English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/98934
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:
Title

Structure and spectroscopy of the He2Cl2 van der Waals cluster

AuthorsHernández, Marta I. ; Halberstadt, Nadine; Sands, William D.; Janda, Kenneth C.
KeywordsCluster analysis
Cluster spectra
Dissociation
Electron spectroscopy
Molecular structure
Issue Date1-Nov-2000
PublisherAmerican Institute of Physics
CitationJournal of Chemical Physics, 113 (17) : 7252-7267 (2000)
AbstractThe rovibrational structure of the He2Cl2 van der Waals cluster in the X and B electronic states is studied by means of full imensional quantum-mechanical calculations. He2Cl2 is the smallest cluster containing helium for which rotationally state-resolved data are available and for which the effects of Bose statistics are important. The He2Cl2 wave functions exhibit quite large amplitude motions, particularly for the He–He bending mode @associated with the angle formed between the two He–~center of mass of Cl2) bonds#. The preferred geometry of the ground van der Waals state is planar, with the He–He axis perpendicular to the Cl2 axis. It is shown that a reduced dimension model for the He–He bending vibration together with a rigid structural model reproduces well the low-lying energy levels of the complex and allows us to assign proper statistical weights to the asymmetric top transitions of the B←X spectra. In particular, the symmetry under He exchange of the rigid rotor levels is shown to depend on the He–He bending evel. The observed excitation spectra are successfully simulated using the proposed model. The effective rigid structure that best reproduces the rotationally excited levels with a rigid rotor analysis is a distorted tetrahedron where the He–He angle is approximately 130°. This difference from the 180° most probable configuration is due to the complex dependence of the moments of inertia on the internal degrees of freedom for such a floppy molecule. Therefore, structural information obtained from observed spectra of this or similar clusters should be carefully analyzed to avoid reaching misleading conclusions. Fragmentation rates for He2Cl2(B,v510– 13) are, for the first time, extracted from experimental data, confirming that the dissociation process is mainly sequential. © 2000 American Institute of Physics.
Description16 p.
Publisher version (URL)http://dx.doi.org/10.1063/1.1313786
URIhttp://hdl.handle.net/10261/98934
DOI10.1063/1.1313786
ISSN0021-9606
Appears in Collections:(CFMAC-IFF) Artículos
Files in This Item:
File Description SizeFormat 
MIHernandez (1).pdf378,68 kBAdobe PDFThumbnail
View/Open
Show full item record
Review this work
 

Related articles:


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.