Insights into photo-induced excited state intramolecular proton transfer behavior for the novel 2-([1, 1'-biphenyl]-4-yl)-3-hydroxy-4H-chromen-4-one system: Effects of solvent polarity

被引:0
作者
Dong, Hao [1 ]
Li, Xiaoxiao [2 ]
Zhao, Shulin [3 ]
Zhao, Jinfeng [2 ,3 ,4 ]
Jin, Bing [2 ]
机构
[1] North China Elect Power Univ, Dept Math & Phys, Hebei Key Lab Phys & Energy Technol, Baoding, Peoples R China
[2] Shandong Univ, Inst Mol Sci & Engn, Inst Frontier & Interdisciplinary Sci, Qingdao, Peoples R China
[3] Shenyang Normal Univ, Coll Phys Sci & Technol, Shenyang, Peoples R China
[4] Shandong Univ, Inst Mol Sci & Engn, Inst Frontier & Interdisciplinary Sci, Qingdao 266237, Peoples R China
基金
中国国家自然科学基金;
关键词
charge redistribution; excited-state intramolecular proton transfer; intramolecular hydrogen bond; photoexcitation; solvent polarity; NONCOVALENT INTERACTIONS; HYDROGEN-BOND; THERMOCHEMISTRY; CONTINUUM; DYNAMICS;
D O I
10.1002/poc.4510
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In the light of potential applications for detecting cysteine in vitro and in vivo, 2-([1, 1'-biphenyl]-4-yl)-3-hydroxy-4H-chromen-4-one (B-bph-fla-OH) is explored about its excited state behaviors. Solvent-polarity-related photo-induced hydrogen bond of B-bph-fla-OH indicates nonpolar aprotic solvents largely enhance S-1-state hydrogen bonding interactions. Charge reorganization stemming from photoexcitation and polarity-dependent energy gap between HOMO and LUMO orbitals further reveals the excited state intramolecular proton transfer (ESIPT) tendency. Insights into potential energy curves along ESIPT paths in solvents with different polarities and emission spectral behaviors of proton-transfer tautomer, we present solvent polarity could harness the excited state behaviors for B-bph-fla-OH system.
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页数:8
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