Jincheng Mao

ORCID: 0000-0003-0301-1322
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Research Areas
  • Catalytic C–H Functionalization Methods
  • Catalytic Cross-Coupling Reactions
  • Hydraulic Fracturing and Reservoir Analysis
  • Enhanced Oil Recovery Techniques
  • Sulfur-Based Synthesis Techniques
  • Surfactants and Colloidal Systems
  • Asymmetric Hydrogenation and Catalysis
  • Synthetic Organic Chemistry Methods
  • Catalytic Alkyne Reactions
  • Cyclopropane Reaction Mechanisms
  • Synthesis and Catalytic Reactions
  • Asymmetric Synthesis and Catalysis
  • Chemical Synthesis and Reactions
  • Petroleum Processing and Analysis
  • Drilling and Well Engineering
  • Hydrocarbon exploration and reservoir analysis
  • Oxidative Organic Chemistry Reactions
  • Chemical Synthesis and Analysis
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Radical Photochemical Reactions
  • Atmospheric and Environmental Gas Dynamics
  • Surface Chemistry and Catalysis
  • Advanced Polymer Synthesis and Characterization
  • Rock Mechanics and Modeling

East China University of Science and Technology
2025

Southwest Petroleum University
2016-2025

State Key Laboratory of Oil and Gas Reservoir Geology and Exploitation
2015-2024

Wuhan Institute of Technology
2022

Beijing University of Civil Engineering and Architecture
2021-2022

Shanxi Jincheng Anthracite Mining Group (China)
2018-2020

Chengdu University
2016-2019

Soochow University
2007-2016

Suzhou Research Institute
2015

City University of New York
2014

A new approach to the selective synthesis of (E)-vinyl sulfones has been developed via a Fe/Cu co-catalyzed sulfonylation arylpropiolic acid or phenylacetylene with sulfonyl hydrazides. variety vinyl have obtained in moderate good yields, comparable best results reported so far. The inexpensive method features simple experimental procedure and tolerance substrate.

10.1021/acs.joc.5b00558 article EN The Journal of Organic Chemistry 2015-04-16

We have successfully developed an example of copper-catalyzed decarboxylative C(sp2)–C(sp3) coupling reactions via C–H functionalization for the first time. It is noteworthy that our catalytic system very stable, low-cost, palladium-free, ligand-free, and easily accessible.

10.1039/c2cc33203e article EN Chemical Communications 2012-01-01

Reported herein is a novel, useful, visible light-promoted ring-opening functionalization of unstrained cycloalkanols.

10.1039/c8sc01763h article EN cc-by Chemical Science 2018-01-01

An example of highly efficient low-cost ferrocene-catalyzed decarboxylative C(sp2)–C(sp3) coupling reactions via C–H functionalization has been developed successfully. It is noteworthy that nanoparticles Fe3O4 could be used as a reusable catalyst for 7 times in the absence ligand.

10.1039/c3gc37131j article EN Green Chemistry 2013-01-01

The highly effective synthesis of methyl esters from benzylic alcohols, aldehydes, or acids via copper-catalyzed C-C cleavage tert-butyl hydroperoxide is reported in this paper for the first time. Our protocol easily accessible and practical, making it a possible supplement traditional way.

10.1021/jo4016387 article EN The Journal of Organic Chemistry 2013-09-02

A hydrophobic associating polymer named DiPHAM (acrylamide/sodium acrylamide-2-methylpropanesulfonic/sodium acrylate/N,N-di-n-dodecylacrylamide) with good salt tolerance was synthesized via photo-initiation polymerization. The critical association concentration (CAC) of determined by viscosity changes to be 490 mg/L different concentrations and particle sizes varied under such dynamic conditions. influences aqueous metal ions charges on its solution were investigated measuring apparent...

10.3390/polym10080849 article EN Polymers 2018-08-01

In order to improve the heat resistance of current clean fracturing fluids, a novel cationic surfactant (VES-T), composed three single-chains and spacer group, was designed synthesized as thickener for fluids. Various performances such VES-T fluid in presence NaSal were evaluated carefully. Study rheological properties demonstrated that fluids with varying concentrations (3⁻5 wt %) have excellent thermal stabilities under ultra-high temperatures ranging from 140 180 °C. Until now, this is...

10.3390/polym10050535 article EN Polymers 2018-05-16

Catalysis is the second largest application for V after its use as an additive to improve steel production. Molecular complexes of vanadium(V) are particularly useful and efficient catalysts oxidation processes; however, their ability catalyze reductive transformations has yet be fully explored. Here we report first examples polar organic functionality reduction mediated by V. Open-shell VIII that feature a π-radical monoanionic 2,2′:6′,2″-terpyridine ligand (Rtpy•)− functionalized at...

10.1021/jacs.9b07062 article EN Journal of the American Chemical Society 2019-09-03

An example of a transition-metal-free, direct, and efficient acetamidosulphenylation reaction alkenes using nitriles as the nucleophiles via radical process is presented. This shows broad substrate scope high regioselectivity provides straightforward access to acetamidosulfide derivatives in moderate yields.

10.1021/acs.orglett.5b02752 article EN Organic Letters 2015-10-29

A novel phosphoric acid -mediated synthesis of vinyl sulfones through decarboxylative coupling reactions sodium sulfinates with phenylpropiolic acids is described. This transformation efficient and environmentally friendly.

10.1021/acs.joc.5b01212 article EN The Journal of Organic Chemistry 2015-07-24

A category of gemini surfactants with novel structures were designed and synthesized as thickening agents clean fracturing fluids good temperature stability in this research.

10.1039/c6ra17823e article EN RSC Advances 2016-01-01

Gemini surfactant, as a functionally flexible polymer-like material in the aqueous solution, has attracted increased attention reservoir stimulation of hydraulic fracturing recent decades. A new cationic viscoelastic surfactant named JS-N-JS, which secondary amine spacer group and two ultra-long hydrophobic tails, was synthesized from erucamidopropyl dimethylamine, diethanolamine, thionyl chloride thickener for fluid. Compared with some methylene spacer, JS-N-JS showed lower critical...

10.3390/polym10111215 article EN Polymers 2018-11-01

Abstract Copper‐catalyzed cross‐coupling reactions of aryl halides and heteroaryl with terminal alkynes were carried out in DMF at 110–130 °C to provide the corresponding coupling products satisfactory‐to‐good yields by using inexpensive 8‐hydoxyquinoline as ligand. Noteworthy is that bifunctional copper catalyst was successfully applied this alkynylation reaction for first time.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)

10.1002/ejoc.200800394 article EN European Journal of Organic Chemistry 2008-07-05

Abstract Ligand‐free iron/copper cocatalyzed cross‐coupling reactions of aryl halides with terminal alkynes were carried out to provide the corresponding coupling products in good yields (up 99%). Noteworthy is that this low‐cost, effective and environmentally friendly protocol was first be employed alkynylation couplings.

10.1002/adsc.200800517 article EN Advanced Synthesis & Catalysis 2008-11-03

Taking control: Selective catalysts for olefin dihydroxylation have been generated by the combination of apo-streptavidin and OsO4. Site-directed mutagenesis allows improvement enantioselectivity even inversion enantiopreference in certain cases. Notably allyl phenyl sulfide cis-β-methylstyrene were converted with unprecedented enantiomeric excess. Detailed facts importance to specialist readers are published as "Supporting Information". Such documents peer-reviewed, but not copy-edited or...

10.1002/anie.201103632 article EN Angewandte Chemie International Edition 2011-09-21
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