Jiajian Peng

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Name: 彭家建
Organization: Hangzhou Normal University , China
Department: Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education
Title: (PhD)
Co-reporter:Jiayun Li;Congbai Niu, ;Yuan Deng;Guodong Zhang;Ying Bai;Chao Ma;Wenjun Xiao ;Guoqiao Lai
Applied Organometallic Chemistry 2014 Volume 28( Issue 6) pp:454-460
Publication Date(Web):
DOI:10.1002/aoc.3149

A series of platinum–acetylide–phosphine complexes were synthesized and their anti-sulfur-poisoning characteristics investigated. In comparison with Speier's and Karstedt's catalysts, the platinum–acetylide–phosphine complexes exhibited both higher catalytic activity and selectivity for the β-adduct for the hydrosilylation reactions under the same conditions. Furthermore, the complexes also exhibited a strong ability to resist to sulfur-poisoning. This indicated that the alkyne ligands containing the silyl group had a strong impact on the hydrosilylation reaction. Copyright © 2014 John Wiley & Sons, Ltd.

Co-reporter:Yisong Xu, Ying Bai, Jiajian Peng, Jiayun Li, Wenjun Xiao, Guoqiao Lai
Journal of Organometallic Chemistry 2014 Volume 765() pp:59-63
Publication Date(Web):15 August 2014
DOI:10.1016/j.jorganchem.2014.05.002
•PEG-DIL had been successfully prepared and applied in the hydrosilylation.•PEG-DIL-Rh catalytic system exhibit both excellent catalytic activity and selectivity.•PEG-DIL-Rh catalytic system is stably and could be recycled.A series of polyethylene glycol-functionalized imidazolium ionic liquids has been prepared and characterized. These ionic liquids have been successfully applied in the hydrosilylation of alkenes catalyzed by rhodium complexes. The effects of the length of the polyether chain, the amount of ionic liquid, and the reaction temperature on the catalytic performance of hydrosilylation have been investigated. Furthermore, the catalytic system has been tested for the hydrosilylation of different alkenes with triethoxysilane. The new catalytic system exhibits both excellent catalytic activity and selectivity under low-temperature conditions. The catalyst system could be recycled five times with slightly deactivation.A series of polyethylene glycol-functionalized imidazolium ionic liquids has been prepared and characterized. These ionic liquids have been successfully applied in the hydrosilylation of alkenes catalyzed by rhodium complexes. The catalytic system exhibits both excellent catalytic activity and selectivity. The catalytic system could be recycled.
Co-reporter:Ying Bai, Shufang Zhang, Yuan Deng, Jiajian Peng, Jiayun Li, Yingqian Hu, Xiaonian Li, Guoqiao Lai
Journal of Colloid and Interface Science 2013 Volume 394() pp:428-433
Publication Date(Web):15 March 2013
DOI:10.1016/j.jcis.2012.11.048
A catalyst containing functionalized polyethylene glycol with 4-aminobenzoic acid (PEG-AMB) stabilized platinum nanoparticles has been synthesized and characterized, and its application in the hydrosilylation of alkenes investigated. It is shown that the functionalized PEG-stabilized Pt nanoparticles form a very efficient catalyst for the hydrosilylation of alkenes. The Pt nanoparticles can be fully immobilized in the PEG-AMB and recycled at least nine times without any obvious loss of catalytic activity.Graphical abstractHighlights► PEG-AMB-Pt nanoparticles catalyst had been synthesized and characterized. ► The PEG-AMB-Pt was very efficient catalyst for hydrosilylation of alkenes. ► The Pt nanoparticles could be immobilized in PEG-AMB stably and recycled.
Co-reporter:Shaofeng Pang;Jiayun Li;Ying Bai;Wenjun Xiao ;Guoqiao Lai
Chirality 2013 Volume 25( Issue 5) pp:275-280
Publication Date(Web):
DOI:10.1002/chir.22137

ABSTRACT

Several chiral ligands containing (R,R)-diaminocyclohexane moieties and pyrrole, furan, or benzene have been synthesized. These ligands were tested in enantioselective zinc-catalyzed hydrosilylation reactions; excellent enantioselectivities were obtained when the ligands containing (R,R)-diaminocyclohexane moieties and furan rings were used. For comparison, zinc chloride combined with different potassium carboxylate salts and ligands were also tested for catalytic hydrosilylation reactions. Chirality 25:275–280, 2013. © 2013 Wiley Periodicals, Inc.

Co-reporter:Chao Ma, Jiayun Li, Jiajian Peng, Ying Bai, Guodong Zhang, Wenjun Xiao, Guoqiao Lai
Journal of Organometallic Chemistry 2013 727() pp: 28-36
Publication Date(Web):
DOI:10.1016/j.jorganchem.2012.12.016
Co-reporter:Weiwei Xia, Yewu Wang, Yafei Luo, Jiayun Li, Yanjun Fang, Lin Gu, Jiajian Peng, Jian Sha
Journal of Power Sources 2012 Volume 217() pp:351-357
Publication Date(Web):1 November 2012
DOI:10.1016/j.jpowsour.2012.05.072
SnO2 nanoparticles (NPs)@carbon nanofibers as anode materials for lithium-ion battery are synthesized by a novel facile route using the commercial filter paper and tin dichloride dehydrate (SnCl2·2H2O). The weight ratio between carbon nanofibers and SnO2 NPs, which seriously affects the battery performance, has been demonstrated to be easily tuned by adjusting the sintering temperature. The electrochemical investigations show that the SnO2 NPs@carbon nanofibers with 9 wt% carbon have the best performance with the highest capacity of 383 mAh g−1 after 30 cycles at a current density of 100 mA g−1. The method introduced in this study provides an easy strategy for the controlled introduction of carbon to optimize the performance of lithium-ion battery using SnO2 NPs@carbon nanofibers as anode materials.Highlights► A simple process to fabricate SnO2 NPs@carbon nanofibers as anode materials. ► Controlled introduction of carbon to optimize the lithium-ion battery performance. ► This method is easy preparation, low cost, and non-toxic source materials.
Co-reporter:Shuai Liu, Jiajian Peng, Hu Yang, Ying Bai, Jiayun Li, Guoqiao Lai
Tetrahedron 2012 68(5) pp: 1371-1375
Publication Date(Web):
DOI:10.1016/j.tet.2011.12.054
Co-reporter:Ying Bai, Jiajian Peng, Yingqian Hu, Jiayun Li, Guoqiao Lai
Journal of Fluorine Chemistry 2011 Volume 132(Issue 2) pp:123-127
Publication Date(Web):February 2011
DOI:10.1016/j.jfluchem.2010.12.007
A novel polymer has been synthesized using 2-vinylpyridine as a functional monomer and allyl polyethylene glycol as a cross-linking agent, and platinum has been immobilized on this synthesized polymer. The resulting immobilized catalyst showed superior catalytic performance for the hydrosilylation of 3,3,3-trifluoropropene with triethoxysilane as compared to homogenous platinum catalyst, polystyrene-immobilized platinum or other hydrosilylation catalysts. The conversion of silane is about 100% and the maximum yield of β-adduct is 92.3% with slightly α-adduct. Furthermore, the catalyst showed sufficient stability that it could be reused three times without noticeable inactivation.Graphical abstractThe novel polymer synthesized immobilized platinum and applied in the catalytic hydrosilylation of 3,3,3-trifluoropropene with triethoxysilane. The catalysts show the excellent activity and the high selectivity of β-adduct.Research highlights▶ Using allyl polyethylene glycol as a cross-linking agent for preparing polymer. ▶ Using 2-vinylpyridine as a functional monomer for preparing polymer. ▶ The catalysts have high catalytic activity and selectivity. ▶ The catalysts could be reused three times without noticeable inactivation.
Co-reporter:Jiayun Li, Jiajian Peng, Guodong Zhang, Ying Bai, Guoqiao Lai and Xiaonian Li  
New Journal of Chemistry 2010 vol. 34(Issue 7) pp:1330-1334
Publication Date(Web):30 Mar 2010
DOI:10.1039/C0NJ00012D
The hydrosilylation of alkenes in a supercritical CO2 (scCO2)/ionic liquid (IL) system was investigated. Rh(PPh3)3Cl exhibited excellent catalytic activity and selectivity. KOtBu was used as an additive, and no hydrogenation by-product (alkane) was detected in the scCO2/IL system. During hydrosilylation in the scCO2/IL system, the reactants were possibly transferred into the IL phase by scCO2, in which the catalyst was dissolved. The products can be flushed with scCO2 after the reaction and the catalyst/IL system reused.
1-BUTYL-3-VINYLIMIDAZOLIUM HEXAFLUOROPHOSPHATE
1-Carboxymethyl-3-methylimidazolium hexafluorophosphate
1H-IMIDAZOLIUM, 1-[3-(ETHOXYDIHYDROXYSILYL)PROPYL]-3-METHYL-, CHLORIDE
1,2-Cyclohexanediamine, N,N'-bis(2-furanylmethyl)-, (1R,2R)-
1H-Imidazolium, 1-(carboxymethyl)-3-methyl-, bromide
1H-Imidazolium, 1-ethyl-3-octyl-, hexafluorophosphate(1-)
Phenol, 2,4-bis(1,1-dimethylethyl)-6-[[[(1S)-1-phenylethyl]imino]methyl]-