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Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9458
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dc.contributor.authorMathur, Pradeepen_US
dc.contributor.authorRai, Dhirendra Kumaren_US
dc.contributor.authorMobin, Shaikh M.en_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:33:13Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:33:13Z-
dc.date.issued2012-
dc.identifier.citationMathur, 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.2012.09.009en_US
dc.identifier.issn0022-328X-
dc.identifier.otherEID(2-s2.0-84869502966)-
dc.identifier.urihttps://doi.org/10.1016/j.jorganchem.2012.09.009-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9458-
dc.description.abstractPhotolysis 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.en_US
dc.language.isoenen_US
dc.sourceJournal of Organometallic Chemistryen_US
dc.subjectChalcogenoleen_US
dc.subjectDemetallationen_US
dc.subjectRedox propertyen_US
dc.subjectTriselenoleen_US
dc.subjectCyclic voltammetryen_US
dc.subjectHexaneen_US
dc.subjectPhotolysisen_US
dc.subjectSynthesis (chemical)en_US
dc.titleSynthesis, structure and redox property of first 1,2,3-triselenoleen_US
dc.typeJournal Articleen_US
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