XueQin Cao

Find an error

Name: 曹雪琴; XueQin Cao
Organization: Soochow University , China
Department: Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, and National Engineering Laboratory for Modern Silk
Title: Associate Professor(PhD)

TOPICS

Co-reporter:Lingling Zhang;Danhua Ge;Genlong Qu;Junwei Zheng;Hongwei Gu
Nanoscale (2009-Present) 2017 vol. 9(Issue 17) pp:5451-5457
Publication Date(Web):2017/05/04
DOI:10.1039/C7NR01425B
Herein, we have developed a facile and effective approach for synthesizing a novel kind of porous nitrogen-doped carbon-coated MnO nanosphere. The porous Mn2O3 nanospheres are initially obtained by the calcination treatment of a coordination self-assembled aggregation precursor (referred to as Mn(OAc)2-C-8). Then, MnO@N-doped carbon composites (MnO@NCs) are obtained by the calcination of the Mn2O3 nanospheres coated with polydopamine (Mn2O3@PDA). The MnO@NCs are evaluated as an anode for lithium ion batteries (LIBs), which exhibit high specific capacity, stable cycling performance (1096.6 mA h g−1 after 100 cycles at 100 mA g−1) and high coulombic efficiency (about 99% over 100 cycles). The unique structure design and synergistic effect not only settle the challenges of low conductivity and poor cycling stability of transition metal oxides but also resolve the imperfection of inferior specific capacity of traditional graphite materials. Importantly, it may provide a commendable conception for developing new-fashioned anode materials to improve the lithium storage capability and electrochemical performance.
Co-reporter:Lingling Zhang;Danhua Ge;Hongbo Geng;Junwei Zheng;Hongwei Gu
New Journal of Chemistry (1998-Present) 2017 vol. 41(Issue 15) pp:7102-7107
Publication Date(Web):2017/07/24
DOI:10.1039/C7NJ01066D
We describe a facile method to prepare porous manganese oxides (Mn2O3) embedded in reduced graphene oxide (rGO). First, the porous Mn2O3 nanospheres were generated from the coordination self-assembled aggregations (referred to as Mn(OAc)2-C-8), serving as precursors via calcination treatment, followed by a graphene-coating approach. The reduced graphene oxide coating Mn2O3 (Mn2O3@rGO) composites not only provide superior conductivity and prevent large volume expansion, resolving the challenges of pure Mn2O3 nanospheres, but also remedy the imperfection of the inferior specific capacity of traditional graphite materials. When evaluated as an anode for lithium-ion batteries (LIBs), the Mn2O3@rGO electrode exhibits a high initial specific capacity (1684.9 mA h g−1), excellent cycling performance (1207.9 mA h g−1 over 150 cycles at a current density of 0.1 A g−1), and high coulombic efficiency (99% after 150 cycles), as well as high rate capacity (730.0 mA h g−1 over 150 cycles at 1 A g−1). The unique structural design and synergistic effect may offer a practical conception for the development of new next-generation LIBs.
Co-reporter:Danhua Ge, Genlong Qu, Xinming Li, Kaiming Geng, Xueqin Cao and Hongwei Gu  
New Journal of Chemistry 2016 vol. 40(Issue 6) pp:5531-5536
Publication Date(Web):18 Apr 2016
DOI:10.1039/C5NJ03544A
A novel type of transition bimetal–organic frameworks was described as a heterogeneous catalyst for the oxidative coupling of amines to imines under mild conditions, which was easily synthesized by the coordination assembly of manganese(II) and cobalt(II) with 1,3,5-benzenetricarboxylic acid (H3BTC) for the first time. The metal–organic framework material was characterized by scanning electron microscopy, energy dispersive spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction, thermogravimetry and N2 sorption. As an environmentally benign heterogeneous catalyst, the catalytic ability of the metal–organic framework material was then detected to be excellent for the tert-butyl hydroperoxide (TBHP) promoted direct oxidative coupling of benzylamines to imines in excellent yields (up to 100%) in methanol for 3 h. More importantly, it could be recycled up to six runs, while still maintaining its high catalytic activity.
Co-reporter:Danhua Ge;Jiaqing Wang;Hongbo Geng;Shuanglong Lu;Dongtao Wang; Xinming Li;Xianli Zhao; Xueqin Cao; Hongwei Gu
ChemPlusChem 2015 Volume 80( Issue 3) pp:511-515
Publication Date(Web):
DOI:10.1002/cplu.201402319

Abstract

The development of highly efficient catalysts for the selective oxidation of styrene to benzaldehyde has attracted great attention in recent years because of its significance in synthetic chemistry. In this study, two different kinds of copper-based metal oxide nanoparticles (NPs), namely, CuO and CuO/Co3O4 NPs, were synthesized by a simple and scalable method, and these nanoparticles demonstrated efficient catalytic abilities for the selective oxidation of styrene and its derivatives to the corresponding aldehydes in the presence of tert-butyl hydroperoxide (TBHP) under mild reaction conditions in excellent yields. Importantly, both of the heterogeneous catalysts can be recycled up to five runs while still maintaining their high catalytic activity.

Co-reporter:Danhua Ge, Hongbo Geng, Jiaqing Wang, Junwei Zheng, Yue Pan, Xueqin Cao and Hongwei Gu  
Nanoscale 2014 vol. 6(Issue 16) pp:9689-9694
Publication Date(Web):10 Jun 2014
DOI:10.1039/C4NR01978D
A simple and scalable coordination-derived method for the synthesis of porous Co3O4 hollow nanospheres is described here. The initially formed coordination-driven self-assembled aggregates (CDSAAs) could act as the precursor followed by calcination treatment. Then the porous hollow Co3O4 nanospheres are obtained, in which the primary Co3O4 nanoparticles are inter-dispersed. When the nanospheres are used as anode materials for lithium storage, they show excellent coulombic efficiency, high lithium storage capacity and superior cycling performance. In view of the facile synthesis and excellent electrochemical performance obtained, this protocol to fabricate special porous hollow frameworks could be further extended to other metal oxides and is expected to improve the practicality of superior cycle life anode materials with large volume excursions for the development of the next generation of LIBs.
Co-reporter:Jiaqing Wang, Shuanglong Lu, Xueqin Cao and Hongwei Gu  
Chemical Communications 2014 vol. 50(Issue 42) pp:5637-5640
Publication Date(Web):01 Apr 2014
DOI:10.1039/C4CC01389A
A novel, efficient, convenient and environmentally friendly approach for the synthesis of nitriles and imines from primary amines has been developed. Using commercially available red copper as the catalyst, ammonium bromide as the co-catalyst and molecular oxygen as the sole oxidant, nitriles and imines can be afforded in high yields through benzylic oxidation.
Co-reporter:Jiaqing Wang, Jing He, Cong Zhi, Bin Luo, Xinming Li, Yue Pan, Xueqin Cao and Hongwei Gu  
RSC Advances 2014 vol. 4(Issue 32) pp:16607-16611
Publication Date(Web):27 Mar 2014
DOI:10.1039/C4RA00749B
A facile and efficient approach to synthesize symmetric, asymmetric and bridged aromatic azo compounds (AAzos) from aromatic amines was developed by using red copper as catalyst. Despite numerous efforts towards the catalytic synthesis of symmetric and asymmetric AAzos derivatives, most reactions present certain drawbacks inhibiting their industrial applications, such as laborious multi-step processes, harsh reaction conditions and expensive reagents. And the synthesis of bridged azos had low yields before. With the presence of ammonium bromide as co-catalyst, pyridine as a ligand and molecular dioxygen as a sole oxidative reagent, red copper, a common and abundant metal in nature, exhibited unexpected catalytic activity towards the preparation of AAzos in high yields via one-step reaction, making this catalyst an attractive candidate for industrial and synthetic applications.
Co-reporter:Tingting Yu;Jiaqing Wang; Xinming Li; Xueqin Cao ; Hongwei Gu
ChemCatChem 2013 Volume 5( Issue 10) pp:2852-2855
Publication Date(Web):
DOI:10.1002/cctc.201300394
Co-reporter:Danhua Ge;Dr. Lei Hu;Jiaqing Wang; Xingming Li;Fenqiang Qi; Jianmei Lu; Xueqin Cao; Hongwei Gu
ChemCatChem 2013 Volume 5( Issue 8) pp:2183-2186
Publication Date(Web):
DOI:10.1002/cctc.201300136
Co-reporter:Linyan Shi, Lei Hu, Jiaqing Wang, Xueqin Cao, and Hongwei Gu
Organic Letters 2012 Volume 14(Issue 7) pp:1876-1879
Publication Date(Web):March 15, 2012
DOI:10.1021/ol300471a
A series of N-substituted isoindolinones have been successfully synthesized through the reductive C–N coupling and intramolecular amidation of 2-carboxybenzaldehyde and amines. This one-pot synthesis gives excellent yields using ultrathin Pt nanowires as catalysts under 1 bar of hydrogen. These unsupported catalysts can also be used for the synthesis of phthalazinones in high yield when hydrazine or phenyl hydrazine is used instead of amines.
Co-reporter:Zhengmao Ye, Lei Hu, Jiang Jiang, Jianxin Tang, Xueqin Cao and Hongwei Gu  
Catalysis Science & Technology 2012 vol. 2(Issue 6) pp:1146-1149
Publication Date(Web):28 Mar 2012
DOI:10.1039/C2CY20138K
Uniform CuO@Ag nanowires were prepared by reduction of Cu(OAc)2 on the surface of Ag nanowires in ethylene glycol. This novel material shows outstanding catalytic activities in the epoxidation of trans-stilbene and the oxidation of alcohols under mild reaction conditions.
Co-reporter:Zhiqiang Guo, Lei Hu, Hsiao-hua Yu, Xueqin Cao and Hongwei Gu  
RSC Advances 2012 vol. 2(Issue 8) pp:3477-3480
Publication Date(Web):29 Feb 2012
DOI:10.1039/C2RA01097F
Aromatic hydrogenation to form cyclohexane derivatives is one of the most important steps in both the petrochemical industry, for clean diesel fuel generation, and the pharmaceutical industry, for safe drug synthesis. We report herein, pure ultra-thin Pt nanowire catalysts with no supporting matrix and their high activities towards the hydrogenation of aromatic compounds (>99% conversion, 1 MPa initial hydrogen pressure, 70 °C). The catalysts can also be recycled up to 40 times with no loss in activity.
Co-reporter:Baoqiang Sheng, Lei Hu, Tingting Yu, Xueqin Cao and Hongwei Gu  
RSC Advances 2012 vol. 2(Issue 13) pp:5520-5523
Publication Date(Web):25 Apr 2012
DOI:10.1039/C2RA20400B
Highly-dispersed ultrafine platinum (Pt) nanoparticles supported on graphene sheets were successfully prepared. Various unsaturated compounds were reduced in excellent yields under mild conditions. Higher pressure (4 atm) accelerated the reaction rate, and complete hydrogenation products were obtained in ten minutes.
Co-reporter:Haiyan Hong;Lei Hu;Min Li;Junwei Zheng;Dr. Xuhui Sun;Xinhua Lu;Dr. Xueqin Cao;Dr. Jianmei Lu;Dr. Hongwei Gu
Chemistry - A European Journal 2011 Volume 17( Issue 31) pp:8726-8730
Publication Date(Web):
DOI:10.1002/chem.201003429

Abstract

Iron oxide coated platinum nanowires (Pt@Fe2O3 NWs) with a diameter of 2.8 nm have been prepared by the oxygen oxidation of FePt NWs in oleylamine. These “cable”-like NWs were characterised by transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy and X-ray absorption fine structure analysis. These Pt@Fe2O3 NWs were used as “non-support” heterogeneous catalysts in oxidation of olefins and alcohols. The results revealed that it is an active and highly selective catalyst. Styrene derivatives were tested with molecular oxygen as the sole oxidant, with benzaldehyde successfully obtained from styrene in an absolute yield of 31 %, whereas the use of tert-butyl hydroperoxide as the sole oxidant in the oxidation of alcohols led to yields of more than 80 % of the corresponding ketone or aldehyde. This unsupported catalyst was found to be more active (TOF=96.5 h−1) than other reported Fe2O3 nanoparticle catalysts and could be recycled multiple times without any notable decrease in activity. Our findings will extend the use of such nanomaterial catalysts to new catalytic systems.

Co-reporter:Lei Hu, Linyan Shi, Haiyan Hong, Min Li, Qinye Bao, Jianxin Tang, Jianfeng Ge, Jianmei Lu, Xueqin Cao and Hongwei Gu  
Chemical Communications 2010 vol. 46(Issue 45) pp:8591-8593
Publication Date(Web):30 Sep 2010
DOI:10.1039/C0CC03204B
A novel FePt@Cu nanowire catalyst was prepared by the reduction of Cu(acac)2 on the surface of FePt nanowires, in oleylamine (OAm). This nanowire catalyst efficiently epoxidised stilbene in the presence of molecular oxygen, and the conversion and selectivity were maintained with repeated use of the catalyst, compared with recycled catalyst.
Co-reporter:Zhengmao Ye, Lei Hu, Jiang Jiang, Jianxin Tang, Xueqin Cao and Hongwei Gu
Catalysis Science & Technology (2011-Present) 2012 - vol. 2(Issue 6) pp:NaN1149-1149
Publication Date(Web):2012/03/28
DOI:10.1039/C2CY20138K
Uniform CuO@Ag nanowires were prepared by reduction of Cu(OAc)2 on the surface of Ag nanowires in ethylene glycol. This novel material shows outstanding catalytic activities in the epoxidation of trans-stilbene and the oxidation of alcohols under mild reaction conditions.
Co-reporter:Jiaqing Wang, Shuanglong Lu, Xueqin Cao and Hongwei Gu
Chemical Communications 2014 - vol. 50(Issue 42) pp:NaN5640-5640
Publication Date(Web):2014/04/01
DOI:10.1039/C4CC01389A
A novel, efficient, convenient and environmentally friendly approach for the synthesis of nitriles and imines from primary amines has been developed. Using commercially available red copper as the catalyst, ammonium bromide as the co-catalyst and molecular oxygen as the sole oxidant, nitriles and imines can be afforded in high yields through benzylic oxidation.
Co-reporter:Lei Hu, Linyan Shi, Haiyan Hong, Min Li, Qinye Bao, Jianxin Tang, Jianfeng Ge, Jianmei Lu, Xueqin Cao and Hongwei Gu
Chemical Communications 2010 - vol. 46(Issue 45) pp:NaN8593-8593
Publication Date(Web):2010/09/30
DOI:10.1039/C0CC03204B
A novel FePt@Cu nanowire catalyst was prepared by the reduction of Cu(acac)2 on the surface of FePt nanowires, in oleylamine (OAm). This nanowire catalyst efficiently epoxidised stilbene in the presence of molecular oxygen, and the conversion and selectivity were maintained with repeated use of the catalyst, compared with recycled catalyst.
Benzenemethanamine, 4-fluoro-N-[(4-fluorophenyl)methylene]-
Benzenemethanamine, 4-(1,1-dimethylethyl)-N-[[4-(1,1-dimethylethyl)phenyl]methylene]-
Benzenemethanamine, 3-chloro-N-[(3-chlorophenyl)methylene]-
Benzenemethanamine, 2-methyl-N-[(2-methylphenyl)methylene]-
Benzenemethanamine, N,2-dimethyl-N-[(2-methylphenyl)methyl]-
Benzenemethanamine, 2-bromo-N-[(2-bromophenyl)methylene]-
BENZENEMETHANAMINE, 4-METHYL-N-[(4-METHYLPHENYL)METHYLENE]-
1-Butanamine, N-[(3-methoxyphenyl)methylene]-
N-HEPTYL-N-METHYLHEPTAN-1-AMINE