Publications

Next-Generation Time-resolved Electron Paramagnetic Resonance for Direct Visualizing Mechanisms in Radical Chemistry
32. Next-Generation Time-resolved Electron Paramagnetic Resonance for Direct Visualizing Mechanisms in Radical Chemistry
Eur. J. Org. Chem. 2024, 27, e202400739 (invited, mini review)
Next-Generation Time-resolved Electron Paramagnetic Resonance for Direct Visualizing Mechanisms in Radical Chemistry
Overestimated Halogen Atom Transfer Reactivity of α-Aminoalkyl Radicals
31. Overestimated Halogen Atom Transfer Reactivity of α-Aminoalkyl Radicals
J. Am. Chem. Soc. 2024, 146, 25860–25869
highlighted by Science:
https://www.science.org/doi/10.1126/science.adu2105#sec-7
Overestimated Halogen Atom Transfer Reactivity of α-Aminoalkyl Radicals
Advancements and Prospects in Continuous Wave Time-Resolved Electron Paramagnetic Resonance
30. Advancements and Prospects in Continuous Wave Time-Resolved Electron Paramagnetic Resonance
Chem. Res. Chinese Universities 2024, 40, 798–805 (invited, mini review)
Advancements and Prospects in Continuous Wave Time-Resolved Electron Paramagnetic Resonance
Characterization and Monitoring of Transient Enamine Radical Intermediates in Photoredox/Chiral Primary Amine Synergistic Catalysis Cycle
29. Characterization and Monitoring of Transient Enamine Radical Intermediates in Photoredox/Chiral Primary Amine Synergistic Catalysis Cycle
CCS Chem. 2024, 6, 2420–2426
Characterization and Monitoring of Transient Enamine Radical Intermediates in Photoredox/Chiral Primary Amine Synergistic Catalysis Cycle
Direct Observation of All Open-Shell Intermediates in a Photo-catalytic Cycle
28. Direct Observation of All Open-Shell Intermediates in a Photo-catalytic Cycle
J. Am. Chem. Soc. 2024, 146, 7140–7145
Direct Observation of All Open-Shell Intermediates in a Photo-catalytic Cycle
Photoinduced Selective B–H Activation of nido-Carboranes
27. Photoinduced Selective B–H Activation of nido-Carboranes
J. Am. Chem. Soc. 2024, 146, 7791–7802
Photoinduced Selective B–H Activation of nido-Carboranes
Time-resolved electron paramagnetic resonance spectrometer based on ultrawide single-sideband phase-sensitive detection
26. Time-resolved electron paramagnetic resonance spectrometer based on ultrawide single-sideband phase-sensitive detection
Rev. Sci. Instrum. 2023, 94, 084101
Time-resolved electron paramagnetic resonance spectrometer based on ultrawide single-sideband phase-sensitive detection
Longevity gene responsible for robust blue organic materials employing thermally activated delayed fluorescence
25. Longevity gene responsible for robust blue organic materials employing thermally activated delayed fluorescence
Nat. Commun. 2023, 14, 3927
Longevity gene responsible for robust blue organic materials employing thermally activated delayed fluorescence
Water-Soluble Tris(cyclometalated) Iridium(III) Complexes for Aqueous Electron and Energy Transfer Photochemistry
24. Water-Soluble Tris(cyclometalated) Iridium(III) Complexes for Aqueous Electron and Energy Transfer Photochemistry
Acc. Chem. Res. 2022, 55, 1290–1300
Water-Soluble Tris(cyclometalated) Iridium(III) Complexes for Aqueous Electron and Energy Transfer Photochemistry
Reductive Amination and Enantioselective Amine Synthesis by Photoredox Catalysis
22. Reductive Amination and Enantioselective Amine Synthesis by Photoredox Catalysis
Eur. J. Org. Chem. 2020, 1288–1293
Reductive Amination and Enantioselective Amine Synthesis by Photoredox Catalysis
Photo-triggered hydrogen atom transfer from an iridium hydride complex to unactivated olefins
23. Photo-triggered hydrogen atom transfer from an iridium hydride complex to unactivated olefins
Chem. Sci. 2020, 11, 8582–8594
Photo-triggered hydrogen atom transfer from an iridium hydride complex to unactivated olefins
Shortcuts for Electron‐Transfer through the Secondary Structure of Helical Oligo‐1,2‐Naphthylenes
21. Shortcuts for Electron‐Transfer through the Secondary Structure of Helical Oligo‐1,2‐Naphthylenes
Chem. Eur. J. 2019, 25, 16748–16754
Shortcuts for Electron‐Transfer through the Secondary Structure of Helical Oligo‐1,2‐Naphthylenes
Unexpected Hydrated Electron Source for Preparative Visible-Light Driven Photoredox Catalysis
20. Unexpected Hydrated Electron Source for Preparative Visible-Light Driven Photoredox Catalysis
J. Am. Chem. Soc. 2019, 141, 2122–2127
Unexpected Hydrated Electron Source for Preparative Visible-Light Driven Photoredox Catalysis
Electron Transfer across o-Phenylene Wires
19. Electron Transfer across o-Phenylene Wires
J. Phys. Chem. 2018, 123, 96–102
Electron Transfer across o-Phenylene Wires
Mixed‐Valent Molecular Triple Deckers
18. Mixed‐Valent Molecular Triple Deckers
Angew. Chem. Int. Ed. 2018, 57, 11688–11691
Mixed‐Valent Molecular Triple Deckers
Charge Accumulation and Multi‐Electron Photoredox Chemistry with a Sensitizer–Catalyst–Sensitizer Triad
17. Charge Accumulation and Multi‐Electron Photoredox Chemistry with a Sensitizer–Catalyst–Sensitizer Triad
Chem. Eur. J. 2018, 24, 14084–14087
Charge Accumulation and Multi‐Electron Photoredox Chemistry with a Sensitizer–Catalyst–Sensitizer Triad
Reductive Amination by Photoredox Catalysis and Polarity‐Matched Hydrogen Atom Transfer
16. Reductive Amination by Photoredox Catalysis and Polarity‐Matched Hydrogen Atom Transfer
Angew. Chem. Int. Ed. 2018, 57, 2469–2473
Reductive Amination by Photoredox Catalysis and Polarity‐Matched Hydrogen Atom Transfer
Enantioselective synthesis of amines by combining photoredox and enzymatic catalysis in a cyclic reaction network
15. Enantioselective synthesis of amines by combining photoredox and enzymatic catalysis in a cyclic reaction network
Chem. Sci. 2018, 9, 5052–5056
Enantioselective synthesis of amines by combining photoredox and enzymatic catalysis in a cyclic reaction network
Electron Accumulation on Naphthalene Diimide Photosensitized by [Ru(2,2′-Bipyridine)$_3$]$^2$$^+$
14. Electron Accumulation on Naphthalene Diimide Photosensitized by [Ru(2,2′-Bipyridine)$_3$]$^2$$^+$
Inorg. Chem. 2017, 56, 2432–2439
Electron Accumulation on Naphthalene Diimide Photosensitized by [Ru(2,2′-Bipyridine)$_3$]$^2$$^+$
A Tris(diisocyanide)chromium(0) Complex Is a Luminescent Analog of Fe(2,2′-Bipyridine)$_3$$^2$$^+$
13. A Tris(diisocyanide)chromium(0) Complex Is a Luminescent Analog of Fe(2,2′-Bipyridine)$_3$$^2$$^+$
J. Am. Chem. Soc. 2017, 139, 985–992
A Tris(diisocyanide)chromium(0) Complex Is a Luminescent Analog of Fe(2,2′-Bipyridine)$_3$$^2$$^+$
A Molybdenum(0) Isocyanide Analogue of Ru(2,2′‐Bipyridine)$_3$$^2$$^+$: A Strong Reductant for Photoredox Catalysis
12. A Molybdenum(0) Isocyanide Analogue of Ru(2,2′‐Bipyridine)$_3$$^2$$^+$: A Strong Reductant for Photoredox Catalysis
Angew. Chem. Int. Ed. 2016, 55, 11247–11250
A Molybdenum(0) Isocyanide Analogue of Ru(2,2′‐Bipyridine)$_3$$^2$$^+$: A Strong Reductant for Photoredox Catalysis
Mechanisms of Hydride Abstractions by Quinones
11. Mechanisms of Hydride Abstractions by Quinones
J. Am. Chem. Soc. 2014, 136, 13863–13873
Mechanisms of Hydride Abstractions by Quinones
Quantification of the Ambident Electrophilicities of Halogen-Substituted Quinones
10. Quantification of the Ambident Electrophilicities of Halogen-Substituted Quinones
J. Am. Chem. Soc. 2014, 136, 11499–11512
Quantification of the Ambident Electrophilicities of Halogen-Substituted Quinones
Manifestation of Polar Reaction Pathways of 2,3-Dichloro-5,6-dicyano-p-benzoquinone
9. Manifestation of Polar Reaction Pathways of 2,3-Dichloro-5,6-dicyano-p-benzoquinone
J. Am. Chem. Soc. 2013, 135, 12377–12387
Manifestation of Polar Reaction Pathways of 2,3-Dichloro-5,6-dicyano-p-benzoquinone
Iron-Catalyzed Oxidation of Tertiary Amines: Synthesis of β-1,3-Dicarbonyl Aldehydes by Three-Component C–C Couplings
8. Iron-Catalyzed Oxidation of Tertiary Amines: Synthesis of β-1,3-Dicarbonyl Aldehydes by Three-Component C–C Couplings
Org. Lett. 2011, 13, 6272–6275
Iron-Catalyzed Oxidation of Tertiary Amines: Synthesis of β-1,3-Dicarbonyl Aldehydes by Three-Component C–C Couplings
Iron‐Catalyzed ortho‐Selective Functionalization of Phenols: A Straightforward Strategy towards the 2′‐Hydroxyphenyl‐1,2‐dione Skeleton
7. Iron‐Catalyzed ortho‐Selective Functionalization of Phenols: A Straightforward Strategy towards the 2′‐Hydroxyphenyl‐1,2‐dione Skeleton
Eur. J. Org. Chem. 2010, 5787–5790
Iron‐Catalyzed ortho‐Selective Functionalization of Phenols: A Straightforward Strategy towards the 2′‐Hydroxyphenyl‐1,2‐dione Skeleton
Iron-Catalyzed N-Alkylation of Azoles via Oxidation of C−H Bond Adjacent to an Oxygen Atom
6. Iron-Catalyzed N-Alkylation of Azoles via Oxidation of C−H Bond Adjacent to an Oxygen Atom
Org. Lett. 2010, 12, 1932–1935
Iron-Catalyzed N-Alkylation of Azoles via Oxidation of C−H Bond Adjacent to an Oxygen Atom
Cross-Dehydrogenative-Coupling (CDC) Reaction
5. Cross-Dehydrogenative-Coupling (CDC) Reaction
Prog. Chem. 2010, 22, 1434-1441
Cross-Dehydrogenative-Coupling (CDC) Reaction
Iron-Catalyzed Tandem Oxidative Coupling and Annulation: An Efficient Approach to Construct Polysubstituted Benzofurans
4. Iron-Catalyzed Tandem Oxidative Coupling and Annulation: An Efficient Approach to Construct Polysubstituted Benzofurans
J. Am. Chem. Soc. 2009, 131, 17387–17393
Iron-Catalyzed Tandem Oxidative Coupling and Annulation: An Efficient Approach to Construct Polysubstituted Benzofurans
One-Pot Synthesis of Symmetric and Unsymmetric 1,1-Bis-indolylmethanes via Tandem Iron-Catalyzed C−H Bond Oxidation and C−O Bond Cleavage
3. One-Pot Synthesis of Symmetric and Unsymmetric 1,1-Bis-indolylmethanes via Tandem Iron-Catalyzed C−H Bond Oxidation and C−O Bond Cleavage
J. Org. Chem. 2009, 74, 8848–8851
One-Pot Synthesis of Symmetric and Unsymmetric 1,1-Bis-indolylmethanes via Tandem Iron-Catalyzed C−H Bond Oxidation and C−O Bond Cleavage
Iron-Catalyzed Selective Oxidation of N-Methyl Amines: Highly Efficient Synthesis of Methylene-Bridged bis-1,3-Dicarbonyl Compounds
2. Iron-Catalyzed Selective Oxidation of N-Methyl Amines: Highly Efficient Synthesis of Methylene-Bridged bis-1,3-Dicarbonyl Compounds
Org. Lett. 2009, 11, 4176–4179
Iron-Catalyzed Selective Oxidation of N-Methyl Amines: Highly Efficient Synthesis of Methylene-Bridged bis-1,3-Dicarbonyl Compounds
C−H Bond Oxidation Initiated Pummerer- and Knoevenagel-Type Reactions of Benzyl Sulfide and 1,3-Dicarbonyl Compounds
1. C−H Bond Oxidation Initiated Pummerer- and Knoevenagel-Type Reactions of Benzyl Sulfide and 1,3-Dicarbonyl Compounds
Org. Lett. 2008, 10, 803–805
C−H Bond Oxidation Initiated Pummerer- and Knoevenagel-Type Reactions of Benzyl Sulfide and 1,3-Dicarbonyl Compounds