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作 者:Xindong Jiang Tingjiang Zhang Changliang Sun Yanqiu Meng Linjiu Xiao
机构地区:[1]College of Applied Chemistry,Key Laboratory of Rare-earth Chemistry and Applying of Liaoning Province,Shenyang University of Chemical Technology,Shenyang 110142,China [2]Department of Chemistry,Graduate School of Science,Hiroshima University,Higashi-Hiroshima 739-8526,Japan [3]Center of Physical and Chemistry Test,Shenyang University of Chemical Technology,Shenyang 110142,China [4]College of Pharmaceutical and Biological Engineering,Shenyang University of Chemical Technology,Shenyang 110142,China
出 处:《Chinese Chemical Letters》2019年第5期1055-1058,共4页中国化学快报(英文版)
基 金:supported by the National Natural Science Foundation of China(Nos.21542004,21372156);Young and middle-aged scientific and technological innovation talents of Shenyang Science and Technology Bureau(No.RC170140);Liaoning Province Natural Science Foundation(No.20170540721);Basic research on the application of Industrial Development of Shenyang Science and Technology Bureau(No.18013027);the Distinguished Professor Project of Liaoning province.We thank the Chinese Scholarship Council(No.20183058);State Administration of Foreign Experts Affairs(No.P183008050)Programme for financial support
摘 要:Using 2-vinylnaphthalene,aza-BODIPYs with the naphthyl groups at 1,7-positions were prepared and their photophysical properties were characterized.Due to attachment of the naphthyl groups at1,7-positions,aza-BODIPYs show long-wavelength absorption and emission in the near-infrared region.The singlet oxygen generation of the dibromo substituted aza-BODIPY with the naphthyl groups at1,7-positions as a photosensitizer was more effective than that of the corresponding aza-BODIPY with the phenyl groups at 1,7-positions.No photobleaching of the naphthyl-containing aza-BODIPY was observed and such NIR aza-BODIPY could be used for the singlet oxygen generation.Using 2-vinylnaphthalene, aza-BODIPYs with the naphthyl groups at 1,7-positions were prepared and their photophysical properties were characterized. Due to attachment of the naphthyl groups at1,7-positions, aza-BODIPYs show long-wavelength absorption and emission in the near-infrared region.The singlet oxygen generation of the dibromo substituted aza-BODIPY with the naphthyl groups at1,7-positions as a photosensitizer was more effective than that of the corresponding aza-BODIPY with the phenyl groups at 1,7-positions. No photobleaching of the naphthyl-containing aza-BODIPY was observed and such NIR aza-BODIPY could be used for the singlet oxygen generation.
关 键 词:Aza-BODIPY NIR Fluorescent DYE NAPHTHYL group PS
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