F NMR study of cis- and trans- effects of substituted triphenylphosphine ligands in trans-(4-fluorophenyl)triarylphosphine- tri(4-fluorophenyl)phosphineplatinum 4-fluorothiophenoxides.

Autor: Kravtsov, D., Pachevskaya, V., Peregudov, A., Fedin, E.
Zdroj: Russian Chemical Bulletin; 1995, Vol. 44 Issue 7, p1311-1315, 5p
Abstrakt: A number of compounds of the type of trans-4-FCHPt(PAr)SCHF-4, where Ar is a substituted phenyl group, have been prepared starting from the corresponding chlorides. By exchange reactions of trans-4-FCHPt[P(CHF-4)]SCHF-4 with the above-mentioned compounds or ArP, trans-4-FCHPt[P(CHF-4)][PAr]SCHF-4 have been generated in solution. For the latter compounds, the effect of ArP on cis- and trans-ligands has been studied by theF NMR technique. It has been shown that the cis- and trans-effects of ArP run parallel and are well described by pK values and ionization potentials of the unshared electron pair in ArP, as well as by σ constants of the aryl groups. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index