Gold(I) and Gold(III) Complexes of Cyclic (Alkyl)(amino)carbenes

被引:65
|
作者
Romanov, Alexander S. [1 ]
Bochmann, Manfred [1 ]
机构
[1] Univ E Anglia, Sch Chem, Norwich NR4 7TJ, Norfolk, England
基金
欧洲研究理事会;
关键词
N-HETEROCYCLIC CARBENE; PI-ACCEPTOR PROPERTIES; ALKYL AMINO CARBENES; OXIDATIVE ADDITION; CRYSTAL-STRUCTURES; CATALYTIC-ACTIVITY; DINUCLEAR GOLD(I); CHEMICAL-SHIFTS; METAL-COMPLEXES; DONOR LIGANDS;
D O I
10.1021/om501211p
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The chemistry of Au(I) complexes with two types of cyclic (alkyl)(amino)carbene (CAAC) ligands has been explored, using the sterically less demanding dimethyl derivative (Me2)CAAC and the 2-adamantyl ligand (Ad)CAAC. The conversion of ((Ad)CAAC)AuCl into ((Ad)CAAC)AuOH by treatment with KOH is significantly accelerated by the addition of tBuOH. ((Ad)CAAC)AuOH is a convenient starting material for the high-yield syntheses of ((Ad)CAAC)AuX complexes by acid/base and C-H activation reactions (X = OAryl, CF3CO2, N(Tf)(2), C2Ph, C6F5, C6HF4, C6H2E3, CH2C(O)C6H4OMe, CH(Ph)C(O)Ph, CH2SO2Ph), while the cationic complexes [((Ad)CAAC)AuL](+) (L = CO, (CNBu)-Bu-t) and ((Ad)CAAC)AuCN were obtained by chloride substitution from ((Ad)CAAC)AuCl. The reactivity toward variously substituted fluoroarenes suggests that ((Ad)CAAC)AuOH is able to react with C-H bonds with pK(a) values lower than about 31.5. This, together with the spectroscopic data, confirm the somewhat stronger electron-donor properties of CAAC ligands in comparison to imidazolylidene-type N-heterocyclic carbenes (NHCs). In spite of this, the oxidation of (Me2)CAAC and (Ad)CAAC gold compounds is much less facile. Oxidations proceed with C-Au cleavage by halogens unless light is strictly excluded. The oxidation of ((Ad)CAAC)AuCl with PhICl2 in the dark gives near-quantitative yields of ((Ad)CAAC)AuCl3, while [Au((Me2)CAAC)(2)]Cl leads to trans-[AuCl2((Me2)CAAC)(2)]Cl. In contrast to the chemistry of imidazolylidene-type gold NHC complexes, oxidation products containing Au-Br or Au I bonds could not be obtained; whereas the reaction with CsBr3 cleaves the Au C bond to give mixtures of [(Ad)CAAC-Br](+)[AuBr2](-) and [((Ad)CAAC-Br)](+) [AuBr4](-), the oxidation of ((Ad)CAAC)AuI with I-2 leads to the adduct ((Ad)CAAC)AuI center dot I-2. Irrespective of the steric demands of the CAAC ligands, their gold complexes proved more resistant to oxidation and more prone to halogen cleavage of the Au C bonds than gold(I) complexes of imidazole-based NHC ligands.
引用
收藏
页码:2439 / 2454
页数:16
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