Literature DB >> 25863481

Second-order nonlinear optical properties of dithienophenazine and TTF derivatives: A butterfly effect of dimalononitrile substitutions.

Shabbir Muhammad1.   

Abstract

Using density functional theory (DFT) methods, the nonlinear optical (NLO) properties have been calculated with strong donor-π-conjugation-acceptor configurations. The static first hyperpolarizability (β0) and dynamic (frequency dependent) electric field induced second harmonic generation (EFISHG) first hyperpolarizability (μβ) are calculated for all designed systems. Our DFT calculations show dithienophenazine merged TTF (2) holds larger β0 amplitudes (β0=21.04×10(3)a.u.) as compared to its corresponding compounds of TTF merged-difurophenazine (1), dicyclopentaphenazine (3) and dipyrrolophenazine (4) derivatives having β0 amplitudes of 16.25×10(3), 12.69×10(3), and 18.38×10(3)a.u., respectively. Furthermore, substitution of dimalononitrile [C(CN)2]2 groups at acceptor end of these compounds results in new derivatives 1a-4a, respectively. Interestingly, a butterfly effect on first hyperpolarizability of all systems 1a-4a has been spotted, which not only results in their robustly larger β0 amplitudes but also changes the increasing order of β0 amplitudes from systems 3<1<4<2 to 1a<2a<3a<4a at both PBE0/6-31G* and CAM-B3LYP/6-31+G* levels of theory. For example, the increase in β0 amplitudes of systems 1a, 2a, 3a and 4a are 3, 3, 5, and 19 times as compared with their corresponding non dimalononitrile derivatives at PBE0/6-31G* level of theory, respectively. Remarkably, unlike the static first hyperpolarizability, the dynamic EFISHG hyperpolarizability (μβω) has the largest value for system 4a with its amplitudes of 1378.59×10(-46) and 1349.40×10(-46)esu, at PBE0/6-31G* and CAM-B3LYP/6-31+G* levels of theory, respectively. TD-DFT calculations have been performed to trace the origin of first hyperpolarizability. It has been found that the lower transition energy and higher oscillator strengths cause robustly large amplitudes especially in systems 3a and 4a, which consequently stems in strong donor-π-conjugation-acceptor configuration of these systems. Thus the present results intrigue the butterfly effect of a two-step substitution on NLO properties of TTF merged dithienophenazine compounds that can be used as an efficient NLO material.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Dithienophenazine merged TTF derivatives; Donor-π-conjugation-acceptor model; Electric field induced second harmonic generation (EFISHG); First hyperpolarizability; Nonlinear optical property

Mesh:

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Year:  2015        PMID: 25863481     DOI: 10.1016/j.jmgm.2015.03.003

Source DB:  PubMed          Journal:  J Mol Graph Model        ISSN: 1093-3263            Impact factor:   2.518


  2 in total

1.  The impact of position and number of methoxy group(s) to tune the nonlinear optical properties of chalcone derivatives: a dual substitution strategy.

Authors:  Shabbir Muhammad; Abdullah G Al-Sehemi; Ahmad Irfan; Aijaz R Chaudhry; Hamid Gharni; S AlFaify; Mohd Shkir; Abdullah M Asiri
Journal:  J Mol Model       Date:  2016-03-12       Impact factor: 1.810

2.  Exploration of CH⋯F & CF⋯H mediated supramolecular arrangements into fluorinated terphenyls and theoretical prediction of their third-order nonlinear optical response.

Authors:  Muhammad Adeel; Muhammad Khalid; Malik Aman Ullah; Shabbir Muhammad; Muhammad Usman Khan; Muhammad Nawaz Tahir; Ilham Khan; Muhammad Asghar; Khawar Shahzad Mughal
Journal:  RSC Adv       Date:  2021-02-17       Impact factor: 3.361

  2 in total

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