Chloro(η2,η2-cycloocta-1,5-diene){1-benzyl-3-[(S)-2-hydroxy-1-methylethyl]benzimidazol-2-ylidene}rhodium(I)

Molbank Pub Date : 2024-04-19 DOI:10.3390/m1811
S. Sakaguchi, Shogo Matsuo
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Abstract

Previously, we demonstrated the synthesis of a well-defined hydroxyalkyl-functionalized N-heterocyclic carbene (NHC)/Ru(II) complex through the transmetalation reaction between [RuCl2(p-cymene)]2 and the corresponding NHC/Ag(I) complex derived from a chiral benzimidazolium salt using the Ag2O method. In this study, we successfully synthesized [RhX(cod)(NHC)] complexes through a one-pot deprotonation route. The hydroxyalkyl-substituted benzimidazolium salt reacted with [Rh(OH)(cod)]2 in THF at room temperature, affording the corresponding monodentate NHC/Rh(I) complex in nearly quantitative yield. The rhodium complex was characterized using NMR, HRMS measurement, and elemental analysis.
氯(η2,η2-环辛烷-1,5-二烯){1-苄基-3-[(S)-2-羟基-1-甲基乙基]苯并咪唑-2-亚基}铑(I)
在此之前,我们利用 Ag2O 方法,通过[RuCl2(p-cymene)]2 与由手性苯并咪唑盐衍生的相应 NHC/Ag(I) 复合物之间的反金属化反应,合成了一种定义明确的羟烷基官能化 N-heterocyclic carbene (NHC)/Ru(II) 复合物。在本研究中,我们通过一锅去质子化路线成功合成了[RhX(cod)(NHC)]配合物。羟烷基取代的苯并咪唑盐在室温下与 THF 中的 [Rh(OH)(cod)]2 反应,得到相应的单价 NHC/Rh(I) 复合物,收率接近定量。该铑络合物通过核磁共振、HRMS 测量和元素分析进行了表征。
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