文献类型：期刊文献

中文题名：硼桥联三氮杂环卡宾配位的铁分子氮配合物:合成、表征和反应性质研究

英文题名：Iron Dinitrogen Complexes Supported by Tris(NHC) borate Ligand:Synthesis,Characterization,and Reactivity Study

作者：凡一明[1];程骏[2];高亚飞[2];施敏[1,2];邓亮[2]

机构：[1]华东理工大学化学与分子工程学院结构可控先进功能材料及其制备教育部重点实验室,上海200237;[2]中国科学院上海有机化学研究所金属有机化学国家重点实验室分子合成科学卓越中心,上海200032

年份：2018

卷号：76

期号：6

起止页码：445

中文期刊名：化学学报

外文期刊名：Acta Chimica Sinica

收录：CSTPCD;;Scopus;WOS:【SCI-EXPANDED(收录号:WOS:000442409600004)】；北大核心:【北大核心2017】；CSCD:【CSCD2017_2018】；

基金：Project supported by the National Key Research and Development Program (No. 2016YFA0202900), the National Natural Science Foundation of China (Nos. 21725104, 21690062, 21432001), the Strategic Priority Research Program of the Chinese Academy of Sciences (No. XDB20000000) and the Fundamental Research Funds for the Central Universities (No. 222201717003).

语种：中文

中文关键词：氮杂环卡宾;铁;分子氮配合物;氮气活化;氮气硅基化

外文关键词：N-heterocyclic carbene;iron;dinitrogen complex;N2 activation;reductive silylation of N2

摘要：研究了氮上取代基为1-金刚烷基的苯基硼桥联三氮杂环卡宾配体在铁促进的氮气活化转化反应中的应用.通过苯基硼桥联三氮杂环卡宾亚铁氯化物[PhB(AdIm)_3FeCl](1)在氮气氛下与KC8反应合成了一价铁分子氮配合物[PhB(AdIm)_3Fe(N_2)](2).进一步通过2与KC_8和18-C-6的反应合成了零价铁分子氮配合物[K(18-C-6)(THF)]-[PhB(AdIm)3Fe(N_2)](4).这些配合物均通过核磁共振、紫外吸收光谱、红外光谱、元素分析等表征,其中配合物2和4的结构经单晶X射线衍射表征确定.配合物2和4的N—N伸缩振动频率分别为1928和1807 cm^(-1),均为同价态铁末端分子氮配合物最低值.在过量KC_8和Me_3SiCl存在下,配合物1,2和4均可催化N2的还原硅基化反应,生成N(SiMe_3)_3.催化体系的TON可达87.
The use of the N-adamantyl-substituted tris（NHC）borate ligand phenyltris（3-（1-adamantylimidazol-2-ylidene））borate（PhB（AdIm）3-） has enabled the preparation of the high-spin tetrahedral iron（I）-and iron（0）-N2 complexes [PhB（AdIm）3Fe（N2）]（2） and [K（18-C-6）（THF）][PhB（AdIm）3Fe（N2）]（4）, from the reduction of the ferrous precursor [PhB（AdIm）3FeCl]（1） and the iron（I） complex 2 with KC8 under N2, respectively. Single-crystal X-ray diffraction studies revealed a distorted tetrahedral coordination geometry for the iron centers in 2 and 4 with the terminally bonded N2 ligand sitting in the cavity composed by the three adamantyl groups of the borate ligand. The frequencies of the N—N stretching resonance（1928 and 1807 cm-1） of 2 and 4 are the lowest among the reported terminal N2 complexes of iron（I） and iron（0）, respectively. 57 Fe M？ssbauer spectrum（δ = 0.59 mms-1; ΔEQ=1.31 mms-1） and solution magnetic susceptibility measurement（μeff=5.2（1） μB） of 2 supported its high-spin iron（I） nature. The cyclic voltammogram of 2 measured in THF shows a quasi-reversible redox waves with E1/2=-2.11 V（vs SCE）, which is assignable to the corresponding redox process of [PhB（AdIm）3Fe（N2）]1-/0. In addition, the reaction of 2 with an excess amount of CO led to the formation of the bis（carbonyl）iron（I） complex, [PhB（AdIm）3Fe（CO）2]（3）, that was characterized by IR spectrum, solution magnetic susceptibility measurement, 1 H NMR, as well as elemental analysis. The protonation of 2 and 4 with HCl or HOTf at-78 ℃ only led to the formation of NH2 NH2 and NH3 in low yields [less than 9（3）% and 5（3）%（per mol Fe）, respectively]. However, 1, 2, and 4 proved effective catalysts for the reductive silylation of N2 by KC8 and Me3SiCl to afford N（SiMe3）3 with comparable catalytic activity. The TON of these catalytic systems could reach 87 using 0.005 mmol of the catalyst, 2000 equiv. of KC8, and 2000 equiv. of Me3SiCl in 10 m L Et2O at room temperature after 24 h.