Synthesis and reaction kinetics of Pd(1,5-cyclooctadiene)Cl2 with N,N′-methylene-bis(2-aminopyridyl): an efficient catalyst for Suzuki-cross-coupling reactions
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Title |
Synthesis and reaction kinetics of Pd(1,5-cyclooctadiene)Cl2 with N,N′-methylene-bis(2-aminopyridyl): an efficient catalyst for Suzuki-cross-coupling reactions
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Creator |
MOHANTY, SASMITA
PUNJI, BENUDHAR BALAKRISHNA, MS |
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Subject |
reaction kinetics
nitrogen donor ligands palladium compounds catalysis |
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Description |
An inexpensive bidentate ligand N,N′-methylene-bis(2-aminopyridyl) (1) has been synthesized. Reaction of 1 with [Pd(COD)Cl2] affords a stable chelate complex, [{NC5H4N(H)(μ-CH2)(H)NC5H4N-κN,κN}PdCl2] (2). The kinetics of the pseudo-unimolecular reaction of N,N′-methylene-bis(2-aminopyridyl) with Pd(1,5-cyclooctadiene)Cl2 has been studied over the range 3.0 less-than-or-equals, slant 103 [1] less-than-or-equals, slant 7.0 mol dm−3, 30 °C less-than-or-equals, slant t less-than-or-equals, slant 40 °C. The rate constants and equilibrium constants were calculated. Entropy and enthalpy of the reaction are found to be −42 ± 1 J K−1 mol−1 and 75 ± 1 kJ mol−1, respectively, which clearly indicates that the substitution reaction follows associative mechanism. The complex 2 was tested for the Suzuki-cross-coupling reaction of a variety of aryl halides with aryl boronic acids in methanol at room temperature or at 60 °C, giving generally high yields for both activated and inactivated aryl bromides. The effect of solvents as well as the effect of base on the Suzuki-coupling reaction is also investigated.
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Publisher |
Elsevier
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Date |
2009-03-20T05:57:17Z
2011-11-25T19:45:52Z 2011-12-26T13:07:38Z 2011-12-27T05:55:40Z 2009-03-20T05:57:17Z 2011-11-25T19:45:52Z 2011-12-26T13:07:38Z 2011-12-27T05:55:40Z 2006 |
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Type |
Article
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Identifier |
Polyhedron 25(3), 815-820
0277-5387 http://dx.doi.org/10.1016/j.poly.2005.08.013 http://hdl.handle.net/10054/1019 http://dspace.library.iitb.ac.in/xmlui/handle/10054/1019 |
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Language |
en
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