439927-43-2Relevant academic research and scientific papers
CO2-Triggered Switchable Hydrophilicity of a Heterogeneous Conjugated Polymer Photocatalyst for Enhanced Catalytic Activity in Water
Byun, Jeehye,Huang, Wei,Wang, Di,Li, Run,Zhang, Kai A. I.
supporting information, p. 2967 - 2971 (2018/02/21)
Water compatibility for heterogeneous photocatalysts has been pursued for energy and environmental applications. However, there exists a trade-off between hydrophilicity and recyclability of the photocatalyst. Herein, we report a conjugated polymer photocatalyst with tertiary amine terminals that reversibly binds CO2 in water, thereby generating switchable hydrophilicity. The CO2-assisted hydrophilicity boosted the photocatalytic efficiency in aqueous medium with minimum dosage. When CO2 was desorbed, the photocatalyst could be simply regenerated from reaction media, facilitating the repeated use of photocatalyst. Hydrophilicity/hydrophobicity control of the polymer photocatalyst was successfully showcased through a variety of organic photoredox reactions under visible-light irradiation in water.
Synthesis and characterization of amino-NHC coinage metal complexes and application for C-H activation of caffeine
Huang, Hsuan-Jui,Lee, Wei-Chih,Yap, Glenn P.A.,Ong, Tiow-Gan
, p. 64 - 73 (2014/05/06)
This paper describes the synthesis and characterization of silver, copper and gold complexes supported by several amino-NHC ligands with different amino side arms. The transmetallation process using silver-NHC complexes can be used to prepare amino-NHC copper and gold complexes easily in high yield. In addition, the catalytic activities of copper complexes are examined for arylation of caffeine via C-H bond activation.
Direct arylation of n-heteroarenes with aryldiazonium salts by photoredox catalysis in water
Xue, Dong,Jia, Zhi-Hui,Zhao, Cong-Jun,Zhang, Yan-Yan,Wang, Chao,Xiao, Jianliang
supporting information, p. 2960 - 2965 (2014/03/21)
A highly effective visible light-promoted "radical-type" coupling of N-heteroarenes with aryldiazonium salts in water has been developed. The reaction proceeds at room temperature with [Ru(bpy)3]Cl 2×6 H2O as a photosensit
Palladium-catalyzed direct arylation of N-heteroarenes with arylsulfonyl hydrazides
Liu, Bo,Li, Jian,Song, Feijie,You, Jingsong
supporting information; experimental part, p. 10830 - 10833 (2012/09/22)
Hydrazides applied: A palladium-catalyzed direct Ci-H arylation of heteroarenes, with arylsulfonyl hydrazides as the arylating reagents, has been developed (see scheme). The reaction is chemoselective, in that arylsulfonyl hydrazides containing halogen substituents can be employed without participation of the halogen substituent in the reaction. The method offers a straightforward approach to a variety of aryl-heteroaryl compounds. Copyright
Palladium-catalyzed desulfitative C-H arylation of heteroarenes with sodium sulfinates
Liu, Bo,Guo, Qiang,Cheng, Yangyang,Lan, Jingbo,You, Jingsong
supporting information; experimental part, p. 13415 - 13419 (2012/01/03)
Desulfitative C-H arylation: Palladium-catalyzed desulfitative C-H arylation of heteroarenes with sodium sulfinates has been disclosed to construct aryl-heteroaryl bonds without the need for any extra ligands (see scheme). Copyright
A palladium/copper bimetallic catalytic system: Dramatic improvement for Suzuki-Miyaura-type direct C-H arylation of azoles with arylboronic acids
Liu, Bo,Qin, Xurong,Li, Kaizhi,Li, Xiyu,Guo, Qiang,Lan, Jingbo,You, Jingsong
supporting information; experimental part, p. 11836 - 11839 (2011/01/12)
Bimetallic catalytic system: Palladium/copper bimetallic-catalyzed Suzuki-Miyaura-type coupling has been disclosed for direct C-H arylation of azoles, instead of azole halides or pseudohalides, with arylboronic acids (see scheme).
Phosphine-free, palladium-catalyzed arylation of heterocycles through C-H bond activation with pivalic acid as a cocatalyst
Zhao, Dongbing,Wang, Weida,Lian, Shuang,Yang, Fei,Lan, Jingbo,You, Jingsong
supporting information; experimental part, p. 1337 - 1340 (2009/09/04)
A new palladium-catalyzed methodology was developed for the direct C-arylation of azoles with a broad spectrum of aryl bromides without the presence of phosphines, the aid of CuI, or other metal additives by using pivalic acid as a cocatalyst. The method also allowed the direct C-arylation of the N-heterocycle N-oxides, and to a lesser degree, the perfluoroaromatics. It was also found that the method can not only be applied to the synthesis of 8-aryl-substituted caffeines, but also 8-arylated theophyllines and theobromines. The result showed thatthe method can tolerate an array of functional groups including ester, nitrile, nitro, aldehyde, methoxy, trifluoromethyl, fluoro, and chloro substituents, and can found its applications in a number of fields such as synthetic and medicinal chemistry both in industry and in academia.
