2,4-Dinitrophenyl phenyl sulfone

Autores
Ellena, J.; Punte, G.; Nudelman, N.S.
Año de publicación
1996
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The crystal structure of the title compound, C12H8-N2O6S, has been determined by single-crystal X-ray diffraction. The compound crystallizes in the noncentrosymmetric P21 space group. The substituted aromatic ring has a slightly deformed boat conformation. The ο-NO2 and p-NO2 groups are twisted out of the plane of the phenyl ring. The unsubstituted aromatic ring is planar and the dihedral angle between the mean plane of the rings is 71.1 (2)○. Short C - H⋯O intermolecular contacts stabilize the three-dimensional structure.
Fil:Ellena, J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fuente
Acta Crystallogr Sect C Cryst Struct Commun 1996;52(11):2929-2932
Materia
Bond strength (chemical)
Chemical bonds
Conformations
Crystal structure
Molecular structure
Single crystals
Sulfur compounds
X ray crystallography
Boat conformations
Phenyl ring
Aromatic compounds
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/2.5/ar
Repositorio
Biblioteca Digital (UBA-FCEN)
Institución
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
OAI Identificador
paperaa:paper_01082701_v52_n11_p2929_Ellena
Acceder
id BDUBAFCEN_96dd491cca89b4d8b89763b76c8b94d1
oai_identifier_str paperaa:paper_01082701_v52_n11_p2929_Ellena
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling 2,4-Dinitrophenyl phenyl sulfoneEllena, J.Punte, G.Nudelman, N.S.Bond strength (chemical)Chemical bondsConformationsCrystal structureMolecular structureSingle crystalsSulfur compoundsX ray crystallographyBoat conformationsPhenyl ringAromatic compoundsThe crystal structure of the title compound, C12H8-N2O6S, has been determined by single-crystal X-ray diffraction. The compound crystallizes in the noncentrosymmetric P21 space group. The substituted aromatic ring has a slightly deformed boat conformation. The ο-NO2 and p-NO2 groups are twisted out of the plane of the phenyl ring. The unsubstituted aromatic ring is planar and the dihedral angle between the mean plane of the rings is 71.1 (2)○. Short C - H⋯O intermolecular contacts stabilize the three-dimensional structure.Fil:Ellena, J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.1996info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12110/paper_01082701_v52_n11_p2929_EllenaActa Crystallogr Sect C Cryst Struct Commun 1996;52(11):2929-2932reponame:Biblioteca Digital (UBA-FCEN)instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesinstacron:UBA-FCENenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/2.5/ar2025-10-16T09:30:07Zpaperaa:paper_01082701_v52_n11_p2929_EllenaInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-10-16 09:30:08.356Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv 2,4-Dinitrophenyl phenyl sulfone
title 2,4-Dinitrophenyl phenyl sulfone
spellingShingle 2,4-Dinitrophenyl phenyl sulfone
Ellena, J.
Bond strength (chemical)
Chemical bonds
Conformations
Crystal structure
Molecular structure
Single crystals
Sulfur compounds
X ray crystallography
Boat conformations
Phenyl ring
Aromatic compounds
title_short 2,4-Dinitrophenyl phenyl sulfone
title_full 2,4-Dinitrophenyl phenyl sulfone
title_fullStr 2,4-Dinitrophenyl phenyl sulfone
title_full_unstemmed 2,4-Dinitrophenyl phenyl sulfone
title_sort 2,4-Dinitrophenyl phenyl sulfone
dc.creator.none.fl_str_mv Ellena, J.
Punte, G.
Nudelman, N.S.
author Ellena, J.
author_facet Ellena, J.
Punte, G.
Nudelman, N.S.
author_role author
author2 Punte, G.
Nudelman, N.S.
author2_role author
author
dc.subject.none.fl_str_mv Bond strength (chemical)
Chemical bonds
Conformations
Crystal structure
Molecular structure
Single crystals
Sulfur compounds
X ray crystallography
Boat conformations
Phenyl ring
Aromatic compounds
topic Bond strength (chemical)
Chemical bonds
Conformations
Crystal structure
Molecular structure
Single crystals
Sulfur compounds
X ray crystallography
Boat conformations
Phenyl ring
Aromatic compounds
dc.description.none.fl_txt_mv The crystal structure of the title compound, C12H8-N2O6S, has been determined by single-crystal X-ray diffraction. The compound crystallizes in the noncentrosymmetric P21 space group. The substituted aromatic ring has a slightly deformed boat conformation. The ο-NO2 and p-NO2 groups are twisted out of the plane of the phenyl ring. The unsubstituted aromatic ring is planar and the dihedral angle between the mean plane of the rings is 71.1 (2)○. Short C - H⋯O intermolecular contacts stabilize the three-dimensional structure.
Fil:Ellena, J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
description The crystal structure of the title compound, C12H8-N2O6S, has been determined by single-crystal X-ray diffraction. The compound crystallizes in the noncentrosymmetric P21 space group. The substituted aromatic ring has a slightly deformed boat conformation. The ο-NO2 and p-NO2 groups are twisted out of the plane of the phenyl ring. The unsubstituted aromatic ring is planar and the dihedral angle between the mean plane of the rings is 71.1 (2)○. Short C - H⋯O intermolecular contacts stabilize the three-dimensional structure.
publishDate 1996
dc.date.none.fl_str_mv 1996
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/20.500.12110/paper_01082701_v52_n11_p2929_Ellena
url http://hdl.handle.net/20.500.12110/paper_01082701_v52_n11_p2929_Ellena
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/2.5/ar
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/2.5/ar
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv Acta Crystallogr Sect C Cryst Struct Commun 1996;52(11):2929-2932
reponame:Biblioteca Digital (UBA-FCEN)
instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
reponame_str Biblioteca Digital (UBA-FCEN)
collection Biblioteca Digital (UBA-FCEN)
instname_str Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron_str UBA-FCEN
institution UBA-FCEN
repository.name.fl_str_mv Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
repository.mail.fl_str_mv ana@bl.fcen.uba.ar
_version_ 1846142845673537536
score 12.712165

Publicaciones similares