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Quantitative Aspects of Gas-Phase Metal Ion Chemistry: Conservation of Spin, Participation of f Orbitals, and C-H Activation and C-C Coupling
被引:0
|作者:
Armentrout, P. B.
[1
]
机构:
[1] Univ Utah, Dept Chem, Salt Lake City, UT 84112 USA
基金:
美国国家科学基金会;
关键词:
COLLISION-INDUCED DISSOCIATION;
STATE-SPECIFIC REACTIONS;
KINETIC-ENERGY DEPENDENCE;
MOLECULE REACTIONS;
ELECTRONIC-ENERGY;
PLUS O;
METHANE ACTIVATION;
CHARGE-TRANSFER;
BOND-ENERGIES;
UNIMOLECULAR REACTIONS;
D O I:
10.1021/acs.jpca.3c06023
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:
In this Featured Article, I reflect on over 40 years of guided ion beam tandem mass spectrometry (GIBMS) studies involving atomic metal cations and their clusters throughout the periodic table. Studies that have considered the role of spin conservation (or lack thereof) are a primary focus with a quantitative assessment of the effects examined. A need for state-specific studies of heavier elements is noted, as is a more quantitative assessment of spin-orbit interactions in reactivity. Because GIBMS experiments explicitly evaluate the kinetic energy dependence of reactions over a wide range, several interesting and unusual observations are highlighted. More detailed studies of such unusual reaction events would be welcome. Activation of C-H bonds and ensuing C-C coupling events are reviewed, with future work encouraged. Finally, studies of lanthanides and actinides are examined with an eye on understanding the role of f orbitals in the chemistry, both as participants (or not) in the bonding and as sources/sinks of electron density. This area seems to be ripe for more quantitative experiments.
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页码:9641 / 9653
页数:13
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