Sun, Baoyun and Ren, Tongxiang and Miao, Xiaopei and Dai, Fucai and Jin, Long and Yuan, Hui and Xing, Gengmei and Li, Meixian and Dong, Jinquan and Chang, Fei and Hu, Jingbo and Chen, Hao and Zhao, Feng and Gao, Xueyun and Zhao, Yuliang (2008) Isomeric and structural impacts on electron acceptability of carbon cages in atom-bridged fullerene dimers. JOURNAL OF PHYSICAL CHEMISTRY C, 112 (3). pp. 741-746.
Full text is not hosted in this archive but may be available via the Official URL, or by requesting a copy from the corresponding author.
Official URL: http://pubs.acs.org/doi/abs/10.1021/jp0771217
The electrochemical properties of the carbon-bridged fullerene dimers C-121(I), C-121(II), C-121(III), C-131, and C-141 were characterized systematically for the first time in this study. Cyclic voltammogram and differential pulse voltammogram analyses revealed that they first underwent three reversible fullerene-unit-based reduction processes where each of the two carbon cages accepted one electron in each step and then possessed a different deep reduction sequence from the fourth to sixth reduction potentials of the fullerene cages. The electronic interactions between cages in the atom-bridged dimers (e.g., C-60-C-C-60) were found to be different from those of dimers in which two cages were connected directly. Comparison studies of the redox properties of the five dimers revealed that the C-60 dimerization via [5.6]-[6.6] connection influenced the cage electron acceptability much more than that of [5.6]-[5.6] or [6.6]-[6.6] connections And the dimerization with C-70 cages influenced the reduction potentials of dimerized products more potently than that with C-60 cages. Further results from controlled potential electrolysis, high-performance liquid chromatography, matrix-assisted laser desorption and ionization time-of-flight mass spectrometry, ultraviolet absorption spectral analyses demonstrated the reduction processes and a dissociation of the dimers based on reductions. The theoretical understanding of the experiments was investigated by using time-dependent density functional calculations for the ionic states Of C-121(I, II, III)(n-) with n = 0, 1, 2, 3, or 4.
|Subjects:||Physical Science > Nano objects|
Material Science > Nanostructured materials
Material Science > Nanochemistry
|Deposited By:||Farnush Anwar|
|Deposited On:||12 Jan 2009 17:36|
|Last Modified:||12 Jan 2009 17:36|
Repository Staff Only: item control page