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CAS: 877615-99-1
MF: C16BN2F2Cl2
MW: 339.8984
Synonyms:

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Yu Zhang

Dalian Institute of Chemical Physics
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Liang Feng

Dalian Institute of Chemical Physics
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Qing Yang

University of Science and Technology of China
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Huayu Qiu

Hangzhou Normal University
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Kezhi Jiang

Hangzhou Normal University
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Dimitri Komiotis

University of Thessaly
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Mario Smet

University of Leuven
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Li-Zhu Wu

Technical Institute of Physics and Chemistry & Graduate University
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Chen-Ho Tung

The Chinese Academy of Sciences
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Santiago De La Moya

Universidad Complutense de Madrid
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Co-reporter: I. Esnal, G. Duran-Sampedro, A. R. Agarrabeitia, J. Bañuelos, I. García-Moreno, M. A. Macías, E. Peña-Cabrera, I. López-Arbeloa, S. de la Moya and M. J. Ortiz  
pp: 8239-8247
Publication Date(Web):23 Feb 2015
DOI: 10.1039/C5CP00193E
Linking amino and hydroxycoumarins to BODIPYs through the amino or hydroxyl group lets the easy construction of unprecedented photostable coumarin–BODIPY hybrids with broadened and enhanced absorption in the UV spectral region, and outstanding wavelength-tunable laser action within the green-to-red spectral region (∼520–680 nm). These laser dyes allow the generation of a valuable tunable UV (∼260–350 nm) laser source by frequency doubling, which is essential to study accurately the photochemistry of biological molecules under solar irradiation. The tunability is achieved by selecting the substitution pattern of the hybrid. Key factors are the linking heteroatom (nitrogen vs. oxygen), the number of coumarin units joined to the BODIPY framework and the involved linking positions.
Co-reporter: I. Esnal, G. Duran-Sampedro, A. R. Agarrabeitia, J. Bañuelos, I. García-Moreno, M. A. Macías, E. Peña-Cabrera, I. López-Arbeloa, S. de la Moya and M. J. Ortiz
pp: NaN8247-8247
Publication Date(Web):2015/02/23
DOI: 10.1039/C5CP00193E
Linking amino and hydroxycoumarins to BODIPYs through the amino or hydroxyl group lets the easy construction of unprecedented photostable coumarin–BODIPY hybrids with broadened and enhanced absorption in the UV spectral region, and outstanding wavelength-tunable laser action within the green-to-red spectral region (∼520–680 nm). These laser dyes allow the generation of a valuable tunable UV (∼260–350 nm) laser source by frequency doubling, which is essential to study accurately the photochemistry of biological molecules under solar irradiation. The tunability is achieved by selecting the substitution pattern of the hybrid. Key factors are the linking heteroatom (nitrogen vs. oxygen), the number of coumarin units joined to the BODIPY framework and the involved linking positions.
Co-reporter: César Ray;Dr. Esther M. Sánchez-Carnerero; Florencio Moreno; Beatriz L. Maroto; Antonia R. Agarrabeitia; María J. Ortiz; Íñigo López-Arbeloa; Jorge Bañuelos;Komlan D. Cohovi;Jamie L. Lunkley; Gilles Muller; Santiago delaMoya
pp: 8805-8808
Publication Date(Web):
DOI: 10.1002/chem.201601463

Abstract

Simple organic molecules (SOM) based on bis(haloBODIPY) are shown to enable circularly polarized luminescence (CPL), giving rise to a new structural design for technologically valuable CPL-SOMs. The established design comprises together synthetic accessibility, labile helicity, possibility of reversing the handedness of the circularly polarized emission, and reactive functional groups, making it unique and attractive as advantageous platform for the development of smart CPL-SOMs.