Hydrogen bonded networks in N–alkyl substituted thiourea platinum (II) oxocarbodianion and carboxylate salts
Hydrogen bonded networks in N–alkyl substituted thiourea platinum (II) oxocarbodianion and carboxylate salts
Crystal structures of ten homoleptic platinum (II) complexes with N-methylthiourea, N,N-dimethylthiourea and 1-methyl-1H-imidazole-2(3H)-thione ligands and squarate, croconate, rhodizonate, terephthalic acid monocarboxylate and 1,4-naphthalene dicarboxylic acid monocarboxylate were determined by X-ray diffraction. The coordinated ligands display hydrogen bonding interactions with the counter anions, leading to the formation of a variety of different hydrogen bonded networks. The thiourea groups adopt different conformations around the metal centre, with a 1,2-alternate arrangement most frequently encountered. Discrete hydrogen bonds are the dominant interactions as a result of the disposition of the alkyl groups preventing the DDAA contacts usually displayed by thiourea ligands and carboxylates.
1180-1190
Fisher, Matthew G.
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Gale, Philip A.
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Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Quesada, Roberto
c7db6299-4eb5-490d-9e6b-be4b9fbc8ca9
2008
Fisher, Matthew G.
d8ab576e-841b-486a-864f-24167a4dd8de
Gale, Philip A.
c840b7e9-6847-4843-91af-fa0f8563d943
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Quesada, Roberto
c7db6299-4eb5-490d-9e6b-be4b9fbc8ca9
Fisher, Matthew G., Gale, Philip A., Light, Mark E. and Quesada, Roberto
(2008)
Hydrogen bonded networks in N–alkyl substituted thiourea platinum (II) oxocarbodianion and carboxylate salts.
CrystEngComm, 10 (9), .
(doi:10.1039/b803260b).
Abstract
Crystal structures of ten homoleptic platinum (II) complexes with N-methylthiourea, N,N-dimethylthiourea and 1-methyl-1H-imidazole-2(3H)-thione ligands and squarate, croconate, rhodizonate, terephthalic acid monocarboxylate and 1,4-naphthalene dicarboxylic acid monocarboxylate were determined by X-ray diffraction. The coordinated ligands display hydrogen bonding interactions with the counter anions, leading to the formation of a variety of different hydrogen bonded networks. The thiourea groups adopt different conformations around the metal centre, with a 1,2-alternate arrangement most frequently encountered. Discrete hydrogen bonds are the dominant interactions as a result of the disposition of the alkyl groups preventing the DDAA contacts usually displayed by thiourea ligands and carboxylates.
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Published date: 2008
Organisations:
Chemistry
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Local EPrints ID: 67665
URI: http://eprints.soton.ac.uk/id/eprint/67665
ISSN: 1466-8033
PURE UUID: 3989eef7-d499-4cd0-807d-4e23a3215a01
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Date deposited: 02 Sep 2009
Last modified: 14 Mar 2024 02:44
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Author:
Matthew G. Fisher
Author:
Philip A. Gale
Author:
Roberto Quesada
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