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Title: | C2-Symmetric ferrocenyl bisthiazoles: Synthesis, photophysical, electrochemical and DFT studies |
Authors: | Mobin, Shaikh M. Misra, Rajneesh |
Keywords: | Chemical bonds;Chemical reactions;Computation theory;Single crystals;Thermodynamic stability;Computational studies;Donor acceptors;Donor-acceptor interaction;Electrochemical studies;Electronic communications;High thermal stability;Sonogashira cross-coupling reaction;Time dependent density functional theory;Density functional theory |
Issue Date: | 2016 |
Publisher: | Royal Society of Chemistry |
Citation: | Maragani, R., Gautam, P., Mobin, S. M., & Misra, R. (2016). C2-symmetric ferrocenyl bisthiazoles: Synthesis, photophysical, electrochemical and DFT studies. Dalton Transactions, 45(11), 4802-4809. doi:10.1039/c5dt04988a |
Abstract: | A series of donor-acceptor ferrocenyl substituted bisthiazoles 3-8 were designed and synthesized by the Pd-catalyzed Suzuki, Heck, and Sonogashira cross-coupling reactions. Their photophysical, electrochemical and computational studies reveal strong donor-acceptor interactions. The photonic and electrochemical studies show that the ferrocenyl bisthiazoles with vinyl linkage ferrocenyl-bisthiazole 4, show better electronic communication compared to rest of the ferrocenyl bisthiazoles. The time dependent density functional theory (TD-DFT) calculation at B3LYP on the ferrocenyl substituted bisthiazoles 3-5 was performed, in which the ferrocenyl-bisthiazole 4 shows strong donor-acceptor interactions compared to the Fc-bisthiazoles 3 and 5. The thermal stability of the ferrocenyl substituted bisthiazoles 3-8 is reported, in which Fc-bisthiazole 8 shows high thermal stability. The single crystal structures of ferrocenyl-bisthiazoles 3 and 5 are reported. © The Royal Society of Chemistry 2016. |
URI: | https://doi.org/10.1039/c5dt04988a https://dspace.iiti.ac.in/handle/123456789/9255 |
ISSN: | 1477-9226 |
Type of Material: | Journal Article |
Appears in Collections: | Department of Chemistry |
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