HYDROGEN BOND NETWORK ISOMERS OF THE WATER NONAMER AND DECAMER OBSERVED BY BROADBAND ROTATIONAL SPECTROSCOPY

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Date

2013

Authors

Perez, Cristobal
Zaleski, Daniel P.
Seifert, Nathan A.
Pate, Brooks H.
Kisiel, Zbigniew
Temelso, Berhane
Shields, George C.

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Ohio State University

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Abstract

After our previous study of the rotational spectrum of water clusters in the 6-18 GHz region, in order to study clusters of larger size ($>8watermolecules),achirpedpulseFouriertransformmicrowavespectrometerinthe2−8GHzfrequencyrangehasbeenusedtoobtainthebroadbandrotationalspectraoffivewaternonamerisomersandfourwaterdecamerisomersinapulsedmolecularbeam.TheoxygenatomframeworkgeometriesforthreenonamersandtwodecamershavealsobeenunambiguouslyidentifiedfromisotopiclabelingmeasurementsusinganH{2}$$^{18}Oenrichedsample.Threeofthefourobservedwaterdecamershowtunnelingeffectassociatedwiththeinternaldynamicsofhydrogenbondnetworkinasimilarfashionastheprismwaterhexamer.ThesetunnelingpathsarequencheduponasingleincorporationofaH{2}$$^{18}Omoleculeinthecluster.DuethelargeamountofcloselyspacedrotationaltransitionsintheH_{2}$$^{18}$O spectrum, automated fitting tools were employed to extract the corresponding rotational spectra, which will be also briefly described.

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Author Institution: Department of Chemistry, University of Virginia, McCormick Rd.; Charlottesville, VA 22904-4319; Institute of Physics, Polish Academy of Sciences, Al. Lotnikow 32/46, 02-668 Warszawa, Poland; Dean's Office, College of Arts and Sciences, and Department of Chemistry, Bucknell University, Lewisburg, PA 17837

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