A Comparison of NH52+ and CH5+ Ions and Deuterated Variants of NHxD(5− x)2+: Real or Artefactual Rotation?
- 作者: Monajjemi M.1
-
隶属关系:
- Department of Chemical Engineering, Central Tehran Branch
- 期: 卷 60, 编号 5 (2019)
- 页面: 713-726
- 栏目: Article
- URL: https://journals.rcsi.science/0022-4766/article/view/162107
- DOI: https://doi.org/10.1134/S0022476619050032
- ID: 162107
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详细
Protonated NH52+ has unusual vibrational and rotational behavior because its three nonequivalent equilibrium structures have nearly identical energies and its five protons scramble freely, while in the CH5+ structure, five hydrogen atoms are bonded to the carbon atom by sharing eight valence electrons. Although a few theoretical papers have been published on quantum mechanics of those systems. Better understanding requires spectral and conformational analyses. CASSCF (8, 9) calculations with the correlation consistent polarized valence double and triple zeta basis sets are accomplished for estimating the vibrational data and zero-point energies of those two ions. The present results indicate that normal modes agree qualitatively with NHxD(5-
x)2+ and one of the normal modes indicates that NH52+ is highly fluxional and has a complex spectrum while the broken N-H bonds are reformed all the time. The spectrum of mode 10 is highly complex with red and some blue shifts. In particular, modes 6 and 12 are attributed to the rapid coupling of the N-H stretching normal mode to motions more closely related to isomerization, i.e., bending or rocking. There have been long debates whether NH52+ has a structure at all or not and if the rotation is real or artefactual.
作者简介
M. Monajjemi
Department of Chemical Engineering, Central Tehran Branch
编辑信件的主要联系方式.
Email: Maj.monajjemi@iauctb.ac.ir
伊朗伊斯兰共和国, Tehran
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