Nondissociative electron capture by disulfide bonds

被引:44
作者
Carles, S
Lecomte, F
Schermann, JP
Desfrançois, C
Xu, S
Nilles, JM
Bowen, KH
Bergès, J
Houée-Levin, C
机构
[1] Univ Paris 13, UMR 7538 CNRS, Phys Lasers Lab, F-93430 Villetaneuse, France
[2] Univ Paris 11, UMR 8600 CNRS, Chim Phys Lab, F-91405 Orsay, France
[3] Univ Paris 06, UMR 7616 CNRS, Chim Theor Lab, F-75005 Paris, France
[4] Johns Hopkins Univ, Dept Chem, Baltimore, MD 21218 USA
关键词
D O I
10.1021/jp0040603
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
By means of Rydberg electron-transfer spectroscopy (RETS), negative ion photoelectron spectroscopy (NIPES), and quantum chemistry calculations, we have studied electron attachment properties of a series of saturated disulfides: dimethyl disulfide, diethyl disulfide, and dipropyl disulfide. Both RETS and NIPES experiments show that the valence anions of these disulfides are stable. RETS further shows that these negative ions result from attachment of nonzero energy electrons (0.2 eV), in contrast to dimers and larger complexes. NIPES experiments provide vertical detachment energies for the three disulfide monomer anions along with their Franck-Condon profiles. Fitting these spectra, using model potentials for the S-S stretch coordinate, finds that the adiabatic electron affinities of these disulfides are positive but rather small, about 0.1 eV. These experimental data compare well with the results of ab initio calculations, performed-at the MP2 level with large basis sets.
引用
收藏
页码:5622 / 5626
页数:5
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