Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/5263
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dc.contributor.authorFausto, Rui-
dc.contributor.authorRibeiro, Maria João S.-
dc.contributor.authorLima, João J. Pedroso de-
dc.date.accessioned2008-09-01T15:06:44Z-
dc.date.available2008-09-01T15:06:44Z-
dc.date.issued1999en_US
dc.identifier.citationJournal of Molecular Structure. 484:1-3 (1999) 181-196en_US
dc.identifier.urihttp://hdl.handle.net/10316/5263-
dc.description.abstractThe results of a series of ab initio (3-21G) and semiempirical (PM3) molecular orbital (MO) calculations on neutral, zwitterionic and cationic forms of dopamine [1,2-benzenediol-4(2-aminoethyl)] are reported. In particular, optimised geometries, relative stabilities, dipole moments and electron charge distributions for the relevant conformational states of the studied molecules are presented and the conformational dependence of some relevant structural parameters is used to characterise the most important intramolecular interactions present in the studied conformers. It is shown that all the studied molecules have a considerably high degree of conformational flexibility, and may exist as a mixture of several conformers of similar energies differing by the relative orientation of the aromatic ring with respect to the alkylamine chain or of the hydroxyl groups. For both neutral dopamine and dopamine cation, the conformational ground state corresponds to a form where the meta-hydroxy group has its hydrogen atom directed towards the para-hydroxy group, the aromatic ring and the alkylamine axis are nearly perpendicular and the C-C-C-N axis assumes a gauche geometry, with the amine group in the same side of the meta-hydroxy group. In turn, the zwitterionic form of dopamine is predicted not to correspond to a minimum in the potential energy surface (PES) for the isolated molecule situation. However, in the zwitterion dimmer, the conformation assumed by the individual molecules is predicted to be similar to that previously observed in crystalline dopamine hydrochloride.en_US
dc.description.urihttp://www.sciencedirect.com/science/article/B6TGS-3XG754G-J/1/fbed16d9d1f1a9d827ebda0183162b1fen_US
dc.format.mimetypeaplication/PDFen
dc.language.isoengeng
dc.rightsopenAccesseng
dc.subjectDopamine [1,2-benzenediol-4(2-aminoethyl)] neutral and zwitterionic formsen_US
dc.subjectDopamine cationen_US
dc.subjectMolecular structureen_US
dc.subjectConformational propertiesen_US
dc.subjectAb initio and semiempirical (PM3) molecular orbital calculationsen_US
dc.titleA molecular orbital study on the conformational properties of dopamine [1,2-benzenediol-4(2-aminoethyl)]and dopamine cationen_US
dc.typearticleen_US
item.fulltextCom Texto completo-
item.grantfulltextopen-
item.languageiso639-1en-
crisitem.author.deptFaculdade de Ciências e Tecnologia, Universidade de Coimbra-
crisitem.author.parentdeptUniversidade de Coimbra-
crisitem.author.researchunitCoimbra Chemistry Center-
crisitem.author.orcid0000-0002-8264-6854-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
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