196213-69-1Relevant academic research and scientific papers
Activation of P-C Bonds in Phosphines and Aromatic C-H Bonds in Toluene by Phosphine Complexes of Dichloro- and Dimethylplatinum(II) in Hydrocarbon Media
Vedernikov, A. N.,Zazybin, A. G.,Solomonov, A. B.,Solomonov, B. N.
, p. 68 - 73 (2008/10/08)
According to GLC and (1)H and (31)P NMR data, lipopholic complexes of cis-dichloro- and cis-dimethylplatinum(II), PtX2(L)2 [X=Cl, L=PPh3 (I); X=Me, L=PPh3 (II); X=Cl, L=P(m-CH3C6H4)3 (III); X=Me, L=P(m-CH3C6H4)3 (IV)], II and III slowly react with toluene at 120°C to give productsof activation of aromatic C-H bonds: tolyl chlorides from the dichlorop latinum complex and tolylplatinum derivatives and methane from the dimethylplatinum complex. Benzene does not react with these complexes. Dichlorobis(tri-m-tolylphosphine)platinum(II) also undergoes cis-trans isomerization. Being almost insoluble in benzene and toluene, cis-dichlorobis(triphenylphosphine)platinum(II) (I) neither undergoes isomerization nor reacts with toluene. The P-C bonds in the phosphine ligands of the dimethylplatinum complexes are cleaved both in benzene and in toluene solutions with formation of the corresponding byaryl and arylplatinum complexes.A scheme of activation of C-H bonds in toluene is proposed, which invol ves oxidative addition of the aromatic hydrocarbon to platinum(II) and formation of unstable aryl hydride platinum(IV) complexes.
Structure - Reactivity correlations for the dissociative uncatalyzed isomerization of monoalkylbis(phosphine)platinum(II) solvento complexes
Romeo, Raffaello,Alibrandi, Giuseppe
, p. 4822 - 4830 (2008/10/09)
Complexes of the type a's-[PtL2Me2] (1-14) (L = an extended series of phosphines of widely different steric and electronic properties) were synthesized, characterized, and used as precursors for the formation of cis-monoalkylplatinum(II) solvente species in methanol. The cleavage of the first platinum-alkyl bond by protonolysis is a fast process, but the subsequent cis to trans isomerization of the cationic solvento species [PtL2- (Me)(MeOH)]+ is relatively slow and it can be monitored using 31P NMR or conventional spectrophotometry. A large collection of 1H and 31P NMR data for cis-[PtL2Me2], cis-[PtL2Me(MeOH)]+, and trans-[PtL2Me(MeOH)]+ complexes showed interesting dependencies upon the size, the α-donor capacity, and the mutual position of the phosphines in the coordination sphere of the metal. The rate constants for isomerization of cis-[PtL2Me(MeOH)]+ were resolved quantitatively into steric and electronic contributions of the phosphine ligands, by means of correlations with parameters which reflect their σ-donor ability (Χ values) and steric requirements (Tolman's cone angles, θ). The electronic and steric profiles obtained for these reactions are discussed within the framework of a mechanism which involves dissociative loss of the solvent molecule and interconversion of two geometrically distinct 3-coordinate T-shaped 14-electron intermediates. The factors controlling the stability of these coordinatively unsaturated species are discussed. The electronic and steric influences of phosphines as spectator ligands in a dissociative process are compared with those shown by these ligands when used as nucleophiles in associative substitution processes. The activation parameters ΔH? and ΔS? were measured using both conventional isothermal and non-isothermal spectrophotometric kinetics.
