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倪勇

姓名 倪勇
性别 发明专利4999代写全部资料
学校 南方科技大学
部门 理学院, 化学系
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学历 版权登记666包过 代写全部资料
职称 副教授
联系方式 南方科技大学理学院化学系C4040
邮箱 niy@sustech.edu.cn
   
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教师主页 团队成员 科研项目 研究领域 学术成果 教学 科研分享 新闻动态 疼痛医学中心 成果介绍 软件 毕业去向 加入我们 联系我们 倪勇 Google Scholar 副教授 理学院, 化学系 倪勇,南方科技大学化学系副教授(研究员)、博士生导师。2010年本科毕业于浙江大学化学系 (导师:黄宪院士,王彦广教授),2015年博士毕业于新加坡国立大学化学系(师从吴继善教授),之后分别在新加坡科技研究局(A-Star)和新加坡国立大学任博士后研究员,主要从事新型有机π共轭功能分子的设计、合成、表征及应用研究,在有机自由基光电磁功能分子、三维芳香性、以及纳米碳结构等领域取得了一系列原创性研究成果。迄今为止,在领域内顶级国际学术刊物(J. Am. Chem. Soc., Nature Chem., Chem, Angew. Chem. Int. Ed., Nat. Rev. Mat., Acc. Chem. Res.等)发表论文40篇,合作撰写专著2本。荣获2021年国家优秀自费留学生奖(B类),2021年新加坡国家化学会优秀青年学者金奖。2021年入选优秀青年科学基金项目(海外),2022年11月加入南方科技大学化学系。 荣誉奖励: 2021年国家优秀自费留学生奖(B类); 2021年新加坡国家化学会优秀青年学者金奖; 2021年国家优秀青年科学基金项目(海外) 近年资助: 2022-2025,国家优秀青年科学基金项目(海外) 个人简介 个人简介 研究领域 1. 有机π共轭自由基体系的设计、合成及功能探索; 2. π共轭分子拓扑学的系统研究及新型芳香性规则的探索; 3. 碳基小分子磁性材料;功能分子材料。 学术成果 查看更多 After Join SUStech [3] Y. Ni and J. Wu*, “Global π-Aromaticity in Open-shell Diradicaloids and Polyradicaloids”, Nat. Rev. Mat. 2022, invited review in press. [2] Z. Gong, Q. Xiang, K. Li, Z. Xu, J. Hu, Y. Ni, S. Sato and Z. Sun*, “Pentagon-Containing Doublet Graphene Fragments with Edge-Dependent Spin/Charge Distribution”, Chin. J. Chem. 2022, 40, 2525-2530. [1] Y. Wang, Y. Huang, T. Huang, J. Zhang, T. Luo, Y. Ni, B. Li, S. Xie and Z. Zeng*, “Perylene-Based Linear Nonalternant Nanoribbons with Bright Emission and Ambipolar Redox Behavior”, Angew. Chem. Int. Ed. 2022, e202200855. Before Join SUStech [36] S. Xin, Y. Han, W. Fan, X. Wang, Y. Ni* and J. Wu*, “Enhanced Aromaticity and Open-Shell Diradical Character in the Dianions of 9-Fluorenylidene-Substituted Expanded Radialenes”, Angew. Chem. Int. Ed. 2022, e202209448. [35] Y. Ni, T. Y. Gopalakrishna, H. Phan, T. Kim, T. S. Herng, Y. Han, T. Tao, J. Ding, D. Kim and J. Wu*, “3D global aromaticity in a fully conjugated diradicaloid cage at different oxidation states”, Nat. Chem. 2020, 12, 242. [34] Y. Ni, T. Y. Gopalakrishna, S. Wu and J. Wu*, “A Stable All-Thiophene-based Core-modified [38]Octaphyrin Diradicaloid: Conformation and Aromaticity Switch at Different Oxidation States”, Angew. Chem. Int. Ed. 2020, 59, 7414. [33] Y. Ni, F. Gordillo-Gámez, M. P. Alvarez, Z. Nan, Z. Li, S. Wu, Y. Han, J. Casado* and J. Wu*, “A Chichibabin’s Hydrocarbon Based Molecular Cage: The Impact of Structural Rigidity on Dynamics, Stability, and Electronic Properties”, J. Am. Chem. Soc. 2020, 142, 12730. [32] Y. Ni, M. E. Sandoval-Salinas, T. Tanaka, H. Phan, T. S. Herng, T. Y. Gopalakrishna, J. Ding, A. Osuka, D. Casanova* and J. Wu*, “[n]Cyclo-para-biphenylmethine Polyradicaloids: [n]Annulene Analogs and Unusual Valence Tautomerization”, Chem 2019, 5, 108. (Also see preview by H. L. Anderson et al in Chem 2019, 5, 9). [31] Y. Ni, T. Y. Gopalakrishna, H. Phan, T. S. Herng, S. Wu, Y. Han, J. Ding and J. Wu*, “A Peri-tetracene Diradicaloid: Synthesis and Properties”, Angew. Chem. Int. Ed. 2018, 57, 9697. (This paper was highlighted in synfacts 2018, 14, 0922). [30] Y. Ni, R. K. Kannadorai, S. W. –K. Yu*, Y. –T. Chang* and J. Wu*, “Push-pull type meso-ester substituted BODIPY near-infrared dyes as contrast agents for photo-acoustic imaging”, Org. Biomol. Chem. 2017, 15, 4531. [29] Y. Ni, S. Lee, M. Son, N. Aratani, M. Ishida, A. Samanta, H. Yamada, Y. –T. Chang, H. Furuta, D. Kim*, J. Wu*, “A Diradical Approach towards BODIPY-Based Dyes with Intense Near-Infrared Absorption around λ=1100 nm”, Angew. Chem. Int. Ed. 2016, 55, 2815. [28] Y. Ni, R. K. Kannadorai, J. Peng, S. W. –K. Yu*, Y. –T. Chang*, J. Wu*, “Naphthalene-fused BODIPY Near-Infrared Dye as A Stable Contrast Agent for In Vivo Photoacoustic Imaging”, Chem. Commun. 2016, 52, 11504. [27] Y. Ni, J. Wu*, “Diradical Approach Toward Organic Near Infrared Dyes”, Tetrahedron Letters 2016, 57, 5426. [26] Y. Ni, J. Wu*, “Diradical Approach Toward Organic Near Infrared Dyes”, ChemInform 2016, 47. [25] Y. Ni, J. Wu*, “Far-red and near infrared BODIPY dyes: synthesis and applications for fluorescent pH probes and bio-imaging”, Org. Biomol. Chem. 2014, 12, 3774. [24] Y. Ni, L. Zeng, N. Kang, K. Huang, L. Wang, Z. Zeng, Y. –T. Chang* and J. Wu*, “meso-Ester and Carboxylic Acid Substituted BODIPYs with Far-Red and Near-Infrared Emission for Bioimaging Applications”, Chem. Eur. J. 2014, 20, 2301. [23] Y. Ni, W. Zeng, K. Huang and J. Wu*, “Benzene-fused BODIPYs: synthesis and the impact of fusion mode”, Chem. Commun. 2013, 49, 1217. [22] S. Wu, Y. Ni, Y. Han, S. Xin, X. Hou, J. Zhu, Z. Li and J. Wu*, “Aromaticity in Fully π-Conjugated Open-Cage Molecules”, J. Am. Chem. Soc. 2022, 144, 23158-23167. [21] Z. Li, X. Hou, Y. Han, W. Fan, Y. Ni, Q. Zhou, J. Zhu, S. Wu, K. Huang and J. Wu*, “[8]Cyclo-para-phenylmethine as a Super-Cyclooctatetraene: Dynamic Behavior, Global Aromaticity, and Open-Shell Diradical Character in the Neutral and Dicationic States”, Angew. Chem. Int. Ed. 2022, e202210697. [20] S. Wu, Y. Ni, Y. Han, X. Hou, C. Wang and J. Wu*, “Hückel‐and Baird‐type 3D Global Aromaticity in a Fully Conjugated Molecular Cage”, Angew. Chem. Int. Ed. 2022, e202115571. [19] L. Ren, Y. Han, Y. Ni and J. Wu*, “All are aromatic: A 3D globally aromatic cage containing five types of 2D aromatic macrocycles”, Chem 2021, 7, 3442-3453. [18] J. Zhu, Y. Han, Y. Ni, S. Wu, Q. Zhang, T. Jiao, Z. Li and J. Wu*, “Facile Synthesis of a Fully Fused, Three-Dimensional π-Conjugated Archimedean Cage with Magnetically Shielded Cavity”, J. Am. Chem. Soc. 2021, 143, 2716-2721. [17] J. Zhu, Y. Han, Y. Ni, G. Li and J. Wu*, “Facile Synthesis of Nitrogen-Doped [(6.)m8]nCyclacene Carbon Nanobelts by a One-Pot Self-Condensation Reaction”, J. Am. Chem. Soc. 2021, 143, 14314-14321. [16] Y. Zou, V. Bonal, S. M. Quintero, P. G. Boj, J. M. Villalvilla, J. A. Quintana, G. Li, S. Wu, Q. Jiang, Y. Ni, J. Casado*, M. A. Díaz-García* and J. Wu*, “Perylene-fused, Aggregation-free Polycyclic Aromatic Hydrocarbons for Solution-processed Distributed Feedback Lasers”, Angew. Chem. Int. Ed. 2020, 59, 14927-14934. [15] Y. Han, Z. Xue, G. Li, Y. Gu, Y. Ni, S. Dong, C. Chi*, “Formation of Azulene-Embedded Nanographene: Naphthalene to Azulene Rearrangement During the Scholl Reaction”,  Angew. Chem. Int. Ed. 2020, 59, 9026-9031. [14] Y. Gu, R. Muñoz-Mármol, S. Wu, Y. Han, Y. Ni, M. A. Díaz-García, J. Casado* and J. Wu*, “Cove-Edged Nanographenes with Localized Double Bonds”, Angew. Chem. Int. Ed. 2020, 59, 8113-8117. [13] C. Liu, Y. Ni, X. Lu, G. Li and J. Wu*, “Global Aromaticity in Macrocyclic Polyradicaloids: Hückel’s Rule or Baird’s Rule?”, Acc. Chem. Res. 2019, 52, 2309. [12] G. Li, H. Yi, Y. Zou, J. J. C. Lee, Y. Ni and J. Wu*, “De-aromatization Approach Toward Superbenzoquinone Based Diradicaloid, Tetraradicaloid, and Hexaradicaloid”, Angew. Chem. Int. Ed. 2019, 58, 14319. [11] X. F. Lu, T. Y. Gopalakrishna, Y. Han, Y. Ni, Y. Zou and J. Wu*, “Bowl-shaped Carbon Nanobelts Showing Size-dependent Properties and Selective Encapsulation of C70”, J. Am. Chem. Soc. 2019, 141, 5934. [10] S. Dong, T. Y. Gopalakrishna, Y. Han, H. Phan, T. Tao, Y. Ni, G. Liu and C. Chi* “Extended Bis(anthraoxa)quinodimethanes with Nine and Ten Consecutively Fused Six-membered Rings: Neutral Diradicaloids and Charged Diradical Dianions/Dications”, J. Am. Chem. Soc. 2019, 141, 62. [9] M. H. Chua, T. Kim, Z. L. Lim, Y. Ni, J. Xu*, D. Kim* and J. Wu*, “BODIPY-based Antiaromatic Macrocycles: Facile Synthesis by Knoevenagel Condensation and Unusual Aggregation-Enhanced Two-Photon Absorption Properites”, Chem. Eur. J. 2018, 24, 2232. [8] X. Gu, T. Y. Gopalakrishna, H. Phan, Y. Ni, T. S. Herng, J. Ding and J. Wu*, “A Three-Dimensionally π-Conjugated Diradical Molecular Cage”, Angew. Chem. Int. Ed. 2017, 56, 15383. [7] F. Miao, S. Uchinomiya, Y. Ni, Y. –T. Chang* and J. Wu*, “Development of pH‐Responsive BODIPY Probes for Staining Late Endosome in Live Cells”, ChemPlusChem 2016, DOI: 10.1002/cplu.201600249. [6] L. Wang, J. Zhang, B. Kim, J. Peng, S. N. Berry, Y. Ni, D. Su, J. Lee, L. Yuan, Y. –T. Chang*,“Boronic Acid: A Bio-Inspired Strategy To Increase the Sensitivity and Selectivity of Fluorescent NADH Probe”,J. Am. Chem. Soc. 2016, 138, 10394. [5] L. Wang, L. Yuan*, X. Zeng, J. Peng, Y. Ni, J. C. Er, W. W. Xu, B. Keshari, D. Su, B. Kinm, Y. –T. Chang*, “A Multisite-Binding Switchable Fluorescent Probe for Monitoring Mitochondrial ATP Level Fluctuation in Live Cells”, Angew. Chem. Int. Ed. 2016, 55, 1773. [4] M. H. Chua, Y. Ni, B. Zheng, K. W. Huang, J. W. Xu* and J. Wu*, “Towards meso -Ester BODIPYs with Aggregation-Induced Emission Properties: The Effect of Substitution Positions”, Chem Asian J. 2015, 10, 1631. [3] W. Zeng, M. Ishida, S. Lee, Y. M. Sung, Z. Zeng, Y. Ni, C. Chi*, D. Kim* and J. Wu*, “A p-Quinodimethane-Bridged Porphyrin Dimer”, Chem. Eur. J. 2013, 19, 16814. [2] Z. Zeng, S. Lee, J. L. Zafra, M. Ishida, X. Zhu, Z. Sun, Y. Ni, R. D. Webster, R. Li, J. T. L_pez Navarrete*, C. Chi*, J. Ding*, J. Casado*, D. Kim* and J. Wu*, “Tetracyanoquaterrylene and Tetracyanohexarylenequinodimethanes with Tunable Ground States and Strong Near-Infrared Absorption”, Angew. Chem. Int. Ed. 2013, 52, 8561. [1] C. Su, Q. Liu, Y. Ni and Xian Huang*, “An efficient synthesis of polysubstituted tetrahydrofuran and indene derivatives via the Lewis acid-mediated cycloadditions of VCPs with aldehydes”, Tetrahedron Letters 2009, 50, 4381. Book Chapters [2] Y. Ni and J. Wu, “Diradicaloids”, Jenny Stanford Publishing 2022. “Chapter 13: Polyradicaloids and 2D/3D GlobalAromaticity”. [1] Y. Ni and J. Wu, “Aromaticity: Modern Computational Methods and Applications”, Elsevier 2021. “Chapter 13: Global aromaticity in 2D macrocyclic polyradicaloids and 3D fully conjugated molecular cages”. 加入团队 查看更多 联系我们 联系地址 南方科技大学理学院化学系C4040 办公电话 13265586205 电子邮箱 niy@sustech.edu.cn

倪勇