教育背景：
2016.10–2020.11 維爾茨堡大學 無機化學 博士
2011.09–2014.07 廈門大學 有機化學 碩士
2006.09–2010.06 齊齊哈爾大學 制藥工程 學士
工作經(jīng)歷：
2025.04–至今 南方科技大學 研究助理教授
2022.04–2025.03 深圳大學 博士后
2021.06–2022.02 南方科技大學 研究學者
2014.12–2016.10 南方科技大學 研究助理
榮譽及獎勵：
2020 深圳市海外高層次人才引進“孔雀計劃”C類人才
研究方向：
·含硼小分子藥物開發(fā)
·芳香稠合borole的設計與合成，側(cè)重于其電化學，光化學性質(zhì)研究?，F(xiàn)階段對于缺電子雜環(huán)稠合的borole更為感興趣
·研究給體-受體化合物的光學及其電化學性質(zhì)。現(xiàn)階段特別是對于具有熱活化延遲熒光的給體-受體化合物產(chǎn)生濃厚興趣
·雜原子摻雜的多環(huán)芳香化合物
·缺電性有機陽離子化合物
發(fā)表論文：
(1) J. He, S. M. Wang, X. F. Song, X. Y. Chang, C. Zou, W. Lu, K. Li, Tetradentate carbene-anilido boron complexes: highly fluorescent dyes with larger stokes shifts than BODIPY dyes. Chem. Commun. 2024, 60, 11524?11527.
(2) J. He, X. Y. Chang, C. Zou, Y. Q. Yu, S. Han, C. F. Wu, S. Ou, W. Lu, K. Li, Tunable Yellow to Near-Infrared Fluorescent Boron-Amino-Chelating Complexes with Stokes Shifts >100 nm. J. Org. Chem. 2023, 88, 14836?14841.
(3) J. He, F. Rauch, A. Friedrich, J. Krebs, I. Krummenacher, R. Bertermann, J. Nitsch, H. Braunschweig, M. Finze, T. B. Marder, Phenylpyridyl-fused Boroles: A Unique Coordination Mode and Weak B–N Coordination-Induced Dual Emission, Angew. Chem. Int. Ed. 2021, 60, 4833–4840. (Designated as a Hot Paper)
(4) J. He, F. Rauch, M. Finze, T. B. Marder, (Hetero)Arene-fused boroles: a broad spectrum of applications, Chem. Sci. 2021, 12, 128–147.
(5) J. He, F. Rauch, I. Krummenacher, H. Braunschweig, M. Finze, T. B. Marder, Two Derivatives of Phenylpyridyl-fused Boroles with Contrasting Electronic Properties: Decreasing and Enhancing the Electron Accepting Ability, Dalton Trans. 2021, 50, 355–361.
(6) J. He, F. Rauch, A. Friedrich, D. Sieh, T. Ribbeck, I. Krummenacher, H. Braunschweig, M. Finze, T. B. Marder, N-Heterocyclic Olefins as Electron Donors in Combination with Triarylborane Acceptors: Synthesis, Optical and Electronic Properties of D-π-A Compounds, Chem. Eur. J. 2019, 25, 13777–13784.
(7) X. Zheng, J. He, H.-H. Li, A. Wang, X.-J. Dai, A.-E Wang, P.-Q. Huang, Umpolung of Amide-based Mannich-Type Reaction: Titanocene(III)-catalyzed Three-Component Reaction of Secondary Amides, Aldehydes and Electrophilic Alkenes, Angew. Chem. Int. Ed. 2015, 54, 13739–13742. (Supervisor is the first author)
