Time-resolved EPR investigation of [70]fulleropyrrolidine nitroxide isomers

被引:12
|
作者
Conti, Fosca [1 ]
Corvaja, Carlo [1 ]
Busolo, Filippo [1 ]
Zordan, Giovanni [1 ]
Maggini, Michele [1 ]
Weber, Stefan [2 ]
机构
[1] Univ Padua, Dipartimento Sci Chim, I-35131 Padua, Italy
[2] Univ Freiburg, Inst Phys Chem, D-79104 Freiburg, Germany
关键词
RADICAL-TRIPLET PAIR; ELECTRON-PARAMAGNETIC-RESONANCE; SPIN POLARIZATION; EXCITED-STATES; FULLERENE DERIVATIVES; EXCHANGE INTERACTION; 1ST OBSERVATION; 95; GHZ; C-60; QUARTET;
D O I
10.1039/b813238k
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
A novel [70]fulleropyrrolidine functionalized with a nitroxide radical has been synthesized. After pulsed photoexcitation, time-resolved electron paramagnetic resonance (EPR) spectra have been recorded in liquid solution at standard X-band (9.5 GHz) and W-band (95 GHz) microwave frequencies. The spectra exhibit strongly electron spin polarized ground and excited states, the latter being arising from the spin coupling of the nitroxide's electron spin with the fullerene's excited triplet state. The EPR parameters such as g-values and hyperfine coupling constants have been discussed in terms of the spin Hamiltonian for excited doublet, triplet and quartet states. On the basis of the strength of the exchange interaction between the fullerene triplet and the radical group, two, out of a possible four [70] fulleropyrrolidine isomeric monoadducts, have been characterized.
引用
收藏
页码:495 / 502
页数:8
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