rac-12-Selena-13,14-di­aza­tri­cyclo­[9.3.0.0(2,4)]tetra­deca-11,13-diene

The centrosymmetric crystal structure of the title compound, C(11)H(16)N(2)Se, is built up from alternating strands of (R,R)- and (S,S)-enanti­omers. These strands, which propagate along the c-axis direction, are composed of homochiral mol­ecules related to each other by twofold screw axes. The shap...

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Detalles Bibliográficos
Autores principales: Detert, Heiner, Schollmeyer, Dieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2020
Materias:
Data Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462238/
https://www.ncbi.nlm.nih.gov/pubmed/36338511
http://dx.doi.org/10.1107/S2414314620010810
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author Detert, Heiner
Schollmeyer, Dieter
author_facet Detert, Heiner
Schollmeyer, Dieter
author_sort Detert, Heiner
collection PubMed
description The centrosymmetric crystal structure of the title compound, C(11)H(16)N(2)Se, is built up from alternating strands of (R,R)- and (S,S)-enanti­omers. These strands, which propagate along the c-axis direction, are composed of homochiral mol­ecules related to each other by twofold screw axes. The shape of the mol­ecule is an almost planar unit around the selena­diazole ring with a hexa­methyl­ene chain as an arched handle. [Image: see text]
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spelling pubmed-94622382022-11-04 rac-12-Selena-13,14-di­aza­tri­cyclo­[9.3.0.0(2,4)]tetra­deca-11,13-diene Detert, Heiner Schollmeyer, Dieter IUCrdata Data Reports The centrosymmetric crystal structure of the title compound, C(11)H(16)N(2)Se, is built up from alternating strands of (R,R)- and (S,S)-enanti­omers. These strands, which propagate along the c-axis direction, are composed of homochiral mol­ecules related to each other by twofold screw axes. The shape of the mol­ecule is an almost planar unit around the selena­diazole ring with a hexa­methyl­ene chain as an arched handle. [Image: see text] International Union of Crystallography 2020-08-11 /pmc/articles/PMC9462238/ /pubmed/36338511 http://dx.doi.org/10.1107/S2414314620010810 Text en © Detert and Schollmeyer 2020 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Data Reports
Detert, Heiner
Schollmeyer, Dieter
rac-12-Selena-13,14-di­aza­tri­cyclo­[9.3.0.0(2,4)]tetra­deca-11,13-diene
title rac-12-Selena-13,14-di­aza­tri­cyclo­[9.3.0.0(2,4)]tetra­deca-11,13-diene
title_full rac-12-Selena-13,14-di­aza­tri­cyclo­[9.3.0.0(2,4)]tetra­deca-11,13-diene
title_fullStr rac-12-Selena-13,14-di­aza­tri­cyclo­[9.3.0.0(2,4)]tetra­deca-11,13-diene
title_full_unstemmed rac-12-Selena-13,14-di­aza­tri­cyclo­[9.3.0.0(2,4)]tetra­deca-11,13-diene
title_short rac-12-Selena-13,14-di­aza­tri­cyclo­[9.3.0.0(2,4)]tetra­deca-11,13-diene
title_sort rac-12-selena-13,14-di­aza­tri­cyclo­[9.3.0.0(2,4)]tetra­deca-11,13-diene
topic Data Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462238/
https://www.ncbi.nlm.nih.gov/pubmed/36338511
http://dx.doi.org/10.1107/S2414314620010810
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