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dc.creatorWeber, J. Mathiasen_US
dc.creatorSchneider, Holgeren_US
dc.date.accessioned2008-07-15T13:50:57Z
dc.date.available2008-07-15T13:50:57Z
dc.date.issued2008en_US
dc.identifier2008-RC-03en_US
dc.identifier.urihttp://hdl.handle.net/1811/33499
dc.descriptionAuthor Institution: JILA, NIST, and Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309en_US
dc.description.abstractWe present data on the microhydration environment of the SF$_6^-$ anion, which can serve as a prototype species to investigate the interaction of an extended negative charge distribution with water ligands. This is particularly interesting, given that there are few data on such large systems, while the hydration of small anions such as halides is already well understood. Our infrared spectra of the SF$_6^- \cdot$ (H$_2$O)$_n$ ($n = 1 - 3$) clusters suggest that the first two water molecules attach to the SF$_6^-$ anion via single ionic H bonds to the same F atom, while signatures of H-bonded networks occur only in the spectrum of the trihydrate. This is an unusual observation as water-water H bonding usually sets in already at the dihydrate level. In addition, we find the SF bond involved in hydrogen bonding considerably weakened upon attachment of the first two ligands, hinting at a possible mechanism for reactions of pre-formed hydrated SF$_6^-$ anions in collisions with water molecules observed in flow-tube experiments.en_US
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleINFRARED SPECTRA OF SF$_6^- \cdot$ (H$_2$O)$_n$ ($n = 1 - 3$): INCIPIENT REACTION AND DELAYED ONSET OF WATER NETWORK FORMATIONen_US
dc.typeArticleen_US


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