Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9465
Title: Synthesis, structure, photophysical, and electrochemical properties of donor-acceptor ferrocenyl derivatives
Authors: Mobin, Shaikh M.
Misra, Rajneesh
Keywords: cyanoacetic acid;ferrocene derivative;ferrocenyl derivative;indanone derivative;malononitrile;unclassified drug;article;chemical structure;crystal structure;electrochemistry;microwave oven;priority journal;synthesis;X ray crystallography
Issue Date: 2012
Citation: Maragani, R., Jadhav, T., Mobin, S. M., & Misra, R. (2012). Synthesis, structure, photophysical, and electrochemical properties of donor-acceptor ferrocenyl derivatives. Tetrahedron, 68(36), 7302-7308. doi:10.1016/j.tet.2012.06.094
Abstract: A series of donor-acceptor compounds 2-6 have been synthesized, via Knoevenagel condensation reaction (using conventional method, as well as microwave method). The ferrocene unit acts as a donor, conjugated phenyl-acetylene linker act as a π-electron relay unit, and malononitrile, cyanoacetic acid, and indanone groups act as acceptor. The electronic absorption spectra displayed a broad intramolecular charge transfer (CT) band in the visible region (450-650 nm). The electrochemical studies suggest considerable donor-acceptor interaction. The single crystal X-ray structure of 2, and 3 are reported, the structure reveals that 2 is nearly planar compared to 3. The supramolecular structure of 2 exhibits intramolecular C-H-π, and C-H-N interaction, which leads to formation of 2D network, whereas compound 3 shows head to tail dimer formation through C-H-π, and π-π interaction. © 2012 Elsevier Ltd. All rights reserved.
URI: https://doi.org/10.1016/j.tet.2012.06.094
https://dspace.iiti.ac.in/handle/123456789/9465
ISSN: 0040-4020
Type of Material: Journal Article
Appears in Collections:Department of Chemistry

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