Synthesis and chiroptical properties of phenanthrene-fused N2O-type BODIPYs |
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Authors: | Yuki Gobo Ryota Matsuoka Yusuke Chiba Takashi Nakamura Tatsuya Nabeshima |
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Affiliation: | Graduate School of Pure and Applied Sciences and Tsukuba Research Center for Energy Materials Science (TREMS), University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8571, Japan |
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Abstract: | A series of phenanthrene-fused N2O-type boron-dipyrrin complexes (BODIPYs) with various substituents were synthesized. The synthesized BODIPYs show light absorption and emission in the red to near-infrared region due to their extended π-system. Furthermore, the first optical resolution of the N2O-type BODIPY was achieved using the phenyl-substituted complex. The separated enantiomers are stable to racemization at room temperature, and exhibited a Cotton effect in the deep-red region. |
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Keywords: | BODIPY Chirality Near-infrared fluorescence Circular dichroism |
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