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Issue 57, 2015
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A fused meso-aminoporphyrin: a switchable near-IR chromophore

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Abstract

An aryl amine attached to the meso position of a porphyrin controls the π-delocalization using a redox process or a protonation/deprotonation centered at the meso-nitrogen. An easily accessible modulated motif affords a switchable near-IR chromophore as reflected by significant changes in absorption and fluorescence spectra.

Graphical abstract: A fused meso-aminoporphyrin: a switchable near-IR chromophore

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Publication details

The article was received on 09 Feb 2015, accepted on 10 Mar 2015 and first published on 10 Mar 2015


Article type: Communication
DOI: 10.1039/C5CC01231G
Citation: Chem. Commun., 2015,51, 11362-11365
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    A fused meso-aminoporphyrin: a switchable near-IR chromophore

    M. Pawlicki, K. Hurej, K. Kwiecińska, L. Szterenberg and L. Latos-Grażyński, Chem. Commun., 2015, 51, 11362
    DOI: 10.1039/C5CC01231G

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