Chengbo Yang

ORCID: 0000-0001-5375-3047
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About
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Research Areas
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
  • Catalytic Cross-Coupling Reactions
  • Organometallic Complex Synthesis and Catalysis
  • Synthesis and characterization of novel inorganic/organometallic compounds
  • Organoboron and organosilicon chemistry
  • Synthetic Organic Chemistry Methods
  • Cyclopropane Reaction Mechanisms
  • Microwave-Assisted Synthesis and Applications
  • Spectroscopy and Chemometric Analyses
  • Asymmetric Hydrogenation and Catalysis
  • Vibrio bacteria research studies
  • Luminescence and Fluorescent Materials
  • Molecular Sensors and Ion Detection
  • Salmonella and Campylobacter epidemiology
  • Surface Chemistry and Catalysis
  • Aquaculture disease management and microbiota
  • Supramolecular Self-Assembly in Materials
  • Catalytic C–H Functionalization Methods
  • Chemical Synthesis and Reactions

Shanghai Institute of Organic Chemistry
2020-2025

Chinese Academy of Sciences
2006-2025

China Academy of Engineering Physics
2024

University of Chinese Academy of Sciences
2022-2023

Nankai University
2016

Institute of Subtropical Agriculture
2006

A novel FRET platform was fabricated based on a macrocyclic amphiphile, reliant the self-sorting complexation of donor periphery assemblies and entrapment an acceptor within inner hydrophobic phase. By tuning subtly donor/acceptor ratio, white light emission successfully achieved with high quantum yield.

10.1039/c6cc09079f article EN Chemical Communications 2016-12-02

Tuning the spin state of metal carbynes, which have broad applications in organic synthesis and material science, presents a formidable challenge for modern chemists as strong field nature carbyne ligands dictates low-spin ground states (S = 0 or 1/2) known carbynes. Through oxidative addition reaction low-coordinate iron(0) N-heterocyclic carbene complex with C-S bond thioazole-2-ylidene, we synthesized first triplet 1) terminal carbyne, an iron cyclic complex. Different from classical...

10.1021/jacs.3c09280 article EN Journal of the American Chemical Society 2023-11-16

The stabilization of reactive anionic main group species utilizing carbenes constitutes a burgeoning and scarcely explored field. Herein, we report the synthesis an triphosphorus [P3]ˉ unit, supported by two cyclic (alkyl)(amino)carbenes (CAACs) in form potassium salts. This anion features planar W-shaped conjugated C-P-P-P-C framework, characterized 5-center-6-electron π delocalization additional σ lone pair located on each three phosphorus atoms. Remarkably, this is not only strongly basic...

10.26434/chemrxiv-2025-n4pfz preprint EN cc-by-nc-nd 2025-02-14

The stabilization of reactive anionic main group species utilizing carbenes constitutes a burgeoning and scarcely explored field. Herein, we report the synthesis an triphosphorus [P3]ˉ unit, supported by two cyclic (alkyl)(amino)carbenes (CAACs) in form potassium salts. This anion features planar W-shaped conjugated C-P-P-P-C framework, characterized 5-center-6-electron π delocalization additional σ lone pair located on each three phosphorus atoms. Remarkably, this is not only strongly basic...

10.1038/s41467-025-57660-6 article EN cc-by-nc-nd Nature Communications 2025-03-08

White phosphorus activation with low-valent metal species has proved to be very effective in converting P4 into small Pn-containing molecules n ≤ 4. Much less developed are metal-mediated P4-coupling reactions that can yield selectively large polyphosphorus clusters. Herein, we report P4-activation three-coordinate N-heterocyclic carbene(NHC)-cobalt(0)-alkene complexes, which produce the P8 complexes of cobalt [(NHC)2Co2(μ-η6:η6-P8)] (NHC = 1,3-dimesitylimidazol-2-ylidene (IMes), 1;...

10.1021/jacs.2c08647 article EN Journal of the American Chemical Society 2022-11-02

Vibrio parahaemolyticus is recognized as a leading human food-borne pathogen. A TaqMan PCR assay based on the gyrase B gene (gyrB) sequence of V. was developed for quantitative detection in seafood. The study involving 27 and 10 strains other species indicated that real-time test highly specific. sensitivity approximately single CFU per pure culture six to eight spiked raw oyster, respectively. Real-time values artificially inoculated oyster homogenates correlated well with plate counts...

10.1111/j.1574-695x.2005.00016.x article EN FEMS Immunology & Medical Microbiology 2006-02-14

Selectivity control in the addition reactions of internal alkynes that bear two similar substituents presents a big challenge modern organic synthesis. Herein we report β-(E)-selective hydrosilylation alk-2-ynes with tertiary silanes can be achieved by using Co2(CO)8 as catalyst. Under catalytic reaction conditions, wide range converted into vinylsilanes β-(E) isomers major or sole products. Mechanistic studies suggest alkyne-bridged dicobalt species are likely intermediates. Steric...

10.1021/acs.organomet.2c00563 article EN Organometallics 2023-01-09

N-heterocyclic carbene (NHC) ligands are intensively used in transition-metal-catalyzed reactions. Their bond-activation reactions, however, much less understood. We now report unprecedented dearylation reactions of N-aryl-substituted NHCs mediated by cobalt(−I) and rhodium(−I) species, which lead to the conversion N-aryl into imidazolate ligands. The reduction [(IMes)Co(η2:η2-dvtms)] (IMes = 1,3-dimesitylimidazol-2-ylidene, dvtms divinyltetramethyldisiloxane) [Rh(cod)Cl]2/IPr (cod...

10.1021/acs.organomet.0c00383 article EN Organometallics 2020-07-24
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