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dc.creatorHarrison, James E.en_US
dc.creatorChristopher, Peter S.en_US
dc.date.accessioned2006-06-15T19:04:40Z
dc.date.available2006-06-15T19:04:40Z
dc.date.issued1998en_US
dc.identifier1998-RG-13en_US
dc.identifier.urihttp://hdl.handle.net/1811/18943
dc.descriptionAuthor Institution: Chemistry Department and Center for Fundamental Materials Research, Michigan State Universityen_US
dc.description.abstractWe will discuss the electronic structure of the ground and low-lying excited states of the titled transition metal hydrides. Of these $ScH^{++}, TiH^{++}$, and $VH^{++}$, are thermodynamically stable while $CrH^{++}$, and $MnH^{++}$ are expected to be very long lived. While the charge distribution for each molecule is approximately $M^{+1.85} H^{+0.15}$ the nature of the bonding changes very rapidly from a conventional sigma bond in $ScH^{++}$. We will discuss trends in $D_{e}$, bond lengths and vibrational frequencies and will compare with the corresponding neutral and monopositive hydrides.en_US
dc.format.extent87731 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleTHE ELECTRONIC STRUCTURE OF $ScH^{++}, TiH^{++}, VH^{++}, CrH^{++}$, AND $MnH^{++}$en_US
dc.typearticleen_US


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