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N-Acryloyl glycinamide
The molecule of the title compound [systematic name: N-(carbamoylmethyl)prop-2-enamide], C(5)H(8)N(2)O(2), which can be radically polymerized to polymers with thermoresponsive behavior in aqueous solution, consists of linked essentially planar acrylamide and amide segments [maximum deviations = 0...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213605/ https://www.ncbi.nlm.nih.gov/pubmed/22091182 http://dx.doi.org/10.1107/S1600536811029758 |
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author | Seuring, Jan Agarwal, Seema Harms, Klaus |
author_facet | Seuring, Jan Agarwal, Seema Harms, Klaus |
author_sort | Seuring, Jan |
collection | PubMed |
description | The molecule of the title compound [systematic name: N-(carbamoylmethyl)prop-2-enamide], C(5)H(8)N(2)O(2), which can be radically polymerized to polymers with thermoresponsive behavior in aqueous solution, consists of linked essentially planar acrylamide and amide segments [maximum deviations = 0.054 (1) and 0.009 (1) Å] with an angle of 81.36 (7)° between their mean planes. In the crystal, N—H⋯O hydrogen bonding leads to an infinite two-dimensional network along (100). |
format | Online Article Text |
id | pubmed-3213605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32136052011-11-16 N-Acryloyl glycinamide Seuring, Jan Agarwal, Seema Harms, Klaus Acta Crystallogr Sect E Struct Rep Online Organic Papers The molecule of the title compound [systematic name: N-(carbamoylmethyl)prop-2-enamide], C(5)H(8)N(2)O(2), which can be radically polymerized to polymers with thermoresponsive behavior in aqueous solution, consists of linked essentially planar acrylamide and amide segments [maximum deviations = 0.054 (1) and 0.009 (1) Å] with an angle of 81.36 (7)° between their mean planes. In the crystal, N—H⋯O hydrogen bonding leads to an infinite two-dimensional network along (100). International Union of Crystallography 2011-07-30 /pmc/articles/PMC3213605/ /pubmed/22091182 http://dx.doi.org/10.1107/S1600536811029758 Text en © Seuring 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 | Organic Papers Seuring, Jan Agarwal, Seema Harms, Klaus N-Acryloyl glycinamide |
title |
N-Acryloyl glycinamide |
title_full |
N-Acryloyl glycinamide |
title_fullStr |
N-Acryloyl glycinamide |
title_full_unstemmed |
N-Acryloyl glycinamide |
title_short |
N-Acryloyl glycinamide |
title_sort | n-acryloyl glycinamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213605/ https://www.ncbi.nlm.nih.gov/pubmed/22091182 http://dx.doi.org/10.1107/S1600536811029758 |
work_keys_str_mv | AT seuringjan nacryloylglycinamide AT agarwalseema nacryloylglycinamide AT harmsklaus nacryloylglycinamide |