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ID 37972
本文ファイル
著者
Muraoka, Azusa
Hammer, Nathan I.
Shin, Joong-Won
Johnson, Mark A.
Nagata, Takashi
キーワード
Infrared photodissociation spectroscopy
cluster anions
structural evolution
hydration
NDC
化学
抄録(英)
The [(CO2)n(H2O)]- cluster anions are studied using infrared photodissociation (IPD) spectroscopy in the 2800-3800 cm-1 range. The observed IPD spectra display a drastic change in the vibrational band features at n = 4, indicating a sharp discontinuity in the structural evolution of the monohydrated cluster anions. The n = 2 and 3 spectra are composed of a series of sharp bands around 3600 cm-1, which are assignable to the stretching vibrations of H2O bound to C2O4- in a double ionic hydrogen-bonding (DIHB) configuration, as was previously discussed [J. Chem. Phys., 122, 094303 (2005)]. In the n ≥ 4 spectrum, a pair of intense bands additionally appears at ≈3300 cm-1. With the aid of ab initio calculations at the MP2/6-31+G* level, the 3300 cm-1 bands are assigned to the bending overtone and the hydrogen-bonded OH vibration of H2O bound to CO2- via a single O-H・・・O linkage. Thus, the structures of [(CO2)n(H2O)]- evolve with cluster size such that DIHB to C2O4- is favored in the smaller clusters with n = 2 and 3 whereas CO2- is preferentially stabilized via the formation of a single ionic hydrogen-bonding (SIHB) configuration in the larger clusters with n ≥ 4.
内容記述
This is a preprint of an article published by American Chemical Society in Journal of Physical Chemistry A, 2009, available online: http://pubs.acs.org/doi/abs/10.1021/jp903578e.
掲載誌名
Journal of Physical Chemistry A
113巻
31号
開始ページ
8942
終了ページ
8948
出版年月日
2009-08-06
出版者
American Chemical Society
ISSN
1089-5639
出版者DOI
PubMedID
言語
英語
NII資源タイプ
学術雑誌論文
広大資料タイプ
学術雑誌論文
DCMIタイプ
text
フォーマット
application/pdf
著者版フラグ
author
権利情報
Copyright (c) 2009 American Chemical Society
関連情報URL(IsVersionOf)
http://dx.doi.org/10.1021/jp903578e
部局名
理学研究科