An Unusual and Facile Synthetic Route to Alumoles

被引:13
|
作者
Li, Jiancheng [1 ]
Wu, Peng [1 ,3 ]
Jiang, Wenjun [1 ]
Li, Bin [1 ]
Wang, Binju [1 ]
Zhu, Hongping [1 ]
Roesky, Herbert W. [2 ]
机构
[1] Xiamen Univ, State Key Lab Phys Chem Solid Surface, Natl Engn Lab Green Chem Prod Alcohols Ethers Est, Coll Chem & Chem Engn, Xiamen 361005, Fujian, Peoples R China
[2] Univ Gcttingen, Inst Anorgan Chem, Tammannstr 4, D-37077 Gottingen, Germany
[3] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
aggregation-induced emission; aluminum; heterocycles; alumoles; tris(pentafluorophenyl)borane; AGGREGATION-INDUCED EMISSION; DIMERIC DIALKYLALUMINUM; TRIORGANOTIN CATIONS; REACTIVITY; ALUMINUM; 1,1-CARBOBORATION; DERIVATIVES; ALUMINACYCLOPROPENE; STANNOLES; 1,1-ORGANOBORATION;
D O I
10.1002/anie.202000899
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Reaction of the aluminum dialkynyl LAl(CCR)(2) (L=N,N-chelate ligand and R=organic group) with B(C6F5)(3) proceeds through an intermediate with Al...eta(2)-C equivalent to C side-on coordination to form the alumoles (2, 4, 6). A distinctive reaction pattern indicates a new facile synthetic route to aluminum-containing heterocycles. The synthetic process is described, and the characterization of compounds and computational calculations were carried out. Furthermore, alumoles 2 and 4 exhibit an aggregation-induced emission (AIE) of the bright yellow fluorescence.
引用
收藏
页码:10027 / 10031
页数:5
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