Yong‐Miao Shen

ORCID: 0000-0002-9382-9744
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About
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Research Areas
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Radical Photochemical Reactions
  • Catalytic C–H Functionalization Methods
  • Sulfur-Based Synthesis Techniques
  • Advanced battery technologies research
  • Synthesis and Reactivity of Heterocycles
  • Crystal structures of chemical compounds
  • Synthesis and pharmacology of benzodiazepine derivatives
  • Cyclopropane Reaction Mechanisms
  • Oxidative Organic Chemistry Reactions
  • Chemical Synthesis and Reactions
  • Fluorine in Organic Chemistry
  • Advanced Photocatalysis Techniques
  • Synthesis and Characterization of Pyrroles
  • Supercapacitor Materials and Fabrication
  • Advanced Battery Materials and Technologies
  • Electrocatalysts for Energy Conversion
  • Advancements in Battery Materials
  • Crystallography and molecular interactions
  • Advanced Battery Technologies Research
  • Synthesis of Organic Compounds
  • Nanomaterials for catalytic reactions
  • Cancer therapeutics and mechanisms
  • Quantum Dots Synthesis And Properties

Zhejiang Sci-Tech University
2018-2025

Zhejiang University
2001-2025

Hangzhou Xixi hospital
2021

Shaoxing University
2008-2018

Jiangsu Normal University
2015-2016

Nanjing University
2005-2010

Institute of Chemistry
2010

State Key Laboratory of Silicon Materials
2001

Surface-modified titanium dioxides by highly dispersed NiO particles have an extended absorption in the visible light region and a reduced hole–electron pair recombination than unmodified TiO2. They now been successfully applied as active heterogeneous photocatalysts mediated direct cyclization of tertiary anilines with maleimides to give tetrahydroquinoline products moderate high yields at ambient temperature. In contrast dioxide catalysts that are conventionally used stoichiometric amount...

10.1021/jo502901h article EN The Journal of Organic Chemistry 2015-02-02

CdSe/CdS core/shell quantum dots (QDs) can be used as stable and highly active photoredox catalysts for efficient transfer hydrogenation of imines to amines with thiophenol a hydrogen atom donor. This reaction proceeds via proton-coupled electron (PCET) from the QDs conduction band protonated imine followed by α-aminoalkyl radical. precious metal free transformation is easy scale up carried out one-pot protocol directly aldehyde, amine, thiophenol. Additional advantageous features this...

10.1021/acs.joc.8b01651 article EN The Journal of Organic Chemistry 2018-08-31

A high-performance aqueous proton battery is fabricated by pairing a dipyridophenazine anode with an indium hexacyanoferrate cathode in pure H<sub>2</sub>SO<sub>4</sub> electrolyte.

10.1039/d1cc01486b article EN Chemical Communications 2021-01-01

Abstract Broadband electroluminescence based on environment-friendly emitters is promising for healthy lighting yet remains an unprecedented challenge to progress. The copper halide-based are competitive candidates broadband emission, but their high-performance shows inadequate broad emission bandwidth of less than 90 nm. Here, we demonstrate efficient ultra-broadband from a halide (CuI) nanocluster single emitter prepared by one-step solution synthesis-deposition process, through dedicated...

10.1038/s41377-024-01427-z article EN cc-by Light Science & Applications 2024-04-07

A one-pot, three-component cascade reaction between pyridine, α-acylmethylbromide, and maleic anhydride leading to direct access of 1-bromoindolizines in high yields has been developed. This protocol is accomplished via a sequence 1,3-dipolar cycloaddition the pyridinium ylide with anhydride, oxidative decarboxylation primary cycloadduct, dehydrogenative bromination resulting 1-unsubstituted indolizine. Copper chloride was used as catalyst oxygen terminal oxidant. represents first example...

10.1021/jo501626b article EN The Journal of Organic Chemistry 2014-09-18

We report a high-performance rechargeable aqueous battery that operates with protons commuting between fused-ring phenazine derivative anode and Prussian blue analogue cathode.

10.1039/d2ta09749d article EN Journal of Materials Chemistry A 2023-01-01

Abstract Indolizino[3,4,5‐ ab ]isoindoles 3a – 3k have been synthesized by [8+2] cycloaddition reactions of the corresponding indolizines 2a 2k with benzyne in moderate yields. Cycloadditions pyrrolo[2,1‐ a ]isoquinolines 4a 4c gave benzo[6,7]pyrrolizino[3,4,5‐ 5a 5c . Compounds 7 and 9 were similarly prepared 6 H ‐[1]benzopyrano[3,4‐ ]indolizine‐6‐one ( ) ‐[1]benzopyrano[3′,4′:3,4]pyrrolo[2,1‐ ]isoquinolin‐6‐one 8 93 62 % yields, respectively. The electronic structures these compounds...

10.1002/ejoc.200700250 article EN European Journal of Organic Chemistry 2007-06-18

We present an efficient and versatile visible light-driven methodology to transform aryl aldehydes ketones chemoselectively either alcohols or pinacol products with CdSe/CdS core/shell quantum dots as photocatalysts. Thiophenols were used proton hydrogen atom donors hole traps for the excited (QDs) in these reactions. The two can be switched from one other simply by changing amount of thiophenol reaction system. QD catalysts are highly a turn over number (TON) larger than 4 × 104 105...

10.1021/acs.joc.0c02627 article EN The Journal of Organic Chemistry 2021-01-08

Indium-based quantum dots (QDs), such as InP, InAs, and CuInS2, are considered the most promising candidates cadmium/lead-free QDs. At present, synthesis of these QDs is limited by unbalanced reactivity various precursors, specifically sluggish indium alkanoates. Here, we demonstrate that, with a phosphine-to-indium molar ratio beyond 3:1, decarboxylation reactions alkanoates aliphatic tertiary organophosphines become apparent, forming series new complexes, instead purely enhancing...

10.1021/acs.chemmater.1c03219 article EN Chemistry of Materials 2021-11-17

3-Acylindolizines (5a–5f) and their benzo- analogues 1-acylpyrrolo[1,2-a]quinolines (6a–6f) 1-acylpyrrolo[2,1-a]isoquinolines (7a–7i) are regioselectively synthesized by a convenient one pot reaction of the corresponding pyridinium (quinolinium, isoquinolinium) ylide with maleic anhydride (MA) in presence mild oxidant tetrakispyridinecobalt(II) dichromate (TPCD). These reactions proceed via tandem sequence 1,3-dipolar cycloaddition azomethine MA, hydrolysis oxidative bisdecarboxylation...

10.1039/c000277a article EN Organic & Biomolecular Chemistry 2010-01-01

We report the photocatalyzed three-component alkene 1,2-alkylpyridylation reaction between alkylboronic acids, 4-cyanopyridine, and an olefin to achieve pyridination alkylation of synthesis structurally diversified 4-alkylpyridines. The readily available easily manipulated acids were used as alkyl radical precursors. reactions take place under mild conditions with a broad substrate scope are easy scale up gram level, they therefore potential practical value for structural modification...

10.1021/acs.joc.4c02600 article EN The Journal of Organic Chemistry 2025-03-03

Electrochemical oxidation of crude ethylene glycol (EG) to commodity chemicals and H2, powered by renewables energy, is a sustainable promising strategy for upcycling the end-of-life polyethylene terephthalate (PET) wastes. Pt/Pd group noble metals are deemed as state-of-the-art catalysts EG electro-oxidation reaction (EGOR). However, these suffer from high affinity carbonyl intermediates, which consequently results in poisoning active sites poor electrochemical stability. Herein, we...

10.1039/d5nr00375j article EN Nanoscale 2025-01-01

A redox-active fused phenazine derivative molecule, hexaazatrinaphthylene, is explored to assemble aqueous organic hybrid flow batteries with high capacity and excellent cycle stability.

10.1039/d1ta06138k article EN Journal of Materials Chemistry A 2021-01-01

An insoluble π-conjugated heterocyclic compound, tribenzo[ a , c i ]phenazine-10,15-dione, is first reported as an anodic capacity booster for aqueous organic redox-targeting flow batteries.

10.1039/d1ta10763a article EN Journal of Materials Chemistry A 2022-01-01
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