Novel Solid‐State Fluorophores, a Series of Cyanostilbene‐Based Amorphous Molecular Materials

Author:

Fukushima Hiroya1,Miyagishi Kou1,Mori Kensuke1,Sagara Yoshimitsu23,Kokado Kenta45,Tamaoki Nobuyuki4,Nakamura Takayoshi4,Nakano Hideyuki1ORCID

Affiliation:

1. Department of Applied Chemistry Muroran Institute of Technology 27-1, Mizumoto-cho, Muroran Hokkaido 050-8585 Japan

2. Department of Materials Science and Engineering Tokyo Institute of Technology 2-12-1 Ookayama, Meguro-ku Tokyo 152-8552 Japan

3. Living Systems Materialogy (LiSM) Research Group International Research Frontiers Initiative (IRFI) Tokyo Institute of Technology 4259 Nagatsuta-cho, Midori-ku Yokohama 226-8501 Japan

4. Research Institute for Electronic Science Hokkaido University N20, W10, Kita-ku, Sapporo Hokkaido 001-0020 Japan

5. Toyota Technological Institute 2-12-1 Hisakata, Tempaku-ku Nagoya 468-8511 Japan

Abstract

AbstractWe have designed and synthesized a novel series of cyanostilbene‐based amorphous molecular materials with different methylene chain lengths, BMAC‐n (n=3,4,5,6), and investigated their emitting properties in solution and various solid states. All BMAC‐n molecules showed solvatochromic fluorescence in solutions. Emission spectra of BMAC‐n molecules in the same solution were identical to one another irrespective of the methylene chain length while the spectra in crystalline states depended on their methylene chain length. As in solutions, emission spectra of their spin‐coated amorphous films were identical to each other irrespective of the methylene chain length. Emission spectra of rubbed amorphous films prepared by grinding their crystals were identical to those for spin‐coated amorphous films; however, comparative studies between spin‐coated and rubbed amorphous films indicated that fluorescence quantum yields and photochemical reactivity depend on the preparation method.

Publisher

Wiley

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