Article ID Journal Published Year Pages File Type
1328088 Journal of Organometallic Chemistry 2007 16 Pages PDF
Abstract

A range of new small bite-angle diphosphine complexes, [M(CO)4{X2PC(R1R2)PX2}] (M = Mo, W; X = Ph, Cy; R1 = H, Me, Et, Pr, allyl, R2 = Me, allyl), have been prepared via elaboration of the methylene backbones in [M(CO)4(X2PCH2PX2)] as a result of successive deprotonation and alkyl halide addition. When X = Ph it proved possible to replace both methylene protons but for X = Cy only one substitution proved possible. This is likely due to the electron-releasing nature of the cyclohexyl groups but may also be due to steric constraints. Attempts to prepare the bis(allyl) substituted complex [Mo(CO)4{Ph2PC(allyl)2PPh2}] were only moderately successful. The crystal structures of nine of these complexes are presented.

Graphical abstractSmall bite-angle diphosphine complexes, [M(CO)4{X2PC(R1R2)PX2}] (M = Mo, W; X = Ph, Cy; R1 = H, Me, Et, Pr, allyl, R2 = Me), have been prepared upon elaboration of the methylene backbones in [M(CO)4(X2PCH2PX2)] via successive deprotonation and alkyl halide addition. The crystal structures of nine examples are presented.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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