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- W2022643480 abstract "Abstract The kinetics of reaction between a series of monosubstituted cobalt carbonyls Co(CO) 2 NOL (with L = Sb(C 6 H 5 ) 3 , As(C 6 H 5 ) 3 , P(C 6 H 5 ) 3 , P(OC 6 H 5 ) 3 , P(OCH 3 ) 3 , and P(−C 4 H 9 ) 3 ) and the same bidentate ligand 1,2-bis(diphenylphosphino)ethane, have been studied. In all cases the end product is the disubstituted chelate complex Co(CO)NOP(C 6 H 5 ) 2 CH 2 CH 2 P(C 6 H 5 ) 2 . For L = P(C 6 H 5 ) 3 and P(OCH 3 ) 3 there are formed to an appreciable extent, at relatively low ligand-to-complex conc. ratios, also the disubstituted complexes Co(CO)NOL 2 . There is good evidence that the associative reaction mechanism goes through a path involving a primary step of substrates ligand displacement, followed by chelation. Only for Co(CO) 2 NOP(OCH 3 ) 3 , a primary step of substrate ligand displacement, follow-ligand again followed by chelation, is competitive with the above one. The order of reactivity for primary ligand displacement is the following: Sb(C 6 H 5 ) 3 >CO> As(C 6 H 5 ) 3 >P(OC 6 H 5 ) 3 >P(C 6 H 5 ) 3 >P(n−C 4 H 9 ) 3 . It is interpreted on the basis of the varied basicity and polarizability of the substrate ligand, and in specific cases of their additional π-bonding ability. Steric factors do not seem to play a relevant role." @default.
- W2022643480 created "2016-06-24" @default.
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- W2022643480 date "1968-03-01" @default.
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- W2022643480 title "Kinetics of disubstitution reactions of 1,2-bis(diphenylphosphino) ethane with monosubstituted derivatives of Co(CO)3NO" @default.
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- W2022643480 doi "https://doi.org/10.1016/s0020-1693(00)87036-x" @default.
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