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Synthesis and characterization of a dicationic dihydrogen complex of iridium with a bis-carbene ligand set

机译:铱与双卡宾配体对的二氢键二氢配合物的合成与表征

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摘要

Reaction of [Cp*lr(CH3CN)(3)] [PF6](2) with methylenebis(N-methylimidazolium) iodide in the presence of Et3N affords [CP*Ir(C-C)I]PF6 (1) (C-C = bis-carbene). The structure of complex 1 was confirmed by X-ray crystallography. The chloride analogue [Cp*Ir(C-C)C1]X (2) was similarly prepared from [Cp*Ir(CH3CN)(3)] [PF6]2 (X = PF6) or [Cp*IrCl2](2) (X = Cl) and methylenebis(N-methylimidazolium) chloride. Reaction of 2 (X = Cl) with Et3SiB(C6F5)(4) under hydrogen gas gives the dicationic dihydrogen complex [Cp*Ir(C-C)(H-2)](2+) (3). Complex 3 is identified as a dihydrogen complex based on T-1(min) = 37 ms for the hydride resonance (240 K, 750 MHz) and J(HD) = 23.5 Hz in the partially deuterated analogue.
机译:[Cp * lr(CH3CN)(3)] [PF6](2)与亚甲基双(N-甲基咪唑鎓)碘化物在Et3N存在下的反应得到[CP * Ir(CC)I] PF6(1)(CC = bis -卡宾)。配合物1的结构通过X射线晶体学确认。氯化物类似物[Cp * Ir(CC)C1] X(2)同样由[Cp * Ir(CH3CN)(3)] [PF6] 2(X = PF6)或[Cp * IrCl2](2)制备( X = Cl)和亚甲基双(N-甲基咪唑鎓)氯化物。 2(X = Cl)与Et3SiB(C6F5)(4)在氢气下反应,生成双阳离子双氢络合物[Cp * Ir(C-C)(H-2)](2+)(3)。根据氢化物共振(240 K,750 MHz)的T-1(min)= 37 ms和部分氘代类似物的J(HD)= 23.5 Hz,将络合物3鉴定为二氢络合物。

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