Molecular Engineering of "Click"-Phospholes Towards Self-Assembled Luminescent Soft Materials

被引:38
作者
He, Xiaoming [1 ,2 ]
Lin, Jian-Bin [1 ,2 ]
Kan, Wang Hay [1 ,2 ]
Dong, Pengcheng [1 ,2 ]
Trudel, Simon [1 ,2 ]
Baumgartner, Thomas [1 ,2 ]
机构
[1] Univ Calgary, Dept Chem, Calgary, AB T2N 1N4, Canada
[2] Univ Calgary, Ctr Adv Solar Mat, Calgary, AB T2N 1N4, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
phospholes; self assembly; luminescence; stimuli-responsive materials; structure-property relationships; EXCITATION-ENERGY TRANSFER; LIQUID-CRYSTALLINE PHASES; ROOM-TEMPERATURE; STRUCTURE-PROPERTY; BUILDING-BLOCKS; POLYMERS; MODULATION; DESIGN; SALTS; COMPLEXATION;
D O I
10.1002/adfm.201302294
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Inspired by the self-assembled bilayer structures of natural amphiphilic phospholipids, a new class of highly luminescent click-phospholes with exocyclic alkynyl group at the phosphorus center is reported. These molecules can be easily functionalized with a self-assembly group to generate neutral phosphole-lipids. This novel approach retains the versatile reactivity of the phosphorus center, allowing further engineering of the photophysical and self-assembly properties of the materials at a molecular level. The results of this study highlight the importance of being able to balance weak intermolecular interactions for controlling the self-assembly properties of soft materials. Only molecules with the appropriate set of intermolecular arrangement/interactions show both organogel and liquid crystal mesophases with well-ordered microstructures. Moreover, an efficient energy transfer of the luminescent materials is demonstrated and applied in the detection of organic solvent vapors.
引用
收藏
页码:897 / 906
页数:10
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