High Turnover Number and Rapid, Room-Temperature Amination of Chloroarenes Using Saturated Carbene Ligands

2000 ◽  
Vol 2 (10) ◽  
pp. 1423-1426 ◽  
Author(s):  
Shaun R. Stauffer ◽  
Sunwoo Lee ◽  
James P. Stambuli ◽  
Sheila I. Hauck ◽  
John F. Hartwig
ChemInform ◽  
2010 ◽  
Vol 31 (36) ◽  
pp. no-no
Author(s):  
Shaun R. Stauffer ◽  
Sunwoo Lee ◽  
James P. Stambuli ◽  
Sheila I. Hauck ◽  
John F. Hartwig

2017 ◽  
Vol 8 (10) ◽  
pp. 7119-7125 ◽  
Author(s):  
Ji Won Han ◽  
Jieun Jung ◽  
Yong-Min Lee ◽  
Wonwoo Nam ◽  
Shunichi Fukuzumi

The present study reports the first example of photocatalytic hydroxylation of benzene with O2 and H2O, both of which are the most green reagents, under visible light irradiation to afford a high turnover number.


2016 ◽  
Vol 6 (12) ◽  
pp. 4077-4080 ◽  
Author(s):  
Shoko Aoi ◽  
Kentaro Mase ◽  
Kei Ohkubo ◽  
Shunichi Fukuzumi

The photocatalytic reduction of CO2 and H2O with triethylamine occurred using a cobalt(ii) chlorin complex adsorbed on multi-walled carbon nanotubes as a catalyst to yield CO and H2 with a high turnover number of 710.


2004 ◽  
Vol 45 (20) ◽  
pp. 3849-3853 ◽  
Author(s):  
Hector Palencia ◽  
Federico Garcia-Jimenez ◽  
James M. Takacs

2014 ◽  
Vol 50 (85) ◽  
pp. 12947-12950 ◽  
Author(s):  
Lei Wang ◽  
Lele Duan ◽  
Ying Wang ◽  
Mårten S. G. Ahlquist ◽  
Licheng Sun

The molecular catalyst Ru(bda)L2 (H2bda = 2,2′-bipyridine-6,6′-dicarboxylic acid, L = 6-bromophthalazine) shows excellent catalytic activity for water oxidation. By using Ce(NH4)2(NO3)6 as an oxidant, the catalyst reached a high turnover number TON = 100 000 in 3 hours.


2014 ◽  
Vol 50 (34) ◽  
pp. 4462-4464 ◽  
Author(s):  
Eun-Gyeong Ha ◽  
Jeong-Ah Chang ◽  
Sung-Min Byun ◽  
Chyongjin Pac ◽  
Dong-Myung Jang ◽  
...  

Higher photocatalytic CO2 conversion to CO with a turnover number of 435 was achieved by the ternary dye-sensitized systems comprising a dye/TiO2/Re platform.


2016 ◽  
Vol 12 ◽  
pp. 863-873 ◽  
Author(s):  
Shaojin Gu ◽  
Jiehao Du ◽  
Jingjing Huang ◽  
Huan Xia ◽  
Ling Yang ◽  
...  

A series of copper complexes (3–6) stabilized by 1,2,3-triazole-tethered N-heterocyclic carbene ligands have been prepared via simple reaction of imidazolium salts with copper powder in good yields. The structures of bi- and trinuclear copper complexes were fully characterized by NMR, elemental analysis (EA), and X-ray crystallography. In particular, [Cu2(L2)2](PF6)2 (3) and [Cu2(L3)2](PF6)2 (4) were dinuclear copper complexes. Complexes [Cu3(L4)2](PF6)3 (5) and [Cu3(L5)2](PF6)3 (6) consist of a triangular Cu3 core. These structures vary depending on the imidazolium backbone and N substituents. The copper–NHC complexes tested are highly active for the Cu-catalyzed azide–alkyne cycloaddition (CuAAC) reaction in an air atmosphere at room temperature in a CH3CN solution. Complex 4 is the most efficient catalyst among these polynuclear complexes in an air atmosphere at room temperature.


2015 ◽  
Vol 5 (2) ◽  
pp. 1181-1186 ◽  
Author(s):  
Jeremy M. John ◽  
Rasu Loorthuraja ◽  
Evan Antoniuk ◽  
Steven H. Bergens

A new, base-free high turnover number (TON) catalyst for hydrogenation of simple and functionalized amides is prepared by reacting [Ru(η3-C3H5)(Ph2P(CH2)2NH2)2]BF4 and BH4− under hydrogen.


2021 ◽  
Author(s):  
Jianguo Liu ◽  
Yanpei Song ◽  
Xiang Wu ◽  
Longlong Ma

<p>N-methylated amines are essential bioactive compounds and have been widely used in the fine and bulk chemical industries, as well as in pharmaceuticals, agrochemicals, and dyes. Developing green, efficient, and low-cost catalysts for methylation of amines by using efficient and easily accessible methylating reagents is highly desired yet remains a significant challenge. Herein, we report the selective N-dimethylation of different functional amines with different functional aldehydes under easily handle-able and industrially applicable conditions using carbon-supported Ru nanoparticles (Ru/C) as a heterogeneous catalyst. A broad spectrum of amines could be efficiently converted to their corresponding N, N-dimethyl amines with good compatibility of various functional groups. This method is widely applicable to N-dimethylation of primary amines including aromatic, aliphatic amines with formaldehyde, and synthesis of tertiary amines from primary, secondary amines with different functional aldehydes. The advantage of this newly described method includes operational simplicity, high turnover number, the ready availability of the catalyst, and good functional group compatibility. This Ru/C catalyzed N-dimethylation reaction possibly proceed through a twice N-methylation reaction process.</p>


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