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有机荧光分子2-氰基-3-(3, 4-二甲氧基苯基)-2-丙烯酰胺的可逆压致变色和质子刺激响应性能
引用本文:边高峰,黄华,占玲玲,吕晓静,曹枫,张诚,张玉建.有机荧光分子2-氰基-3-(3, 4-二甲氧基苯基)-2-丙烯酰胺的可逆压致变色和质子刺激响应性能[J].物理化学学报,2016,32(2):589-594.
作者姓名:边高峰  黄华  占玲玲  吕晓静  曹枫  张诚  张玉建
作者单位:1 浙江工业大学化学工程学院, 杭州 3100142 杭州师范大学有机硅化学及材料技术重点实验室, 杭州 3100123 湖州师范学院材料化学系, 浙江湖州 313000
基金项目:the National Natural Science Foundation of China(51203138, 51273179, 51573165, 51406030);Natural ScienceFoundation of Zhejiang Province, China(LY15E030006, LY15E030002);Natural Science Foundation of Zhejiang University of Technology, China(1401101002408);Natural Science Foundation of Huzhou, China(2014YZ02)
摘    要:设计合成了3-芳基-2-腈基丙烯酰胺类有机发光小分子2-氰基-3-(3, 4-二甲氧基苯基)-2-丙烯酰胺(CDMPA)。经研究发现, CDMPA化合物具有明显的压致变色和酸致变色现象。在外力刺激下,化合物CDMPA荧光最大发射峰发生20 nm的红移,经过加热或蒸汽处理后可恢复初始状态。对样品研磨前后粉末的X射线衍射图谱及荧光寿命衰减曲线进行测试分析得出, CDMPA压致变色现象归因于分子构型由晶态到无定形态的转化。另外,在酸刺激下CDMPA发光颜色由蓝光红移至黄光,最大发射波长红移33 nm。经过二甲基甲酰胺(DMF)处理后可恢复到初始状态。由测试得到的红外光谱及分子轨道理论计算推测,酸致变色现象是由氨基取代基的质子化影响了CDMPA前线分子轨道引起的。本研究可使人们深入了解这种类型材料的多刺激响应发光机制,且显著的颜色变化性能使CDMPA在传感器和检测装置方面具有潜在的应用前景。

关 键 词:丙烯酰胺衍生物  多刺激响应  荧光转换  前线分子轨道  荧光寿命  
收稿时间:2015-10-14

Reversible Piezochromism and Protonation Stimuli-Response of (Z)-2-Cyano-3-(3,4-dimethoxyphenyl)acrylamide
Gao-Feng BIAN,Hua HUANG,Ling-Ling ZHAN,Xiao-Jing Lü,Feng CAO,Cheng ZHANG,Yu-Jian ZHANG.Reversible Piezochromism and Protonation Stimuli-Response of (Z)-2-Cyano-3-(3,4-dimethoxyphenyl)acrylamide[J].Acta Physico-Chimica Sinica,2016,32(2):589-594.
Authors:Gao-Feng BIAN  Hua HUANG  Ling-Ling ZHAN  Xiao-Jing Lü  Feng CAO  Cheng ZHANG  Yu-Jian ZHANG
Institution:1. College of Chemical Engineering, Zhejiang University of Technology, Hangzhou 310014, P. R. China;2. Key Laboratory of Organosilicon Chemistry and Material Technology, Hangzhou Normal University, Hangzhou 310012, P. R. China;3. Department of Materials Chemistry, Huzhou University, Huzhou 313000, Zhejiang Province, P. R. China
Abstract:A 3-aryl-2-cyano acrylamide derivative (Z)-2-cyano-3-(3, 4-dimethoxy-phenyl)acrylamide (CDMPA) was designed and synthesized, which exhibited piezochromism and acidchromism properties. Under external mechanical force stimuli, CDMPA showed a red-shift of 20 nm in its fluorescence emission and the mechanically induced luminescence color could return to the original state via heating or solvent vapor treatment. Powder X-ray diffraction (XRD) and fluorescence lifetime experiments indicated that the piezochromic luminescence could be attributed to the transformation from the crystalline to the amorphous phase. Additionally, the fluorescence color changed from blue to yellow with a red-shift of 33 nm using the stimulus of protonation. The emission color was recovered upon fuming with dimethyl formamide (DMF) vapor. Infrared (IR) spectra of CDMPA powder and theoretical calculation of the frontier molecular orbitals showed that protonation of the amino moieties in CDMPA had a significant effect on the frontier molecular orbitals and, thus, caused the acidchromism phenomenon. This study provides comprehensive insight into the stimuli-responsive luminescent mechanisms within this type of compound and the reversible switching of emission color may enable discovery of novel applications of CDMPA for detection and sensing devices.
Keywords:Acrylamide derivative  Multi-stimuli response  Fluorescence switching  Frontier molecular orbital  Fluorescence lifetime  
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