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Synthesis and characterization of thiazole-containing chromophores for second-order nonlinear optics

dc.citation.epage1452en_US
dc.citation.issue7en_US
dc.citation.spage1449en_US
dc.citation.volume9en_US
dc.citation.woscount42
dc.contributor.authorWang, YKen_US
dc.contributor.authorShu, CFen_US
dc.contributor.authorBreitung, EMen_US
dc.contributor.authorMcMahon, RJen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:46:23Z
dc.date.available2014-12-08T15:46:23Z
dc.date.issued1999-07-01en_US
dc.description.abstractPush-pull thiazole-containing nonlinear optical chromophores with dicyanovinyl and tricyanovinyl accepters, along with their thiophene analogs, have been synthesized and characterized. The onset temperatures of thermal decomposition of these chromophores determined by DSC are:above;240 degrees C. The;redox properties of the chromophores were studied by cyclic voltammetry and the results reveal the electron-deficient (thiazole) and electron-excessive (thiophene) nature of the heterocycles. Experimental measurements of second-order nonlinear optical response (mu.beta) indicate that the combination of either,a thiazole or thiophene conjugating,unit and a tricyanovinyl acceptor results in a nonlinear optical chromephore exhibiting substantial molecular hyperpolarizability (mu.beta ca 7000 x 10(-48) cm(6) at 1907 nm).en_US
dc.identifier.doi10.1039/a900820ien_US
dc.identifier.issn0959-9428en_US
dc.identifier.journalJOURNAL OF MATERIALS CHEMISTRYen_US
dc.identifier.urihttp://dx.doi.org/10.1039/a900820ien_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/31216
dc.identifier.wosnumberWOS:000081372600012
dc.language.isoen_USen_US
dc.titleSynthesis and characterization of thiazole-containing chromophores for second-order nonlinear opticsen_US
dc.typeArticleen_US

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