Dicarbonylrhodium(I) complexes of benzoylpyridine ligands: Synthesis, reactivity and catalytic carbonylation reaction

被引:14
|
作者
Borah, Bibek Jyoti [1 ]
Deb, Biswajit [1 ]
Sarmah, Podma Pollov [1 ]
Dutta, Dipak Kumar [1 ]
机构
[1] CSIR, NE Inst Sci & Technol, Div Mat Sci, Jorhat 785006, Assam, India
关键词
Rhodium(I); Dicarbonyl complexes; Benzoylpyridine; Oxidative addition; Carbonylation; OXIDATIVE ADDITION; METHANOL CARBONYLATION; RHODIUM(I) CARBONYL; ACID LIGANDS; PYRIDINE; CHEMISTRY;
D O I
10.1016/j.molcata.2009.11.022
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
The new complexes of the type [Rh(CO)(2)ClL] (1a-c), where L = 2-Benzoylpyridine (a), 3-Benzoylpyridine (b) and 4-Benzoylpyridine (c) have been synthesized and characterized. Oxidative addition (OA) of 1a-c with CH3I, C2H5I and C6H5CH2Cl afford penta coordinated Rh(III) complexes, [Rh(CO)(CORn)ClXL]{R-1 = -CH3 (2a-c), R-2 = -C2H5 (3a-c); X = I and R-3 = -CH2C6H5 (4a-c); X = CI}. Kinetic data for the reaction of 1a-c with CH3I indicate a pseudo-first order reaction. The la-c exhibit high catalytic activity in the carbonylation of methanol to acetic acid and its ester and show a higher turn over number (TON = 1529-1748) than the well known commercial species [Rh(CO)(2)I-2](-) (TON = 1000) under the reaction conditions: temperature 130 +/- 2 degrees C, pressure 30 +/- 2 bar and time 1 h. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:66 / 70
页数:5
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