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https://hdl.handle.net/1822/14432
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Campo DC | Valor | Idioma |
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dc.contributor.author | Raposo, M. Manuela M. | - |
dc.contributor.author | Castro, M. Cidália R. | - |
dc.contributor.author | Belsley, M. | - |
dc.contributor.author | Fonseca, A. Maurício C. | - |
dc.date.accessioned | 2011-11-17T14:00:46Z | - |
dc.date.available | 2011-11-17T14:00:46Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 0143-7208 | por |
dc.identifier.uri | https://hdl.handle.net/1822/14432 | - |
dc.description.abstract | Three series of bithiophene azo dyes functionalized with thiazol-2-yl or benzothiazol-2-yl-diazene acceptor moieties were synthesized through azo coupling reaction using 2,2´-bithiophene, 5-alkoxy-2,2´-bithiophenes, 5-N,N-dialkylamino-2,2´-bithiophenes and thiazolyl and benzothiazolyl diazonium salts as coupling components. The 5-alkoxy-2,2´-bithiophene precursors yielded the 5-thiazolylazo-5´-alkoxy-2,2´-bithiophenes, while the azo coupling reaction of 5-N,N-dialkylamino-2,2´-bithiophenes with the thiazolyldiazonium salt gave 4-thiazolyl-azo-5-N,N-dialkylamino-2,2´-bithiophenes. A different reactivity behavior was observed for 2,2-bithiophene with thiazolyl diazonium salts which gave rise to the expected azo dyes together with several arylation products. The redox behavior, thermal stability, and the first hyperpolarizability of the novel chromophores were evaluated through cyclic voltammetry, thermogravimetric analysis (TGA) and hyper-Rayleight scattering (HRS) respectively. By varying the position of the thiazolyldiazene acceptor group on the bithiophene system, the electrochemical behavior as well as the optical (linear and nonlinear) properties of the donor-acceptor -conjugated systems can readily be tuned. Push-pull 5-thiazolylazo-5´-alkoxy-2,2´-bithiophenes exhibit the most promising redox and the solvatochromic properties and second order nonlinear optical response. The redox and the optical properties also show notable variations for the different heterocyclic spacers and were also sensitive to the electronic acceptor strength of the (benzo)thiazolyldiazene moieties. | por |
dc.description.sponsorship | Thanks 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 a research grant to M. C. R. Castro (UMINHO/BI/142/2009). 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.iso | eng | por |
dc.publisher | Elsevier 1 | por |
dc.relation | info:eu-repo/grantAgreement/FCT/5876-PPCDTI/66251/PT | - |
dc.rights | openAccess | por |
dc.subject | Heterocyclic azo dyes | por |
dc.subject | Bithiophene | por |
dc.subject | (Benzo)thiazole | por |
dc.subject | Auxiliary donor/acceptor heterocycles | por |
dc.subject | Hyper-Rayleigh scattering (HRS) | por |
dc.subject | Nonlinear optical (NLO) materials | por |
dc.title | Push-pull bithiophene azo-chromophores bearing thiazole and benzothiazole acceptor moieties: synthesis and evaluation of their redox and nonlinear optical properties | eng |
dc.type | article | por |
dc.peerreviewed | yes | por |
sdum.publicationstatus | published | por |
oaire.citationStartPage | 454 | por |
oaire.citationEndPage | 465 | por |
oaire.citationIssue | 3 | por |
oaire.citationTitle | Dyes and Pigments | por |
oaire.citationVolume | 91 | por |
dc.identifier.doi | 10.1016/j.dyepig.2011.05.007 | por |
dc.subject.wos | Science & Technology | por |
sdum.journal | Dyes and Pigments | por |
Aparece nas coleções: | CDQuim - Artigos (Papers) |
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Ficheiro | Descrição | Tamanho | Formato | |
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Push-pull bithiophene azo-chromophores bearing thiazole and benzothiazole acceptor moieties synthesis and evaluation of their redox and nonlinear optical properties.pdf | 856,43 kB | Adobe PDF | Ver/Abrir |