Literature DB >> 21322608

Quinoline-annulated porphyrins.

Joshua Akhigbe1, Matthias Zeller, Christian Brückner.   

Abstract

Porphyrin-2,3-dione mono- and dioximes were used as starting materials for the efficient syntheses of mono- and bis-quinoline-annulated porphyrins and their corresponding N-oxides. Owing to an extended π-system, these novel porphyrinoid chromophores show significantly red-shifted UV-vis spectra compared to the parent porphyrins. A crystal structure exemplifies the nonplanar conformation of the macrocycle.

Entities:  

Year:  2011        PMID： 21322608     DOI： 10.1021/ol1031848

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  3 in total

1.  The evaluation of NIR-absorbing porphyrin derivatives as contrast agents in photoacoustic imaging.

Authors:  Akram Abuteen; Saeid Zanganeh; Joshua Akhigbe; Lalith P Samankumara; Andres Aguirre; Nrusingh Biswal; Marcel Braune; Anke Vollertsen; Beate Röder; Christian Brückner; Quing Zhu
Journal:  Phys Chem Chem Phys       Date:  2013-11-14       Impact factor: 3.676

2.  In vivo photoacoustic tumor tomography using a quinoline-annulated porphyrin as NIR molecular contrast agent.

Authors:  Michael Luciano; Mohsen Erfanzadeh; Feifei Zhou; Hua Zhu; Tobias Bornhütter; Beate Röder; Quing Zhu; Christian Brückner
Journal:  Org Biomol Chem       Date:  2017-01-25       Impact factor: 3.876

3.  An unusual [4 + 2] fusion strategy to forge meso-N/O-heteroarene-fused (quinoidal) porphyrins with intense near-infrared Q-bands.

Authors:  Chengming Li; Lei Zhu; Wenbo Liang; Rongchuan Su; Jiangliang Yin; Yanmei Hu; Yu Lan; Di Wu; Jingsong You
Journal:  Chem Sci       Date:  2019-06-17       Impact factor: 9.825
  3 in total

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