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成果及论文

35. Du, D.#; Chen, Y.#; Zhang, H.; Zhao, J.; Jin L.; Ji, W.*; Huang, H.*; Pang, S.* High-Performance Azo Cathodes Enabled by N-Heteroatomic Substitution for Zinc Batteries with a Self-Charging Capability. Angew. Chem. Int. Ed.2024, e202408292.


34. Du, D.#; Zhou J.#; Yin Z.; Feng, G.; Ji, W.*; Huang, H.*; Pang, S.* High-Voltage Recyclable Organic Cathode Enabled by Heteroatomic Substitution for Aqueous Zinc-Ion Batteries. Advanced Energy Materials, 2024, 2400580.


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33. Ji, W.*, Du, D., Liang J., Li G., Feng G., Yin Z., Zhou J., Zhao J., Shen Y., Huang H.*Pang S.* Aqueous Zn−organic batteries: Electrochemistry and design strategies. Battery Energy2023, 20230020.



32. Ji, W.*, Liang, J., Zhou, J., Huang, H., Qu, D.*, Pang, S., Ai, X*. Built-In Stimuli-Responsive Designs for Safe and Reliable Electrochemical Energy Storage Devices-A Review. Energy Stor. Mater.2023, 102945.


31. Huang, H.; Lambert, T. H.* Regiodivergent Electrophotocatalytic Aminooxygenation of Aryl Olefins. J. Am. Chem. Soc2022, 144, 18803-18809. 

Figure 1

(Highlighted by Synfacts 2022, 18, 1360-1360)


Before BIT

30. Huang, H.; Steiniger, K. A.; Lambert, T. H.* Electrophotocatalysis: Combining Light and Electricity to Catalyze Reactions. J. Am. Chem. Soc. 2022, 144, 12567–12583. 


29. Ji, W.; Zhang, X.; Zheng, D.; Huang, H.*; Lambert, T. H.; Qu, D.* Practically Accessible All‐Solid‐State Batteries Enabled by Organosulfide Cathodes and Sulfide Electrolytes. Adv. Funct. Mater. 2022, 2202919.



28. Ji, W.; Zhang, X.; Qu, H.; Xin, L.; Luedtke, A.; Huang, H.*; Lambert, T. H.; Qu, D.* Polyimide as A Durable Cathode for All-Solid-State Li (Na)−Organic Batteries with Boosted Cell-Level Energy Density. Nano Energy 2022, 96, 107130.

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27. Ji, W.; Zhang, X.; Xin, L.; Luedtke, A.; Zheng, D.; Huang, H.*; Lambert, T. H.; Qu, D.* A High-performance Organic Cathode Customized for Sulfide-Based All-Solid-State Batteries. Energy Storage Mater. 2022, 45, 680-686.


26. Huang, H.; Lambert, T. H.* Electrophotocatalytic Acetoxyhydroxylation of Aryl Olefins. J. Am. Chem. Soc. 2021, 143, 7247-7252.

Abstract Image


25. Huang, H.; Lambert, T. H.* Electrophotocatalytic C–H Heterofunctionalization of Arenes. Angew. Chem. Int. Ed. 2021, 60, 11163-11167.


24. Huang, H.; Zhang, Y.; Ji, P.; Mariano, P. S.*; Wang, W.*, Organophotocatalyzed E and Z Stereoselective Csp3-Csp2 Bond Forming Cross Coupling Reactions of Carboxylic Acids with β-Aryl-vinyl Halides. Green Synth. and Catal. 2021, 2, 27-31.


23. Huang, H.; Strater, Z. M.; Lambert, T. H.* Electrophotocatalytic C–H Functionalization of Ethers with High Regioselectivity. J. Am. Chem. Soc. 2020, 142, 1698-1703.

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22. Huang, H.; Lambert, T. H.* Electrophotocatalytic SNAr Reactions of Unactivated Aryl Fluorides at Ambient Temperature and Without Base. Angew. Chem. Int. Ed. 2020, 59, 658-662.


21. Ji, W.#; Huang, H.#; Zhang, X.; Zheng, D.; Ding, T.; Lambert, T. H.*; Qu, D.* A Redox-active Organic Salt for Safer Na-ion Batteries. Nano Energy 2020, 104705. (# co-first)


20. Ji, W.#; Huang, H.#; Zheng, D.; Zhang, X.; Ding, T.; Lambert, T. H.*; Qu, D.* A Redox-active Organic Cation for Safer Metallic Lithium-based Batteries. Energy Storage Mater. 2020, 32, 185-190. (# co-first)


19. Ji, W.#; Huang, H.#; Huang, X.; Zhang, X; Zheng, D.; Ding, T.; Chen, J.; Lambert, T. H.*; Qu, D.* A Redox-active Organic Cation for Safer High Energy Density Li-ion Batteries. J. Mater. Chem. A, 2020, 8, 17156-17162. (# co-first)

Graphical abstract: A redox-active organic cation for safer high energy density Li-ion batteries


18. Huang, H.; Strater, Z. M.; Rauch, M.; Shee, J.; Sisto, T. J.; Nuckolls, C.; Lambert, T. H.* Electrophotocatalysis with a Trisaminocyclopropenium Radical Dication. Angew. Chem. Int. Ed. 2019, 58, 13318-13322. 

Description unavailable

(Highlighted by Angew. Chem. Int. Ed. 2019, 58, 17508-17510)

(Highlighted by Synfacts 2019, 15, 1181-1181)

(Highlighted by Org. Chem. Front., 2019, 7, 131-135)


17. Huang, H.; Yu, C.; Zhang, Y.; Zhang, Y.; Mariano, P. S.*; Wang, W.*, Chemo- and Regioselective Organo-Photoredox Catalyzed Hydroformylation of Styrenes via a Radical Pathway. J. Am. Chem. Soc. 2017, 139, 9799-9802

Abstract Image

(Highlighted by Synfacts 201713, 1089-1089.)


16. Huang, H.; Yu, C.; Li, X.; Zhang, Y.; Zhang, Y.; Chen, X.; Mariano, P. S.*; Xie, H.*; Wang, W.*, Synthesis of Aldehydes by Organocatalytic

Formylation Reactions of Boronic Acids with Glyoxylic Acid. Angew. Chem. Int. Ed. 2017, 56, 8201-8205.

Description unavailable


15. Huang, H.; Li, X.; Yu, C.; Zhang, Y.; Mariano, P. S.*; Wang, W.*, Visible-Light-Promoted Nickel- and Organic-Dye-Cocatalyzed Formylation Reaction of Aryl Halides and Triflates and Vinyl Bromides with Diethoxyacetic Acid as a Formyl Equivalent. Angew. Chem. Int. Ed. 2017, 56, 1500-1505.


14. Huang, H.#; Zhang, X.#; Yu, C.; Li, X.; Zhang, Y.; Wang, W.*, Highly Regio-and Stereoselective Synthesis of Z and E Enol Esters by an Amine Catalyzed Conjugate Addition-rearrangement Reaction of Ynals with Carboxylic Acids. ACS Catal. 2016, 6, 8030-8035. (# co-first)

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13. Zhang, Y., Ji, P., Gao, F., Dong, Y., Huang, H., Wang, C., Zhou, Z. and Wang, W.*, Organophotocatalytic Dearomatization of Indoles, Pyrroles and Benzo(thio)furans via a Giese-type Transformation. Commun. Chem., 2021, 4.

12. Zhang, Y., Ji, P., Gao, F., Huang, H., Zeng, F., Wang, W.*, Photoredox Asymmetric Nucleophilic Dearomatization of Indoles with Neutral Radicals. ACS Catal. 2021, 11, 998-1007.

11. Ji, P.; Zhang, Y.; Dong, Y.; Huang, H.; Wei, Y.; Wang, W.*, Synthesis of Enantioenriched α-Deuterated α-Amino Acids Enabled by an Organophotocatalytic Radical Approach. Org. Lett. 2020, 22, 1557-1562.

10. Zhang, Y.; Ji, P.; Hu, W.; Wei, Y.; Huang, H.; Wang, W.*, Organocatalytic Transformation of Aldehydes to Thioesters with Visible Light. Chem-Eur J. 2019, 25, 8225-8228.

9. Ji, P.; Zhang, Y.; Wei, Y.; Huang, H.; Hu, W.; Mariano, P. S.*; Wang, W.*, Visible-Light-Mediated, Chemo- and Stereoselective Radical Process for the Synthesis of C-Glycoamino Acids. Org. Lett. 2019, 21, 3086-3092.

8. Yu, C.; Huang, H.; Li, X.; Zhang, Y.; Wang, W.*, Dynamic Kinetic Resolution of Biaryl Lactones via a Chiral Bifunctional Amine Thiourea-Catalyzed Highly Atropo-Enantioselective Transesterification. J. Am. Chem. Soc. 2016, 138, 6956-6959.

7. Yu, C.; Huang, H.; Li, X.; Zhang, Y.; Li, H.; Wang, W.*, Aniline-Promoted Cyclization-Replacement Cascade Reactions of 2- Hydroxycinnamaldehydes with Various Carbonic Nucleophiles through In Situ Formed N, O-Acetals. Chem-Eur J. 2016, 22, 9240-9246.

6. Li, X.; Huang, H.; Yu, C.; Zhang, Y.; Li, H.; Wang, W.*, Synthesis of Tryptanthrins by Organocatalytic and Substrate Co-catalyzed Photochemical Condensation of Indoles and Anthranilic Acids with Visible Light and O2. Org. Lett. 2016, 18, 5744-5747.

5. Song, A.; Zhang, X.; Song, X.; Chen, X.; Yu, C.; Huang, H.; Li, H.; Wang, W.*, Construction of Chiral Bridged Tricyclic Benzopyrans: Enantioselective Catalytic Diels–Alder Reaction and a One‐Pot Reduction/Acid‐Catalyzed Stereoselective Cyclization. Angew. Chem. Int.

Ed. 2014, 53, 4940-4944.

4. Teng, H.-L.; Huang, H.; Wang, C.-J.*, Catalytic Asymmetric Construction of Spiro (γ-butyrolactam-γ-butyrolactone) Moieties through Sequential Reactions of Cyclic Imino Esters with Morita–Baylis–Hillman Bromides. Chem-Eur J. 2012, 18, 12614-12618.

3. Teng, H.-L.; Huang, H.; Tao, H.-Y.; Wang, C.-J.*, Morita–Baylis–Hillman Adducts as Effective Dipolarophiles in Copper (I)-catalyzed 1,3-Dipolar Cycloaddition with Azomethine Ylides: Asymmetric Construction Of Pyrrolidine Derivatives Containing Quaternary Stereogenic Center. Chem. Commun. 2011, 47, 5494-5496.

2. Xue, Z.-Y.; Liu, T.-L.; Lu, Z.; Huang, H.; Tao, H.-Y.; Wang, C.-J.*, exo-Selective Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides with Alkylidene Malonates Catalyzed by AgOAc/TF-BiphamPhos. Chem. Commun. 2010, 46, 1727-1729.

1. Dong, X.-Q.; Teng, H.-L.; Tong, M.-C.; Huang, H.; Tao, H.-Y.; Wang, C.-J.*, Organocatalytic Asymmetric Michael Addition of α-aryl Cyclopentanones to Nitroolefins for Construction of Adjacent Quaternary and Tertiary Stereocenters. Chem. Commun. 2010, 46, 6840-6842.