Co-reporter:Lei Huang;Pingfei Luo;Man Xiong;Rizhi Chen;Yong Wang;Weihong Xing
Chinese Journal of Chemistry 2013 Volume 31( Issue 8) pp:987-991
Publication Date(Web):
DOI:10.1002/cjoc.201300310
Abstract
Commercial MoS2 was found to be a highly selective catalyst for the reduction of nitrobenzenes to the corresponding anilines with hydrazine under mild conditions. MoS2 is not only much cheaper, but also more selective than noble metal catalysts for the reduction of functional nitrobenzenes to the corresponding anilines. Nitrobenzenes with halides (F, Cl, Br and I) were reduced selectively, and the corresponding anilines were obtained in excellent yields, and no dehalogenation was detected. Functional groups such as NH2, OH, alkene groups were tolerated during the reduction of the nitro compounds. The reduction of p-chloronitrobenzene was studied over MoS2 and Pd/C respectively with hydrazine. The yield of p-chloroaniline was much higher with MoS2 than that with Pd/C at full conversion.
Co-reporter:Lei Huang;Pingfei Luo;Weige Pei;Xiaoyun Liu;Yong Wang;Jun Wang;Weihong Xing
Advanced Synthesis & Catalysis 2012 Volume 354( Issue 14-15) pp:2689-2694
Publication Date(Web):
DOI:10.1002/adsc.201200330
Abstract
We have demonstrated a highly active and selective nanocatalyst, Rh/HAP (rhodium supported on hydroxyapatite), for the reduction of nitroarenes with hydrazine and for the hydrogenation of olefins with hydrogen gas under mild conditions. Nitroarenes were hydrogenated selectively to the corresponding anilines over the Rh/HAP catalyst with hydrazine as reducing agent, and reducible groups, such as halides (fluorine, chlorine, bromine and iodine), cyano and alkene were untouched. Moreover, olefins can be hydrogenated selectively to the corresponding alkanes in good yields over the Rh/HAP catalyst in the presence of reducible nitro, carbonyl and cyano groups when H2 was used.
Co-reporter:Pingfei Luo, Kunling Xu, Rui Zhang, Lei Huang, Jun Wang, Weihong Xing and Jun Huang
Catalysis Science & Technology 2012 vol. 2(Issue 2) pp:301-304
Publication Date(Web):01 Dec 2011
DOI:10.1039/C1CY00358E
A highly efficient and selective Rh nanocatalyst was demonstrated for the reduction of nitroarenes with hydrazine monohydrate under mild conditions. Functional groups such as halides (F, Cl, Br and I), CN, NH2, OH, alkene, ester and amide groups were untouched during the hydrogenation of the nitroarenes, and the corresponding anilines were obtained quantitatively.
Co-reporter:Rui Zhang;Lei Huang;Yanfang Zhang;Xiaorong Chen;Weihong Xing
Catalysis Letters 2012 Volume 142( Issue 3) pp:378-383
Publication Date(Web):2012 March
DOI:10.1007/s10562-011-0764-2
A heterogeneous silver catalyst was prepared and applied efficiently for the selective bromination of aromatics with NBS. The silver nanoparticles combined with the acidic support HMB can activate both the aromatic ring and NBS, and the synergistic effects between the silver nanoparticles and the HMB highly enhanced the efficiency of the bromination reaction.
Co-reporter:Yanpeng Yu, Tongjie Hu, Xiaorong Chen, Kunling Xu, Junli Zhang and Jun Huang
Chemical Communications 2011 vol. 47(Issue 12) pp:3592-3594
Publication Date(Web):07 Feb 2011
DOI:10.1039/C0CC04498A
A porous copolymer of an IL with divinylbenzene was prepared and applied as a support for Pd nanoparticles. The supported Pd nanocatalyst was found to be extremely active for Suzuki–Miyaura reaction of aryl bromides and chlorides with phenylboronic acid even with 10 ppm Pd loading under air in water.
Co-reporter:Kunling Xu;Yuan Zhang;Xiaorong Chen;Lei Huang;Rui Zhang
Advanced Synthesis & Catalysis 2011 Volume 353( Issue 8) pp:1260-1264
Publication Date(Web):
DOI:10.1002/adsc.201100007
Abstract
A convenient and highly selective platinum nanocatalyst was developed for the hydrogenation of nitro aromatics into the corresponding anilines at room temperature under ambient pressure. The platinum catalyst was highly active and selective for the hydrogenation of nitro aromatic compounds. Reducible groups such as aldehyde, ketone and nitrile were untouched during the hydrogenation of the corresponding nitro compounds, and the corresponding anilines were obtained quantitatively.
Co-reporter:Tongjie Hu;Xiaorong Chen;Dr. Jun Wang;Dr. Jun Huang
ChemCatChem 2011 Volume 3( Issue 4) pp:661-665
Publication Date(Web):
DOI:10.1002/cctc.201000416
Co-reporter:Junli Zhang;Xiaorong Chen;Tongjie Hu;Yuan Zhang;Kunling Xu
Catalysis Letters 2010 Volume 139( Issue 1-2) pp:56-60
Publication Date(Web):2010 October
DOI:10.1007/s10562-010-0385-1
A highly improved Pd-catalyzed cyanation of aryl chlorides to corresponding benzonitriles was demonstrated in aqueous media. Moreover, Pd-catalyzed cyanation of aryl tosylates and benzenesulfonates with K4[Fe(CN)6] was developed under the similar conditions, which extended application scope of the cyanation.
Co-reporter:Tongjie Hu, Thomas Schulz, Christian Torborg, Xiaorong Chen, Jun Wang, Matthias Beller and Jun Huang
Chemical Communications 2009 (Issue 47) pp:7330-7332
Publication Date(Web):02 Nov 2009
DOI:10.1039/B915249K
A convenient and general palladium-catalyzed coupling reaction of aryl bromides and chlorides with phenols was developed. Various functional groups such as nitriles, aldehydes, ketones and esters are well tolerated and the corresponding products are obtained in good to excellent yield.
Co-reporter:Pingfei Luo, Kunling Xu, Rui Zhang, Lei Huang, Jun Wang, Weihong Xing and Jun Huang
Catalysis Science & Technology (2011-Present) 2012 - vol. 2(Issue 2) pp:NaN304-304
Publication Date(Web):2011/12/01
DOI:10.1039/C1CY00358E
A highly efficient and selective Rh nanocatalyst was demonstrated for the reduction of nitroarenes with hydrazine monohydrate under mild conditions. Functional groups such as halides (F, Cl, Br and I), CN, NH2, OH, alkene, ester and amide groups were untouched during the hydrogenation of the nitroarenes, and the corresponding anilines were obtained quantitatively.
Co-reporter:Yanpeng Yu, Tongjie Hu, Xiaorong Chen, Kunling Xu, Junli Zhang and Jun Huang
Chemical Communications 2011 - vol. 47(Issue 12) pp:NaN3594-3594
Publication Date(Web):2011/02/07
DOI:10.1039/C0CC04498A
A porous copolymer of an IL with divinylbenzene was prepared and applied as a support for Pd nanoparticles. The supported Pd nanocatalyst was found to be extremely active for Suzuki–Miyaura reaction of aryl bromides and chlorides with phenylboronic acid even with 10 ppm Pd loading under air in water.
Co-reporter:Tongjie Hu, Thomas Schulz, Christian Torborg, Xiaorong Chen, Jun Wang, Matthias Beller and Jun Huang
Chemical Communications 2009(Issue 47) pp:NaN7332-7332
Publication Date(Web):2009/11/02
DOI:10.1039/B915249K
A convenient and general palladium-catalyzed coupling reaction of aryl bromides and chlorides with phenols was developed. Various functional groups such as nitriles, aldehydes, ketones and esters are well tolerated and the corresponding products are obtained in good to excellent yield.