Статья

Influence of acceptor tethering on the performance of nonlinear optical properties for pyrene-based materials with A-π-D-π-D architecture

Muhammad Usman KhanDepartment of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai 201620, ChinaMuhammad KhalidDepartment of Chemistry, Khwaja Fareed University of Engineering & Information Technology, Rahim Yar Khan 64200, PakistanRasheed Ahmad KheraDepartment of Chemistry, University of Agriculture, 38000 Faisalabad, PakistanMuhammad Nadeem AkhtarDivision of Inorganic Chemistry, Institute of Chemistry, Baghdad-ul-Jadeed Campus, The Islamia University of Bahawalpur, Bahawalpur 63100, PakistanAmna AbbasDepartment of Chemistry, Khwaja Fareed University of Engineering & Information Technology, Rahim Yar Khan 64200, PakistanMuhammad Fayyaz ur RehmanInstitute of Chemistry, University of Sargodha, Sargodha 40100, PakistanAtaualpa Albert Carmo BragaDepartamento de Química Fundamental, Instituto de Química, Universidade de São Paulo, Av. Prof. Lineu Prestes, 748, São Paulo 05508-000, BrazilMohammed Mujahid AlamDepartment of Chemistry, Faculty of Science, King Khalid University, P.O. Box 9004, Abha 61413, Saudi ArabiaMuhammad ImranDepartment of Chemistry, Faculty of Science, King Khalid University, P.O. Box 9004, Abha 61413, Saudi ArabiaYao WangDepartment of Assisted Reproduction, Shanghai Ninth People’s Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai, ChinaChangrui LuDepartment of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai 201620, China

2022en

ABI

Аннотация

In this study, we designed a series of pyrene-based donor-π-donor-π-acceptor compounds (HPTC1-HPTC7) by structural tailoring the reference compound (HPTC) using acceptor units. Nonlinear optical (NLO) properties, frontier molecular orbitals (FMOs), natural bonding orbital (NBO), transition density matric (TDM) analysis, and absorption spectra of reference and proposed derivatives were calculated at M06/6-31G(d,p) functional. All the designed compounds have smaller energy bandgaps than the HPTC compound. Moreover, the designed compounds exhibited larger global softness values than the reference. The absorption maxima of HPTC2, HPTC3, and HPTC7 are blue shifted with respect to HPTC. NBO analysis revealed that prolonged hyper conjugative associations and strong interactions between the donor (π) and acceptor (π*) moieties play a crucial part in their stabilization. The FMO and NBO findings supported the NLO responses of entitled compounds, and consequently, the linear and nonlinear properties of designed derivatives elevate compared to the reference molecule. Promisingly, the NLO response for HPTC7 comprises of highest values of <α>, βtotal and < γ > as 1.92 × 10−22 esu, 1.95 × 10−27 esu, and 4.69 × 107 (a.u). This NLO behavior shows push–pull NLO chromophores for HPTC7 predicting its role in pursuing NLO materials for optoelectronic applications.

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Идентификаторы

DOI: 10.1016/j.arabjc.2021.103673

Цитирования и источники

Цитирований: 2Использованных источников: 0

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