1,2 -二(4-吡啶基)乙烯在水溶液中pH控制的荧光开关行为

IF 3.1 4区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Wen-sheng ZOU , Qian-jin SHEN , Yu WANG , Wei-jun JIN
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引用次数: 5

摘要

随着pH值从8.45降低到−1.0,1,2-双(4-吡啶基)乙烯(BPE)的紫外-可见吸收光谱和荧光光谱在8.45 - 7.20、7.20-5.62、5.62-2.60和2.60-1.0四个不同的连续pH阶段呈现相同的变化趋势,即不变化、减小、增大、再减小。其中,在7.20 ~ 5.62范围内,荧光波长由418 nm蓝移至359 nm,而UV-Vis吸收波长则由285 nm红移至298 nm。当pH值从2.60降至- 1.0时,BPE的荧光强度下降甚至猝灭,这可能是由于其阳离子-π相互作用降低了BPE的π电子云密度。根据荧光数据得到两个解离常数pKa1(4.30±0.01)和pKa2(5.65±0.04)。荧光光谱的变化表明BPE具有“off-on-off”的开关行为。BPE的荧光光谱几乎与α-和β-环糊精的存在无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fluorescent Switch Behavior of 1, 2-Bis(4-pyridyl) Ethylene Controlled by pH in Aqueous Solution

With the decrease of pH value from 8.45 to −1.0, the UV-Vis absorption and fluorescent spectra of 1,2-bis(4-pyridyl) ethylene(BPE) took on the same changing trend at four different successive pH stages: 8.45—7.20, 7.20—5.62, 5.62—2.60, and 2.60—1.0, namely, no change, decrease, increase, and decrease again. Among these, in a range of 7.20—5.62, the fluorescence wavelength blueshifted from 418 to 359 nm, but the UV-Vis absorption wavelength, in contrast, redshifted from 285 to 298 nm. The fluorescence intensity of BPE had a drop even to quench upon a decline in the pH value from 2.60 to −1.0 probably owing to its cation-π interaction to reduce the π electron cloud density of BPE. Two dissociation constants, pKa1(4.30±0.01) and pKa2(5.65±0.04), were obtained based on fluorescence data. The changes of fluorescence spectra indicate that BPE has “off-on-off” switch behavior. The fluorescent spectra of BPE were nearly independent on the presence of α- and β-cyclodextrins.

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来源期刊
CiteScore
5.30
自引率
6.50%
发文量
152
审稿时长
3.0 months
期刊介绍: The journal publishes research articles, letters/communications and reviews written by faculty members, researchers and postgraduates in universities, colleges and research institutes all over China and overseas. It reports the latest and most creative results of important fundamental research in all aspects of chemistry and of developments with significant consequences across subdisciplines. Main research areas include (but are not limited to): Organic chemistry (synthesis, characterization, and application); Inorganic chemistry (bio-inorganic chemistry, inorganic material chemistry); Analytical chemistry (especially chemometrics and the application of instrumental analysis and spectroscopy); Physical chemistry (mechanisms, catalysis, thermodynamics and dynamics); Polymer chemistry and polymer physics (mechanisms, material, catalysis, thermodynamics and dynamics); Quantum chemistry (quantum mechanical theory, quantum partition function, quantum statistical mechanics); Biochemistry; Biochemical engineering; Medicinal chemistry; Nanoscience (nanochemistry, nanomaterials).
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