Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/14810

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dc.contributor.authorRaposo, M. Manuela M.-
dc.contributor.authorFonseca, A. Maurício C.-
dc.contributor.authorCastro, M. Cidália R.-
dc.contributor.authorBelsley, M.-
dc.contributor.authorCardoso, M. Fátima S.-
dc.contributor.authorCarvalho, Luís M.-
dc.contributor.authorCoelho, Paulo J.-
dc.date.accessioned2011-12-05T14:07:03Z-
dc.date.available2011-12-05T14:07:03Z-
dc.date.issued2011-
dc.identifier.issn0143-7208por
dc.identifier.urihttps://hdl.handle.net/1822/14810-
dc.description.abstractTwo series of novel thermally stable second-order nonlinear optical (NLO) and photochromic chromophores have been designed and synthesized. The two series of compounds were based on different combinations of donor groups (pyrrole or thienylpyrrole) which act simultaneously as Π-conjugated bridges, together with diazoaryl or diazothiazolyl as acceptor moieties. Their photochromic and electrochemical behavior were characterized, while hyper-Rayleigh scattering (HRS) was employed to evaluate their second-order nonlinear optical properties. The results of these studies have been critically analyzed together with two other related compounds reported earlier from our laboratories in which the thienylpyrrole system was used as the donor group keeping the functionalized diazoaryl as acceptor moiety. The measured molecular first hyperpolarizabilities and the observed photochromic behavior showed strong variations for the different donor systems used (pyrrole or thienylpyrrole) and were also sensitive to the acceptor strength of the diazenehetero(aryl) moiety. The thienylpyrrole based compounds endowed with extended Π-conjugated bridges and stronger donor auxiliary effects in comparison to the pyrrole compounds, when coupled to the stronger acceptor diazo(hetero)aryl groups gave rise to significantly larger hyperpolarizabilities (β= 274 - 415 x 10-30 esu) for an incident wavelength of 1064nm). These compounds also displayed improved photochromic behavior with very fast response to the visible light stimulus (1.5 s) and fast thermal return to the original forms (2-3 s).por
dc.description.sponsorshipThanks are due to the Fundacao para a Ciencia e Tecnologia (Portugal) and FEDER for financial support through the Centro de Quimica and Centro de Fisica- Universidade do Minho, Project PTDC/QUI/66251/2006 (FCOMP-01-0124-FEDER-007429), Project PTDC/CTM/105597/2008 with funding from COMPETE/FEDER and research grants to M. C. R. Castro (UMINHO/BI/142/2009) and M. F. S. Cardoso (UMINHO/BII/249/2009). The NMR spectrometer Bruker Avance III 400 is part of the National NMR Network and was purchased within the framework of the National Program for Scientific Re-equipment, contract REDE/1517/RMN/2005 with funds from POCI 2010 (FEDER) and FCT.por
dc.language.isoengpor
dc.publisherElsevier 1por
dc.relationinfo:eu-repo/grantAgreement/FCT/5876-PPCDTI/66251/PT-
dc.relationinfo:eu-repo/grantAgreement/FCT/5876-PPCDTI/105597/PT-
dc.rightsopenAccesspor
dc.subjectThiazolepor
dc.subjectDonor-acceptor chromophorespor
dc.subjectSolvatochromic probespor
dc.subjectHyper-Rayleigh scattering (HRS)por
dc.subjectNonlinear optical (NLO) materialspor
dc.subjectRedox potentialspor
dc.subjectPhotochromismpor
dc.subjectThermal stabilitypor
dc.subjectHeterocyclic azo dyespor
dc.subjectHyper-Rayleigh scaterring (HRS) techniquepor
dc.titleSynthesis and characterization of novel diazenes bearing pyrrole, thiophene and thiazole heterocycles as efficient photochromic and nonlinear optical (NLO) materialspor
dc.typearticlepor
dc.peerreviewedyespor
sdum.publicationstatuspublishedpor
oaire.citationStartPage62por
oaire.citationEndPage73por
oaire.citationIssue1por
oaire.citationTitleDyes and Pigmentspor
oaire.citationVolume91por
dc.identifier.doi10.1016/j.dyepig.2011.02.012por
dc.subject.wosScience & Technologypor
sdum.journalDyes and Pigmentspor
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