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Impact of extended π-conjugated acceptor moieties on non-linear optical behavior in polar medium for designed 4,4-dimethyl-4 H-indeno[1,2-b] thiophene based materials

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Autor(es):
Khalid, Muhammad ; Wu, Gang ; Umber, Areeha ; Khan, Mashal ; Braga, Ataualpa A. C. ; Alhokbany, Norah ; Ojha, Suvash Chandra
Número total de Autores: 7
Tipo de documento: Artigo Científico
Fonte: JOURNAL OF MOLECULAR LIQUIDS; v. 401, p. 13-pg., 2024-04-06.
Resumo

In the current study, the organic compounds (D2-D9) with D1-pi-D2-pi-A configuration were designed by structural modeling with various end-capped acceptor moieties for nonlinear optical (NLO) study. TD-DFT/DFT approaches at CAM-B3LYP/6-311G(d,p) level were accomplished to investigate the NLO behavior of these compounds. For this, various analyses: frontier molecular orbitals (FMOs), density of states (DOS), UV-Vis absorption, natural bond orbitals (NBOs), transition density matrix (TDMs) and non-linear optical (NLO) investigations were performed. These findings revealed that all designed chromophores exhibited comparable band gaps (3.962-4.182 eV) and absorption spectra (lambda(max) = 441.6-460.7 nm) with reference chromophore (band gap = 4.008 eV). An efficient charge transfer from central core in HOMO was transferred towards terminal acceptors in LUMO that was also supported by DOS and TDM maps. Among all studied chromophores, the significant linear and nonlinear polarizability properties were examined in D5 (<alpha>=2.213 x 10(-22) esu), D6 (beta(tot) = 3.339 x 10(-28) esu) and D4 (gamma(tot) = 3.068 x 10(-33) esu) chromophores. The NLO results indicated that the designed compounds (D5, D6 and D4) possess promising NLO behavior via effective charge delocalization. It is inferred that the current computational work might be helpful for further developments in non-linear optic field. (AU)

Processo FAPESP: 14/25770-6 - Novas fronteiras em reações de acoplamento cruzado mediadas por paládio: associando catálise enantiosseletiva, ativações C-H, novos materiais e reações em fluxo visando alta eficiência e sustentabilidade em processos sintéticos
Beneficiário:Carlos Roque Duarte Correia
Modalidade de apoio: Auxílio à Pesquisa - Temático
Processo FAPESP: 15/01491-3 - Estudo teórico das reações de acoplamento-cruzado: catálise homogênea e heterogênea
Beneficiário:Ataualpa Albert Carmo Braga
Modalidade de apoio: Auxílio à Pesquisa - Regular