Theoretical investigation of solvent-polarity-dependent excited-state intramolecular proton transfer behavior for incorporated bulky -CF3 side semi-aliphatic polyimide.

IF 2.5 4区 化学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xiaoyu Zhang, Qingfang Zhang, Yujian Zhang, Qiuhe Ren, Hengyi Yuan
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引用次数: 0

Abstract

Context: In this work, the molecular properties of the novel semi-aliphatic polyimide derivative with incorporating bulky -CF3 side groups (3H-6F) in gas, chloroform and acetonitrile have been studied by DFT and TDDFT methods. The optimal reaction path could be found to regulate the occurrence of excited-state intramolecular proton transfer (ESIPT) reaction. In S1 state, the strength of O1-H2···O3 hydrogen bond increases significantly and contributes to the ESIPT reaction providing the driving force. We calculated the infrared (IR) vibrational spectrum to analyze the movement of O1-H2 bond expansion vibration and then studied the variations of hydrogen bonding strength. In addition, from the rearrangement of frontier molecular orbital (MOs), the electron density distribution should be also an extremely important positive factor in ESIPT process. According to potential energy curves (PECs), ESIPT reaction occurs after the molecule absorbs the photon to reach the first excited state, and the hydrogen atom of the O1-H2 bond combines with the adjacent O3 atom to form an isomer. After the completion of the ESIPT reaction process, the S1 state returns to S0 state with recovering the original structure. The barrier size and photoexcitation characteristics in different surroundings are also compared, based on which we present that the increase of solvent polarity promotes occurrence of ESIPT reaction process for 3H-6F fluorophore.

Methods: All molecular structures have been optimized using DFT and TDDFT method with B3LYP/6-311 +  + G(d,p) level by Gaussian 16 software. Vertical excitation simulations were based on TDDFT method with analyzing charge redistributions. Using Multiwfn 3.8 software, the core-valence bifurcation indexes were performed. Further, potential energy surfaces have been constructed, based on which the transition state configurations were found at the same level.

溶质-CF3侧半脂肪族聚酰亚胺分子内激发态质子转移行为的理论研究。
背景:本文采用DFT和TDDFT方法,研究了含-CF3侧基(3H-6F)的新型半脂肪族聚酰亚胺衍生物在气体、氯仿和乙腈中的分子性质。找到了调控激发态分子内质子转移(ESIPT)反应发生的最佳反应路径。S1态下,O1-H2··O3氢键强度显著增加,为ESIPT反应提供动力。通过计算红外(IR)振动谱来分析O1-H2键膨胀振动的运动,进而研究氢键强度的变化。此外,从前沿分子轨道(MOs)的重排来看,电子密度分布也应该是ESIPT过程中一个极其重要的积极因素。根据势能曲线(PECs), ESIPT反应发生在分子吸收光子达到第一激发态后,O1-H2键上的氢原子与相邻的O3原子结合形成同分异构体。ESIPT反应过程完成后,S1态恢复到S0态,恢复了原来的结构。对比了3H-6F荧光团在不同环境下的势垒大小和光激发特性,发现溶剂极性的增加促进了ESIPT反应过程的发生。方法:采用高斯16软件,采用B3LYP/6-311 + + G(d,p)水平的DFT和TDDFT方法对所有分子结构进行优化。基于TDDFT方法进行了纵向激励仿真,并对电荷重分布进行了分析。采用Multiwfn 3.8软件计算核心价分岔指数。此外,我们还构造了势能面,在此基础上发现了在同一能级上的过渡态构型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Molecular Modeling
Journal of Molecular Modeling 化学-化学综合
CiteScore
3.50
自引率
4.50%
发文量
362
审稿时长
2.9 months
期刊介绍: The Journal of Molecular Modeling focuses on "hardcore" modeling, publishing high-quality research and reports. Founded in 1995 as a purely electronic journal, it has adapted its format to include a full-color print edition, and adjusted its aims and scope fit the fast-changing field of molecular modeling, with a particular focus on three-dimensional modeling. Today, the journal covers all aspects of molecular modeling including life science modeling; materials modeling; new methods; and computational chemistry. Topics include computer-aided molecular design; rational drug design, de novo ligand design, receptor modeling and docking; cheminformatics, data analysis, visualization and mining; computational medicinal chemistry; homology modeling; simulation of peptides, DNA and other biopolymers; quantitative structure-activity relationships (QSAR) and ADME-modeling; modeling of biological reaction mechanisms; and combined experimental and computational studies in which calculations play a major role.
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