Synthesis of zwitterionic palladium complexes and their application as catalysts in cross-coupling reactions of aryl, heteroaryl and benzyl bromides with organoboron reagents in neat water
作者:V. Ramakrishna、N. Dastagiri Reddy
DOI:10.1039/c7dt01433c
日期:——
found to be highly active for carrying out these reactions between aryl bromides and organoboron reagents. Further, the scope of the catalyst I was also examined by employing (hetero)aryl bromides, hydrophilic aryl bromides, benzylbromides and various organoboron reagents. More than 80 aryl/benzyl bromide-arylboronic acid combinations were screened in neat water/K2CO3 and found that I is a versatile catalyst
N-(3-氯-2-喹喔啉基)-N'-芳基咪唑鎓盐(芳基= 2,6-二异丙基苯基[HL1Cl] Cl,芳基=甲苯基[HL2Cl] Cl)已通过将2,3-二氯喹喔啉与N'-芳基咪唑纯净。这些咪唑鎓盐与Pd(PPh 3)4和Pd 2(dba)3 / PPh 3(dba =二苄基苯丙酮)在50 o C的容易反应,得到两性离子钯(II)络合物[Pd(HL1)(PPh 3) Cl 2 ](I)和[Pd(HL2)(PPh 3)Cl 2 ](II)的收率极高。已测试I和II在纯水/ K中催化Suzuki-Miyaura交叉偶联(SMC)反应的能力2 CO 3,对在芳基溴化物和有机硼试剂之间进行这些反应具有很高的活性。此外,还通过使用(杂)芳基溴化物,亲水性芳基溴化物,苄基溴化物和各种有机硼试剂来检查催化剂I的范围。在纯水/ K 2 CO 3中筛选了80多种芳基/苄基溴-芳基硼酸组合,发现I是一种多用途催化
A Zwitterionic Palladium(II) Complex as a Precatalyst for Neat-Water-Mediated Cross-Coupling Reactions of Heteroaryl, Benzyl, and Aryl Acid Chlorides with Organoboron Reagents
A zwitterionic palladium(II) complex has been found to be an efficient catalyst for Suzuki–Miyaura cross‐coupling reactions of aryl and heteroaryl organoboron reagents with various heteroaryl chlorides, aryl‐ and heteroarylmethyl chlorides, and aryl acid chlorides in neat water.
COMPOUND FOR ORGANIC OPTOELECTRONIC DEVICE, COMPOSITION FOR ORGANIC OPTOELECTRONIC DEVICE, ORGANIC OPTOELECTRONIC DEVICE, AND DISPLAY DEVICE
申请人:SAMSUNG SDI CO., LTD.
公开号:US20220140257A1
公开(公告)日:2022-05-05
A compound for an organic optoelectronic device, a composition for an organic optoelectronic device including the same, an organic optoelectronic device, and a display device, the compound being represented by a combination of Chemical Formula 1 and Chemical Formula 2,
Pd-NHC catalyzed Suzuki cross-coupling of benzyl ammonium salts
作者:Chuntao Zhong、Huiling Tang、Benqiang Cui、Yanhui Shi、Changsheng Cao
DOI:10.1007/s11164-022-04795-6
日期:2022.10
palladium-catalyzed Suzukicross-coupling of benzyl ammonium triflates via activation of a Csp3–N bond to construct a Csp3–Csp2 bond is described. Various boronicacids can be coupled with a range of benzylamine-derived quaternary ammonium salts in 1:1 molar ratio by the bench-stable N-heterocyclic carbene palladium complex, SIPr-PdCl2-Py to afford diarylmethane derivatives. This reaction exhibits a wide
The present invention relates to a process to produce compounds of the formula (1) which are suitable for use in electronic devices, as well as to intermediate compounds of formula (Int-1) and compounds of formula (1-1) and (1-2) obtained via the process. These compounds are particularly suitable for use organic electroluminescent devices. The present invention also relate to electronic devices, which comprise these compounds.