000165328 001__ 165328
000165328 005__ 20260107201858.0
000165328 0247_ $$2doi$$a10.1016/j.dyepig.2015.02.026
000165328 0248_ $$2sideral$$a97720
000165328 037__ $$aART-2015-97720
000165328 041__ $$aeng
000165328 100__ $$0(orcid)0000-0001-7341-0033$$aGonzález-Lainez, M.$$uUniversidad de Zaragoza
000165328 245__ $$aUsing functionalized nonlinear optical chromophores to prepare NLO-active polycarbonate films
000165328 260__ $$c2015
000165328 5060_ $$aAccess copy available to the general public$$fUnrestricted
000165328 5203_ $$aNovel functionalized second order nonlinear optical (NLO) chromophores have been prepared with functionalized aniline as electron donor, thiophene or isophorone as a p-spacer and 1,3-diethyl-2- thiobarbituric acid as electron acceptor. The films prepared from dyes with alkylsilyl bulky groups gave better performance than the corresponding non functionalized chromophores due to the reduction of the intermolecular electrostatic interactions. The incorporation of chromophores 4 and 10 in a poly- carbonate matrix allowed the preparation of good optical-quality films. Nonlinear coefficients d33 and d31 as high as 17 and 5.6 pm V-1, respectively, were obtained. Moreover, the temporal stability of these host- guest films was confirmed up to eight months (>80%).
000165328 536__ $$9info:eu-repo/grantAgreement/ES/DGA/E04$$9info:eu-repo/grantAgreement/ES/DGA/E39$$9info:eu-repo/grantAgreement/ES/MINECO/CTQ2011-22727$$9info:eu-repo/grantAgreement/ES/MINECO/MAT2011-27978-C02-02
000165328 540__ $$9info:eu-repo/semantics/openAccess$$aby-nc-nd$$uhttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
000165328 590__ $$a4.055$$b2015
000165328 591__ $$aCHEMISTRY, APPLIED$$b6 / 72 = 0.083$$c2015$$dQ1$$eT1
000165328 591__ $$aMATERIALS SCIENCE, TEXTILES$$b1 / 23 = 0.043$$c2015$$dQ1$$eT1
000165328 591__ $$aENGINEERING, CHEMICAL$$b17 / 135 = 0.126$$c2015$$dQ1$$eT1
000165328 592__ $$a0.957$$b2015
000165328 593__ $$aProcess Chemistry and Technology$$c2015$$dQ1
000165328 593__ $$aChemical Engineering (miscellaneous)$$c2015$$dQ1
000165328 655_4 $$ainfo:eu-repo/semantics/article$$vinfo:eu-repo/semantics/acceptedVersion
000165328 700__ $$aJiménez-Ruiz, M.T.
000165328 700__ $$aMartínez de Baroja, N.
000165328 700__ $$0(orcid)0000-0001-8265-8970$$aGarín, J.$$uUniversidad de Zaragoza
000165328 700__ $$0(orcid)0000-0003-3514-2570$$aOrduna, J.$$uUniversidad de Zaragoza
000165328 700__ $$0(orcid)0000-0001-9814-0834$$aVillacampa, B.$$uUniversidad de Zaragoza
000165328 700__ $$0(orcid)0000-0001-7193-1732$$aBlesa, M.J.$$uUniversidad de Zaragoza
000165328 7102_ $$12010$$2760$$aUniversidad de Zaragoza$$bDpto. Química Inorgánica$$cÁrea Química Inorgánica
000165328 7102_ $$12013$$2765$$aUniversidad de Zaragoza$$bDpto. Química Orgánica$$cÁrea Química Orgánica
000165328 7102_ $$12003$$2395$$aUniversidad de Zaragoza$$bDpto. Física Materia Condensa.$$cÁrea Física Materia Condensada
000165328 773__ $$g119 (2015), 30-40$$pDyes pigm.$$tDyes and Pigments$$x0143-7208
000165328 8564_ $$s2859749$$uhttps://zaguan.unizar.es/record/165328/files/texto_completo.pdf$$yPostprint
000165328 8564_ $$s911734$$uhttps://zaguan.unizar.es/record/165328/files/texto_completo.jpg?subformat=icon$$xicon$$yPostprint
000165328 909CO $$ooai:zaguan.unizar.es:165328$$particulos$$pdriver
000165328 951__ $$a2026-01-07-18:52:29
000165328 980__ $$aARTICLE