Title Controllable multicolor switching of oligopeptide-based mechanochromic molecules: from gel phase to solid powder
Authors Ma, Zhiyong
Wang, Zhijian
Xu, Zejun
Jia, Xinru
Wei, Yen
Affiliation Peking Univ, Beijing Natl Lab Mol Sci, Key Lab Polymer Chem & Phys, Minist Educ,Coll Chem & Mol Engn, Beijing 100871, Peoples R China.
Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China.
Keywords PHOTOLUMINESCENT POLYMER BLENDS
ENHANCED EMISSION COMPOUNDS
INDUCED COLOR CHANGES
SUPRAMOLECULAR HYDROGEL
FLUORESCENT ORGANOGELS
LIQUID-CRYSTALS
PHOTONIC GELS
LUMINESCENCE
AGGREGATION
GELATION
Issue Date 2015
Publisher journal of materials chemistry c
Citation JOURNAL OF MATERIALS CHEMISTRY C.2015,3,(14),3399-3405.
Abstract A series of molecules with pyrene and rhodamine B as color-producing mechanophores linked by different spacers were synthesized and their mechanochromic properties were studied. Interestingly, we found that the molecule with diphenylalanine as a linker (PHE-2) showed a sequential multicolored switch from deep blue to bluish green and further to a reddish color, which was associated with the phase change from gel to xerogel as the solvent evaporated, and to a solid powder triggered by grinding. However, the gel and xerogel of the molecule with the pentaphenylalanine linker (PHE-5) exhibited the same deep blue color that switched to bluish green and further to a reddish powder by virtue of continuously grinding the xerogel sample in situ. The multicolored switching of PHE-2 and PHE-5 was realized by the variation of the self-assembled structures, which induced the transition of the pyrene excimers from excimer 1 (deep blue) to excimer 2 (bluish green), and by the chemical reaction of rhodamine B from a spirolactam to a ring-opened amide (red). From the experimental results, we may conclude that the crucial point for controlling and tuning the tricolored fluorescent switch of this system is to constrict the pyrene excimer in an overlapped packing mode, which can be achieved (1) by controlling the molecular structure; and (2) by confining the excimers of pyrene in a restricted environment.
URI http://hdl.handle.net/20.500.11897/150329
ISSN 2050-7526
DOI 10.1039/c5tc00148j
Indexed SCI(E)
EI
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