Mostrar el registro sencillo del ítem

dc.contributor.author
Freire Espeleta, Eleonora  
dc.contributor.author
Polla, Griselda Ines  
dc.contributor.author
Baggio, Ricardo Fortunato  
dc.date.available
2019-05-22T15:17:36Z  
dc.date.issued
2013-02  
dc.identifier.citation
Freire Espeleta, Eleonora; Polla, Griselda Ines; Baggio, Ricardo Fortunato; Aripiprazole salts. III. Bis(aripiprazolium) oxalate-oxalic acid (1/1); Wiley Blackwell Publishing, Inc; Acta Crystallographica Section C-Crystal Structure Communications; 69; 2; 2-2013; 186-190  
dc.identifier.issn
0108-2701  
dc.identifier.uri
http://hdl.handle.net/11336/76846  
dc.description.abstract
The asymmetric unit of the title salt [systematic name: bis(4-(2,3-dichlorophenyl)-1-{4-[(2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)oxy] butyl}piperazin-1-ium) oxalate-oxalic acid (1/1)], 2C23H28Cl2N3O2 +·C2O4 2-·C2H2O4, consists of one protonated aripiprazole unit (HArip+), half an oxalate dianion and half an oxalic acid molecule, the latter two lying on inversion centres. The conformation of the HArip+ cation differs from that in other reported salts and resembles more the conformation of neutral Arip units in reported polymorphs and solvates. The intermolecular interaction linking HArip + cations is also similar to those in reported Arip compounds crystallizing in the space group P , with head-to-head N - H ⋯O hydrogen bonds generating centrosymmetric dimers, which are further organized into planar ribbons parallel to (01 ). The oxalate anions and oxalic acid molecules form hydrogen-bonded chains running along [010], which 'pierce' the planar ribbons, interacting with them through a number of stronger N - H ⋯O and weaker C - H ⋯O hydrogen bonds, forming a three-dimensional network.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Wiley Blackwell Publishing, Inc  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Aripiprazol  
dc.subject
Salts  
dc.subject
Oxalate  
dc.subject.classification
Otras Ciencias Químicas  
dc.subject.classification
Ciencias Químicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
Aripiprazole salts. III. Bis(aripiprazolium) oxalate-oxalic acid (1/1)  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2019-05-21T20:50:13Z  
dc.journal.volume
69  
dc.journal.number
2  
dc.journal.pagination
186-190  
dc.journal.pais
Reino Unido  
dc.journal.ciudad
Londres  
dc.description.fil
Fil: Freire Espeleta, Eleonora. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Universidad Nacional de San Martín. Escuela de Ciencia y Tecnología; Argentina  
dc.description.fil
Fil: Polla, Griselda Ines. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina  
dc.description.fil
Fil: Baggio, Ricardo Fortunato. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina  
dc.journal.title
Acta Crystallographica Section C-Crystal Structure Communications  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://scripts.iucr.org/cgi-bin/paper?S0108270113001133  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1107/S0108270113001133