Facile Access to Novel [60]Fullerenyl Diethers and [60]Fullerene-Sugar Conjugates via Annulation of Diol Moieties

被引:31
作者
Zhai, Wen-Qiang [1 ,2 ]
Jiang, Sheng-Peng [1 ,2 ]
Peng, Ru-Fang [3 ]
Jin, Bo [3 ]
Wang, Guan-Wu [1 ,2 ,3 ]
机构
[1] Univ Sci & Technol China, CAS Key Lab Soft Matter Chem, iChEM Collaborat Innovat Ctr Chem Energy Mat, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Dept Chem, Hefei 230026, Anhui, Peoples R China
[3] Southwest Univ Sci & Technol, State Key Lab Cultivat Base Nonmet Composites & F, Mianyang 621010, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
PERCHLORATE-MEDIATED SYNTHESIS; CYCLOADDITION; FULLERENES; HETEROANNULATION; SULFONAMIDES; DERIVATIVES; CHEMISTRY; CHLORIDE; ESTERS; C-60;
D O I
10.1021/acs.orglett.5b00536
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A general and facile annulation of various diol motifs to [60]fullerene has been developed. This protocol can afford not only 6- to 10-membered-ring fullerenyl diethers in one step from simple acyclic diols but also directly couple [60]fullerene with a variety of structurally diverse sugars. The [60]fullerene-sugar conjugates formed do not require any linker moiety and maintain their inherent structural integrity. The electrochemistry of the fullerenyl diethers and [60]fullerene-sugar conjugates has also been investigated.
引用
收藏
页码:1862 / 1865
页数:4
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