Issue 65, 2019

meso-Alkylidenyl dibenzihexaphyrins: synthesis and protonation studies

Abstract

The synthesis and characterization of the alkylidenyl-dibenzihexaphyrins bearing four indanedionyl groups at the meso-positions linked via four meso-exocyclic double bonds is reported. Treatment with trifluoroacetic acid at 50 °C leads to C(α)-protonation of the two indanedionyl groups resulting increased macrocyclic conjugation with dramatic red shifted absorption spectra.

Graphical abstract: meso-Alkylidenyl dibenzihexaphyrins: synthesis and protonation studies

Supplementary files

Article information

Article type
Communication
Submitted
16 Jun 2019
Accepted
21 Jul 2019
First published
22 Jul 2019

Chem. Commun., 2019,55, 9693-9696

Author version available

meso-Alkylidenyl dibenzihexaphyrins: synthesis and protonation studies

S. Hong, R. Dutta, R. Kumar, Q. He, V. M. Lynch, J. L. Sessler and C. Lee, Chem. Commun., 2019, 55, 9693 DOI: 10.1039/C9CC04607K

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