The University of Southampton
University of Southampton Institutional Repository

Crystal structures of two palladacycles from the C–H activation of 2-(Thiophen-2-yl)pyridine

Crystal structures of two palladacycles from the C–H activation of 2-(Thiophen-2-yl)pyridine
Crystal structures of two palladacycles from the C–H activation of 2-(Thiophen-2-yl)pyridine
A C,N-bound palladacycle dimer has been synthesised by reaction of 2-(thiophen-2-yl)pyridine, LH, with palladium acetate in acetic acid. Characterisation by single crystal X-ray diffraction showed the palladacycle dimer, [(L)Pd(OAc)](2), to crystallise in the monoclinic space group P2(1)/n with cell parameters a = 9.5853(1) , b = 19.1332(3) , c = 12.3889(2) , beta = 103.732(1)A degrees. Reaction of [(L)Pd(OAc)](2) with triphenylphosphine afforded a trans-substituted monomeric complex, [(L)PdPPh(3)(OAc)] which was also analysed using single crystal X-ray diffraction. [(L)PdPPh(3)(OAc)] crystallises in the monoclinic space group P2(1)/c with cell parameters a = 9.4839(1) , b = 11.0427(2) , c = 26.0770(4) , beta = 95.022(1)A degrees.
crystal structure, palladacycle, 2-(thiophen-2-yl) pyridine, dimer, triphenylphosphine
1074-1542
523-527
Callear, Samantha K.
5af7f651-0ff0-4163-80b3-34996d62022a
Spencer, John
a3cf55cd-a4c7-4af6-b16c-96c8fb8c4cf4
Patel, Hiren
73682df0-69ba-44c9-88b2-5c19f7f23677
Deadman, John J.
6ec79e7a-322c-4d5c-99fd-25480e53ec05
Hursthouse, Michael B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Callear, Samantha K.
5af7f651-0ff0-4163-80b3-34996d62022a
Spencer, John
a3cf55cd-a4c7-4af6-b16c-96c8fb8c4cf4
Patel, Hiren
73682df0-69ba-44c9-88b2-5c19f7f23677
Deadman, John J.
6ec79e7a-322c-4d5c-99fd-25480e53ec05
Hursthouse, Michael B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da

Callear, Samantha K., Spencer, John, Patel, Hiren, Deadman, John J. and Hursthouse, Michael B. (2011) Crystal structures of two palladacycles from the C–H activation of 2-(Thiophen-2-yl)pyridine. Journal of Chemical Crystallography, 41 (4), 523-527. (doi:10.1007/s10870-010-9913-5).

Record type: Article

Abstract

A C,N-bound palladacycle dimer has been synthesised by reaction of 2-(thiophen-2-yl)pyridine, LH, with palladium acetate in acetic acid. Characterisation by single crystal X-ray diffraction showed the palladacycle dimer, [(L)Pd(OAc)](2), to crystallise in the monoclinic space group P2(1)/n with cell parameters a = 9.5853(1) , b = 19.1332(3) , c = 12.3889(2) , beta = 103.732(1)A degrees. Reaction of [(L)Pd(OAc)](2) with triphenylphosphine afforded a trans-substituted monomeric complex, [(L)PdPPh(3)(OAc)] which was also analysed using single crystal X-ray diffraction. [(L)PdPPh(3)(OAc)] crystallises in the monoclinic space group P2(1)/c with cell parameters a = 9.4839(1) , b = 11.0427(2) , c = 26.0770(4) , beta = 95.022(1)A degrees.

This record has no associated files available for download.

More information

Published date: April 2011
Keywords: crystal structure, palladacycle, 2-(thiophen-2-yl) pyridine, dimer, triphenylphosphine
Organisations: Organic Chemistry: Synthesis, Catalysis and Flow

Identifiers

Local EPrints ID: 347412
URI: http://eprints.soton.ac.uk/id/eprint/347412
ISSN: 1074-1542
PURE UUID: bca5c5c0-7deb-4a42-91ba-4efc80c5d4d2

Catalogue record

Date deposited: 04 Feb 2013 14:50
Last modified: 14 Mar 2024 12:47

Export record

Altmetrics

Contributors

Author: Samantha K. Callear
Author: John Spencer
Author: Hiren Patel
Author: John J. Deadman

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×