2′-Amino-3,6-dihydroxyxanthene-9-spiro-1′-isoindolin-3′-one monohydrate

The title compound, C(20)H(14)N(2)O(4)·H(2)O, was synthesized by the reaction of fluorescein and hydrazine hydrate in ethanol. In the crystal structure, the organic mol­ecules are linked into extended two-dimensional networks by inter­molecular hydrogen bonding. Additional face-to-face π–π stacking...

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Detalles Bibliográficos
Autores principales: Wang, Dong-Xiang, Wu, Gen-Hua
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960396/
https://www.ncbi.nlm.nih.gov/pubmed/21201425
http://dx.doi.org/10.1107/S1600536808000032
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author Wang, Dong-Xiang
Wu, Gen-Hua
author_facet Wang, Dong-Xiang
Wu, Gen-Hua
author_sort Wang, Dong-Xiang
collection PubMed
description The title compound, C(20)H(14)N(2)O(4)·H(2)O, was synthesized by the reaction of fluorescein and hydrazine hydrate in ethanol. In the crystal structure, the organic mol­ecules are linked into extended two-dimensional networks by inter­molecular hydrogen bonding. Additional face-to-face π–π stacking inter­actions between the phenolic benzene rings in two adjacent mol­ecules [centroid-to-centroid separation = 3.773 (3) Å] link the mol­ecules into a three-dimensional framework.
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spelling pubmed-29603962010-12-30 2′-Amino-3,6-dihydroxyxanthene-9-spiro-1′-isoindolin-3′-one monohydrate Wang, Dong-Xiang Wu, Gen-Hua Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(20)H(14)N(2)O(4)·H(2)O, was synthesized by the reaction of fluorescein and hydrazine hydrate in ethanol. In the crystal structure, the organic mol­ecules are linked into extended two-dimensional networks by inter­molecular hydrogen bonding. Additional face-to-face π–π stacking inter­actions between the phenolic benzene rings in two adjacent mol­ecules [centroid-to-centroid separation = 3.773 (3) Å] link the mol­ecules into a three-dimensional framework. International Union of Crystallography 2008-01-09 /pmc/articles/PMC2960396/ /pubmed/21201425 http://dx.doi.org/10.1107/S1600536808000032 Text en © Wang and Wu 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
Wang, Dong-Xiang
Wu, Gen-Hua
2′-Amino-3,6-dihydroxyxanthene-9-spiro-1′-isoindolin-3′-one monohydrate
title 2′-Amino-3,6-dihydroxyxanthene-9-spiro-1′-isoindolin-3′-one monohydrate
title_full 2′-Amino-3,6-dihydroxyxanthene-9-spiro-1′-isoindolin-3′-one monohydrate
title_fullStr 2′-Amino-3,6-dihydroxyxanthene-9-spiro-1′-isoindolin-3′-one monohydrate
title_full_unstemmed 2′-Amino-3,6-dihydroxyxanthene-9-spiro-1′-isoindolin-3′-one monohydrate
title_short 2′-Amino-3,6-dihydroxyxanthene-9-spiro-1′-isoindolin-3′-one monohydrate
title_sort 2′-amino-3,6-dihydroxyxanthene-9-spiro-1′-isoindolin-3′-one monohydrate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960396/
https://www.ncbi.nlm.nih.gov/pubmed/21201425
http://dx.doi.org/10.1107/S1600536808000032
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AT wugenhua 2amino36dihydroxyxanthene9spiro1isoindolin3onemonohydrate

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