<i>trans</i>-1,4-dibromocyclohexane-1,4-dicarboxylic acid

Autores
Echeverría, Gustavo Alberto; Goeta, Andrés Eduardo; Barón, Máximo; Punte, Graciela María del Carmen
Año de publicación
2003
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Molecules of the title compound, C8H10Br2O4, located on symmetry centers, are in a rigid chair conformation, with the COOH and Br substituents axial and equatorial, respectively. The carboxylic acid groups form hydrogen bonds, in a cyclic motif, leading to infinite chains along the b axis.
Facultad de Ciencias Exactas
Materia
Ciencias Exactas
Física
Química
crystallization
fourier transform infrared spectroscopy
halogen compounds
hydrogen bonds
symmetry centers
carboxylic acids
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/3.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/34715
Acceder
id SEDICI_32c6d06296e9414d5b9f6b62623ebe88
oai_identifier_str oai:sedici.unlp.edu.ar:10915/34715
network_acronym_str SEDICI
repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling <i>trans</i>-1,4-dibromocyclohexane-1,4-dicarboxylic acidEcheverría, Gustavo AlbertoGoeta, Andrés EduardoBarón, MáximoPunte, Graciela María del CarmenCiencias ExactasFísicaQuímicacrystallizationfourier transform infrared spectroscopyhalogen compoundshydrogen bondssymmetry centerscarboxylic acidsMolecules of the title compound, C<SUB>8</SUB>H<SUB>10</SUB>Br<SUB>2</SUB>O<SUB>4</SUB>, located on symmetry centers, are in a rigid chair conformation, with the COOH and Br substituents axial and equatorial, respectively. The carboxylic acid groups form hydrogen bonds, in a cyclic motif, leading to infinite chains along the b axis.Facultad de Ciencias Exactas2003info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf959-961http://sedici.unlp.edu.ar/handle/10915/34715enginfo:eu-repo/semantics/altIdentifier/url/http://journals.iucr.org/e/issues/2003/07/00/wn6160/wn6160.pdfinfo:eu-repo/semantics/altIdentifier/issn/1600-5368info:eu-repo/semantics/altIdentifier/doi/10.1107/S160053680301239Xinfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/3.0/Creative Commons Attribution 3.0 Unported (CC BY 3.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T10:57:03Zoai:sedici.unlp.edu.ar:10915/34715Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 10:57:03.281SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv <i>trans</i>-1,4-dibromocyclohexane-1,4-dicarboxylic acid
title <i>trans</i>-1,4-dibromocyclohexane-1,4-dicarboxylic acid
spellingShingle <i>trans</i>-1,4-dibromocyclohexane-1,4-dicarboxylic acid
Echeverría, Gustavo Alberto
Ciencias Exactas
Física
Química
crystallization
fourier transform infrared spectroscopy
halogen compounds
hydrogen bonds
symmetry centers
carboxylic acids
title_short <i>trans</i>-1,4-dibromocyclohexane-1,4-dicarboxylic acid
title_full <i>trans</i>-1,4-dibromocyclohexane-1,4-dicarboxylic acid
title_fullStr <i>trans</i>-1,4-dibromocyclohexane-1,4-dicarboxylic acid
title_full_unstemmed <i>trans</i>-1,4-dibromocyclohexane-1,4-dicarboxylic acid
title_sort <i>trans</i>-1,4-dibromocyclohexane-1,4-dicarboxylic acid
dc.creator.none.fl_str_mv Echeverría, Gustavo Alberto
Goeta, Andrés Eduardo
Barón, Máximo
Punte, Graciela María del Carmen
author Echeverría, Gustavo Alberto
author_facet Echeverría, Gustavo Alberto
Goeta, Andrés Eduardo
Barón, Máximo
Punte, Graciela María del Carmen
author_role author
author2 Goeta, Andrés Eduardo
Barón, Máximo
Punte, Graciela María del Carmen
author2_role author
author
author
dc.subject.none.fl_str_mv Ciencias Exactas
Física
Química
crystallization
fourier transform infrared spectroscopy
halogen compounds
hydrogen bonds
symmetry centers
carboxylic acids
topic Ciencias Exactas
Física
Química
crystallization
fourier transform infrared spectroscopy
halogen compounds
hydrogen bonds
symmetry centers
carboxylic acids
dc.description.none.fl_txt_mv Molecules of the title compound, C<SUB>8</SUB>H<SUB>10</SUB>Br<SUB>2</SUB>O<SUB>4</SUB>, located on symmetry centers, are in a rigid chair conformation, with the COOH and Br substituents axial and equatorial, respectively. The carboxylic acid groups form hydrogen bonds, in a cyclic motif, leading to infinite chains along the b axis.
Facultad de Ciencias Exactas
description Molecules of the title compound, C<SUB>8</SUB>H<SUB>10</SUB>Br<SUB>2</SUB>O<SUB>4</SUB>, located on symmetry centers, are in a rigid chair conformation, with the COOH and Br substituents axial and equatorial, respectively. The carboxylic acid groups form hydrogen bonds, in a cyclic motif, leading to infinite chains along the b axis.
publishDate 2003
dc.date.none.fl_str_mv 2003
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
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://sedici.unlp.edu.ar/handle/10915/34715
url http://sedici.unlp.edu.ar/handle/10915/34715
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://journals.iucr.org/e/issues/2003/07/00/wn6160/wn6160.pdf
info:eu-repo/semantics/altIdentifier/issn/1600-5368
info:eu-repo/semantics/altIdentifier/doi/10.1107/S160053680301239X
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/3.0/
Creative Commons Attribution 3.0 Unported (CC BY 3.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/3.0/
Creative Commons Attribution 3.0 Unported (CC BY 3.0)
dc.format.none.fl_str_mv application/pdf
959-961
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
collection SEDICI (UNLP)
instname_str Universidad Nacional de La Plata
instacron_str UNLP
institution UNLP
repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
repository.mail.fl_str_mv alira@sedici.unlp.edu.ar
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score 13.070432

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