Palladacycles of Thioethers Catalyzing Suzuki-Miyaura C-C Coupling: Generation and Catalytic Activity of Nanoparticles

被引:88
作者
Rao, Gyandshwar Kumar [1 ]
Kumar, Arun [1 ]
Kumar, Satyendra [1 ]
Dupare, Umesh B. [1 ]
Singh, Ajai K. [1 ]
机构
[1] Indian Inst Technol Delhi, Dept Chem, New Delhi 110016, India
关键词
SULFUR-CONTAINING PALLADACYCLES; N-HETEROCYCLIC CARBENES; SCHIFF-BASE LIGANDS; ARYL CHLORIDES; PALLADIUM(II) COMPLEXES; AEROBIC CONDITIONS; ARYLBORONIC ACIDS; EFFICIENT CATALYSTS; PHENYLBORONIC ACID; ROOM-TEMPERATURE;
D O I
10.1021/om4001956
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Tridentate thioether ligands, 2-HO-4-R-C6H3-(C6H4)CHNH(CH2)(3)SPh [R = H (L1) or -OMe (L2,)] react with Na2PdCl4, giving palladacycles [PdCl(C-,N,S)] (1: (C-,N,S) = L1-H; 2: (C-,N,S) = L2-H). The H-1 and C-13{H-1} NMR spectra of ligands and their palladacycles have been found to be characteristic. Complexes I and 2 have also been characterized with HR-MS. The crystal structure of 2 has been solved. The Pd-S bond length is 2.428(2) angstrom, and palladium has a nearly square planar geometry. During the course of catalysis of Suzuki-Miyaura C-C coupling using 1 and 2 as catalysts, unexpected formation of Pd16S7 nanoparticles (NPs) has been observed with both complexes. This is the first time that such an observation has been made with palladacycles of thioethers used in this coupling reaction. The efficiency of 2 in carrying out the coupling is significantly lower than that of 1. Complex 2 has an additional -OMe group in the ligand structure, and the size of Pd16S7 NPs formed from this complex are larger (6 nm) than those obtained from 1 (2 nm).
引用
收藏
页码:2452 / 2458
页数:7
相关论文
共 56 条
[41]   Palladium(II)-selenated Schiff base complex catalyzed Suzuki-Miyaura coupling: Dependence of efficiency on alkyl chain length of ligand [J].
Rao, Gyandshwar Kumar ;
Kumar, Arun ;
Kumar, Bharat ;
Kumar, Dinesh ;
Singh, Ajai Kumar .
DALTON TRANSACTIONS, 2012, 41 (07) :1931-1937
[42]   3-PHASE TEST FOR REACTIVE INTERMEDIATES - CYCLOBUTADIENE [J].
REBEK, J ;
GAVINA, F .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1974, 96 (22) :7112-7114
[43]   3-PHASE TEST FOR REACTION INTERMEDIATES - NUCLEOPHILIC CATALYSIS AND ELIMINATION-REACTIONS [J].
REBEK, J ;
BROWN, D ;
ZIMMERMAN, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1975, 97 (02) :454-455
[44]   Syntheses, oxidations, and palladium complexes of fluorous dialkyl sulfides: new precursors to highly active catalysts for the Suzuki coupling [J].
Rocaboy, C ;
Gladysz, JA .
TETRAHEDRON, 2002, 58 (20) :4007-4014
[45]   1,1′-P/O-ferrocenyl ligands in palladium-catalyzed suzuki coupling of aryl chlorides [J].
Teo, SH ;
Weng, ZQ ;
Hor, TSA .
ORGANOMETALLICS, 2006, 25 (05) :1199-1205
[46]   Mesoporous silica-supported Pd catalysts: An investigation into structure, activity, leaching and heterogeneity [J].
Webb, Jonathan D. ;
MacQuarrie, Stephanie ;
McEleney, Kevin ;
Crudden, Cathleen M. .
JOURNAL OF CATALYSIS, 2007, 252 (01) :97-109
[47]   A review of the problem of distinguishing true homogeneous catalysis from soluble or other metal-particle heterogeneous catalysis under reducing conditions [J].
Widegren, JA ;
Finke, RG .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2003, 198 (1-2) :317-341
[48]   Highly active palladium catalysts for Suzuki coupling reactions [J].
Wolfe, JP ;
Singer, RA ;
Yang, BH ;
Buchwald, SL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (41) :9550-9561
[49]  
Wolfe JP, 1999, ANGEW CHEM INT EDIT, V38, P2413, DOI 10.1002/(SICI)1521-3773(19990816)38:16<2413::AID-ANIE2413>3.0.CO
[50]  
2-H