Palladium salicylaldimine complexes derived from 2,3-dihydroxybenzaldehyde

Eric G. Bowes; Graham M. Lee; Christopher M. Vogels; Andreas Decken; Stephen A. Westcott

doi:10.1016/j.ica.2011.07.051

Palladium salicylaldimine complexes derived from 2,3-dihydroxybenzaldehyde

Eric G. Bowes
, Graham M. Lee
, Christopher M. Vogels
, Andreas Decken
, Stephen A. Westcott

Research output: Contribution to journal › Article › peer-review

37 Scopus citations

Abstract

Schiff bases derived from condensation of 2,3-dihydroxybenzaldehyde with various primary amines, such as 1-adamantanamine hydrochloride, 2,6-dimethylaniline, 2,6-diethylaniline and 2,6-diisopropylaniline, react with palladium(II) acetate to give the corresponding bis(N-arylsalicylaldiminato) palladium(II) complexes. These complexes have been found to be active catalyst precursors for the Suzuki-Miyaura cross-coupling of aryl bromides and iodides with aryl boronic acids using water as a solvent. © 2011 Elsevier B.V. All rights reserved.

Original language	English
Pages (from-to)	84-90
Number of pages	7
Journal	Inorganica Chimica Acta
Volume	377
Issue number	1
DOIs	https://doi.org/10.1016/j.ica.2011.07.051
State	Published - Nov 1 2011
Externally published	Yes

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title = "Palladium salicylaldimine complexes derived from 2,3-dihydroxybenzaldehyde",

abstract = "Schiff bases derived from condensation of 2,3-dihydroxybenzaldehyde with various primary amines, such as 1-adamantanamine hydrochloride, 2,6-dimethylaniline, 2,6-diethylaniline and 2,6-diisopropylaniline, react with palladium(II) acetate to give the corresponding bis(N-arylsalicylaldiminato) palladium(II) complexes. These complexes have been found to be active catalyst precursors for the Suzuki-Miyaura cross-coupling of aryl bromides and iodides with aryl boronic acids using water as a solvent. {\textcopyright} 2011 Elsevier B.V. All rights reserved.",

author = "Bowes, \{Eric G.\} and Lee, \{Graham M.\} and Vogels, \{Christopher M.\} and Andreas Decken and Westcott, \{Stephen A.\}",

year = "2011",

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doi = "10.1016/j.ica.2011.07.051",

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journal = "Inorganica Chimica Acta",

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T1 - Palladium salicylaldimine complexes derived from 2,3-dihydroxybenzaldehyde

AU - Bowes, Eric G.

AU - Lee, Graham M.

AU - Vogels, Christopher M.

AU - Decken, Andreas

AU - Westcott, Stephen A.

PY - 2011/11/1

Y1 - 2011/11/1

N2 - Schiff bases derived from condensation of 2,3-dihydroxybenzaldehyde with various primary amines, such as 1-adamantanamine hydrochloride, 2,6-dimethylaniline, 2,6-diethylaniline and 2,6-diisopropylaniline, react with palladium(II) acetate to give the corresponding bis(N-arylsalicylaldiminato) palladium(II) complexes. These complexes have been found to be active catalyst precursors for the Suzuki-Miyaura cross-coupling of aryl bromides and iodides with aryl boronic acids using water as a solvent. © 2011 Elsevier B.V. All rights reserved.

AB - Schiff bases derived from condensation of 2,3-dihydroxybenzaldehyde with various primary amines, such as 1-adamantanamine hydrochloride, 2,6-dimethylaniline, 2,6-diethylaniline and 2,6-diisopropylaniline, react with palladium(II) acetate to give the corresponding bis(N-arylsalicylaldiminato) palladium(II) complexes. These complexes have been found to be active catalyst precursors for the Suzuki-Miyaura cross-coupling of aryl bromides and iodides with aryl boronic acids using water as a solvent. © 2011 Elsevier B.V. All rights reserved.

UR - https://www.scopus.com/pages/publications/80053925221

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DO - 10.1016/j.ica.2011.07.051

M3 - Article

SN - 0020-1693

VL - 377

SP - 84

EP - 90

JO - Inorganica Chimica Acta

JF - Inorganica Chimica Acta

IS - 1

ER -

Palladium salicylaldimine complexes derived from 2,3-dihydroxybenzaldehyde

Abstract

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