Xiaodong Jin

ORCID: 0009-0008-2133-0128
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About
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Research Areas
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Catalytic Cross-Coupling Reactions
  • Catalytic C–H Functionalization Methods
  • Copper-based nanomaterials and applications
  • Advanced Photocatalysis Techniques
  • Nanomaterials for catalytic reactions
  • Asymmetric Hydrogenation and Catalysis
  • Chemical Synthesis and Reactions
  • Cyclopropane Reaction Mechanisms
  • Carbon dioxide utilization in catalysis
  • Crystallography and molecular interactions
  • Asymmetric Synthesis and Catalysis
  • Synthesis of Indole Derivatives
  • MXene and MAX Phase Materials
  • Synthesis and Catalytic Reactions
  • ZnO doping and properties
  • Synthetic Organic Chemistry Methods
  • Catalytic Alkyne Reactions
  • Sulfur-Based Synthesis Techniques

Xi’an Jiaotong-Liverpool University
2024

Lanzhou Jiaotong University
2020-2021

Imperial College London
2017

Transnational Press London
2017

Nanjing Tech University
2014

Lanzhou University
2012-2013

Development of highly efficient photocatalysts is a primary goal in the photocatalysis domain among which reusable composites with synergistic photocatalytic effect have attracted extensive interest. The ability catalysts to capture light determines their effect, and porous or hollow are more conducive entry reflection light. this research develop type visible-light-driven, double-shell photocatalyst high antibacterial activity excellent cycling stability. Photocatalysts were fabricated...

10.1021/acsami.0c01476 article EN ACS Applied Materials & Interfaces 2020-04-22

Phenylpyrazole derivatives were designed and synthesized to fabricate novel herbicides containing strobilurin moieties. Most compounds demonstrated good inhibition on A. retroflexus , which speculated as PPO inhibitors.

10.1039/d5ra02377g article EN cc-by RSC Advances 2025-01-01

Abstract An efficient iodine‐mediated oxidation reaction for ynamides has been developed to produce N ‐monosubstituted α‐ketoamides and α‐ketoimides. This oxidative method, which exhibits good functional group tolerance, was performed under mild conditions without a metal catalyst.

10.1002/ejoc.201402538 article EN European Journal of Organic Chemistry 2014-09-24

An efficient and low-cost ligand, diethylenetriamine, is shown to promote the copper catalysed Finkelstein reaction without requirement of inert atmosphere conditions.

10.1039/c7cy00538e article EN Catalysis Science & Technology 2017-01-01

A coral-like ZnO/C-ZnFe2O4 (Z/C-ZFO) photocatalyst was synthesized by simulating the structural characteristics of coral since its structure is conducive to capture and absorption light. The synthesis process involves a two-step process. First, flowerlike hierarchical precursors were through hydrothermal self-assembled route. Next, thermally annealed in nitrogen atmosphere after doping with zinc source. In addition forming heterojunctions that enhance photocatalytic properties,...

10.1021/acs.iecr.0c00939 article EN Industrial & Engineering Chemistry Research 2020-05-14

Skeletal editing is an important approach for the modification and diversification of biologically active molecules. The utilization nitrogen deletion strategies in skeletal has recently emerged as a new method compound modification. Here, we report unexpected isoindolines. Contrary to anticipated outcome cyclobutane formation via intramolecular radical couplings, isoindoline triggers Diels–Alder cycloaddition facilitated by situ ortho-xylylene yield tetraline. Inspired this reaction,...

10.1021/acs.joc.4c01959 article EN cc-by The Journal of Organic Chemistry 2024-11-21

A combination of solid-state structural studies and kinetic profiling have been used to study the copper( i )-catalysed intramolecular Ullmann N -arylation reaction leading new mechanistic insights an improved protocol for benzimidazole synthesis.

10.1039/d3cy00767g article EN cc-by-nc Catalysis Science & Technology 2023-01-01

The structures of novel copper( i ) complexes which are potential intermediates in copper-catalysed benzoxazole and benzothiazole synthesis reported their relative reactivities studied.

10.1039/d4dt01418a article EN cc-by-nc Dalton Transactions 2024-01-01
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