Issue 77, 2016

NIR absorbing diferrocene-containing meso-cyano-BODIPY with a UV-Vis-NIR spectrum remarkably close to that of magnesium tetracyanotetraferrocenyltetraazaporphyrin

Abstract

Diferrocene-containing meso-cyano-BODIPY (4) was prepared by the direct cyanation/oxidation reaction of symmetric BODIPY 1 followed by Knoevenagel condensation with ferrocenealdehyde. Ferrocene-containing BODIPY 4 was characterized by a variety of spectroscopic, electrochemical, and theoretical methods and its UV-Vis-NIR spectrum has a striking similarity with a UV-Vis-NIR spectrum of the previously reported magnesium 2(3),7(8),12(13),17(18)-tetracyano-3(2),8(7),13(12),18(17)-tetraferrocenyl-5,10,15,20-tetraazaporphyrin.

Graphical abstract: NIR absorbing diferrocene-containing meso-cyano-BODIPY with a UV-Vis-NIR spectrum remarkably close to that of magnesium tetracyanotetraferrocenyltetraazaporphyrin

Supplementary files

Article information

Article type
Communication
Submitted
01 Aug 2016
Accepted
30 Aug 2016
First published
30 Aug 2016

Chem. Commun., 2016,52, 11563-11566

NIR absorbing diferrocene-containing meso-cyano-BODIPY with a UV-Vis-NIR spectrum remarkably close to that of magnesium tetracyanotetraferrocenyltetraazaporphyrin

N. O. Didukh, Y. V. Zatsikha, G. T. Rohde, T. S. Blesener, V. P. Yakubovskyi, Y. P. Kovtun and V. N. Nemykin, Chem. Commun., 2016, 52, 11563 DOI: 10.1039/C6CC06344F

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