| Literature DB >> 16704272 |
Takahiro Tsuchiya1, Kumiko Sato, Hiroki Kurihara, Takatsugu Wakahara, Tsukasa Nakahodo, Yutaka Maeda, Takeshi Akasaka, Kei Ohkubo, Shunich Fukuzumi, Tatsuhisa Kato, Naomi Mizorogi, Kaoru Kobayashi, Shigeru Nagase.
Abstract
Complexation of endohedral metallofullerene La@C(82)-A (1) with macrocyclic compounds, such as 1,4,7,10,13,16-hexaazacyclooctadecane (2), 1,4,7,10,13,16-hexamethyl-1,4,7,10,13,16-hexaazacyclooctadecane (3), mono-aza-18-crown-6 ether (4), 18-crown-6 ether (5), and p-tert-butylcalix[n]arenes (n = 4-8, 6-10), for the first time is examined. Among them, 1 forms a complex with azacrown ethers 2-4 while accompanying the electron transfer between them. This is characteristic of endohedral metallofullerene and caused by its low reduction potential. Activation energies, DeltaG(et), for the electron transfer from 2-4 to 1 are 4.6, 2.8, and 11 kcal/mol, respectively. These small DeltaG(et) values indicate that the electron transfer from the azacrown ethers to 1 is facile in the ground state. Furthermore, the selective isolation of lanthanum endohedral metallofullerenes from the extracts of soot is accomplished by utilizing the complexation of 1 with 2.Entities:
Year: 2006 PMID: 16704272 DOI: 10.1021/ja0608390
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419