Issue 32, 2010

Palladacycle containing nitrogen and selenium: highly active pre-catalyst for the Suzuki–Miyaura coupling reaction and unprecedented conversion into nano-sized Pd17Se15

Abstract

Newly synthesized, air and moisture insensitive palladacycle [PdCl(L–H)] (L = (C6H5)(2-HOC6H4)CHNH(CH2)3SePh; a (N, Se, C) ligand) shows high catalytic activity for the Suzuki–Miyaura coupling reaction of phenylboronic acid with aryl/heteroaryl chlorides/bromides (TON for aryl chlorides up to 9200) and is converted to ∼8 nm size particles of Pd17Se15 (probably the real catalyst).

Graphical abstract: Palladacycle containing nitrogen and selenium: highly active pre-catalyst for the Suzuki–Miyaura coupling reaction and unprecedented conversion into nano-sized Pd17Se15

Supplementary files

Article information

Article type
Communication
Submitted
22 Apr 2010
Accepted
21 Jun 2010
First published
12 Jul 2010

Chem. Commun., 2010,46, 5954-5956

Palladacycle containing nitrogen and selenium: highly active pre-catalyst for the Suzuki–Miyaura coupling reaction and unprecedented conversion into nano-sized Pd17Se15

G. K. Rao, A. Kumar, J. Ahmed and A. K. Singh, Chem. Commun., 2010, 46, 5954 DOI: 10.1039/C0CC01075H

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