Intact Four-atom Organic Tetracation Stabilized by Charge Localization in the Gas Phase

被引:10
|
作者
Yatsuhashi, Tomoyuki [1 ,2 ]
Toyota, Kazuo [1 ]
Mitsubayashi, Naoya [1 ]
Kozaki, Masatoshi [1 ]
Okada, Keiji [1 ]
Nakashima, Nobuaki [1 ]
机构
[1] Osaka City Univ, Grad Sch Sci, Sumiyoshi Ku, 3-3-138 Sugimoto, Osaka 5588585, Japan
[2] Japan Sci & Technol Agcy, PRESTO, 4-1-8 Honcho, Kawaguchi, Saitama 3320012, Japan
关键词
active species; density functional calculations; laser chemistry; polycations; tunneling; COULOMB EXPLOSION; MOLECULAR-IONS; IONIZATION; SPECTROSCOPY; SPECTRUM; CATIONS; C2H22+;
D O I
10.1002/cphc.201600555
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
Several features distinguish intact multiply charged molecular cations (MMCs) from other species such as monocations and polycations: high potential energy, high electron affinity, a high density of electronic states with various spin multiplicities, and charge-dependent reactions. However, repulsive Coulombic interactions make MMCs quite unstable, and hence small organic MMCs are currently not readily available. Herein, we report that the isolated four-atom molecule diiodoacetylene survives after the removal of four electrons via tunneling. We show that the tetracation remains metastable towards dissociation because of the localization (91-95%) of the positive charges on the terminal iodine atoms, ensuring minimum Coulomb repulsion between adjacent atoms as well as maximum charge-induced attractive dipole interactions between iodine and carbon. Our approach making use of iodines as the positively charged sites enables small organic MMCs to remain intact.
引用
收藏
页码:2977 / 2981
页数:5
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