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공공누리This item is licensed Korea Open Government License

dc.contributor.author
오데
dc.contributor.author
김광수
dc.contributor.author
민병진
dc.contributor.author
이식
dc.contributor.author
이한명
dc.date.accessioned
2019-08-28T07:40:23Z
dc.date.available
2019-08-28T07:40:23Z
dc.date.issued
2004-05-22
dc.identifier.issn
0021-9606
dc.identifier.uri
https://repository.kisti.re.kr/handle/10580/13572
dc.identifier.uri
http://www.ndsl.kr/ndsl/search/detail/article/articleSearchResultDetail.do?cn=NART21705534
dc.description.abstract
To understand the mechanism of aqueous acid dissociation, which plays a fundamental role in aqueous chemistry, the ionic dissociation of HX acids (X5F, Cl, Br, and I) in water clusters up to hexamer is examined using density functional theory and M?ªller.Plesset second-order perturbation methods ~MP2!. Further accurate analysis based on the coupled clusters theory with singles and doubles excitations agrees with the MP2 results. The equilibrium structures, binding energies, electronic properties, stretching frequencies, and rotational constants of HX(H2O)n and X2(H3O)1(H2O)n21 are calculated. The issociated structures of HF and HCl can be formed for n>4, while those of HBr and HI can be formed for n>3. Among these, the dissociated structures of HX (X5Cl, Br, and I) are more stable than the undissociated ones for n>4, while such cases for HF would require much more than six water molecules, in agreement with previous reports. The IR spectra of stable...
dc.language
eng
dc.relation.ispartofseries
The Journal of chemical physics
dc.title
Dissociation chemistry of hydrogen halides in water
dc.citation.endPage
9535
dc.citation.number
20
dc.citation.startPage
9524
dc.citation.volume
120
Appears in Collections:
7. KISTI 연구성과 > 학술지 발표논문
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