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(m-Phenyl­enedimethyl­ene)diammonium p-nitro­phenyl­phosphate perchlorate

The title compound, C(8)H(14)N(2) (2+)·C(12)H(8)N(2)O(8)P(−)·ClO(4) (−), was formed by the reaction of α,α-bis-m-xylenediamine and sodium bis-p-nitro­phenyl­phosphate in the presence of Zn(ClO(4))·6H(2)O in methanol solution. The two amine groups of the m-xylenediammonium ion are each protonated and...

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Autores principales: Tesema, Yohannes T., Yisgedu, Teshome B., Butcher, Ray J., Gultneh, Yilma, Ahvazi, Bijan
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960385/
https://www.ncbi.nlm.nih.gov/pubmed/21201408
http://dx.doi.org/10.1107/S1600536807068638
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author Tesema, Yohannes T.
Yisgedu, Teshome B.
Butcher, Ray J.
Gultneh, Yilma
Ahvazi, Bijan
author_facet Tesema, Yohannes T.
Yisgedu, Teshome B.
Butcher, Ray J.
Gultneh, Yilma
Ahvazi, Bijan
author_sort Tesema, Yohannes T.
collection PubMed
description The title compound, C(8)H(14)N(2) (2+)·C(12)H(8)N(2)O(8)P(−)·ClO(4) (−), was formed by the reaction of α,α-bis-m-xylenediamine and sodium bis-p-nitro­phenyl­phosphate in the presence of Zn(ClO(4))·6H(2)O in methanol solution. The two amine groups of the m-xylenediammonium ion are each protonated and each hydrogen-bonded to two O atoms of the phosphate anion, which acts as a 1,3-bridge. The ammonium groups are arranged matched face to face and each pair is doubly bridged by two perchlorate ions through hydrogen bonding. In addition, there are also weak C—H⋯O inter­actions. Both the N—H⋯O and C—H⋯O inter­actions are contained in a channel down the a axis. The perchlorate oxygen atoms are disordered over two positions with site occupancy factors of ca 0.7 and 0.3.
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spelling pubmed-29603852010-12-30 (m-Phenyl­enedimethyl­ene)diammonium p-nitro­phenyl­phosphate perchlorate Tesema, Yohannes T. Yisgedu, Teshome B. Butcher, Ray J. Gultneh, Yilma Ahvazi, Bijan Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(8)H(14)N(2) (2+)·C(12)H(8)N(2)O(8)P(−)·ClO(4) (−), was formed by the reaction of α,α-bis-m-xylenediamine and sodium bis-p-nitro­phenyl­phosphate in the presence of Zn(ClO(4))·6H(2)O in methanol solution. The two amine groups of the m-xylenediammonium ion are each protonated and each hydrogen-bonded to two O atoms of the phosphate anion, which acts as a 1,3-bridge. The ammonium groups are arranged matched face to face and each pair is doubly bridged by two perchlorate ions through hydrogen bonding. In addition, there are also weak C—H⋯O inter­actions. Both the N—H⋯O and C—H⋯O inter­actions are contained in a channel down the a axis. The perchlorate oxygen atoms are disordered over two positions with site occupancy factors of ca 0.7 and 0.3. International Union of Crystallography 2008-01-04 /pmc/articles/PMC2960385/ /pubmed/21201408 http://dx.doi.org/10.1107/S1600536807068638 Text en © Tesema et al. 2008 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 Organic Papers
Tesema, Yohannes T.
Yisgedu, Teshome B.
Butcher, Ray J.
Gultneh, Yilma
Ahvazi, Bijan
(m-Phenyl­enedimethyl­ene)diammonium p-nitro­phenyl­phosphate perchlorate
title (m-Phenyl­enedimethyl­ene)diammonium p-nitro­phenyl­phosphate perchlorate
title_full (m-Phenyl­enedimethyl­ene)diammonium p-nitro­phenyl­phosphate perchlorate
title_fullStr (m-Phenyl­enedimethyl­ene)diammonium p-nitro­phenyl­phosphate perchlorate
title_full_unstemmed (m-Phenyl­enedimethyl­ene)diammonium p-nitro­phenyl­phosphate perchlorate
title_short (m-Phenyl­enedimethyl­ene)diammonium p-nitro­phenyl­phosphate perchlorate
title_sort (m-phenyl­enedimethyl­ene)diammonium p-nitro­phenyl­phosphate perchlorate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960385/
https://www.ncbi.nlm.nih.gov/pubmed/21201408
http://dx.doi.org/10.1107/S1600536807068638
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