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

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Date

2024

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Royal Society of Chemistry

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. © 2024 The Royal Society of Chemistry.

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Keywords

Computation theory, Copper compounds, Density functional theory, Iron compounds, Organometallics, Red Shift, % reductions, Click reaction, Computational studies, Emission bands, Ethynylferrocene, Ferrocenes, Photoinduced electron-transfer process, Porphyrin rings, Red-shifted, Thienyl, Porphyrins, dichloromethane, ferrocene, porphyrin, proton, pyrrole derivative, trifluoroacetic acid, absorption, absorption spectroscopy, Article, carbon nuclear magnetic resonance, catalysis, click chemistry, column chromatography, comparative study, conjugate, cyclic voltammetry, density functional theory, differential pulse voltammetry, electrochemical analysis, fluorescence, oxidation, oxidation reduction potential, polymerization, proton nuclear magnetic resonance, purification, quantum yield, reduction (chemistry), substitution reaction, synthesis

Citation

New Journal of Chemistry, 2024, 48, 25, pp. 11349-11359

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