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Updated: Jul 14, 2025

Amide Coupling Reaction for the Synthesis of Bispyridine-based Ligands and Their Complexation to Platinum as Dinuclear Anticancer Agents
Published on: May 28, 2014
Four- and three-coordinate planar iron(II) complexes supported by bulky organosilyl ligands
Reon Ishii1, Minesato Nakagawa1, Yoshimasa Wada1,2
1Department of Applied Chemistry, School of Engineering, The University of Tokyo, 4-6-1, Komaba, Meguro-ku, Tokyo 153-8505, Japan. sunada@iis.u-tokyo.ac.jp.
Abstract:
The ligand exchange reaction of (THF)2Fe[Si(SiMe3)3]2 with 2 equivalents of an N-heterocyclic carbene (NHC) led to the formation of a square-planar iron(II) complex with trans-oriented -Si(SiMe3)3 ligands. Conversely, the introduction of a cis-coordinate bidentate organosilyl ligand instead of -Si(SiMe3)3 resulted in the formation of a square planar iron(II) complex supported by a cis-coordinate bidentate organosilyl ligand. A three-coordinate planar iron(II) bis(silyl) complex was also synthesized using a cis-coordinate bidentate organosilyl ligand and a cyclic (alkyl)(amino)carbene auxiliary ligand. Investigation of the catalytic performance of these complexes in the hydrosilylation of acetophenone revealed that the square-planar iron(II) complex with trans-oriented -Si(SiMe3)3 ligands exhibits superior reactivity relative to its tetrahedral precursor.
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