23055-77-8Relevant articles and documents
Aromatic amine derivative organic electroluminescent material and device thereof
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Paragraph 0143-0146, (2021/09/29)
The invention discloses an aromatic amine derivative organic electroluminescent material and a device thereof. The compound is an aromatic amine substituted pyrene compound, and a longer arylene group or heteroarylene group and other structures are introduced among one arylamine and pyrene to prolong the molecular length of the luminescent material. The compound can be used as a luminescent material in an organic electroluminescent device. These novel compounds provide better device performance, such as light emission efficiency and external quantum efficiency. An electroluminescent device and a compound formulation are also disclosed.
Highly efficient palladium-catalyzed cross-coupling of diarylborinic acids with arenediazoniums for practical diaryl synthesis
Wang, Fengze,Wang, Chen,Sun, Guoping,Zou, Gang
, (2019/12/25)
A highly efficient cross-coupling of cost-effective diarylborinic acids with both isolatable and latent arenediazoniums, i.e. tetrafluoroborates and aryltriazenes, respectively, has been developed with a practical palladium catalyst system under base-free conditions in open flask at room temperature. A variety of electronically and sterically various biaryls, in particular, those bearing a coordinative ortho-substituent, could be obtained in good to excellent yields by using 0.3 mol% palladium acetate as catalyst. Features of the protocol including cost-effectiveness of diarylborinic acids, efficacy to heteroatom ortho-substituted substrates and high chemoselectivity to aryl chlorides have been clearly demonstrated in practical synthesis of fungicide Boscalid.
Immobilized Pd on Eggshell Membrane: A powerful and recyclable catalyst for Suzuki and Heck cross-coupling reactions in water
Wu, Shang,Jiang, Hongyan,Zhang, Hong,Zhao, Lianbiao,Yuan, Peilin,Zhang, Ying,Su, Qiong,Wang, Yanbin,Wu, Lan,Yang, Quanlu
, (2020/09/09)
A stable heterogeneous palladium catalysts, the waste eggshell membrane (ESM) anchored Pd complex, was synthesized by a simple and green technique. The catalyst obtained can display an outstanding catalytic activity for Suzuki and Heck coupling reactions in water media. The reactions of various aryl halides with aryl boronic acids and terminal alkenes provided the corresponding products in moderate to excellent yields. More importantly, this novel and efficient catalyst with high stability can be easily reused for at least twelve times with no decrease of the catalytic activity, performing an endurable and wide tolerance of the substrates. Facile synthesis, high catalytic activity, and recyclability make these catalysts interesting for further studies.