Meso-tris(2-furyl/2-thienyl) substituted porphyrin-ferrocene ‘click’ conjugates: synthesis, experimental, and computational studies
| dc.contributor.author | Shet, S.N. | |
| dc.contributor.author | Patil, M. | |
| dc.contributor.author | Shetti, V.S. | |
| dc.date.accessioned | 2026-02-04T12:24:49Z | |
| dc.date.issued | 2024 | |
| dc.description.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. | |
| dc.identifier.citation | New Journal of Chemistry, 2024, 48, 25, pp. 11349-11359 | |
| dc.identifier.issn | 11440546 | |
| dc.identifier.uri | https://doi.org/10.1039/d4nj01788a | |
| dc.identifier.uri | https://idr.nitk.ac.in/handle/123456789/21126 | |
| dc.publisher | Royal Society of Chemistry | |
| dc.subject | Computation theory | |
| dc.subject | Copper compounds | |
| dc.subject | Density functional theory | |
| dc.subject | Iron compounds | |
| dc.subject | Organometallics | |
| dc.subject | Red Shift | |
| dc.subject | % reductions | |
| dc.subject | Click reaction | |
| dc.subject | Computational studies | |
| dc.subject | Emission bands | |
| dc.subject | Ethynylferrocene | |
| dc.subject | Ferrocenes | |
| dc.subject | Photoinduced electron-transfer process | |
| dc.subject | Porphyrin rings | |
| dc.subject | Red-shifted | |
| dc.subject | Thienyl | |
| dc.subject | Porphyrins | |
| dc.subject | dichloromethane | |
| dc.subject | ferrocene | |
| dc.subject | porphyrin | |
| dc.subject | proton | |
| dc.subject | pyrrole derivative | |
| dc.subject | trifluoroacetic acid | |
| dc.subject | absorption | |
| dc.subject | absorption spectroscopy | |
| dc.subject | Article | |
| dc.subject | carbon nuclear magnetic resonance | |
| dc.subject | catalysis | |
| dc.subject | click chemistry | |
| dc.subject | column chromatography | |
| dc.subject | comparative study | |
| dc.subject | conjugate | |
| dc.subject | cyclic voltammetry | |
| dc.subject | density functional theory | |
| dc.subject | differential pulse voltammetry | |
| dc.subject | electrochemical analysis | |
| dc.subject | fluorescence | |
| dc.subject | oxidation | |
| dc.subject | oxidation reduction potential | |
| dc.subject | polymerization | |
| dc.subject | proton nuclear magnetic resonance | |
| dc.subject | purification | |
| dc.subject | quantum yield | |
| dc.subject | reduction (chemistry) | |
| dc.subject | substitution reaction | |
| dc.subject | synthesis | |
| dc.title | Meso-tris(2-furyl/2-thienyl) substituted porphyrin-ferrocene ‘click’ conjugates: synthesis, experimental, and computational studies |
