共 73 条
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.
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页码:897 / 906
页数:10
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