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Investigation of Excited State Intramolecular Proton Transfer and Structural Dynamics in Bis-Benzimidazole Derivative (BBM) Using Femtosecond Stimulated Raman Spectroscopy
2023-04-25
状态已发表
摘要

Bis-benzimidazole derivative (BBM) molecule, consisting of two 2-(2'-Hydroxyphenyl) benzimidazole (HBI) halves, has been synthesized and successfully utilized as a ratiometric fluorescence sensor for the sensitive detection of Cu2+ based on enol-keto excited state intramolecular proton transfer (ESIPT). In this study, we strategically implement femtosecond stimulated Raman spec-troscopy and several time-resolved electronic spectroscopies, aided by quantum chemical calcula-tions to investigate the detailed primary photodynamics of BBM molecule. The results demonstrate that the ESIPT from BBM-enol* to BBM-keto* was observed in only one of HBI halves with a time constant of 300 fs, after that, the rotation of the dihedral angle between two HBI halves generate a planarized BBM-keto* isomer in 3 ps, leading to dynamics red shift of BBM-keto* emission.

关键词excited state intramolecular proton transfer structural dynamics transient absorption femtosecond fluorescence up-conversion femtosecond stimulated Raman spectroscopy
DOI10.20944/preprints202304.0894.v1
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出处Preprints
WOS记录号PPRN:67070790
WOS类目Chemistry, Physical
资助项目Natural Science Foundation of Shanghai[
文献类型预印本
条目标识符https://kms.shanghaitech.edu.cn/handle/2MSLDSTB/348135
专题物质科学与技术学院
物质科学与技术学院_PI研究组_刘伟民组
物质科学与技术学院_PI研究组_黄逸凡组
物质科学与技术学院_PI研究组_任毅组
物质科学与技术学院_博士生
大科学中心_PI研究组_翁祖谦组
大科学中心_公共科研平台_大科学装置建设部
作者单位
1.ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
2.STU & SIOM Joint Lab Superintense Lasers & Applicat, Shanghai 201210, Peoples R China
3.Shandong Univ, Key Lab Colloid & Interface Chem, Minist Educ, Jinan 250100, Peoples R China
推荐引用方式
GB/T 7714
Xie, Junhan,Wang, Ziyu,Zhu, Ruixue,et al. Investigation of Excited State Intramolecular Proton Transfer and Structural Dynamics in Bis-Benzimidazole Derivative (BBM) Using Femtosecond Stimulated Raman Spectroscopy. 2023.
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