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Lichengjie

PhD

化学与分子工程学院

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Office Location:

Email: chengjie.li@ecust.edu.cn

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Resume

Chengjie Li, Associate Professor

Contact Information:

  • Phone: +86-21-64253530

  • Email:chengjie.li@ecust.edu.cn

  • Office: Room 110A&110B, Laboratory Building 13, Xuhui Campus, East China University of Science and Technology


Professional Experience:

  • 2007–2012 | Ph.D.
    Tianjin University, Tianjin, China
    Supervisor: Prof. Dr. Yaqing Feng

  • 2012–2016 | Postdoctoral Researcher
    University of Innsbruck, Innsbruck, Austria
    Supervisor: Prof. Dr. Bernhard Kräutler

  • 2016–2018 | Asistance Professor
    East China University of Science and Technology, Shanghai, China

  • 2018–Present | Associate Professor

    East China University of Science and Technology, Shanghai, China



Research

Synthesis of novel conjugated systems and their applications in catalysis

Publications

发表论文详情



[43]    Li, Z.; Lu, Q.; Zhang, Y.; Li, Q.; Wu, W.;* Li, S.; Wang, H.; Jiang, J.; Li, C.;* Xie, Y.* Solar cells sensitized with doubly concerted companion dyes with optimized donors to achieve high efficiencies up to 12.5%: a record efficiency for iodine electrolyte-based DSSCs. Journal of Material Chemistry A, 2025, 13: 4176-4185.

[42]    Liu, J.; Zhang, Y.; Fan, P.; Feng, Y.; Duan, T.; Zhou, Y.; Zheng, S.; Li, Q.; Li, Y.; Liu. X.*; Wu, X.; Li, C.* Adjustable regio-selectivity for the Diels-Alder reactions of sulfolenodipyrrins upon molecular engineering on H-bonds. Journal of Organic Chemistry, 2024, 89(21): 15678-15685.

[41]    Huang, S.; Li, Q.; Li, S.; Li, C.;* Tan, H.;* Xie, Y.* Recent advances in the approaches for improving the photovoltaic performance of porphyrin-based DSSCs. Chemical Communications, 2024, 60: 4521-4536.

[40]    Ma, W.; Chen, C.; Qin, Z.; Zhu, S.; Qiu, N.; Baryshnikov, G.;* Li, Q.; Li, C.;  Liu, X.* Rational construction of perylenequinone annulated porphyrins via cycloaddition reactions. Dyes and Pigments,2024, 227: 112144.

[39]    Lin, Q.#; Ma, W.#; Yu, Y.; Tang, Y.; Mo, W.; Li, C.*; Li. Q.; Li, Y.; Liu, X. * Anthraquinone fused sulfolenoporphyrins: Regulation of reactivity and property through annulations. Journal of Porphyrins and Phthalocyanines, 2024, 28(4): 243-251.

[38]    马文静#,叶兆雯#,李其兆,刘秀军,解永树*李成杰*. 芳香稠环卟啉染料的合成与性质研究进展,化学反应工程与工艺,202440(3)255-273.

Ma, W.#; Ye, Z.#; Li, Q.; Liu, X.; Xie, Y.*; Li, C.* Research Progress on Synthesis and Properties of of Peripheral Aromatic Ring Fused Porphyrins, Chemical Reaction Engineering and Technology, 2024, 40(3): 255-273.

[37]    Wang, Y.; Li, Z.; Lu, Q.; Li, Q.; Luo, J.; Li, C.*; Xie, Y.* Solar cells based on doubly concerted companion dyes with the efficiencies modulated by inserting an ethynyl group at different positions. Chinese Chemical Letters, 2024, 35(5): 109093.

[36]    Liu, J.; Wang, Y.; Qiu, N.; Liu, X.*; Li, Q.; Li, Y.; Wu, X.; Li, C.* Aromatic ring-fused dipyrrins: Programmed [4+2]-cycloaddition pathway with regio-selectivity upon alkylamino-substitution. Journal of Organic Chemistry, 2023, 88(24): 17381-17388.

[35]    Luo, J.; Lu, Q.; Li, Q.; Li, Z.; Wang, Y.; Wu, X.*; Li, C.*; Xie, Y.* Efficient solar cells based on porphyrin and concerted companion dyes featuring benzo 12-crown-4 for suppressing charge recombination and enhancing dye loading. ACS Applied Materials & Interfaces, 2023, 15(35): 41569-41579.

[34]    Luo, J.; Wang, Y.; Shi, S.; Wu, Y.; Ma, T.; Wang, L.; Baryshnikov, G.; Wu, X.*; Li, C.*; Xie, Y.* Solar cells sensitized by donor-linked concerted companion dyes. Journal of Materials Chemistry C, 2023, 11: 5450-5460.

[33]    Li, C.; Kräutler, B.* Facile retro-Dieckmann cleavage of a pink phyllobilin: new type of potential downstream steps of natural chlorophyll breakdown. Monatshefte für Chemie - Chemical Monthly, 2023, 154: 1359-1368.



[32]    Xue, R.; Zhou, Y.*; Lin, Q.; Zhang, L.; Li, C.; Chen, Y.; Xie, Y.; Liu X.* Loading phlorins with fullerenes by a [4 + 2]-cycloaddition reaction: Regulation of the regioselectivity by pyrrole linkage modes. Journal of Organic Chemistry, 2022, 87(5): 2758-2766.

[31]    Zou, J.#; Wang, Y.#; Baryshnikov, G.; Luo, J.; Wang, X.; Ågren, H.; Li, C.*; Xie, Y.* Efficient dye sensitized solar cells based on a new class of doubly concerted companion dyes. ACS Applied Materials & Interfaces, 2022, 14(29): 33274-33284.

[30]    Wang, X.; Wang, Y.; Zou, J.; Luo, J.; Li, C.*; Xie, Y.* Efficient solar cells sensitized by organic concerted companion dyes suitable for indoor lamps. ChemSusChem, 2022, 15(16): e202201116.

[29]    Cao, G.; Baryshnikov, G.; Chen, C.; Chen, L.; Zhao, T.; Fu, S.; Jiang, Z.; Liu, X.*; Li, Q.; Xie, Y.; Li, C.* Porphyrindiene-based tandem Diels-Alder reaction for preparing low-symmetry π-extended porphyrins with push-pull skeletons. Journal of Organic Chemistry, 2022, 87(14): 9001-9010.

[28]    Luo, J.; Xie, Z.; Zou, J.; Wu, X.*; Gong, X.*; Li, C.*; Xie, Y.* Efficient dye-sensitized solar cells based on concerted companion dyes: Systematic optimization of thiophene units in the organic dye components. Chinese Chemical Letters, 2022, 33(9): 4313-4316.

[27]    Zou, J.; Tang, Y.; Baryshnikov, G.; Yang, Z.; Mao, R.; Feng, W.; Guan, J.; Li, C.*; Xie, Y.* Porphyrins containing a tetraphenylethylene-substituted phenothiazine donor for fabricating efficient dye sensitized solar cells with high photovoltages. Journal of Materials Chemistry A, 2022, 10(3): 1320-1328.

[26]    Chen, C.; Li, D.; Cao, G.; Qin, Z.; Xu, Y.; Liu, X.*; Li, Q.; Xie, Y.; Li, C.* Solvent-regulated biomorphs from the intense ,-mediated assemblies of tetracenequinone fused porphyrin. CrystEngComm, 2021, 23(43): 7565-7569. (Cover story)

[25]    Chen, Y.#; Tang, Y.#; Zou, J.; Zeng, K.; Baryshnikov, G.; Li, C.*; Xie, Y.* Fluorenyl indoline as an efficient electron donor for concerted companion dyes: Enhanced light-harvesting and photocurrent. ACS Applied Materials & Interfaces, 2021, 13(42): 49828-49839.

[24]    Li, C.; Podewitz, M.; Kräutler, B.* A blue zinc complex of a dioxobilin-type pink chlorophyll catabolite exhibiting bright chelation-enhanced red fluorescence. Eurpean Journal of Inorganic Chemistry, 2021, 2021(20): 1904-1912. (Cover story)

[23]    Li, C.#; Li, Q.#; Shao, J.; Tong, Z.; Ishida, M.; Baryshnikov, G.; Ågren, H.; Furuta, H.*; Xie, Y.* Expanded N-confused phlorin: A platform for a multiply fused polycyclic ring system via oxidation within the macrocycle. Journal of the American Chemical Society, 2020, 142(40): 17195-17205.

[22]    Li, C.#; Zhang, K.#; Ishida, M.; Li, Q. Z.; Shimomura, K.; Baryshnikov, G.; Li, X.; Savage, M.; Wu, X.-Y.; Yang, S. H.; Furuta, H.*; Xie, Y.* Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion. Chemical Science, 2020, 11(10): 2790-2795.

[21]    Ma, F.; Zhou, L.; Liu, Q.; Li, C.*; Xie, Y.* Selective photocatalysis approach for introducing ArS units into BODIPYs through thiyl radicals. Organic Letters, 2019, 21(3): 733-736.

[20]    Li, C.; Erhart, T.; Liu, X.; Kräutler, B.* Yellow dioxobilin-type tetrapyrroles from chlorophyll breakdown in higher plants-A new class of colored phyllobilins. Chemistry-a European Journal, 2019, 25(16): 4052-4057.

[19]    Li, C.; Kräutler, B.* A pink colored dioxobilin-type phyllobilin from breakdown of chlorophyll. Monatshefte Für Chemie - Chemical Monthly, 2019, 150(5): 813-820.

[18]    Shao, J.; Li, C.*; Kong, J.; Jiang, H.; Zhao, S.; Li, M.; Liang, X.; Zhu, W.; Xie, Y.* Regioselective oxidative ring cleavage of a phlorin analogue: An approach for synthesizing linear tetrapyrroles. Organic Letters, 2018, 20(7): 1941-1944.

[17]    Li, C.; Wurst, K.; Kräutler, B.* A dipyrrin programmed for covalent loading with fullerenes. Chemistry-a European Journal, 2018, 24(40): 10032-10037.

[16]    Li, C.; Wurst, K.; Berghold, J.; Podewitz, M.; Liedl, K. R.; Kräutler, B.* Pyro-phyllobilins: elusive chlorophyll catabolites lacking a critical carboxylate function of the natural chlorophylls. Chemistry-a European Journal, 2018, 24(12): 2987-2998.

[15]    Erhart, T.#; Mittelberger, C.#; Liu, X.#; Podewitz, M.#; Li, C.#; Scherzer, G.; Stoll, G.; Valls, J.; Robatscher, P.; Liedl, K. R.; Oberhuber, M.; Kräutler, B.* Novel types of hypermodified fluorescent phyllobilins from breakdown of chlorophyll in senescent leaves of grapevine (Vitis vinifera). Chemistry-a European Journal, 2018, 24(65): 17268-17279.

[14]    Li, C.; Zhang, J.; Song, J.; Xie, Y.*; Jiang, J. Synthetic porphyrin chemistry in China. Science China-Chemistry, 2018, 61(5): 511-514.



[13]    Wang, Q.; Wei, X.; Li, C.*; Xie, Y.* A novel p-aminophenylthio- and cyano-substituted BODIPY as a fluorescence turn-on probe for distinguishing cysteine and homocysteine from glutathione. Dyes and Pigments, 2018, 148: 212-218.

[12]    Wang, Q.; Ma, F.; Tang, W.; Zhao, S.; Li, C.*; Xie, Y.* A novel nitroethylene-based porphyrin as a NIR fluorescence turn-on probe for biothiols based on the Michael addition reaction. Dyes and Pigments, 2018, 148: 437-443.

[11]    Li, C.; Liu, X.; Shao, J.; Su, G.; Xie, Y.* Synthesis of a doubly SO2-fused phlorin: Tuning the structure and properties by the SO2 groups. Journal of Porphyrins and Phthalocyanines, 2018, 22(9-10): 799-806.

[10]    Kong, J.; Shao, J.; Li, C.*; Qi, D.; Li, M.; Liang, X.; Zhu, W.; Jiang, J.; Xie, Y.* Neo-N-confused phlorins and phlorinone: rational synthesis and tunable properties. Organic Letters, 2017, 19(3): 650-653.

[9]    Li, C.; Wurst, K.; Jockusch, S.; Gruber, K.; Podewitz, M.; Liedl, K. R.; Kräutler, B.* Chlorophyll-derived yellow phyllobilins of higher plants as medium-responsive chiral photoswitches. Angewandte Chemie-International Edition, 2016, 55(51): 15760-15765. (Inside cover story)

[8]    Li, C.; Kräutler, B.* Zn-complex of a natural yellow chlorophyll catabolite. Journal of Porphyrins and Phthalocyanines, 2016, 20(1-4): 388-396.



[7]    Li, C.; Wurst, K.; Feng, Y.; Kräutler, B.* Synthesis, spectroscopic and crystallographic analysis of the Zn-complex of a di(beta,beta'-sulfoleno)pyrrin: model for Zn-complexes of bilirubin and of phylloxanthobilins. Monatshefte Für Chemie, 2016, 147(6): 1031-1036.

[6]    Li, C.; Kräutler, B.* Transition metal complexes of phyllobilins-A new realm of bioinorganic chemistry. Dalton Transactions, 2015, 44(22): 10116-10127.

[5]    Li, C.; Zhang, J.; Liu, X.; Zhou, Y.; Sun, D.; Cheng, P.; Zhang, B.; Feng, Y.* Synthesis of corrole-fullerene dyads via [4+2] cycloaddition reaction. RSC Advances, 2014, 4(77): 40758-40762.

[4]    Li, C.; Ulrich, M.; Liu, X.; Wurst, K.; Müller, T.; Kräutler, B.* Blue transition metal complexes of a natural bilin-type chlorophyll catabolite. Chemical Science, 2014, 5(9): 3388-3395.

[3]    Li, C.; Zhang, T.; Zeng, Z.; Liu, X.; Zhao, Y.; Zhang, B.; Feng, Y.* A New Route to Indazolone via Amidation Reaction of o-Carboxyazobenzene. Organic Letters, 2012, 14(2): 479-481.

[2]    Li, C.; Fechtel, M.; Feng, Y.; Kräutler, B.* Corroles programmed for regioselective cycloaddition chemistry-Synthesis of a bisadduct with C60-fullerene. Journal of Porphyrins and Phthalocyanines, 2012, 16(5-6): 556-563.

[1]    Li, C.; Feng, Y.*; Liu, X.; Zhang, T. The synthesis of porphyrin-anthraquinone dyad via an azo-rearrangement. Chinese Chemical Letters, 2011, 22: 539-542.