Donor-Acceptor Stenhouse Adduct-Polydimethylsiloxane-Conjugates for Enhanced Photoswitching in Bulk Polymers

被引:11
|
作者
Clerc, Michele [1 ,2 ,3 ]
Tekin, Cem [1 ]
Ulrich, Sebastian [1 ]
Freire, Rafael V. M. [2 ]
Salentinig, Stefan [2 ]
Bruns, Nico [3 ]
Boesel, Luciano F. [1 ]
机构
[1] Empa, Swiss Fed Labs Mat Sci & Technol, Lab Biomimet Membranes & Text, Lerchenfeldstr 5, CH-9014 St Gallen, Switzerland
[2] Univ Fribourg, Dept Chem, Chemin Musee 9, CH-1700 Fribourg, Switzerland
[3] Univ Strathclyde, Dept Pure & Appl Chem, Thomas Graham Bldg,295 Cathedral St, Glasgow G1 1XL, Lanark, Scotland
基金
瑞士国家科学基金会;
关键词
donor-acceptor Stenhouse adducts; PDMS; photochromic materials; photoswitches; polysiloxanes; stimuli responsive polymers; LIGHT RESPONSIVE POLYMER; RIGID HOST MATRIX; VISIBLE-LIGHT; SWITCHING SPEEDS; DRUG-RELEASE; PHOTOCHROMISM; SURFACE;
D O I
10.1002/marc.202200120
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Donor-acceptor Stenhouse adducts (DASAs) are a rapidly emerging class of visible light-activated photochromes and DASA-functionalized polymers hold great promise as biocompatible photoresponsive materials. However, the photoswitching performance of DASAs in solid polymer matrices is often low, particularly in materials below their glass transition temperature. To overcome this limitation, DASAs are conjugated to polydimethylsiloxanes which have a glass transition temperature far below room temperature and which can create a mobile molecular environment around the DASAs for achieving more solution-like photoswitching kinetics in bulk polymers. The dispersion of DASAs conjugated to such flexible oligomers into solid polymer matrices allows for more effective and tunable DASA photoswitching in stiff polymers, such as poly(methyl methacrylate), without requiring modifications of the matrix. The photoswitching of conjugates with varying polymer molecular weight, linker type, and architecture is characterized via time-dependent UV-vis spectroscopy in organic solvents and blended into polymethacrylate films. In addition, DASA-functionalized polydimethylsiloxane networks, accessible via the same synthetic route, provide an alternative solution for achieving fast and efficient DASA photoswitching in the bulk owing to their intrinsic softness and flexibility. These findings may contribute to the development of DASA-functionalized materials with better tunable, more effective, and more reversible modulation of their optical properties.
引用
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页数:13
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