Cytenamide–formic acid (1/1)

In the crystal structure of the title compound [systematic name: 5H-dibenzo[a,d]cyclo­hepta­triene-5-carboxamide–meth­anoic acid (1/1)], C(16)H(13)NO·CH(2)O(2), the cytenamide and solvent mol­ecules form a hydrogen-bonded R (2) (2)(8) dimer motif, which is further connected to form a centrosymmetric...

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Detalles Bibliográficos
Autores principales: Johnston, Andrea, Florence, Alastair J., Miller, Gary J., Kennedy, Alan R., Bedford, Colin T.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962013/
https://www.ncbi.nlm.nih.gov/pubmed/21203100
http://dx.doi.org/10.1107/S1600536808019181
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author Johnston, Andrea
Florence, Alastair J.
Miller, Gary J.
Kennedy, Alan R.
Bedford, Colin T.
author_facet Johnston, Andrea
Florence, Alastair J.
Miller, Gary J.
Kennedy, Alan R.
Bedford, Colin T.
author_sort Johnston, Andrea
collection PubMed
description In the crystal structure of the title compound [systematic name: 5H-dibenzo[a,d]cyclo­hepta­triene-5-carboxamide–meth­anoic acid (1/1)], C(16)H(13)NO·CH(2)O(2), the cytenamide and solvent mol­ecules form a hydrogen-bonded R (2) (2)(8) dimer motif, which is further connected to form a centrosymmetric double-motif arrangement. The asymmetric unit contains two formula units.
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spelling pubmed-29620132010-12-30 Cytenamide–formic acid (1/1) Johnston, Andrea Florence, Alastair J. Miller, Gary J. Kennedy, Alan R. Bedford, Colin T. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound [systematic name: 5H-dibenzo[a,d]cyclo­hepta­triene-5-carboxamide–meth­anoic acid (1/1)], C(16)H(13)NO·CH(2)O(2), the cytenamide and solvent mol­ecules form a hydrogen-bonded R (2) (2)(8) dimer motif, which is further connected to form a centrosymmetric double-motif arrangement. The asymmetric unit contains two formula units. International Union of Crystallography 2008-07-05 /pmc/articles/PMC2962013/ /pubmed/21203100 http://dx.doi.org/10.1107/S1600536808019181 Text en © Johnston 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
Johnston, Andrea
Florence, Alastair J.
Miller, Gary J.
Kennedy, Alan R.
Bedford, Colin T.
Cytenamide–formic acid (1/1)
title Cytenamide–formic acid (1/1)
title_full Cytenamide–formic acid (1/1)
title_fullStr Cytenamide–formic acid (1/1)
title_full_unstemmed Cytenamide–formic acid (1/1)
title_short Cytenamide–formic acid (1/1)
title_sort cytenamide–formic acid (1/1)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962013/
https://www.ncbi.nlm.nih.gov/pubmed/21203100
http://dx.doi.org/10.1107/S1600536808019181
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AT florencealastairj cytenamideformicacid11
AT millergaryj cytenamideformicacid11
AT kennedyalanr cytenamideformicacid11
AT bedfordcolint cytenamideformicacid11

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