Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9442
Title: β-Substituted ferrocenyl porphyrins: Synthesis, structure, and properties
Authors: Mobin, Shaikh M.
Misra, Rajneesh
Keywords: Cyclic voltammetric;Electronic communications;Ferrocenes;Ferrocenyl;Fluorescence quantum yield;Single crystal x-ray structures;Sonogashira cross-coupling reaction;UV-vis absorptions;Organometallics;Porphyrins
Issue Date: 2013
Citation: Sharma, R., Gautam, P., Mobin, S. M., & Misra, R. (2013). β-Substituted ferrocenyl porphyrins: Synthesis, structure, and properties. Dalton Transactions, 42(15), 5539-5545. doi:10.1039/c3dt00003f
Abstract: β-Substituted ferrocenyl porphyrins were designed and synthesized by the Pd-catalyzed Sonogashira cross-coupling reaction. The UV-vis absorption, emission, and cyclic voltammetric results indicate strong electronic communication between ferrocene and porphyrin. The porphyrin 4a is non-emissive in nature, while 4b and 4c show reduced fluorescence quantum yield. The single crystal X-ray structure of 4b is reported, which shows extensive C-H-π interactions. © 2013 The Royal Society of Chemistry.
URI: https://doi.org/10.1039/c3dt00003f
https://dspace.iiti.ac.in/handle/123456789/9442
ISSN: 1477-9226
Type of Material: Journal Article
Appears in Collections:Department of Chemistry

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