Theoretical study of the absorption and nonradiative deactivation of 1-nitronaphthalene in the low-lying singlet and triplet excited states including methanol and ethanol solvent effects


Autoria(s): Orozco-Gonzalez, Yoelvis; Coutinho, Kaline Rabelo; Peon, Jorge; Canuto, Sylvio Roberto Accioly
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

07/11/2013

07/11/2013

2012

Resumo

The photophysics of the 1-nitronaphthalene molecular system, after the absorption transition to the first singlet excited state, is theoretically studied for investigating the ultrafast multiplicity change to the triplet manifold. The consecutive transient absorption spectra experimentally observed in this molecular system are also studied. To identify the electronic states involved in the nonradiative decay, the minimum energy path of the first singlet excited state is obtained using the complete active space self-consistent field//configurational second-order perturbation approach. A near degeneracy region was found between the first singlet and the second triplet excited states with large spin-orbit coupling between them. The intersystem crossing rate was also evaluated. To support the proposed deactivation model the transient absorption spectra observed in the experiments were also considered. For this, computer simulations using sequential quantum mechanic-molecular mechanic methodology was used to consider the solvent effect in the ground and excited states for proper comparison with the experimental results. The absorption transitions from the second triplet excited state in the relaxed geometry permit to describe the transient absorption band experimentally observed around 200 fs after the absorption transition. This indicates that the T-2 electronic state is populated through the intersystem crossing presented here. The two transient absorption bands experimentally observed between 2 and 45 ps after the absorption transition are described here as the T-1 -> T-3 and T-1 -> T-5 transitions, supporting that the intermediate triplet state (T-2) decays by internal conversion to T-1. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.4738757]

nBioNet

Instituto Nacional de Ciencia e Tecnologia de Fluidos Complexos (INCT-FCx)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Coordenacao de Aperfiecoamento de Pessoal de Nivel Superior (CAPES)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Identificador

JOURNAL OF CHEMICAL PHYSICS, MELVILLE, v. 137, pp. 1564-1569, AUG 7, 2012

0021-9606

http://www.producao.usp.br/handle/BDPI/43095

10.1063/1.4738757

http://dx.doi.org/10.1063/1.4738757

Idioma(s)

eng

Publicador

AMER INST PHYSICS

MELVILLE

Relação

JOURNAL OF CHEMICAL PHYSICS

Direitos

restrictedAccess

Copyright AMER INST PHYSICS

Palavras-Chave #ELECTRON-TRANSFER REACTIONS #MOLECULAR WAVE-FUNCTIONS #PI-ASTERISK TRANSITION #SELF-CONSISTENT-FIELD #ANO BASIS-SETS #LIQUID WATER #MONTE-CARLO #CONFIGURATION-INTERACTION #RADIATIONLESS PROCESSES #QUANTUM-MECHANICS #PHYSICS, ATOMIC, MOLECULAR & CHEMICAL
Tipo

article

original article

publishedVersion