In this study, a heterogeneous catalyst including palladium nanoparticles supported on nitrogen-doped mesoporous carbon (Pd@N-C) is synthesized from palladium salts as palladium precursor, colloidal silica as template, and chitosan as carbon source. N2 sorption isotherm results show that the prepared Pd@N-C had a high BET surface area (640m(2)g(-1)) with large porosity. The prepared Pd@N-C is high nitrogen-rich as characterized with element analysis. X-ray photoelectron spectroscopy (XPS), high-resolution transmission electron microscopy (HR-TEM), and Raman spectroscopy characterization of the catalyst shows that the palladium species with different chemical states are well dispersed on the nitrogen-containing mesoporous carbon. The Pd@N-C is high active and shows excellent stability as applied in Heck coupling reactions. This work supplies a successful method to prepare Pd heterogeneous catalysts with high performance from bulk biopolymer/Pd to high porous nitrogen-doped carbon supported palladium catalytic materials.
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http://dx.doi.org/10.1016/j.ijbiomac.2016.05.011 | DOI Listing |
Inorg Chem
February 2020
Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials, Department of Chemistry, School of Chemistry and Chemical Engineering , Jiangsu Normal University, Xuzhou , 221116 , P. R. China.
Catalysts based on metallic NPs have shown high activities in heterogeneous catalysis, due to their high fractions of surface-active atoms, which, however, will lead to the sacrifices in stability and recycle of catalysts. In order to balance well the relationship between activity, stability, and recovery, in this paper, we have constructed a 3D mesoporous sphere structure assembled by N-doped carbon coated Ni/Pd NP heterojunctions (Ni/Pd@N-C). This obtained Ni/Pd@N-C has shown high catalytic activity, durability and recyclability for the hydrolytic dehydrogenation of ammonia borane (AB).
View Article and Find Full Text PDFInt J Biol Macromol
August 2016
Zhejiang Key Laboratory of Alternative Technologies for Fine Chemicals Process, Shaoxing University, Shaoxing 312000, China.
In this study, a heterogeneous catalyst including palladium nanoparticles supported on nitrogen-doped mesoporous carbon (Pd@N-C) is synthesized from palladium salts as palladium precursor, colloidal silica as template, and chitosan as carbon source. N2 sorption isotherm results show that the prepared Pd@N-C had a high BET surface area (640m(2)g(-1)) with large porosity. The prepared Pd@N-C is high nitrogen-rich as characterized with element analysis.
View Article and Find Full Text PDFChemSusChem
June 2014
Key Laboratory of Applied Chemistry of Zhejiang Province, Zhejiang University, Hangzhou 310028 (PR China).
A composite catalyst including palladium nanoparticles on titania (TiO2) and on nitrogen-modified porous carbon (Pd/TiO2@N-C) is synthesized from palladium salts, tetrabutyl titanate, and chitosan. N2 sorption isotherms show that the catalyst has a high BET surface area (229 m(2) g(-1)) and large porosity. XPS and TEM characterization of the catalyst shows that palladium species with different chemical states are well dispersed across the TiO2 and nitrogen-modified porous carbon, respectively.
View Article and Find Full Text PDFJ Am Chem Soc
October 2009
Department of Chemistry and Biotechnology, Graduate School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-Ku, Tokyo 113-8656, Japan.
Linear polyethylene propagation starting from Pd phosphine-sulfonate complexes, Pd(CH(3))(L)(Ar(2)PC(6)H(4)SO(3)) (L = 2,6-lutidine, Ar = o-MeOC(6)H(4) (2a) and L = pyridine, Ar = Ph (2b)), was studied both experimentally and theoretically. Experimentally, highly linear polyethylene was obtained with Pd(CH(3))(L)(Ar(2)PC(6)H(4)SO(3)) complexes 2a and 2b. Formation of a long alkyl-substituted palladium complex (3) was detected as a result of ethylene oligomerization on a palladium center starting from methylpalladium complex.
View Article and Find Full Text PDFJ Am Chem Soc
August 2009
Department of Chemistry, University of Michigan, 930 North University Avenue, Ann Arbor, Michigan 48109, USA.
This contribution describes the substrate scope and mechanism of Pd-catalyzed ligand-directed C-H arylation with diaryliodonium salts. This transformation was applied to the synthesis of a variety of different biaryl products, using directing groups including pyridines, quinolines, pyrrolidinones, and oxazolidinones. Electronically and sterically diverse aryl groups (Ar) were transferred in high yield using iodine(III) reagents of general structure [Mes-I-Ar]BF(4).
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