Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9413
Title: Donor-acceptor meso-alkynylated ferrocenyl BODIPYs: Synthesis, structure, and properties
Authors: Misra, Rajneesh
Mobin, Shaikh M.
Keywords: Computational studies;Conjugation length;Donor-acceptors;Electronic communications;Palladium-catalyzed;Single crystal x-ray structures;Sonogashira cross-coupling reaction;Supramolecular interactions;Electronic structure;Organometallics;4,4 difluoro 4 bora 3a,4a diaza s indacene;4,4-difluoro-4-bora-3a,4a-diaza-s-indacene;alkyne;boron derivative;ferrous ion;article;chemical structure;chemistry;quantum theory;synthesis;Alkynes;Boron Compounds;Ferrous Compounds;Models, Molecular;Molecular Structure;Quantum Theory
Issue Date: 2013
Citation: Misra, R., Dhokale, B., Jadhav, T., & Mobin, S. M. (2013). Donor-acceptor meso-alkynylated ferrocenyl BODIPYs: Synthesis, structure, and properties. Dalton Transactions, 42(37), 13658-13666. doi:10.1039/c3dt51374b
Abstract: meso-Alkynylated ferrocenyl BODIPYs (3-6) with varying conjugation length have been designed, and synthesized using the palladium catalyzed Sonogashira cross-coupling reaction of meso-chloro BODIPY with the corresponding ferrocenylethynes. These BODIPYs have been designed to improve the electronic communication between the donor ferrocene, and the acceptor BODIPY. The photonic and electrochemical properties indicate charge transfer (CT) from the ferrocene to the BODIPY. Single crystal X-ray structures of 2′, 3, and 6 show interesting supramolecular interactions. Computational studies were used to study the electronic structure of the BODIPYs. © 2013 The Royal Society of Chemistry.
URI: https://doi.org/10.1039/c3dt51374b
https://dspace.iiti.ac.in/handle/123456789/9413
ISSN: 1477-9226
Type of Material: Journal Article
Appears in Collections:Department of Chemistry

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