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李春举 教授
2023-03-22 09:29 新葡萄3522登录网页版 


姓名:李春举  

出生日期:197912

实验室:明理楼B217225232202

职称:教授、博士生导师

学历:博士

通信地址:天津市西青区宾水西道393新葡萄3522登录网页版明理楼B221

Emailcjli@shu.edu.cn; cjli@tjnu.edu.cn

[个人简历]  

李春举,男,博士,教授。197912月生,1998年~2007年在南开大学化学系学习,获理学学士和博士学位;20072008年从事药物研发合成工作;2008年进入上海大学化学系;2010年晋升为副教授;2015年晋升为教授;20142015年美国德克萨斯大学奥斯汀分校博士后201812月全职调动到新葡萄3522登录网页版工作;20208月起任新葡萄3522登录网页版院长、天津市功能分子结构与性能重点实验室主任。

一直从事超分子化学和有机合成化学方面的研究,5年在Acc. Chem. Res.1篇)、Nat. Commun.3篇)、Angew. Chem. Int. Ed.8篇)、Chem. Sci.2篇)等权威期刊上发表SCI论文50余篇;研究工作被ACS 的“Noteworthy Chemistry”、RSC 的“ChemistryWorld”和Wiley的“ChemViews”等知名学术媒体评价报道;论文累计共被他人引用5000多次,H指数为46;主持国家自然科学基金项目5项。

获得全国大环芳烃超分子化学新星奖、天津市特聘教授、天津市高校“学科领军人才培养计划”、上海市曙光学者、浦江人才计划和上海市青年岗位能手等荣誉;目前担任《中国化学快报》等期刊编委和中国化学会超分子化学专委会委员。

在学生培养方面,指导的本科生两次获得“挑战杯”全国大学生课外学术科技作品竞赛国家级一等奖,并获“挑战杯”累进创新奖;指导的团队获得全国大学生“小平科技创新团队”;指导的博/硕士研究生11人次获得国家奖学金。


[研究领域]

新型有机超分子主体分子合成

基于分子识别及自组装的生物医药应用

超分子智能材料


[代表性论文]  

1. Biphen[n]arenes: Modular Synthesis, Customizable Cavity Sizes, and Diverse Skeletons

Z.-Y. Zhang and C. Li*

Acc. Chem. Res. 2022, 55, 916−929.

2. Synthesis of Cationic Biphen[4, 5]arenes as Biofilm Disruptors

X. Du,# M. Ma,# Y. Zhang, X. Yu, L. Chen, H. Zhang, Z. Meng, X. Jia, J. Chen,* Q. Meng* and C. Li*

Angew. Chem. Int. Ed. DOI: 10.1002/anie.202301857.

3. Macrocyclization-Induced Phosphorescence Enhancement of Pyridinium-based Macrocycle

S. Li#, Z.-Y. Zhang#, J.-F. Lv, L. Li, J. Li and C. Li*

J. Mater. Chem. A. DOI: 10.1039/D2TA09993D.

4. Modular Introduction of Endo-Binding Sites in Macrocyclic Cavity towards Selective Recognition of Neutral Azacycles

K. Xu, B. Li, S. Yao, Z. Li, Y. Lu, M. Dong, J. Qiu, L. Luo* and C. Li*

Angew. Chem. Int. Ed. 2022, 61, e202203016.

5. Synthesis and macrocyclization-induced emission enhancement of benzothiadiazole-based macrocycle

S. Li, K. Liu, X.-C. Feng, Z.-X. Li, Z.-Y. Zhang, B. Wang, M. Li, Y.-L. Bai*, L. Cui* and C. Li*

Nat. Commun. 2022, 13, 2850.

6. Supramolecular Detoxification of Macromolecular Biotoxin through the Complexation by a Large-Sized Macrocycle

L. Zhao, J. Chen, L. Tian, Y. Zhang, L. Chen, X. Du, M. Ma, J. Li, Q. Meng,* and C. Li*

Adv. Healthc. Mater. 2022, 11, 2200270.  

7. Switchable Supramolecular Jalousie Constructed from a Fluorenone Macrocycle

C.-M. Yu, X. Meng, X. Liu, Z.-Y. Zhang, and C. Li*

Chem. Mater. 2022, 34, 358–365.

8. One-pot and Shape-controlled Synthesis of Organic Cages  

X. Zhao, Y. Liu, Z.-Y. Zhang, Y. Wang, X. Jia, and C. Li*

Angew. Chem. Int. Ed. 2021, 60, 17904-17909..

9. Complexation of an Antimicrobial Peptide by Large-Sized Macrocycles for Decreasing Hemolysis and Improving Stability

J. Chen, Q. Meng, Y. Zhang, M. Dong, L. Zhao, Y. Zhang, L. Chen, Y. Chai, Z. Meng, C. Wang, X. Jia, and C. Li* .

Angew. Chem. Int. Ed. 2021, 60, 11288-11293.

10. Synergistic Enhancement for Emergency Treatment Effect of Organo-phosphate Poisoning by A Supramolecular Strategy

J. Chen, Y. Zhang, Y. Chai, Z. Meng, Y. Zhang, L. Chen, D. Quan,* Y. Wang,* Q. Meng,* and C. Li*

Chem. Sci., 2021, 12, 5202-5208.

11. A Modular Synthetic Strategy for Functional Macrocycles

K. Xu, Z.-Y. Zhang, C. Yu, B. Wang, M. Dong, X. Zeng, R. Gou, L. Cui, and C. Li*

Angew. Chem. Int. Ed. 2020, 59, 7214-7218.

12. Macrocycle Co-Crystals Showing Vapochromism to Haloalkanes

B. Li, L. Cui, and C. Li*

Angew. Chem. Int. Ed. 2020, 59, 22012-22016.

13. A Cyclic Bis[2]catenane Metallacage

Y. Wang, Y. Zhang, Z. Zhou, R. Vanderlinden, B. Li, B. Song, X. Li, L. Cui, J. Li, X. Jia, J. Fang, C. Li*, and P. J. Stang*

Nat. Commun. 2020, 11, 2727.

14. Supramolecular Combination Chemotherapy: A pH-Responsive Co-Encapsulation Drug Delivery System

JChen, Y. Zhang, Z. Meng, L. Guo, X. Yuan, Y. Zhang, Y. Chai, J. L. Sessler,* Q. Meng * and C. Li*

Chem. Sci., 2020, 11, 6275-6282.

15. Supramolecular trap for catching polyamines in cells as an anti-tumor strategy

J. Chen, H. Ni, Z. Meng, J. Wang, X. Huang, Y. Dong, C. Sun, Y. Zhang, L. Cui, J. Li, X. Jia, Q. Meng,* and C. Li*

Nat. Commun. 2019, 10, 3546.

16. Efficient Separation of Cis- and Trans-1,2-dichloroethene Isomers by Adaptive Biphen[3]arene Crystals

Y. Wang,# K. Xu, # B. Li, L. Cui, J. Li, X. Jia, H. Zhao, J. Fang, and C. Li*

Angew. Chem. Int. Ed. 2019, 58, 10281–10284.

17. Terphen[n]arenes and Quaterphen[n]arenes (n = 3‒6): One-pot Synthesis, Self-assembly into Supramolecular Gels, and Iodine Capture

B. Li, B. Wang, X. Huang, L. Dai, L. Cui, J. Li, X. Jia, and C. Li*

Angew. Chem. Int. Ed. 2019, 58, 3885–3889.


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