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个人简介韩勰老师主要从事有机合成和分子发光领域的工作,研究兴趣含括超分子合成及功能化、智能材料的构建(如光致变色材料和机械变色材料)和荧光分子在生命科学(如细胞成像、生物探针)等领域的拓展应用等。在过去的几年中,韩老师基于荧光染料分子的光物理特性和超分子结构骨架特点,开展了包括细胞成像、荧光探针、传感和超分子功能化等方面的研究工作,先后在J. Mater. Chem. B、Org. Biomol. Chem.、Chem. Commun、Dyes Pigm、Chem 等知名期刊上发表研究论文10余篇。目前,韩老师的研究工作主要集中在主客体作用对分子发光性能的调控和刺激响应型材料的研究。 | ||
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学术成果
1. Han, X.; Hu, F.; Chi, W.; Ma, X.; Liu, S. H.; Liu, X.*; Yin, J.* “Unusual intermolecular charge transfer enables supramolecular fluorescent viscosity sensors” Accept by Sensor Actuat B-Chem.
2. Han, X.; Li, D.; Ma, X.; Liu, S. H.; Yin, J.* “Photoactivatable Fluorescence Enhanced Behaviour of Benzo[c][1,2,5]oxadiazole-dressing Tetraphenylethene” New J. Chem. 2018, 42, 6609-6612.
3 Han, X.; Zhang, B.; Chen, J.; Liu, S. H.; Tan, C.; Liu, H.; Lang, M. J.; Tan, Y.*; Liu, X.*; Yin, J.* “Modulating aggregation-induced emission via a non-conjugated linkage of fluorophores to tetraphenylethenes”J. Mater. Chem. B 2017, 5, 5096-5100.
4. Han, X.; Li, Z.; Xu, Z.; Zhao, Z.; Liu, S. H.; Yin, J.* “Construction of Crown Ether-Stoppering [3]Rotaxanes Based on N-Hetero Crown Ether Host” Chin. J. Chem. 2017, 35, 1050-1056.
5. Han, X.; Liu, G.; Liu, S. H.; Yin, J.* “Synthesis of rotaxanes and catenanes using an imine clipping reaction” Org. Biomol. Chem. 2016, 14, 10331-10351.
6. Han, X.; Cao, M.; Xu, Z.; Wu, D.; Chen, Z.; Wu, A.; Liu, S. H.; Yin, J.* “Aggregation-induced emission behavior of a pH-controlled molecular shuttle based on a tetraphenylethene moiety” Org. Biomol. Chem. 2015, 13, 9767-9774.
7. Han, X.; Lv, X.; Chen, Z.; Yu, G.; Yin, J.; Liu, S.* “A Fluorescent Probe for Hg2+ Based on Gold(I) Complex with An Aggregation-Induced Emission Feature” Chin. J. Chem. 2015, 33, 1064-1068.
8. Han, X.; Hu, F.; Ge, H.; Liu, S.; Yin, J.* “The Application of Templated-Directed Clipping Approach in Constructing Mechanically Interlocked Molecules Based on N-Hetero Crown Ether” Prog. Chem. 2015, 27, 675-686.
9. Li, Z.#; Han, X. #; Chen, H.; Wu, D.; Hu, F.; Liu, S. H.; Yin, J.* “Construction of photoswitchable rotaxanes and catenanes containing dithienylethene fragments” Org. Biomol. Chem. 2015, 13, 7313-7322.
10. Xu, Z.#; Huang, X.#; Han, X.#; Wu, D.; Zhang, B.; Tan, Y.*; Cao, M.; Liu, S. H.; Yin, J.*; Yoon, J.* “A visible and near-Infrared, dual channel fluorescence-on probe for highly selective tracking of mitochondrial glutathione” Chem. 2018, 4, 1609-1628.
11. Liu, G.; Han, X.; Zhang, J.; Xu, Z.; Liu, S. H.; Zeng, L.*; Yin, J.* “Oxidized-morpholine dressing ratiometric fluorescent probe for specifically visualizing the intracellular glutathione” Dyes Pigm. 2018, 148, 292-297.
12. Chen, Z.; Han, X.; Zhang, J.; Wu, D.; Yu, G.-A.*; Yin, J.; Liu, S. H.* “Fluorene-based novel gold(I) complexes with aggregation-induced emission (AIE) or aggregate fluorescence change characteristics: from green to white emission” RSC Adv. 2015, 5, 15341-15349.
13. Chen, Z.; Wu, D.; Han, X.; Liang, J.; Yin, J.*; Yu, G.-A.; Liu, S. H.* “A novel fluorene-based gold(I) complex with aggregate fluorescence change: a single-component white light-emitting luminophor”Chem. Commun. 2014, 50, 11033-11035.
14. Chen, Z.; Wu, D.; Han, X.; Nie, Y.; Yin, J.*; Yu, G.-A.; Liu, S. H.* “1,8-Naphthalimide-based highly blue-emissive fluorophore induced by a bromine atom: reversible thermochromism and vapochromism characteristics” RSC Adv. 2014, 4, 63985-63988.
15. Cao, M.; Hu, F.; Han, X.; Zhang, Y.; Wu, D.; Liu, S. H.; Yin, J.* “Aggregation Control of Hemicyanine Fluorescent Dye by Using of Cucurbit[7]uril and Pillar[6]arene” Chin. J. Chem. 2015, 33, 351-355.
16. Xu, Z.; Ge, H.; Han, X.; Liu, S. H.; Meng, X.-G.*; Yin, J.* “Self-recognition behavior of novel frameworks containing both urea and carboxylate anion motifs” Tetrahedron 2017, 73, 6386-6391.
17. Liu, G.; Liu, D.; Han, X.; Sheng, X.; Xu, Z.; Liu, S. H.; Zeng, L.*; Yin, J.* “A hemicyanine-based colorimetric and ratiometric fluorescent probe for selective detection of cysteine and bioimaging in living cell” Talanta 2017, 170, 406-412.
18. Liu, G.; Wu, D.; Liang, J.; Han, X.; Liu, S. H.; Yin, J.* “Tetraphenylethene modified [n]rotaxanes: synthesis, characterization and aggregation-induced emission behavior” Org. Biomol. Chem. 2015, 13, 4090-4100.