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孙跃老师概况
孙跃老师概况

姓名:孙跃

学科专业:有机化学

研究方向:仿生纳米通道;超分子智能材料;生物医药材料

学者概况:孙跃,博士,教授。2017.6年毕业于华中师范大学,获理学博士学位。2017. 6?2019. 8于美国犹他大学从事博士后研究。20198?至今,于威尼斯手机网站工作。

目前发表SCI论文20余篇。其中,第一编辑或通讯编辑SCI论文14篇,含化学类国际顶级期刊7篇,包括2PNAS; 2Nature Communications2J. Am. Chem. Soc1Angew. Chem. Int. Ed。研究工作受到国内外同行的广泛关注,多篇工作被选为“热点文章”和“封面文章”,部分工作被Wiley数据库Materials Views网站、科学网等重点报道。

独立工作:

1.Sun, Y.; +Ding F.; + Chen, Z.; + Zhang, R.; + Li, C.; Xu, Y.; Zhang, Y.; Ni, R.; Li, X.; Yang, G.; Sun, Y.; Stang, P. J. Melanin-dot–mediated delivery of metallacycle for NIR-II/photoacoustic dual-modal imaging-guided chemo-photothermal synergistic therapy. Proc. Natl. Acad. Sci. USA, 2019, 116, 16729. (+equal contribution)

独立前工作:

2.Sun, Y.;Zhang, F.; Tian, D. M.; Li, H. B. A biomimetic chiral-driven ionic gate constructed by pillar[6]arene-based host-guest systems, Nat. Commun., 2018, 9, 2617.

3.Sun, Y.;Ma, J. K.; Zhang, F.; Zhu, F.; Mei, Y. X.; Liu, L.; Tian, D. M.; Li, H. B. A light-regulated host–guest-based nanochannel system inspired by channelrhodopsins protein,Nat. Commun., 2017, 8, 260.

4.Sun, Y.;+Li, S.;+ Zhou, Z. X.; Saha, M.; Datta, S.; Zhang, M.; Yan, X.; Tian, D. M.; Li, X. P.; Liu, M. H.; Li, H. B.; Stang, P. J; Alanine-based chiral metallogels via supramolecular coordination complex platforms: metallogelation induced chirality transfer, J. Am. Chem. Soc., 2018, 140, 3257. (+equal contribution)

5.Sun, Y.; Ding, F.; Zhou, Z.; Li, C.; Pu, M.; Xu, X.; Zhan, Y.; Lu, X.; Li, H.; Yang, G.; Sun, Y.; Stang, P. J. Rhomboidal Pt(II) metallacycle-based NIR-II theranostic nanoprobe for tumor diagnosis and image-guided therapy. Proc. Natl. Acad. Sci. USA. 2019, 116, 1968.

6.Wang, R.; Sun, Y.;* Zhang, F.; Song, M. M.; Tian, D. M.; Li, H. B.* Temperature-sensitive artificial channels through pillar[5]arene-based host–guest interactions. Angew. Chem. Int. Ed., 2017, 56, 5294. (*通讯编辑)

7.Tang, J. H.;+Sun, Y.;+Gong, Z. L.; Li, Z. Y.; Zhou, Z. X.; Wang, H.; Li, X. P.; Saha, M. L.; Zhong, Y. W.; Stang, P. J. Temperature-responsive fluorescent organoplatinum(II) metallacycles, J. Am. Chem. Soc., 2018, 140, 7723. (+equal contribution)

8.Tang, J. H.; Ni, R.; He, Y. Q.; Vanderlinden, R. T.; Li, Y.; Shi, B.; Li, Z. Y.; Wang, H.;* Li, X.; Sun, Y.;* Zhong, Y. W.;* Stang, P. J.* Metal–Organic Pt(II) Hexagonal-Prism Macrocycles and Their Photophysical Properties. Inorg. Chem. 2019, 58, 13376. (*通讯编辑)

9.Sun, Y.;Mei, Y. X.; Quan, J. X.; Xiao, X.; Zhang, L.; Tian, D. M.; Li, H. B. The macroscopic wettable surface: fabricated by calix[4]arene-based host–guest interaction and chiral discrimination of glucose. Chem. Commun., 2016, 52, 14416.

10.Sun, Y.; Mei, Y. X.; Quan, J. X.; Xiao, X.; Zhang, L.; Tian, D. M.; Li, H. B. Macroscopic switches constructed through host–guest chemistry, Chem. Commun., 2016, 52, 4602.

11.Sun, Y.;Zhao, H. Y.; Boussouar, I.; Zhang, F.; Tian, D. M.; Li, H. B. Highly sensitive chiral sensing by calix[4]arene-modified silver nanoparticles via dynamic light scattering,Sensors and Actuators B: Chemical., 2015, 216, 235.

12.Sun, Y.; Mao, X. W.; Luo, L.; Tian, D. M.; Li, H. B. Calix[4]arene triazole-linked pyrene: click synthesis, assembly on graphene oxide, and highly sensitive carbaryl sensing in serum,Org. Biomol. Chem.,2015, 13, 9294.

13.Sun, Y.;Yan, M. Q.; Liu, Y.; Lian, Z. Y.; Meng, T.; Liu, S-H.; Chen, J.; Yu, G-A. Phenylphosphinacalix[3]trifuran: synthesis, coordination and application in the Suzuki-Miyaura cross-coupling reaction in water, RSC Adv., 2015, 5, 71437.

14.Sun, Y.; Zhang, F.; Zhang, L.; Luo, L.; Zou, Z-L.; Cao, X. L.; Tan, S. L.; Bi, J. H.; Tian, D. M; Li, H. B. Synthesis of calix[4]arene derivatives via a Pd-catalyzed sonogashira reaction and their recognition properties towards phenols, Chinese Chemical Letters., 2014, 25, 226.

15.Zhang, F.; Sun, Y.; Tian, D. M.; Li, H. B. Chiral Selective Transport of Proteins by Cysteine-Enantiomer-Modified Nanopores, Angew Chem. Int. Ed. 2017, 56, 7186.

16.Zhang, F.; Sun, Y.;Tian, D. M.; Shin, W. S.; Kim, J. S.; Li, H. B. Selective molecular recognition on calixarene-functionalized 3D surfaces,Chem. Commun., 2016, 52, 12685.


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