OXIDATIVE METAL-METAL BOND-CLEAVAGE IN TP(2)RU(2)(CO)(4) (TP=HYDRIDOTRIS(PYRAZOLY)BORATE)

被引：11

作者：

SORLIE, M ^{[1
]}

TILSET, M ^{[1
]}

机构：

[1] UNIV OSLO, DEPT CHEM, N-0315 OSLO, NORWAY

来源：

INORGANIC CHEMISTRY | 1995年 / 34卷 / 21期

关键词：

D O I：

10.1021/ic00125a018

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The Ru-Ru bonded dimer Tp(2)Ru(2)(CO)(4) (1) is oxidized at E degrees = 0.15 V vs Cp(2)Fe/Cp(2)Fe(+) in acetonitrile. The chemical or electrochemical 2-electron oxidation of 1 results in the formation of the solvent adducts TpRu(CO)(2)(Sol)(+) (Sol: MeCN, 2; THF, 3; Me(2)CO, 4; H2O, 5). A derivative cyclic voltammetry investigation of the oxidation process has established that the metal-metal bond cleavage occurs from 1(.+) following the rate law -d[1(.+)]/dt = k[1(.+)][Sol] (Sol = MeCN, THF, Me(2)CO). An associative mechanism is furthermore implicated by large and negative entropies of activation. The rate of Ru-Ru bond cleavage is strongly solvent dependent and decreases in the order Me(2)CO > MeCN > THF > CH2Cl2. The order of stabilities of the monomeric solvent adducts was established by observation of ligand-exchange reactions by H-1 NMR spectroscopy in nitromethane-d(3), and the stabilities decrease in the order MeCN > H2O > THF > Me(2)CO.

引用

页码：5199 / 5204

页数：6

共 48 条

[1] INVOLVEMENT OF 19-ELECTRON SPECIES IN OXIDATIVELY INDUCED HOMOLYTIC METAL-CARBON BOND-CLEAVAGE REACTIONS - DECOMPOSITION OF 17-ELECTRON CYCLOPENTADIENYLRUTHENIUM METHYL CATIONS [J].