作者: Helmut G. Alt , Heidi E. Engelhardt , Wolfgang Kläui , Arnold Müller
DOI: 10.1016/0022-328X(87)80004-9
关键词: Stereochemistry 、 Trimethylphosphine 、 Cis–trans isomerism 、 Chemistry 、 Cis trans isomerization
摘要: Abstract Tricarbonylhydrido complexes of the type LM(CO) 3 H (L − η 5 -C , Me [C Co{;P(O)(OEt) 2 }; ] ; M Cr, Mo, W) react thermally or photochemically with PMe in solution to form monosubstitution products (PMe )H, and disubstitution LM(CO)(PMe ) H. The C derivatives (R H, Me) consists cis trans isomers. tripod analogs, however, give only more stable isomer. In all cases, showed one isomer, probably form. energy barrier for pseudo-rotation carbonyl hydrido ligands starting materials substitution is higher R than compounds O -tripod ligands. dinuclear L(CO)(PMe MM(CO) L could be detected as by-products from photoinduced reactions.