Issue 25, 2024

Meso-tris(2-furyl/2-thienyl) substituted porphyrin–ferrocene ‘click’ conjugates: synthesis, experimental, and computational studies

Abstract

The chemical synthesis of 5-(4-azidophenyl)-10,15,20-tris(2-furyl/2-thienyl)porphyrins and their utilization in a Cu(I) catalyzed alkyne-azide ‘click’ reaction (CuAAC) with ethynylferrocene to obtain the hitherto unknown meso-tris(2-furyl/2-thienyl) substituted porphyrin–ferrocene ‘click’ conjugates are reported. These new ‘click’ conjugates were studied along with the reference ‘click’ conjugates containing all-meso-aryl substituted porphyrins by experimental and computational methods. Compared to the reference, the new conjugates displayed red-shifted absorption/emission bands, easier porphyrin ring reduction, and an efficient photoinduced electron transfer (PET) process from ferrocene to a porphyrin unit. Density functional theory (DFT) calculations performed on these conjugates revealed a good correlation with the experimental results.

Graphical abstract: Meso-tris(2-furyl/2-thienyl) substituted porphyrin–ferrocene ‘click’ conjugates: synthesis, experimental, and computational studies

Supplementary files

Article information

Article type
Paper
Submitted
18 Apr 2024
Accepted
24 May 2024
First published
27 May 2024

New J. Chem., 2024,48, 11349-11359

Meso-tris(2-furyl/2-thienyl) substituted porphyrin–ferrocene ‘click’ conjugates: synthesis, experimental, and computational studies

S. N. Shet, M. Patil and V. S. Shetti, New J. Chem., 2024, 48, 11349 DOI: 10.1039/D4NJ01788A

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