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Aripiprazole salts IV. Anionic plus solvato networks defining molecular

cnea.tipodocumentoARTÍCULO CIENTÍFICO
dc.contributor.authorFreire Espeleta, Eleonora
dc.contributor.authorPolla, Griselda Ines
dc.contributor.authorBaggio, Ricardo Fortunato
dc.date.accessioned2025-12-11T23:27:00Z
dc.date.available2025-12-11T23:27:00Z
dc.date.issued2014-04
dc.description.abstractFive new examples of aripiprazole (arip) salts are presented, viz., the Harip phthalate [Harip+·C8H5O4− (I)], homophthalate [Harip+·C9H7O4− (II)] and thiosalicilate [Harip+·C7H4O2S− (III)] salts on one side, and two different dihidrogenphosphates, Harip+·H2PO4−·2(H3PO4)·H2O (IV) and Harip+·H2PO4−·H3PO4 (V). Regarding the internal structure of the aripH+ cations, they do not differ from the already known moieties in bond distances and angles, while interesting differences in conformation can be observed, setting them apart in two groups: those in I, II and III present similar conformations to those in the so far reported arip salts presenting the same centrosymmetric R(8)22 dimeric synthon, but different to those in IV and V. In parallel, the anion (+ acid) groups define bulky systems of different dimensionality (1D in the former group, 2D in the latter). The correlation between arip molecular conformation and anionic network type is discussed. An interesting feature arises with the water solvato molecule in IV, disordered around an inversion center, in regard with its interaction with an (also disordered) phosphato O–H, in a way that an “orderly disordered” H-bonding scheme arises, complying with the S.G. symmetry requirements only on average.
dc.description.institutionalaffiliationFil: Freire Espeleta, Eleonora. Universidad Nacional de San Martín. Escuela de Ciencia y Tecnología; Argentina. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes. Gerencia de Investigación y Aplicaciones; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
dc.description.institutionalaffiliationFil: Polla, Griselda Ines. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes. Gerencia de Investigación y Aplicaciones; Argentina
dc.description.institutionalaffiliationFil: Baggio, Ricardo Fortunato. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes. Gerencia de Investigación y Aplicaciones; Argentina
dc.identifier.issn0022-2860
dc.identifier.urihttps://nuclea.cnea.gob.ar/handle/20.500.12553/8304
dc.publisherElsevier
dc.relationinfo:eu-repo/semantics/reference/hdl/11336/33514
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.molstruc.2014.03.062
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0022286014003305
dc.rights.licenseinfo:eu-repo/semantics/openAccess
dc.rights.licensehttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subjectAripiprazole Salts
dc.subjectCrystal Structures
dc.subjectAnionic/Solvate Network
dc.subjectOtras Ciencias Químicas
dc.subjectCiencias Químicas
dc.subjectCIENCIAS NATURALES Y EXACTAS
dc.titleAripiprazole salts IV. Anionic plus solvato networks defining molecular
dc.typeARTÍCULO
dc.type.versionVersión publicada

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