个人简介
2005/09-2008/07，中国科学院化学研究所，分子识别与功能院重点实验室，博士
2002/09-2005/07，吉林大学，化学学院，硕士
1998/09-2002/07，吉林大学，化学学院，学士
近期论文
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Rong Wang, Ju Ding, Yuxiu Wang,and YanrongZhang*，Effect of Conjugation Mode on Intramolecular Charge Transfer in Fabricating Acid-ResponsiveFluorophores， Chem.Asian J. 2019, 14,3883–3892.
Yahui Niu, Rong Wang, Liang Pu, Yanrong Zhang∗,Pyrene meets 2-(2-hydroxyphenyl)benzothiazole: Creation of highly efficient solid-state monomeric emitter for organic light-emitting diode, Dyes and Pigments , 2019, 170, 107594.
Rong Wang, Ju Ding and Yanrong Zhang*,Naphthalimide/benzimide-based excited-state intramolecular proton transfer active luminogens: aggregation-induced enhanced emission and potential for chemical modification, New J. Chem., 2019, 43, 9152--9161
Yahui Niu, Rong Wang, Panlin Shao, Yuxiu Wang, and Yanrong Zhang*, Nitrostyrene-Modified 2-(2-Hydroxyphenyl)benzothiazole: Enol-Emission Solvatochromism by ESICT-ESIPT and Aggregation-Induced Emission Enhancement , Chem. Eur. J. 2018, 24, 16670 -16676.(IF: 5.160)
Qin Wang, Yahui Niu, Rong Wang, Haoran Wu, and Yanrong Zhang*, A cid-Induced Shift of Intramolecular Hydrogen Bonding Responsible for Excited-State Intramolecular Proton Transfer, Chem. Asian J. 2018, 13, 1735-1743. (IF: 3.692)
Yahui Niu, Longfei Xu, Qin Wang, Haoran Wu and Yanrong Zhang*, Planar 2-(2-hydroxyphenyl)benzothiazole-based dyes functionalized via triple bonds as exceedingly efficient solid-state fluorophores , CrystEngComm , 2017, 19, 5178-5183. (IF: 3.474)
Yahui Niu, Qin Wang, Haoran Wu, Yuxiu Wang and Yanrong Zhang*, Experimental and DFT studies of disubstituted 2-(2-hydroxyphenyl)benzothiazole-based fluorophores synthesized by Suzuki coupling , New J. Chem. , 2017, 41, 9796-9805. (IF: 3.269)
L. F. Xu, Q. Wang, Y. R. Zhang*, Electronic effect on the photophysical properties of 2-(2-hydroxyphenyl)benzothiazole-based excited state intramolecular proton transfer fluorophores synthesized by sonogashira-coupling reaction ， Dyes and Pigments 136, 732-741,2017. (IF: 4.066)
Qin Wang, Longfei Xu, Yahui Niu, Mao-Sen Yuan, and Yanrong Zhang*, Exceedingly Large Stokes Shift Induced by Low-Barrier H-Bond-Assisted Internal Charge Transfer , Asian J. Org. Chem. 2017, 6, 794-797.
Q. Wang, L. F. Xu, Y. H Niu, Y. X. Wang M. S. Yuan, Y. R. Zhang*, Excited State Intramolecular Proton Transfer in Ethynyl-extended Regioisomers of 2-(2'-hydroxyphenyl)benzothiazole: Effects of Position and Electronic Nature of Substituent Group , Chem. Asian J. 11, 3454–3464,2016. (IF: 4.592)
Q. Wang, L. F. Xu, Y. R. Zhang*, Perpendicular Phenyl-induced Exceedingly Efficient Solid-state ESIPT Fluorophore Based on 2-(2-hydroxyphenyl)benzothiazole, Dyes and Pigments 2017,142, 365-370. (IF: 4.066)
L.F. Xu, Q. Wang, Ma.-S. Yuan, Y. R. Zhang*. Dicyanomethylene-benzopyran-based alkynyl conjugatable near–infrared fluorescent probe for detection of fluoride anion . ChemistrySelect , 2016,1, 114–117.
Y. R. Zhang, L. Ren, Q. Tu, X. Q. Wang, R. Liu, L. Li, J. C. Wang, W. M. Liu, J. Xu, J. Y. Wang*. Fabrication of reversible poly(dimethylsiloxane) surfaces via host-guest chemistry and their repeated utilization in cardiac biomarker analysis . Analytical Chemistry , 2011, 83(24), 9651-9659. (IF: 5.886)
Y. R. Zhang, L. Pang, C. Ma, Q. Tu, R. Zhang, E. Saeed, A. E. Mahmoud, J. Y. Wang*. Small molecule-initiated light-activated semiconducting polymer dots: an integrated nanoplatform for targeted photodynamic therapy and imaging of cancer cells . Analytical Chemistry , 86(6), 3092--3099, 2014(IF: 5.886).
Y. R. Zhang, Q. Tu, D. E. Wang, Y. Chen, B. Z. Lu, M. S. Yuan, J. Y. Wang*. Adamantyl-terminated dendronized molecules: synthesis and interaction with b-cyclodextrinfunctionalized poly(dimethylsiloxane) interface . New Journal of Chemistry , 2013, 37, 2358-2368. (IF: 2.966)
Y. R. Zhang, L. He, X. Wu, P. L. Shao, S. Ye*. Chiral N-heterocyclic carbene catalyzed Staudinger reaction of ketenes with imines: highly enantioselective synthesis of N-boc β-lactams . Organic. Letters , 2008,10(2), 277-280. (IF: 6.732)
Y. R. Zhang, H. Lv, D. Zhou, S. Ye*, Chiral N-heterocyclic carbene-catalyzed formal [4+2] cycloaddition of ketenes with enones: highly enantioselective synthesis of trans- and cis-δ-lactones . Chemistry-A European Journal , 2008, 14(28), 8473-8476. (IF: 5.771)
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