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高翔
单位:中国科学院长春应用化学研究所电分析化学国家重点实验室
地址:吉林省长春市人民大街5625号
邮编:130022
电话:86-431-85262946
个人主页: http://yjsb.ciac.jl.cn/daoshi_read.php?brow=59&lb=%B5%BC%CA%A6%BC%F2%BD%E9
实验室介绍:
 
个人简历 Personal resume
 
研究方向 Research direction
1、富勒烯化学
 
招生信息 Enrollment information
 
 
论文专著 The monograph
1) Methoxylation of Singly Bonded 1,4-1’,4’-BnC60-C60Bn Dimer: Preferential Formation of 1,4-C60 Adduct with Sterically Less Demanding Addends and Stability Difference between 1,2- and 1,4-OMe(Bn)C60 - J. Org. Chem. - 2016 - 81
2) Multifunctionalization of C70 at the two polar regions with a high regioselectivity via oxazolination and benzylation reactions - Chem. Commun. - 2016 - 52
3) Base-Promoted Oxidative Cycloaddition Reaction of [60]Fullerene with Ethyl Acetoacetate for C60 Bis-2’,3’-Dihydrofuran Derivatives: Effect of Bulky Addends - J. Org. Chem. - 2016 - 81
4) Base-Promoted Consecutive Enolate Addition Reaction of [60]Fullerene with Ketones - Org. Lett. - 2015 - 17
5) Vis-NIR Spectroscopic and DFT Study of Reduced Singly Bonded C60 Species - J. Phys. Chem. A - 2015 - 119
6) Preparation of a C70 Bis-heterocyclic Derivative with High Chemio- and Regioselectivity - J. Org. Chem. - 2015 - 80
7) Reductive Benzylation of Singly Bonded 1,2,4,15‒C60 Dimers with an Oxazoline or Imidazoline Heterocycle: Unexpected Formation of 1,2,3,16‒C60 Adducts and Insights into the Reactivity of Singly Bonded C60 Dimers - J. Org. Chem. - 2015 - 80
8) Electronic vs Steric Effect on the Stability of Anionic Species: A Case Study on the Ortho- and Para-regioisomers of Organofullerenes - J. Org. Chem. - 2015 - 80
9) Approach to High Open-circuit Voltage in Organic Solar Cells Utilizing Structural Change of Oxazolino-C70 Derivative - Chem.Eur.J. - 2015 - 21
10) Reductive Benzylation of C70 Imidazoline with a Bulky Addend - J. Org. Chem. - 2014 - 79
11) Reductive Benzylation of C60 Imidazoline with a Bulky Addend - Org. Lett. - 2014 - 16
12) Oxazoline and Imidazoline Functionalization of a C60 Dimer via the Reaction of C60HBn and Aromatic Nitriles with Bifunctional Hydroxide - J. Org. Chem. - 2014 - 79
 
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