Modular Synthesis of Diarylalkynes and Their Efficient Conversion into Luminescent Tetraarylbutadienes

被引:11
|
作者
Shynkaruk, Olena [1 ]
Qi, Yanyu [2 ]
Cottrell-Callbeck, Aiden [1 ]
Delgado, William Torres [1 ]
McDonald, Robert [1 ]
Ferguson, Michael J. [1 ]
He, Gang [2 ]
Rivard, Eric [1 ]
机构
[1] Univ Alberta, Dept Chem, 11227 Saskatchewan Dr, Edmonton, AB T6G 2G2, Canada
[2] Xi An Jiao Tong Univ, Frontier Inst Sci & Technol, Xian 710054, Shaanxi Provinc, Peoples R China
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
AGGREGATION-INDUCED EMISSION; CROSS-COUPLING REACTIONS; CATALYZED SUZUKI-MIYAURA; METAL-FREE; REGIOSELECTIVE SYNTHESIS; SONOGASHIRA REACTIONS; PROPIOLIC ACID; ARYL HALIDES; SOLID-STATE; ALKYNES;
D O I
10.1021/acs.organomet.6b00298
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A series of electronically distinct symmetrical diarylalkynes were prepared via a general Suzuki-Miyaura cross coupling protocol. These alkynes underwent zirconium-mediated coupling to yield zirconacycles that afford new tetraaryl-1,3-butadienes upon subsequent protonolysis; these butadienes display deep blue or green emission and represent promising building blocks for light-emitting devices. The presented synthetic pathway allows access to new libraries of molecular light emitters with tunable luminescence and considerable thermal-and photostabilities.
引用
收藏
页码:2232 / 2241
页数:10
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