Ph, 1,2-C6H4(NCCH2)2, NCCH2(C4H3S-3)} react in CH2Cl2 at room temperature to give the nitrile exchanged products, [WI(CO)L{P(OiPr)3}2(η2-MeC2Me)][BPh4] (1–7). The complexes for L=NCiPr (2), NCtBu (3), NCCH2Ph (5), and 1,2-C6H4(NCCH2)2 (6) have all been crystallographically characterised. The geometry of all four complexes is psuedo-octahedral with the alkyne ligand occupying one site trans- to an iodo ligand, with the triisopropylphosphite ligand mutually trans and the carbonyl ligand trans to the nitrile group. |
Databáze: | OpenAIRE |
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