ENERGIES OF THE LOWEST SINGLET AND TRIPLET-STATES OF MOLECULAR DICATIONS DETERMINED USING O+ AND C+ ION DOUBLE-CHARGE-TRANSFER SPECTROSCOPY

被引:13
作者
REID, CJ
机构
[1] SERC Mass Spectrometry Service Centre, Chemistry Department, University College of Swansea, Swansea, SA2 8PP, Singleton Park
来源
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES | 1991年 / 110卷 / 03期
关键词
D O I
10.1016/0168-1176(91)80028-L
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
The potential for using O+ and C+ ions as projectiles in double-charge-transfer (DCT) spectroscopy has been investigated. Target-gas molecules of CO2, OCS and CS2 are shown to be double ionized into triplet states in reactions with ground-state O+ and C+ ions whereas the metastable ions in these beams populate singlet dication states. The superpositions of spectral peaks arising from these processes have allowed precise determinations to be made of the energy separations between lowest singlet and triplet states which are consistent with previous experimental and theoretical values. CH4 target gas was also studied, the vertical double ionization energy to the 3T1 state being found to be 38.3 +/- 0.4 eV and the separation between this state and the lowest singlet state 1E being 0.3 +/- 0.2 eV. Additional peaks observed in the DCT spectra of C+ (2P) ions have been tentatively attributed to spin-disallowed processes or to reactions involving radiative loss.
引用
收藏
页码:195 / 214
页数:20
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