Reactivity of a Fe(III)-Bound Methoxide Supported with a Tris(thiolato)phosphine Ligand: Activation of C-Cl Bond in CH2Cl2 by Nucleophilic Attack of a Fe(III)-OCH3 Moiety

Kai Chun Chang, Ching Ju Huang, Ya Ho Chang, Zong Han Wu, Ting Shen Kuo, Hua Fen Hsu

研究成果: Article同行評審

8 引文 斯高帕斯(Scopus)

摘要

Two mononuclear nonheme FeIII complexes, [PPh4][FeIII(PS3′)(OCH3)] (1) and [PPh4][FeIII(PS3′)(Cl)] (2), supported by a tris(benzenethiolato)phosphine derivative PS3′ (PS3′ = P(C6H3-3-Me3Si-2-S)33-) have been synthesized and characterized. The structures resolved from X-ray crystallography show that FeIII centers in both complexes adopt distorted trigonal-bipyramidal geometry with a methoxide or a chloride binding in the axial position. The magnetic data for both are consistent with intermediate-spin FeIII centers with a C3 symmetry (S = 3/2 ground state). The bound methoxide in 1 is labile and can be replaced by a CH3CN molecule. The forming FeIII-CH3CN species can be further reduced by cobaltcene quantitatively to a stable FeII-CH3CN complex, [Fe(PS3′)(CH3CN)]-. One-electron oxidation of 2 by ferrocenium gave a FeIV analogue, [FeIV(PS3′)(Cl)]. Importantly, the FeIII-OCH3 moiety in complex 1 acts as a strong nucleophile that activates the C-Cl bond in CH2Cl2, leading to the formation of complex 2 quantitatively. Complex 1 also reacts with other electrophiles, benzyl chloride and benzyl bromide, to generate FeIII-X species (X = Cl or Br). The reactions were investigated and monitored by UV-vis-NIR, NMR, and ESI-MS spectroscopies.

原文English
頁(從 - 到)566-572
頁數7
期刊Inorganic Chemistry
55
發行號2
DOIs
出版狀態Published - 2016 1月 19

All Science Journal Classification (ASJC) codes

  • 物理與理論化學
  • 無機化學

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