4.8 Article

Spontaneous and Fast Molecular Motion at Room Temperature in the Solid State

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 58, 期 14, 页码 4536-4540

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201813554

关键词

aggregation-induced emission; ESIPT; molecular motion; polymer microphase visualization

资金

  1. National Science Foundation of China [21788102]
  2. Research Grants Council of Hong Kong [16308016, 16305015, 16305518, C2014-15G, C6009 -17G, A-HKUST605/16]
  3. Innovation and Technology Commission [ITC-CNERC14SC01, ITC/254/17]
  4. Science and Technology Plan of Shenzhen [J CYJ20160229205601482, JCYJ20170818113602462]

向作者/读者索取更多资源

The development of molecular machines requires new building blocks which are easy to characterize and visualize to realize a complexity comparable to their natural counterparts such as biological enzymes. Furthermore, with the desire to build functional nanobots capable of navigating living organisms, it is necessary that the building blocks show mobility even in the solid state. Herein we report a system which is emissive in the amorphous state but is non-fluorescent in the crystalline state due to the formation of extensive pi-pi interactions. This dual nature could be exploited for easy visualization of its solid-state molecular rearrangement. The emission of the amorphous film was quenched as the molecules spontaneously formed pi-pi interactions even in the solid state. Scratching the non-emissive film destroyed the interactions and restored the emission of the film. The emission quickly disappeared with an average lifetime of 20s as the compound reformed the pi-network even at room temperature.

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