李成杰 (1984. 12)，教授 (博士生导师)
联系方式：chengjie.li@ecust.edu.cn
研究方向：精细有机合成化学与催化应用
招生专业：应用化学（硕博）、有机化学（博士）、材料与化工（硕博）
教育经历：
2003.09-2012.06天津大学 (本、博) 导师：冯亚青 教授
2009.10-2010.10奥地利因斯布鲁克大学 联合培养 导师：B. Kräutler 教授
工作经历：
2012.10-2016.10奥地利因斯布鲁克大学 博士后 导师：B. Kräutler 教授
2016.12-2018.08 华东理工大学 化学与分子工程学院 助理研究员
2018.09-2026.08 华东理工大学 化学与分子工程学院 副教授
2026.09-至今 华东理工大学 化学与分子工程学院 教授
项目情况：
1. 上海市科学技术委员会上海市浦江人才计划17PJ1401700，基于BODIPY和卟啉的生物硫醇荧光探针研究 (2017-07 至 2019-06、结题、主持)
2. 国家自然科学基金委员会青年项目 21702062，新型稠环BODIPY近红外生物硫醇荧光探针的研究 (2018-01 至 2020-12、结题、主持)
3. 上海市科学技术委员会面上项目 20ZR1414100，基于环加成反应构建新型缺电子芳香稠环卟啉 (2020-07 至 2023-06、结题、主持)
4. 国家自然科学基金委员会面上项目 22075077，新型缺电子芳香稠环卟啉分子的合成与性质研究 (2021-01 至 2024-12、结题、主持)
5. 上海市科学技术委员会面上项目 23ZR1415600，基于砜基卟啉的分子内骈连反应构建融合型芳香稠环卟啉 (2023-07 至 2026-06、结题、主持)
6. 杭州传化精细化工有限公司横向（在研）
论文情况：
[47]Ye, Z.; Hu, M.; Gong, D.; Li, Q. S.; Luo, J.; Li, Q. L.; Liu, X.; Li, Q.; Li, C.* Masked-diene strategy for constructing aromatic ring-fused corroles: SOMO(cor)-HOMO(cor) inversion. Organic Letters, 2026, 28(25): 8240-8245.
[46]Liu, C.; Li, Y.; Hu, Y.; Li, Q.*; Li, C.*; Xie, Y.*Efficient dye-sensitized solar cells based on doubly concerted companion dyes with bulky branched chains on the donors and optimized linkage length. Chinese Chemical Letters, 2026, 37(03): 111863.
[45]Lu, Q.; Hu, Y.; Zheng, B.; Li, Z.; Li, C.*; Li, Q.*; Xie, Y.* Concerted companion organic dyes with benzothiadiazole–ethynyl units for high-performance indoor dye-sensitized solar cells. New Journal of Chemistry, 2025, 49: 20063-20072.
[44]Liu, J.; Liang, X.; Zhang, Y.; Li, Q.; Li, Y.; Perrin, T.; D’Herbillié, R.; Liu. X.; Wu, X.; Li, C.* Loading Thiacorrole with Various Aromatic Rings: Enhanced NIR Absorption and Improved OER Activity. Organic Letters, 2025, 27(23): 6151-6156.
[43]Liang, X.; Liu, J.; Dong, C.; Li, Y.; Zhao, C.; Li, C.* Dihydrophenazines with push-pull frameworks: Synthesis, photophysical properties and photoredox catalysis. Dyes and Pigments, 2025, 242: 112940.
[42]Fan, P.; Peng, H.; Liu, J.; Gao, X.; Zhu, S.; Zhang, Y.; Li, C.* Polypyrrole as a Photothermal Reactor to Conduct Solvent-Free Pericyclic Reactions. Chemistry-A European Journal., 2025, 31: e202500995.
[41]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 Materials Chemistry A, 2025, 13: 4176-4185.
[40]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.
[39]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.
[38]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.
[37]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，2024，40(3)：255-273.
Ma, W.#; Ye, Z.#; Li, Q.; Liu, X.; Xie, Y.*; Li, C.* Research Progress on Synthesis and Properties of Peripheral Aromatic Ring Fused Porphyrins, Chemical Reaction Engineering and Technology, 2024, 40(3): 255-273.
[36]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.
[35]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.
[34]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.
[33]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.
[32]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.
[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.