Photodissociation spectroscopy of phenol dimer ion. Lack of resonance interaction between the aromatic rings
Use this link to cite this item : https://ir.lib.hiroshima-u.ac.jp/00038221
ID | 38221 |
file | |
creator |
Ohashi, Kazuhiko
Nishi, Nobuyuki
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NDC |
Chemistry
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abstract | Electronic spectra of a homo-molecular but inequivalent dimer ion, (C6H5OH)2+, are measured by photodissociation spectroscopy. A broad band appeared in the 340–440 nm region is characteristic of the C←X transition of a phenol ion chromophore, suggesting that the dimer ion consists of a phenol ion and a neutral phenol. No strong band is observed in the 450–1400 nm region, whereas other aromatic dimer ions usually show charge resonance bands in near-infrared region. Owing to the geometrical constraint of an O–H・・・O hydrogen bond in (C6H5OH)2+, the two aromatic rings cannot be in a parallel configuration suitable for the resonance interaction.
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description | This is a postprint of an article published by Elsevier B.V. in Chemical Physics Letters, 1996, available online: http://doi.org/10.1016/0009-2614(96)00522-2
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journal title |
Chemical Physics Letters
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volume | Volume 257
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issue | Issue 1–2
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start page | 137
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end page | 142
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date of issued | 1996-07-19
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publisher | Elsevier B.V.
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issn | 0009-2614
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publisher doi | |
language |
eng
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nii type |
Journal Article
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HU type |
Journal Articles
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DCMI type | text
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format | application/pdf
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text version | author
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rights | Copyright (c) 1996 Elsevier Science B.V. All rights reserved
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relation is version of URL | http://doi.org/10.1016/0009-2614(96)00522-2
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department |
Graduate School of Science
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