An H2O2 Molecule Stabilized inside Open-Cage C60 Derivatives by a Hydroxy Stopper

被引:7
|
作者
Huang, Guanglin [1 ]
Hasegawa, Shota [1 ]
Hashikawa, Yoshifumi [1 ]
Ide, Yuki [1 ]
Hirose, Takashi [1 ]
Murata, Yasujiro [1 ]
机构
[1] Kyoto Univ, Inst Chem Res, Uji, Kyoto 6110011, Japan
关键词
hydrogen bonding; hydrogen peroxide; intramolecular interaction; open-cage fullerene derivatives; peroxosolvates; PEROXIDE; WATER; EXPANSION; OXIDES;
D O I
10.1002/chem.202103836
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An H2O2 molecule was isolated inside hydroxylated open-cage fullerene derivatives by mixing an H2O2 solution with a precursor molecule followed by reduction of one of carbonyl groups on its orifice. Depending on the reduction site, two structural isomers for H2O2@open-fullerenes were obtained. A high encapsulation ratio of 81 % was attained at low temperature. The structures of the peroxosolvate complexes thus obtained were studied by H-1 NMR spectroscopy, X-ray analysis, and DFT calculations, showing strong hydrogen bonding between the encapsulated H2O2 and the hydroxy group located at the center of the orifice. This OH group was found to act as a kinetic stopper, and the formation of the hydrogen bonding caused thermodynamic stabilization of the H2O2 molecule, both of which prevent its escape from the cage. One of the peroxosolvates was isolated by HPLC, affording H2O2@open-fullerene with 100 % encapsulation ratio, likely due to the intramolecular hydrogen-bonding interaction.
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页数:5
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