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CAS: 1281983-52-5
MF: C18H15BN2F2Cl2
MW: 379.0389
Synonyms:

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Yoshihiro Matano

Niigata University
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Co-reporter: Takaharu Satoh;Dr. Mao Minoura;Dr. Haruyuki Nakano;Dr. Ko Furukawa;Dr. Yoshihiro Matano
pp: 2235-2238
Publication Date(Web):
DOI: 10.1002/anie.201510734

Abstract

The first examples of air-stable 20π-electron 5,10,15,20-tetraaryl-5,15-diaza-5,15-dihydroporphyrins, their 18π-electron dications, and the 19π-electron radical cation were prepared through metal-templated annulation of nickel(II) bis(5-arylamino-3-chloro-8-mesityldipyrrin) complexes followed by oxidation. The neutral 20π-electron derivatives are antiaromatic and the cationic 18π-electron derivatives are aromatic in terms of the magnetic criterion of aromaticity. The meso N atoms in these diazaporphyrinoids give rise to characteristic redox and optical properties for the compounds that are not typical of isoelectronic 5,10,15,20-tetraarylporphyrins.

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.