Detailed Study of C-O and C-C Bond-Forming Reductive Elimination from Stable C2N2O2-Ligated Palladium(IV) Complexes

被引:322
|
作者
Racowski, Joy M. [1 ]
Dick, Allison R. [1 ]
Sanford, Melanie S. [1 ]
机构
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
OXYGEN-ATOM TRANSFER; CARBON-CARBON; OXIDATIVE ADDITION; NITROUS-OXIDE; PT(IV); MECHANISM; ACETOXYLATION; OXIDANTS; IODIDE; PD;
D O I
10.1021/ja9014474
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This paper describes the synthesis of a series of Pd-IV complexes of general structure (N similar to C)(2)Pd-IV(O2CR)(2) (N similar to C = a rigid cyclometalated ligand; O2CR = carboxylate) by reaction of (N similar to C)(2)Pd-II with Phl(O2CR)(2). The majority of these complexes undergo clean C-O bond-forming reductive elimination, and the mechanism of this process has been investigated. A variety of experiments, including Hammett plots, Eyring analysis, crossover studies, and investigations of the influence of solvent and additives, suggest that C-O bond-forming reductive elimination proceeds via initial carboxylate dissociation followed by C-O coupling from a 5-coordinate cationic Pd-IV intermediate. The mechanism of competing C-C bond-forming reductive elimination from these complexes has also been investigated and is proposed to involve direct reductive elimination from the octahedral Pd-IV centers.
引用
收藏
页码:10974 / 10983
页数:10
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