4.8 Article

MVS-derived palladium nanoparticles deposited on polydimethylphosphazene as recyclable catalysts for Heck-type reactions: Preparation, structural study, and catalytic activity

Journal

JOURNAL OF CATALYSIS
Volume 246, Issue 2, Pages 351-361

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2006.12.017

Keywords

Heck reaction; alkylative cyclization; palladium; polydimethylphosphazene; metal vapor synthesis; P-31, C-13, N-15 solid-state NMR; HRTEM

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Palladium nanoparticles, obtained by the metal vapor synthesis (MVS) technique, were deposited on polydimethylphosphazene (PDMP). The Pd/PDMP system showed high catalytic activity in the Heck C-C Coupling of iodobenzene and methyl acrylate, with greater activity than commercially available catalysts such as Pd(OAc)(2) and Pd on carbon. The Pd/PDMP is soluble in the reaction solvent, 1-methyl-2-pyrrolidinone, and can be quantitatively recovered at the end of the reaction by precipitation without loss of metal. When reused, the recovered Pd/PDMP retains its catalytic activity. A multinuclear (P-31, C-13, N-15) solid-state NMR study identified and characterized the strong structural and dynamic modifications induced by Pd nanoparticles on PDMP. Moreover, solid-state NMR Studies and HRTEM analyses, performed on the pristine catalyst and on the catalyst recovered after the reaction, highlighted the almost complete structural invariability of the Pd/PDMP, pointing out the high stability toward agglomeration of the palladium nanoparticles in such a system. Pd/PDMP in the presence of triphenylphosphine was also active in the alkylative cyclization of 7-octen-1-ynes, an important C-C coupling reaction to obtain substituted 1,2-bis(alkylidene)cyclohexanes, which are valuable building blocks in fine chemistry. (c) 2007 Elsevier Inc. All rights reserved.

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