{"title":"作为光电和非线性光学材料的 N-(1H-苯并[d]咪唑-2-基)-1-(3-取代苯基)甲亚胺:光谱和计算方法","authors":"Nathanael Damilare Ojo, Olaide Deborah Adekusibe, Nnenna Winifred Odozi, Nelson Okpako Obi-Egbedi","doi":"10.1007/s11696-024-03625-w","DOIUrl":null,"url":null,"abstract":"<div><p>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 (<b>1</b>) and N-(1H-benzo[d]imidazole(-2-yl)-1-(3-nitrophenyl))methanimine (<b>2</b>), were synthesized via one-pot single-step condensation and characterized using spectrometric (<sup>1</sup>H NMR, <sup>13</sup>C NMR, HRMS and FTIR) techniques. The optoelectronic, nonlinear optical (NLO), adsorption properties and natural bond orbital (NBO) analysis of <b>1</b> and<b> 2</b> 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 (<i>V</i><sub>oc</sub> and Δ<i>G</i><sub>inj</sub>) were computed using the time-dependent DFT/B3LYP/6–311++<i>G</i>(d,p) method. Hyperpolarizabilities were compared with those of urea (standard). The binding properties of <b>1</b> and<b> 2</b> on TiO<sub>2</sub> (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 <b>2</b>. Dye <b>2</b> displayed a high <i>V</i><sub>oc</sub>, while <b>1</b> exhibited a more negative Δ<i>G</i><sub>inj</sub>. The negative adsorption energies of the <b>1</b>-TiO<sub>2</sub> (− 52.9 kJ/mol) and <b>2</b>-TiO<sub>2</sub> (– 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.</p></div>","PeriodicalId":513,"journal":{"name":"Chemical Papers","volume":null,"pages":null},"PeriodicalIF":2.2000,"publicationDate":"2024-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"N-(1H-Benzo[d]imidazol-2-yl)-1-(3-substituted phenyl) methanimines as optoelectronic and nonlinear optical materials: spectroscopic and computational approaches\",\"authors\":\"Nathanael Damilare Ojo, Olaide Deborah Adekusibe, Nnenna Winifred Odozi, Nelson Okpako Obi-Egbedi\",\"doi\":\"10.1007/s11696-024-03625-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>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 (<b>1</b>) and N-(1H-benzo[d]imidazole(-2-yl)-1-(3-nitrophenyl))methanimine (<b>2</b>), were synthesized via one-pot single-step condensation and characterized using spectrometric (<sup>1</sup>H NMR, <sup>13</sup>C NMR, HRMS and FTIR) techniques. The optoelectronic, nonlinear optical (NLO), adsorption properties and natural bond orbital (NBO) analysis of <b>1</b> and<b> 2</b> 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 (<i>V</i><sub>oc</sub> and Δ<i>G</i><sub>inj</sub>) were computed using the time-dependent DFT/B3LYP/6–311++<i>G</i>(d,p) method. Hyperpolarizabilities were compared with those of urea (standard). The binding properties of <b>1</b> and<b> 2</b> on TiO<sub>2</sub> (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 <b>2</b>. Dye <b>2</b> displayed a high <i>V</i><sub>oc</sub>, while <b>1</b> exhibited a more negative Δ<i>G</i><sub>inj</sub>. The negative adsorption energies of the <b>1</b>-TiO<sub>2</sub> (− 52.9 kJ/mol) and <b>2</b>-TiO<sub>2</sub> (– 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.</p></div>\",\"PeriodicalId\":513,\"journal\":{\"name\":\"Chemical Papers\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2024-09-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Papers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11696-024-03625-w\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Engineering\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Papers","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11696-024-03625-w","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Engineering","Score":null,"Total":0}
N-(1H-Benzo[d]imidazol-2-yl)-1-(3-substituted phenyl) methanimines as optoelectronic and nonlinear optical materials: spectroscopic and computational approaches
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.
Chemical PapersChemical Engineering-General Chemical Engineering
CiteScore
3.30
自引率
4.50%
发文量
590
期刊介绍:
Chemical Papers is a peer-reviewed, international journal devoted to basic and applied chemical research. It has a broad scope covering the chemical sciences, but favors interdisciplinary research and studies that bring chemistry together with other disciplines.