Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9458
Title: Synthesis, structure and redox property of first 1,2,3-triselenole
Authors: Mathur, Pradeep
Rai, Dhirendra Kumar
Mobin, Shaikh M.
Keywords: Chalcogenole;Demetallation;Redox property;Triselenole;Cyclic voltammetry;Hexane;Photolysis;Synthesis (chemical)
Issue Date: 2012
Citation: Mathur, P., Rai, D. K., Tauqeer, M., Joshi, R. K., Lahiri, G. K., & Mobin, S. M. (2012). Synthesis, structure and redox property of first 1,2,3-triselenole. Journal of Organometallic Chemistry, 721-722, 144-147. doi:10.1016/j.jorganchem.2012.09.009
Abstract: Photolysis of [Fe3Se2(CO)9] with 3-ferrocenylpropynal in hexane yields an adduct of [Fe2Se 2(CO)6] and FcC2CHO, [(CO)6Fe 2{μ-SeC(Fc)C(CHO)Se}] (1). Subsequent reaction of 1 with [Fe 2Se2(CO)6] in presence of excess of Me 3NO·2H2O in THF leads to formation of a novel 5-ferrocenyl-4-carbaldehyde-1,2,3-triselenole (2). Its electrochemistry has been investigated by cyclic voltammetry, which shows two successive quasi-reversible oxidations. © 2012 Elsevier B.V. All rights reserved.
URI: https://doi.org/10.1016/j.jorganchem.2012.09.009
https://dspace.iiti.ac.in/handle/123456789/9458
ISSN: 0022-328X
Type of Material: Journal Article
Appears in Collections:Department of Chemistry

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