4.5 Article

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

Journal

JOURNAL OF MOLECULAR GRAPHICS & MODELLING
Volume 59, Issue -, Pages 14-20

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jmgm.2015.03.003

Keywords

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

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Using density functional theory (DFT) methods, the nonlinear optical (NLO) properties have been calculated with strong donor-pi-conjugation-acceptor configurations. The static first hyperpolarizability (no) and dynamic (frequency dependent) electric field induced second harmonic generation (EFISHG) first hyperpolarizability (mu beta) are calculated for all designed systems. Our DFT calculations show dithienophenazine merged TTF (2) holds larger beta(0) amplitudes (beta(0) =21.04 x 10(3) a.u.) as compared to its corresponding compounds of TTF merged-difurophenazine (1), dicyclopentaphenazine (3) and dipyrrolophenazine (4) derivatives having beta(0) amplitudes of 16.25 x 10(3), 12.69 x 10(3), and 18.38 x 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 beta(0) amplitudes but also changes the increasing order of beta(0) 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 beta(0) amplitudes of systems 1a, 2a, 3a and 4a are 3, 3, 5, and 19 times as compared with their corresponding non dimalononitrile derivatives at PBEO/6-31G* level of theory, respectively. Remarkably, unlike the static first hyperpolarizability, the dynamic EFISHG hyperpolarizability (to.) has the largest value for system 4a with its amplitudes of 1378.59 x 10(-46) and 1349.40 x 10(-46) esu, at PBEO/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-pi-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. (C) 2015 Elsevier Inc. All rights reserved.

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