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https://olympias.lib.uoi.gr/jspui/handle/123456789/16990Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Robertson, E. G. | en |
| dc.contributor.author | Martin, D. E. | en |
| dc.contributor.author | Thompson, C. D. | en |
| dc.contributor.author | Morrison, R. J. S. | en |
| dc.contributor.author | Philis, J. G. | en |
| dc.date.accessioned | 2015-11-24T18:34:46Z | - |
| dc.date.available | 2015-11-24T18:34:46Z | - |
| dc.identifier.issn | 0009-2614 | - |
| dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/16990 | - |
| dc.rights | Default Licence | - |
| dc.subject | 2-photon spectroscopy | en |
| dc.subject | aromatic-molecules | en |
| dc.subject | n-propylbenzene | en |
| dc.subject | gas-phase | en |
| dc.subject | alkylbenzenes | en |
| dc.subject | transition | en |
| dc.subject | phenylacetylene | en |
| dc.subject | ethylbenzene | en |
| dc.subject | benzenes | en |
| dc.subject | spectra | en |
| dc.title | Structure determination of sec-butylbenzene rotamers by UV spectroscopy and ab initio calculations | en |
| heal.type | journalArticle | - |
| heal.type.en | Journal article | en |
| heal.type.el | Άρθρο Περιοδικού | el |
| heal.identifier.primary | DOI 10.1016/j.cplett.2008.08.006 | - |
| heal.identifier.secondary | <Go to ISI>://000259150400004 | - |
| heal.identifier.secondary | http://ac.els-cdn.com/S0009261408010841/1-s2.0-S0009261408010841-main.pdf?_tid=58f66c07352fd2922450047fe40cbe13&acdnat=1334231904_b023043c37fc796a25603a782faee028 | - |
| heal.language | en | - |
| heal.access | campus | - |
| heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών και Τεχνολογιών. Τμήμα Βιολογικών Εφαρμογών και Τεχνολογιών | el |
| heal.publicationDate | 2008 | - |
| heal.abstract | Sec-butylbenzene has been investigated using resonant two-photon ionization (R2PI) and UV-UV hole-burning spectroscopy aided by ab initio calculations. All three conformers predicted from theory are observed in the spectrum, and are assigned by rotational band contour analysis. The most strongly populated conformer (G1) has a gauche arrangement of the side chain dihedral angle tau(2)(C(1)C(alpha)C(beta)C(gamma)). The populations of the anti (A) and the remaining gauche conformer (G2) are about 7% and 2%, respectively. The alpha methyl group is found to significantly affect the conformational preferences in sec-butylbenzene (sec-BB), compared to n-propylbenzene in which the anti conformer is favored. (c) 2008 Elsevier B.V. All rights reserved. | en |
| heal.journalName | Chemical Physics Letters | en |
| heal.journalType | peer reviewed | - |
| heal.fullTextAvailability | TRUE | - |
| Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Robertson-2008-Structure determinat.pdf | 334.26 kB | Adobe PDF | View/Open Request a copy |
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