N-(1H-Benzo[d]imidazol-2-yl)-1-(3-substituted phenyl) methanimines as optoelectronic and nonlinear optical materials: spectroscopic and computational approaches
Publication type: Journal Article
Publication date: 2024-09-02
scimago Q2
wos Q3
SJR: 0.431
CiteScore: 4.3
Impact factor: 2.5
ISSN: 03666352, 13369075, 25857290
Abstract
The negative environmental impact of fossil fuel and the ever-increasing need for renewable energy materials necessitate a rigorous search for optoelectronic materials. Photon reabsorption due to a small Stokes shift limits the light-emitting potentials of many optical materials. In this research, two benzimidazole Schiff bases, 3-(((1H-benzo[d]imidazol-2-yl)imino)methyl)phenol (1) and N-(1H-benzo[d]imidazole(-2-yl)-1-(3-nitrophenyl))methanimine (2), were synthesized via one-pot single-step condensation and characterized using spectrometric (1H NMR, 13C NMR, HRMS and FTIR) techniques. The optoelectronic, nonlinear optical (NLO), adsorption properties and natural bond orbital (NBO) analysis of 1 and 2 were explored using spectroscopic, density functional theory (DFT) and Monte Carlo (MC) simulation approaches. The absorption, light-harvesting efficiency (LHE) and fluorescence properties were studied in solution. Static and dynamic first and second hyperpolarizabilities and parameters for power conversion efficiency (Voc and ΔGinj) were computed using the time-dependent DFT/B3LYP/6–311++G(d,p) method. Hyperpolarizabilities were compared with those of urea (standard). The binding properties of 1 and 2 on TiO2 (anatase 101) were investigated using the MC method. The calculated electronic properties agree with the experimental results. The compounds display large Stokes shifts (> 200 nm), appreciable quantum yields and low band gaps. High LHE (87%) and large hyperpolarizabilities were obtained for 2. Dye 2 displayed a high Voc, while 1 exhibited a more negative ΔGinj. The negative adsorption energies of the 1-TiO2 (− 52.9 kJ/mol) and 2-TiO2 (– 57.1 kJ/mol) interfaces indicate their strong binding interactions with anatase. NBO analysis revealed that conjugation and hyperconjugation were the primary interactions responsible for the stabilization of the dyes. These dyes have the potential for use in optoelectronic and nonlinear optical applications.
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6
Citations from 2024:
6
(100%)
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Ojo N. D. et al. N-(1H-Benzo[d]imidazol-2-yl)-1-(3-substituted phenyl) methanimines as optoelectronic and nonlinear optical materials: spectroscopic and computational approaches // Chemical Papers. 2024. Vol. 78. No. 14. pp. 7775-7789.
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Ojo N. D., Adekusibe O. D., Odozi N. W., Obi Egbedi N. O. N-(1H-Benzo[d]imidazol-2-yl)-1-(3-substituted phenyl) methanimines as optoelectronic and nonlinear optical materials: spectroscopic and computational approaches // Chemical Papers. 2024. Vol. 78. No. 14. pp. 7775-7789.
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TY - JOUR
DO - 10.1007/s11696-024-03625-w
UR - https://link.springer.com/10.1007/s11696-024-03625-w
TI - N-(1H-Benzo[d]imidazol-2-yl)-1-(3-substituted phenyl) methanimines as optoelectronic and nonlinear optical materials: spectroscopic and computational approaches
T2 - Chemical Papers
AU - Ojo, Nathanael Damilare
AU - Adekusibe, Olaide Deborah
AU - Odozi, Nnenna Winifred
AU - Obi Egbedi, Nelson Okpako
PY - 2024
DA - 2024/09/02
PB - Springer Nature
SP - 7775-7789
IS - 14
VL - 78
SN - 0366-6352
SN - 1336-9075
SN - 2585-7290
ER -
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@article{2024_Ojo,
author = {Nathanael Damilare Ojo and Olaide Deborah Adekusibe and Nnenna Winifred Odozi and Nelson Okpako Obi Egbedi},
title = {N-(1H-Benzo[d]imidazol-2-yl)-1-(3-substituted phenyl) methanimines as optoelectronic and nonlinear optical materials: spectroscopic and computational approaches},
journal = {Chemical Papers},
year = {2024},
volume = {78},
publisher = {Springer Nature},
month = {sep},
url = {https://link.springer.com/10.1007/s11696-024-03625-w},
number = {14},
pages = {7775--7789},
doi = {10.1007/s11696-024-03625-w}
}
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MLA
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Ojo, Nathanael Damilare, et al. “N-(1H-Benzo[d]imidazol-2-yl)-1-(3-substituted phenyl) methanimines as optoelectronic and nonlinear optical materials: spectroscopic and computational approaches.” Chemical Papers, vol. 78, no. 14, Sep. 2024, pp. 7775-7789. https://link.springer.com/10.1007/s11696-024-03625-w.