Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/32119

TítuloNonlinear optical materials formed by push-pull (bi)thiophene derivatives functionalized with di(tri)cyanovinyl acceptor groups
Autor(es)Wojciechowski, A.
Raposo, M. Manuela M.
Castro, M. Cidália R.
Kuznik, W.
Janczrek, I. Fuks
Bureš, F.
Kityk, I. V.
Palavras-chaveSynthesis
Bithiophene
Nonlinear optical (NLO) materials
Polymethylmethacrylate (PMMA) matrices
UV-visible spectroscopy
DFT studies
Second order susceptibilities
Push-pull conjugated heterocyclic systems
Di(tri)cyanovinyl acceptor groups
PMMA
Structure-property relationships
Data2014
EditoraSpringer
RevistaJournal of Materials Science: Materials in Electronics
Resumo(s)Studies of the second-order nonlinear optical susceptibilities of six NLOphores bearing di(tri)cyanovinyl acceptor groups linked to (bi)thiophene heterocyclic donor systems were performed for the first time in polymethyl methacrylate (PMMA) matrices with a 1064 nm laser working in the 20 ns time pulse regime. Absorption spectra and DFT calculations were also performed. This multidisciplinary study showed that modulation of the optical (linear and nonlinear) properties can be achieved by increasing the length of the -conjugated heterocyclic system (thiophene vs. bithiophene), the strength of the electron donor groups (HMeO/EtOEt2N) as well as the strength of the electron acceptor moieties (DCV vs. TCV, two vs. three electron withdrawing cyano groups). Due to the relatively high second-order susceptibilities (0.08 to 6.45 pm/V), the studied push-pull chromophores can be denote as very potent NLOphores.
TipoArtigo
URIhttps://hdl.handle.net/1822/32119
DOI10.1007/s10854-014-1793-6
ISSN0957-4522
1573-482X
Arbitragem científicayes
AcessoAcesso aberto
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