Zhenjiang Li

ORCID: 0000-0002-1100-7297
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Research Areas
  • Carbon dioxide utilization in catalysis
  • biodegradable polymer synthesis and properties
  • Advanced Polymer Synthesis and Characterization
  • Synthetic Organic Chemistry Methods
  • Chemical Synthesis and Reactions
  • Synthesis and Catalytic Reactions
  • Multicomponent Synthesis of Heterocycles
  • Chemical Synthesis and Analysis
  • CO2 Reduction Techniques and Catalysts
  • Sulfur-Based Synthesis Techniques
  • Chemistry and Chemical Engineering
  • Catalytic C–H Functionalization Methods
  • Enzyme Catalysis and Immobilization
  • Asymmetric Synthesis and Catalysis
  • Organometallic Complex Synthesis and Catalysis
  • Synthesis and biological activity
  • Microbial Metabolic Engineering and Bioproduction
  • Polymer Surface Interaction Studies
  • Advanced Radiotherapy Techniques
  • Organoboron and organosilicon chemistry
  • Click Chemistry and Applications
  • Nanomaterials for catalytic reactions
  • Synthesis and pharmacology of benzodiazepine derivatives
  • Polyoxometalates: Synthesis and Applications
  • Crystallization and Solubility Studies

Nanjing Tech University
2016-2025

Henan Normal University
2024-2025

Shandong First Medical University
2023-2024

Shandong Tumor Hospital
2023-2024

Shandong University of Science and Technology
2024

Shanghai Institute of Applied Physics
2024

University of Chinese Academy of Sciences
2024

Qingdao University of Science and Technology
2009-2023

Institute of New Materials
2023

Beijing Jingshida Electromechanical Equipment Research Institute
2022

ADVERTISEMENT RETURN TO ISSUEPREVArticlePersonal Experience with Four Kinds of Chemical Structure Drawing Software: Review on ChemDraw, ChemWindow, ISIS/Draw, and ChemSketchZhenjiang Li, Honggui Wan, Yuhu Shi, Pingkai OuyangView Author Information College Life Science Pharmaceutical Engineering, Nanjing University Technology, 210009, China, Chemistry Xinjiang University, Urumqi 830008, ChinaCite this: J. Chem. Inf. Comput. Sci. 2004, 44, 5, 1886–1890Publication Date (Web):August 7,...

10.1021/ci049794h article EN Journal of Chemical Information and Computer Sciences 2004-08-07

In this study, we aimed to dissolve microcrystalline cellulose (MCC) with phosphoric acid obtain high-quality fermentable saccharides. MCC was directly dissolved in (the concentration 83%) for 10 hours at temperatures of 30, 50, and 70 °C. The structural changes were determined detail X-ray powder diffraction, solid-state cross-polarization magic angle spinning 13C-NMR, photoelectron spectroscopy. kinetics decrystallization during treatment also compared With the assumption first order...

10.3390/molecules14125027 article EN cc-by Molecules 2009-12-04

Abstract Background Acinetobacter baumannii , a significant nosocomial pathogen, has evolved resistance to almost all conventional antimicrobial drugs. Bacteriophage therapy is potential alternative treatment for multidrug-resistant bacterial infections. In this study, one lytic bacteriophage, ZZ1, which infects A. and broad host range, was selected characterization. Results Phage ZZ1 3 of its natural hosts, baumanni clinical isolates AB09V, AB0902, AB0901, are described in study. The...

10.1186/1471-2180-12-156 article EN cc-by BMC Microbiology 2012-07-28

The anionic ring-opening polymerizations (AROPs) of N-sulfonyl aziridines, in the presence organic superbases including phosphazene (t-Bu-P4), Verkade's base (P(i-PrNCH2CH2)3N, TiPP), DBU, MTBD, and N,N,N′,N′-tetramethylguanidine (TMG), using N-benzyl-p-toluenesulfonamide (BnN(H)Ts) as initiator were explored to produce metal-free poly(sulfonylaziridine)s. Among used, catalytic activity was found directly proportional their basicity. Remarkably, t-Bu-P4 TiPP gave a living/controlled AROP...

10.1021/acsmacrolett.7b00775 article EN ACS Macro Letters 2017-11-14

A hydrogen-bond motif based on a squaramide and sparteine efficiently promoted the ring-opening polymerization of <sc>l</sc>-lactide at ambient temperature.

10.1039/c5py00508f article EN Polymer Chemistry 2015-01-01

Abstract Halogen bonding, parallel to hydrogen was introduced into the catalytic cycloaddition of carbon dioxide epoxide (CCE) reactions. A series halogen‐bond donor (XBD) catalysts N ‐iodopyridinium halide featured with N−I bond were synthesized and evaluated in CCE The optimal XBD catalyst, 4‐(dimethylamino)‐ bromide ([DMAPI]Br), under screened conditions at 100 °C, ambient pressure, 1 mol % catalyst loading, realized 93 conversion styrene oxide cyclic carbonate 6 h. substrate scope...

10.1002/cssc.202002525 article EN ChemSusChem 2020-11-19

Here, we report an unprecedented regioselective, intermolecular 1,2-cyanoalkylacylation of feedstock alkenes with readily available oxime esters and aldehydes by N-heterocyclic carbene (NHC) organocatalysis. The crux this success is the exquisite control over radical relay process NHC organocatalyst. This protocol offers a general platform for diversity-oriented synthesis valuable ketonitriles under mild, transition-metal-free, redox-neutral conditions highlights its potential in late-stage...

10.1021/acs.orglett.0c03907 article EN Organic Letters 2020-12-18

Sulfur mustard is one of the most harmful chemical warfare agents and can induce skin, eye, lung injuries. However, it hard for medical stuff to diagnose sulfur poisoning early because incubation period after exposure. Detecting intact in vivo might be an effective approach diagnosis poisoning. A series fluorescent probes detection were developed this study. All could react with selectivity. Among these probes, SiNIR-SM exhibited extremely good response rate a high off/on contrast. To best...

10.1021/acssensors.9b01424 article EN ACS Sensors 2019-09-24

The cycloadditions of carbon dioxide into epoxides to afford cyclic carbonates by H-bond donor (HBD) and onium halide (X) cocatalysis have emerged as a key strategy for CO2 fixation. However, if the HBD is also receptor, two will quench each other, decreasing catalytic activity. Here, we propose strained ion pair tris(alkylamino)cyclopropenium (TAC·X), in which TAC repels X. possesses positively charged cyclopropenium core that makes vicinal C–H or N–H nonclassical HBD. interionic strain...

10.1021/acs.joc.0c02790 article EN The Journal of Organic Chemistry 2021-01-29

Zwitterionic catalytic model for ring-opening polymerization (ROP) was unveiled. Among the designed quaternary ammonium carboxylate zwitterionic catalysts, carnitine, a natural product zwitterion, showed optimal performance in ROPs of cyclic esters.

10.1039/d4gc01171f article EN Green Chemistry 2024-01-01

A halide-free ionic pair organocatalyst was proposed for the cycloaddition of CO

10.1021/acs.joc.3c02609 article EN The Journal of Organic Chemistry 2024-05-24

Currently, the development of suitable transition metal chalcogenides (TMDs) for aqueous zinc ion batteries (AZIBs) is plagued by terrible conductivity and electrochemical properties. Herein, a one-step ball milling method applied to enhance commercial MnTe cathode constructing three dimensional (3D) carbon nanotubes (CNTs) interweaved nanoparticles (abbreviated as MnTe@CNTs), which can achieve ultrafast conduction. The stable electrochemistry properties benefit from synergistic effects...

10.1002/chem.202404600 article EN Chemistry - A European Journal 2025-01-15

The growing demand for sustainable, biodegradable, and low-toxicity products has accelerated innovations in bioderived chemicals materials. Since the restriction of alkylphenol polyoxyethylene ethers, substituting these surfactants with safer, greener, more eco-friendly been a goal researchers to strive. Herein, we report three biobased nonionic (PAHA-EO, PAOA-EO, PAIA-EO) derived from esterification renewable biomass phloretic acid straight- or branched-chain fatty alcohols followed by...

10.1021/acs.langmuir.4c05232 article EN Langmuir 2025-03-20

10.1007/s12083-025-01960-7 article EN Peer-to-Peer Networking and Applications 2025-03-28

The ring-opening polymerization (ROP) of trimethylene carbonate (TMC) using a base–acid binary organocatalyst system 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (MTBD) and Brønsted acid trifluoromethanesulfonic (TFA) with benzyl alcohol (BnOH) as the initiator has been investigated. MTBD its conjugate-acid pair H-bonding bifunctional synergistic activation mechanism was demonstrated by NMR measurements, living/controlled nature MTBD/TFA catalyzed ROP TMC confirmed kinetic chain extension...

10.1039/c4py00773e article EN Polymer Chemistry 2014-06-27
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