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First theoretical probe for efficient enhancement of optical nonlinearity via structural modifications into phenylene based D–π–A configured molecules

The design of nonlinear optical (NLO) materials using conjugated molecules via different techniques is reported in the literature to boost the use of these systems in NLO. Therefore, in the current study, designed phenylene based non-fullerene organic compounds with a D–π–A framework were selected f...

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Autores principales: Khalid, Muhammad, Naz, Salma, Mahmood, Khalid, Hussain, Shabbir, Carmo Braga, Ataualpa Albert, Hussain, Riaz, Ragab, Ahmed H., Al-Mhyawi, Saedah R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9623554/
https://www.ncbi.nlm.nih.gov/pubmed/36349029
http://dx.doi.org/10.1039/d2ra04844b
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author Khalid, Muhammad
Naz, Salma
Mahmood, Khalid
Hussain, Shabbir
Carmo Braga, Ataualpa Albert
Hussain, Riaz
Ragab, Ahmed H.
Al-Mhyawi, Saedah R.
author_facet Khalid, Muhammad
Naz, Salma
Mahmood, Khalid
Hussain, Shabbir
Carmo Braga, Ataualpa Albert
Hussain, Riaz
Ragab, Ahmed H.
Al-Mhyawi, Saedah R.
author_sort Khalid, Muhammad
collection PubMed
description The design of nonlinear optical (NLO) materials using conjugated molecules via different techniques is reported in the literature to boost the use of these systems in NLO. Therefore, in the current study, designed phenylene based non-fullerene organic compounds with a D–π–A framework were selected for NLO investigation. The initial compound (PMD-1) was taken as a reference and its seven derivatives (PMDC2–PMDC8) were made by introducing different acceptor moieties into the chemical structure of PMD-1. To explain the NLO findings, frontier molecular orbital (FMO), transition density matrix (TDM), density of states (DOS), natural bond orbital (NBO) and UV-Vis study of the title compounds was executed by applying the PBE1PBE functional with the 6-311G(d,p) basis set. The descending order of band gaps (E(gap)) was reported as PMDC7 (2.656) > PMDC8 (2.485) > PMD-1 (2.131) > PMDC3 (2.103) > PMDC2 (2.079) > PMDC4 (2.065) > PMDC5 (2.059) > PMDC6 (2.004), in eV. Global reactivity parameters (GRPs) were associated with E(gap) values as PMDC6 with the lowest band gap showed less hardness (0.0368 E(h)) and high softness (13.5785 E(h)). The UV-Vis investigation revealed that the maximum λ(max) (739.542 nm) was exhibited by PMDC6 in dichloromethane (DCM) as compared to other derivatives. Additionally, natural bond orbital (NBO) based findings revealed that PMDC6 exhibited the highest stability value (34.98 kcal mol(−1)) because of prolonged hyper-conjugation. The dipole moment (μ), average linear polarizability 〈α〉, first hyperpolarizability (β(tot)) and second hyperpolarizability (γ(tot)) were evaluated for the reference and its derivatives. Consequently, among the designed compounds, the highest β(tot) (4.469 × 10(−27) esu) and γ(tot) (5.600 × 10(−32) esu) values were shown by PMDC6. Hence, it's concluded from said results that these structural modifications proved PMDC6 as the best second and third order NLO candidate for various applications like fiber optics, signal processing and data storage.
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spelling pubmed-96235542022-11-07 First theoretical probe for efficient enhancement of optical nonlinearity via structural modifications into phenylene based D–π–A configured molecules Khalid, Muhammad Naz, Salma Mahmood, Khalid Hussain, Shabbir Carmo Braga, Ataualpa Albert Hussain, Riaz Ragab, Ahmed H. Al-Mhyawi, Saedah R. RSC Adv Chemistry The design of nonlinear optical (NLO) materials using conjugated molecules via different techniques is reported in the literature to boost the use of these systems in NLO. Therefore, in the current study, designed phenylene based non-fullerene organic compounds with a D–π–A framework were selected for NLO investigation. The initial compound (PMD-1) was taken as a reference and its seven derivatives (PMDC2–PMDC8) were made by introducing different acceptor moieties into the chemical structure of PMD-1. To explain the NLO findings, frontier molecular orbital (FMO), transition density matrix (TDM), density of states (DOS), natural bond orbital (NBO) and UV-Vis study of the title compounds was executed by applying the PBE1PBE functional with the 6-311G(d,p) basis set. The descending order of band gaps (E(gap)) was reported as PMDC7 (2.656) > PMDC8 (2.485) > PMD-1 (2.131) > PMDC3 (2.103) > PMDC2 (2.079) > PMDC4 (2.065) > PMDC5 (2.059) > PMDC6 (2.004), in eV. Global reactivity parameters (GRPs) were associated with E(gap) values as PMDC6 with the lowest band gap showed less hardness (0.0368 E(h)) and high softness (13.5785 E(h)). The UV-Vis investigation revealed that the maximum λ(max) (739.542 nm) was exhibited by PMDC6 in dichloromethane (DCM) as compared to other derivatives. Additionally, natural bond orbital (NBO) based findings revealed that PMDC6 exhibited the highest stability value (34.98 kcal mol(−1)) because of prolonged hyper-conjugation. The dipole moment (μ), average linear polarizability 〈α〉, first hyperpolarizability (β(tot)) and second hyperpolarizability (γ(tot)) were evaluated for the reference and its derivatives. Consequently, among the designed compounds, the highest β(tot) (4.469 × 10(−27) esu) and γ(tot) (5.600 × 10(−32) esu) values were shown by PMDC6. Hence, it's concluded from said results that these structural modifications proved PMDC6 as the best second and third order NLO candidate for various applications like fiber optics, signal processing and data storage. The Royal Society of Chemistry 2022-11-01 /pmc/articles/PMC9623554/ /pubmed/36349029 http://dx.doi.org/10.1039/d2ra04844b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Khalid, Muhammad
Naz, Salma
Mahmood, Khalid
Hussain, Shabbir
Carmo Braga, Ataualpa Albert
Hussain, Riaz
Ragab, Ahmed H.
Al-Mhyawi, Saedah R.
First theoretical probe for efficient enhancement of optical nonlinearity via structural modifications into phenylene based D–π–A configured molecules
title First theoretical probe for efficient enhancement of optical nonlinearity via structural modifications into phenylene based D–π–A configured molecules
title_full First theoretical probe for efficient enhancement of optical nonlinearity via structural modifications into phenylene based D–π–A configured molecules
title_fullStr First theoretical probe for efficient enhancement of optical nonlinearity via structural modifications into phenylene based D–π–A configured molecules
title_full_unstemmed First theoretical probe for efficient enhancement of optical nonlinearity via structural modifications into phenylene based D–π–A configured molecules
title_short First theoretical probe for efficient enhancement of optical nonlinearity via structural modifications into phenylene based D–π–A configured molecules
title_sort first theoretical probe for efficient enhancement of optical nonlinearity via structural modifications into phenylene based d–π–a configured molecules
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9623554/
https://www.ncbi.nlm.nih.gov/pubmed/36349029
http://dx.doi.org/10.1039/d2ra04844b
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