Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Seuring, Jan, Agarwal, Seema, Harms, Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
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
_version_ 1782216161276985344
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