Oxidative addition transition states of Pd(0) complexes in polar solvent-a DFT study involving implicit and explicit solvation

被引:32
|
作者
Lyngvi, Eirik [1 ]
Schoenebeck, Franziska [1 ]
机构
[1] ETH, Organ Chem Lab, CH-8093 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
Oxidative addition; Palladium; Computational; Transition state; Acetonitrile; EFFECTIVE CORE POTENTIALS; MOLECULAR CALCULATIONS; ARYL CHLORIDES; PALLADIUM(0) COMPLEX; DENSITY FUNCTIONALS; BOND ACTIVATION; C-C; PHOSPHINE; MECHANISM; REACTIVITY;
D O I
10.1016/j.tet.2013.03.095
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Previous reports in the literature have suggested that concerted transition states for oxidative addition would not exist in solution. By contrast, this report describes the successful location of transition states for the oxidative addition of monoligated Pd((PBu3)-Bu-t), bisligated Pd((PBu3)-Bu-t)(MeCN), and anionic Pd((PBu3)-Bu-t)F- complexes to C-Cl and C-OTf of an aryl chloro triflate in polar solvent (MeCN). Optimizations were done with implicit salvation and a combined implicit/explicit solvation approach in which six acetonitrile molecules were additionally involved in the optimization. The geometries obtained from optimizations employing an implicit solvation model are structurally largely analogous to those found using a combination of implicit and explicit solvation. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5715 / 5718
页数:4
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