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{μ-1,2-Bis[bis­(4-meth­oxy­phen­yl)phosphan­yl]-1,2-diethyl­hydrazine-κ(2) P:P′}bis­[chloridogold(I)] tetra­hydro­furan disolvate

The title compound, [Au(2)Cl(2)(C(32)H(38)N(2)O(4)P(2))]·2C(4)H(8)O, is formed from a bidentate phosphine ligand complexed to two linear gold(I) nuclei [P—Au—Cl = 175.98 (3)°]. The nuclei are 3.1414 (2) Å apart. The mol­ecule exhibits a twofold symmetry axis. Stacks of the compound are formed throug...

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Detalles Bibliográficos
Autores principales: Kriel, Frederik H., Fernandes, Manuel A., Coates, Judy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201433/
https://www.ncbi.nlm.nih.gov/pubmed/22064923
http://dx.doi.org/10.1107/S1600536811038499
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author Kriel, Frederik H.
Fernandes, Manuel A.
Coates, Judy
author_facet Kriel, Frederik H.
Fernandes, Manuel A.
Coates, Judy
author_sort Kriel, Frederik H.
collection PubMed
description The title compound, [Au(2)Cl(2)(C(32)H(38)N(2)O(4)P(2))]·2C(4)H(8)O, is formed from a bidentate phosphine ligand complexed to two linear gold(I) nuclei [P—Au—Cl = 175.98 (3)°]. The nuclei are 3.1414 (2) Å apart. The mol­ecule exhibits a twofold symmetry axis. Stacks of the compound are formed through inter­molecular C—H⋯Cl inter­actions, while the tetra­hydro­furan (THF) solvate is further attached to the stacks through weak C—H⋯O hydrogen bonding from the THF O atom to two separate H atoms on the complex.
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spelling pubmed-32014332011-11-06 {μ-1,2-Bis[bis­(4-meth­oxy­phen­yl)phosphan­yl]-1,2-diethyl­hydrazine-κ(2) P:P′}bis­[chloridogold(I)] tetra­hydro­furan disolvate Kriel, Frederik H. Fernandes, Manuel A. Coates, Judy Acta Crystallogr Sect E Struct Rep Online Metal-Organic Papers The title compound, [Au(2)Cl(2)(C(32)H(38)N(2)O(4)P(2))]·2C(4)H(8)O, is formed from a bidentate phosphine ligand complexed to two linear gold(I) nuclei [P—Au—Cl = 175.98 (3)°]. The nuclei are 3.1414 (2) Å apart. The mol­ecule exhibits a twofold symmetry axis. Stacks of the compound are formed through inter­molecular C—H⋯Cl inter­actions, while the tetra­hydro­furan (THF) solvate is further attached to the stacks through weak C—H⋯O hydrogen bonding from the THF O atom to two separate H atoms on the complex. International Union of Crystallography 2011-09-30 /pmc/articles/PMC3201433/ /pubmed/22064923 http://dx.doi.org/10.1107/S1600536811038499 Text en © Kriel et al. 2011 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Metal-Organic Papers
Kriel, Frederik H.
Fernandes, Manuel A.
Coates, Judy
{μ-1,2-Bis[bis­(4-meth­oxy­phen­yl)phosphan­yl]-1,2-diethyl­hydrazine-κ(2) P:P′}bis­[chloridogold(I)] tetra­hydro­furan disolvate
title {μ-1,2-Bis[bis­(4-meth­oxy­phen­yl)phosphan­yl]-1,2-diethyl­hydrazine-κ(2) P:P′}bis­[chloridogold(I)] tetra­hydro­furan disolvate
title_full {μ-1,2-Bis[bis­(4-meth­oxy­phen­yl)phosphan­yl]-1,2-diethyl­hydrazine-κ(2) P:P′}bis­[chloridogold(I)] tetra­hydro­furan disolvate
title_fullStr {μ-1,2-Bis[bis­(4-meth­oxy­phen­yl)phosphan­yl]-1,2-diethyl­hydrazine-κ(2) P:P′}bis­[chloridogold(I)] tetra­hydro­furan disolvate
title_full_unstemmed {μ-1,2-Bis[bis­(4-meth­oxy­phen­yl)phosphan­yl]-1,2-diethyl­hydrazine-κ(2) P:P′}bis­[chloridogold(I)] tetra­hydro­furan disolvate
title_short {μ-1,2-Bis[bis­(4-meth­oxy­phen­yl)phosphan­yl]-1,2-diethyl­hydrazine-κ(2) P:P′}bis­[chloridogold(I)] tetra­hydro­furan disolvate
title_sort {μ-1,2-bis[bis­(4-meth­oxy­phen­yl)phosphan­yl]-1,2-diethyl­hydrazine-κ(2) p:p′}bis­[chloridogold(i)] tetra­hydro­furan disolvate
topic Metal-Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201433/
https://www.ncbi.nlm.nih.gov/pubmed/22064923
http://dx.doi.org/10.1107/S1600536811038499
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