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5,5,7,12,12,14-Hexamethyl-1,8-bis­(4-nitro­benz­yl)-1,4,8,11-tetra­aza­cyclo­tetra­deca­ne

The asymmetric unit of the title compound, C(30)H(46)N(6)O(4), contains one half-mol­ecule. The C(benzene)—C(CH(2))—N—C(—Me) torsion angle is −79.89 (13)° suggesting a synclinal orientation of the nitro­benzene ring with respect to the macrocycle. The conformation of the macrocycle is stabilized by...

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Detalles Bibliográficos
Autores principales: Gayathri, K., Sathya, S., Usha, G., Ramanjaneya Reddy, G., Balasubramanian, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914089/
https://www.ncbi.nlm.nih.gov/pubmed/24526993
http://dx.doi.org/10.1107/S1600536813031164
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author Gayathri, K.
Sathya, S.
Usha, G.
Ramanjaneya Reddy, G.
Balasubramanian, S.
author_facet Gayathri, K.
Sathya, S.
Usha, G.
Ramanjaneya Reddy, G.
Balasubramanian, S.
author_sort Gayathri, K.
collection PubMed
description The asymmetric unit of the title compound, C(30)H(46)N(6)O(4), contains one half-mol­ecule. The C(benzene)—C(CH(2))—N—C(—Me) torsion angle is −79.89 (13)° suggesting a synclinal orientation of the nitro­benzene ring with respect to the macrocycle. The conformation of the macrocycle is stabilized by intra­molecular N—H⋯N hydrogen bonds.
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spelling pubmed-39140892014-02-13 5,5,7,12,12,14-Hexamethyl-1,8-bis­(4-nitro­benz­yl)-1,4,8,11-tetra­aza­cyclo­tetra­deca­ne Gayathri, K. Sathya, S. Usha, G. Ramanjaneya Reddy, G. Balasubramanian, S. Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(30)H(46)N(6)O(4), contains one half-mol­ecule. The C(benzene)—C(CH(2))—N—C(—Me) torsion angle is −79.89 (13)° suggesting a synclinal orientation of the nitro­benzene ring with respect to the macrocycle. The conformation of the macrocycle is stabilized by intra­molecular N—H⋯N hydrogen bonds. International Union of Crystallography 2013-12-14 /pmc/articles/PMC3914089/ /pubmed/24526993 http://dx.doi.org/10.1107/S1600536813031164 Text en © Gayathri et al. 2014 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
Gayathri, K.
Sathya, S.
Usha, G.
Ramanjaneya Reddy, G.
Balasubramanian, S.
5,5,7,12,12,14-Hexamethyl-1,8-bis­(4-nitro­benz­yl)-1,4,8,11-tetra­aza­cyclo­tetra­deca­ne
title 5,5,7,12,12,14-Hexamethyl-1,8-bis­(4-nitro­benz­yl)-1,4,8,11-tetra­aza­cyclo­tetra­deca­ne
title_full 5,5,7,12,12,14-Hexamethyl-1,8-bis­(4-nitro­benz­yl)-1,4,8,11-tetra­aza­cyclo­tetra­deca­ne
title_fullStr 5,5,7,12,12,14-Hexamethyl-1,8-bis­(4-nitro­benz­yl)-1,4,8,11-tetra­aza­cyclo­tetra­deca­ne
title_full_unstemmed 5,5,7,12,12,14-Hexamethyl-1,8-bis­(4-nitro­benz­yl)-1,4,8,11-tetra­aza­cyclo­tetra­deca­ne
title_short 5,5,7,12,12,14-Hexamethyl-1,8-bis­(4-nitro­benz­yl)-1,4,8,11-tetra­aza­cyclo­tetra­deca­ne
title_sort 5,5,7,12,12,14-hexamethyl-1,8-bis­(4-nitro­benz­yl)-1,4,8,11-tetra­aza­cyclo­tetra­deca­ne
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914089/
https://www.ncbi.nlm.nih.gov/pubmed/24526993
http://dx.doi.org/10.1107/S1600536813031164
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