Catalytic activity of PdCl2 complexes with pyridines in nitrobenzene carbonylation

被引：24

作者：

Krogul, Agnieszka ^{[1
]}

Skupinska, Jadwiga ^{[1
]}

Litwinienko, Grzegorz ^{[1
]}

机构：

[1] Univ Warsaw, Fac Chem, PL-02093 Warsaw, Poland

来源：

JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL | 2011年 / 337卷 / 1-2期

关键词：

Carbonylation; Reduction of nitrobenzene; Palladium complexes; Carbamates; Substituted pyridines; REDUCTIVE CARBONYLATION; STRUCTURAL-CHARACTERIZATION; OXIDATIVE CARBONYLATION; CARBON-MONOXIDE; CARBONYLRHODIUM COMPLEXES; PALLADIUM COMPLEXES; NITRO-COMPOUNDS; LIGANDS; AMINES; NITROARENES;

D O I：

10.1016/j.molcata.2011.01.007

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

Synthesis of square planar palladium(II) complexes of general structure PdCl2(XnPy)(2) (where: Py = pyridine; XnPy = 2-MePy: 3-MePy; 4-MePy; 2,4-Me2Py; 2,6-Me2Py; 2-CIPy; 3-CIPy and 3,5-Cl2Py) has been performed in order to study activity of these complexes as catalysts of nitrobenzene (NB) carbonylation - a process of industrial importance leading to production of ethyl N-phenylcarbamate (EPC). Electron withdrawing/electron donating properties of XnPy ligands (described by experimentally determined acidity parameter pK(a)) have been correlated with activities of PdCl2(X Py)2 complexes during NB carbonylation in presence of catalytic system PdCl2(XnPy)(2)/Fe/I-2/XnPy. We observed that conversions of substrates and yields of EPC increase within increasing basicity of XnPy ligand (for not sterically hindered XnPy's). On the basis of current work and our previous studies a detailed mechanism of catalytic carbonylation of NB is proposed. (C) 2011 Elsevier B.V. All rights reserved.

引用

页码：9 / 16

页数：8

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[1] Platinum group antitumor chemistry: Design and development of new anticancer drugs complementary to cisplatin [J].