SPS-Ni(II) pincer compounds of the type [Ni(phPS2)(P(C6H4-4-R)3)] Synthesis, characterization and catalytic evaluation in C-S cross-coupling reactions

被引:19
作者
Gomez-Benitez, Valente [1 ]
Valdes, Hugo [2 ]
Hernandez-Ortega, Simon [2 ]
Manuel German-Acacio, Juan [3 ]
Morales-Morales, David [2 ]
机构
[1] Univ Autonoma Chihuahua, Fac Ciencias Quim, Circuito Univ S-N, Chihuahua 31125, Chihuahua, Mexico
[2] Univ Nacl Autonoma Mexico, Inst Quim, Ciudad Univ, Ciudad De Mexico 04510, DF, Mexico
[3] UNAM, Inst Nacl Ciencias Med & Nutr SZ, Red Apoyo Invest, CIC, Ciudad De Mexico 14000, DF, Mexico
关键词
SPS-pincer nickel complex; C-S cross-coupling; Thioether synthesis; Nickel catalyst; Thioetherification reaction; PHP(C6H4-SH-2)(2) PHPS(2)H(2); COMPLEXES; NICKEL; BOND; HYDROGENATION; ALCOHOLS; LIGAND; MONONUCLEAR; THIOLATE; CLEAVAGE;
D O I
10.1016/j.poly.2017.09.026
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis and characterization of a series of SPS-Ni(II) pincer complexes with different para-substituted triphenylphosphines has been performed. The molecular structure of [Ni(phPS(2))(PPh3)] (1) (phPS(2)H(2) = PhP(C6H4-2-SH)(2), bis(phenyl-2-thiol)phenylphosphine) was unequivocally determined by single crystal X-ray diffraction analysis. The metal centre exhibited a slightly distorted square planar geometry. The complexes showed a high catalytic activity in the C-S cross-coupling reaction of both alkyl-and aryl-disulfides with iodobenzenes for the production of non-symmetric sulfides. In general, the different para-substituted triphenylphosphine ligands do not affect the catalytic performance of the SPS-Ni(II) complexes. However, activity of the catalyst decreases with the steric hindrance of the different alkyl groups in the disulphide substrates. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:144 / 148
页数:5
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