摘要
[tBuN=TaCl3(py)2]和氮杂环卡宾(IPr=1,3-bis(2,6-diisoproylphenyl)imidazol-2-ylidene)的反应得到预料之外的叔丁基亚胺四氯合钽髨阴离子配合物[IPrH]+[tBuN=TaCl4(py)]-(1)。利用核磁共振波谱,红外吸收光谱,荧光光谱,元素分析和X-Ray单晶衍射对配合物1的结构进行了表征。X-射线单晶衍射分析表明,Ta(V)中心与4个氯和2个分别来自亚胺和吡啶配体的氮原子以八面体构型配位。
[IPrH]+[tBuN=TaC14(py)]- (1) (IPr=1,3-bis(2,6-diisoproylphenyl)imidazol-2-ylidene) was obtained unexpe- etedly by the reaction of 'BuN=TaC13(py)2 and IPr. Complex 1 was structurally eharaeterized by NMR, IR, fluores- cence speetra, elemental analysis and single-crystal X-ray diffraction. The erystal structure of 1 shows that the Ta(V) center is octahedrally eoordinated by four chlorides and two nitrogen atoms from imido and pyridyl ligands, respectively. CCDC: 873803.
出处
《无机化学学报》
SCIE
CAS
CSCD
北大核心
2013年第5期953-957,共5页
Chinese Journal of Inorganic Chemistry
基金
国家自然科学基金(No.20861007)
江西省教育厅基金(No.GJJ08026)资助项目
关键词
亚胺
氮杂环卡宾
钽化合物
荧光
imido complex
N-heterocyclic-carbene
Ta complex
luminescence