Department of Chemistry, School of Life Sciences, University of Sussex, Brighton BN1 9QJ, U.K.
Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Renmin Street 5626, 130022 Changchun, China.
J Am Chem Soc. 2020 Mar 4;142(9):4104-4107. doi: 10.1021/jacs.9b13571. Epub 2020 Feb 20.
Addition of Lewis acidic [CpM] (M = Y, Gd) to the dinitrosyliron complexes (DNICs) [(NacNac)Fe(NO)] (Ar = mesityl, 2,6-diisopropylphenyl) results in formation of the isonitrosyl-bridged DNICs [(Cp)M(μ-ON)Fe(NacNac)]. When Ar = 2,6-diisopropylphenyl, coupling of the NO ligands and release of NO occur. Two factors contribute to this previously unobserved DNIC reactivity mode. First, the oxophilic rare-earth elements drive the formation of isonitrosyl bonds, forcing the DNIC nitrogen atoms into proximity. Second, the bulky substituents further squeeze the DNIC, which ultimately overcomes the barrier to NO coupling, demonstrating that NO elimination can occur from a single iron center.
路易斯酸性[CpM](M = Y,Gd)的添加到二亚硝酰铁配合物(DNICs)[(NacNac)Fe(NO)](Ar = 均三甲苯基,2,6-二异丙基苯基)中,会形成异亚硝酰桥联的 DNICs[(Cp)M(μ-ON)Fe(NacNac)]。当 Ar = 2,6-二异丙基苯基时,NO 配体发生偶联并释放出 NO。有两个因素促成了这种以前未观察到的 DNIC 反应模式。首先,亲氧稀土元素驱动异亚硝酰键的形成,迫使 DNIC 的氮原子靠近。其次,庞大的取代基进一步挤压 DNIC,最终克服了 NO 偶联的障碍,表明可以从单个铁中心消除 NO。