Dipyrene-Terminated Oligosilanes Enable Ratiometric Fluorescence Response in Polymers toward Mechano- and Thermo-Stimuli

Developing fluorescent motifs capable of displaying mechano-and thermo-stimuli reversibly and ratiometrically is appealing for monitoring the deformation or temperature to which polymers are subjected. Here, a series of excimer-type chromophores Sin-Py (n = 1-3) consisting of two pyrenes linked with oligosilanes of one to three silicon atoms is developed as the fluorescent motif incorporated in a polymer. The fluorescence of Sin-Py is steered with the linker length where Si2-Py and Si3-Py with disilane and trisilane linkers display prominent excimer emission accompanied by pyrene monomer emission. Covalent incorporation of Si2-Py and Si3- Py in polyurethane gives fluorescent polymers PU-Si2-Py and PU-Si3-Py, respectively, where intramolecular pyrene excimers and corresponding combined emission of excimer and monomer are obtained. Polymer films of PU-Si2-Py and PU-Si3-Py display instant and reversible ratiometric fluorescence change during the uniaxial tensile test. The mechanochromic response arises from the reversible suppression of excimer formation during the mechanically induced separation of the pyrene moieties and relaxation. Furthermore, PU-Si2-Py and PU-Si3-Py show thermochromic response toward temperature, and the inflection point from the ratiometric emission as a function of temperature gives an indication of the glass transition temperature (Tg) of the polymers. The design of the excimer-based mechanophore with oligosilane provides a generally implementable way to develop mechano-and thermo-dual-responsive polymers.

Automated summary

The development of fluorescent motifs that can reversibly and ratiometrically display mechano- and thermo-stimuli is attractive for monitoring the deformation or temperature of polymers. In this study, a series of excimer-type chromophores called Sin-Py (n = 1-3) was developed and incorporated into a polymer. The fluorescence of Sin-Py was controlled by the linker length, and the resulting fluorescent polymers, PU-Si2-Py and PU-Si3-Py, exhibited mechano- and thermo-responsive behavior. The mechanochromic response of the polymer films was due to the reversible suppression of excimer formation during mechanical deformation, while the thermochromic response indicated the glass transition temperature (Tg) of the polymers. This design provides a generally implementable way to develop dual-responsive polymers.