Spectroscopy and photophysics of C60H18 and C60H36

被引:50
作者
Bensasson, RV
Hill, TJ
Land, EJ
Leach, S
McGarvey, DJ
Truscott, TG
Ebenhoch, J
Gerst, M
Ruchardt, C
机构
[1] OBSERV PARIS, CNRS URA 812, DAMAP, F-92195 MEUDON, FRANCE
[2] INSERM U201, CNRS UA481, MUSEUM NATL HIST NAT, BIOPHYS LAB, F-75231 PARIS 05, FRANCE
[3] UNIV KEELE, DEPT CHEM, KEELE ST5 5BG, STAFFS, ENGLAND
[4] CHRISTIE HOSP NHS TRUST, PATERSON INST CANC RES, CRC, DEPT BIOPHYS CHEM, MANCHESTER M20 9BX, LANCS, ENGLAND
[5] UNIV FREIBURG, INST ORGAN CHEM & BIOCHEM, D-79014 FREIBURG, GERMANY
关键词
D O I
10.1016/S0301-0104(96)00343-6
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ground and triplet state spectroscopic and photophysical properties of C60H18 and C60H36 have been studied using the complementary techniques of nanosecond pulse radiolysis and laser flash photolysis to determine triplet-triplet (T-T) absorption spectra, triplet lifetimes, T-T molar absorption coefficients and triplet quantum yields, in particular for C60H18. The spectroscopic and photophysical properties of C60H18 are similar to those of an sp(2) network species such as C-60, whereas those of C60H36 resemble benzene. No T-T absorption was observed for C60H36 at lambda > 300 nm, so that its triplet state parameters could not be measured. The most probable assignment of the C60H36 samples studied, on the basis of vibrational and electronic spectra and structure, is to an S-6 symmetry isomer, but the lowest energy T and D-3d isomers are not entirely excluded, Our partially hydrogenated fullerene samples were prepared by a transfer hydrogenation method. Other preparation techniques may have produced other isomers of these species, thus accounting for some differences in reported spectroscopic results.
引用
收藏
页码:111 / 123
页数:13
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