Affiliation:
1. Beijing Advanced Innovation Center for Soft Matter Science and Engineering State Key Laboratory of Organic‐Inorganic Composites College of Chemical Engineering Beijing University of Chemical Technology Beijing 100029 China
2. College of Engineering Peking University Beijing 100871 China
3. Department of Chemical Engineering & Chemistry and Institute for Complex Molecular Systems Eindhoven University of Technology P.O. Box 513 Eindhoven 5600 MB The Netherlands
4. Guangdong Provincial Key Laboratory of Functional and Intelligent Hybrid Materials and Devices South China University of Technology Guangzhou 510640 China
Abstract
AbstractAn ultrasensitive concentration‐dependent ESIPT mechanochromic mechanophore (MM) NaMz (4‐amino‐2‐(1H‐naphtho[2,3‐d]imidazol‐2‐yl)phenol), which exhibits real‐time and reversible multicolor mechanochromism in polyurethane is reported. NaMz has one single link point and can be obtained facilely by one‐step reaction. As the concentration of NaMz increased from 0.01 to 0.05 mol%, the intensity ratio IE/IK of enol emission to keto emission changed significantly and concentration‐dependent multicolor fluorescence (yellow, white, blue) can be realized. Then, a simple strategy, force‐tuning the aggregation state of NaMz molecules, to adjust the ESIPT process to achieve ultrasensitive colorful mechanochromism is proposed. Intriguingly, force‐tuned white light emitting can be realized for 0.035 mol%NaMz@PU. Because the extended conjugation structure, NaMz@PU shows a red‐shifted keto emission at 541 nm with a larger Stoke shift compared with PhMz‐NH2@PU, which is also the key to multicolor concentration‐dependent polymer mechanochromism of NaMz@PU. Control experiments of NaMz‐OH@PU and NaMz‐3OH@PU show that the aliphatic hydroxyl group on the naphthimidazole moiety impedes the planarization of molecular structure and thus hinders aggregation, further verifying that the multicolor concentration‐dependent mechanochromism of NaMz@PU is indeed caused by force induced disaggregation. The excellent color‐changing effect, real‐time reversible force‐optical coupling and precise regulation of this study will make a new contribution to polymer mechanochemistry.
Funder
National Natural Science Foundation of China
Natural Science Foundation of Beijing Municipality
Fundamental Research Funds for the Central Universities