Tetrapyridinium μ-oxido-di-μ-sulfato-bis[chloridodioxidomolybdate(VI)]
The title salt, (C5H6N)4[Mo2Cl2O5(SO4)2], comprises four pyridinium cations for each [(MoClO2)2(μ-O)(μ-SO4)2]4− anionic unit. The asymmetric unit consists of three aggregates of the empirical formula. The tetraanionic bimetallic molybdenum(VI) cluster is unpre...
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International Union of Crystallography
2010-08-01
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Series: | Acta Crystallographica Section E |
Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536810028254 |
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doaj-cc5cbeb529ae4b8bb2dfbb6b310ba97e2020-11-24T21:32:46ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682010-08-01668m1005m100610.1107/S1600536810028254Tetrapyridinium μ-oxido-di-μ-sulfato-bis[chloridodioxidomolybdate(VI)]José A. FernandesAna C. GomesSónia FigueiredoSandra GagoAndré D. LopesMartyn PillingerPaulo J. A. Ribeiro-ClaroIsabel S. GonçalvesFilipe A. Almeida PazThe title salt, (C5H6N)4[Mo2Cl2O5(SO4)2], comprises four pyridinium cations for each [(MoClO2)2(μ-O)(μ-SO4)2]4− anionic unit. The asymmetric unit consists of three aggregates of the empirical formula. The tetraanionic bimetallic molybdenum(VI) cluster is unprecedented and contains two sulfate and one oxide bridges. This structure constitutes the first example of a non-polymeric compound with terminal oxide, sulfate and halide ligands bonded to the same metal. The hydrogen bonds connecting the pyridinium cations to the molybdenum clusters are diverse, varying from strong and directional interactions to bifurcated bonds with a subsequent loss of directionality. http://scripts.iucr.org/cgi-bin/paper?S1600536810028254 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
José A. Fernandes Ana C. Gomes Sónia Figueiredo Sandra Gago André D. Lopes Martyn Pillinger Paulo J. A. Ribeiro-Claro Isabel S. Gonçalves Filipe A. Almeida Paz |
spellingShingle |
José A. Fernandes Ana C. Gomes Sónia Figueiredo Sandra Gago André D. Lopes Martyn Pillinger Paulo J. A. Ribeiro-Claro Isabel S. Gonçalves Filipe A. Almeida Paz Tetrapyridinium μ-oxido-di-μ-sulfato-bis[chloridodioxidomolybdate(VI)] Acta Crystallographica Section E |
author_facet |
José A. Fernandes Ana C. Gomes Sónia Figueiredo Sandra Gago André D. Lopes Martyn Pillinger Paulo J. A. Ribeiro-Claro Isabel S. Gonçalves Filipe A. Almeida Paz |
author_sort |
José A. Fernandes |
title |
Tetrapyridinium μ-oxido-di-μ-sulfato-bis[chloridodioxidomolybdate(VI)] |
title_short |
Tetrapyridinium μ-oxido-di-μ-sulfato-bis[chloridodioxidomolybdate(VI)] |
title_full |
Tetrapyridinium μ-oxido-di-μ-sulfato-bis[chloridodioxidomolybdate(VI)] |
title_fullStr |
Tetrapyridinium μ-oxido-di-μ-sulfato-bis[chloridodioxidomolybdate(VI)] |
title_full_unstemmed |
Tetrapyridinium μ-oxido-di-μ-sulfato-bis[chloridodioxidomolybdate(VI)] |
title_sort |
tetrapyridinium μ-oxido-di-μ-sulfato-bis[chloridodioxidomolybdate(vi)] |
publisher |
International Union of Crystallography |
series |
Acta Crystallographica Section E |
issn |
1600-5368 |
publishDate |
2010-08-01 |
description |
The title salt, (C5H6N)4[Mo2Cl2O5(SO4)2], comprises four pyridinium cations for each [(MoClO2)2(μ-O)(μ-SO4)2]4− anionic unit. The asymmetric unit consists of three aggregates of the empirical formula. The tetraanionic bimetallic molybdenum(VI) cluster is unprecedented and contains two sulfate and one oxide bridges. This structure constitutes the first example of a non-polymeric compound with terminal oxide, sulfate and halide ligands bonded to the same metal. The hydrogen bonds connecting the pyridinium cations to the molybdenum clusters are diverse, varying from strong and directional interactions to bifurcated bonds with a subsequent loss of directionality. |
url |
http://scripts.iucr.org/cgi-bin/paper?S1600536810028254 |
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