Show simple item record

dc.creatorDecius, J. C.en_US
dc.date.accessioned2006-06-15T12:45:27Z
dc.date.available2006-06-15T12:45:27Z
dc.date.issued1955en_US
dc.identifier1955-K-2en_US
dc.identifier.urihttp://hdl.handle.net/1811/7400
dc.descriptionAuthor Institution: Department of Chemistry, Oregon State Collegeen_US
dc.description.abstractVaritation of the $C^{12} - C^{13}$ ratio in carbonates of the aragonite lattice leads to fine structure in the 12$\mu$ region whose spacing and qualitative intensity can be fitted satisfactorily by the introduction of a nearest neighbor coupling constant in the potential energy. The coupling constant is believed to arise from dipole-dipole forces. From the coupling constant the value of the CO bond moment is found to be $1.52 \pm 0.1$ debyes in $BaCO_{3}$, $1.56 \pm 0.1$ debyes in $SrCO_{3}$. The coupling is so large in $CaCO_{3}$ (on account of the inverse cube dependence upon interdipole distance) that the perturbation theory cannot be applied without modification.en_US
dc.format.extent66652 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleCO BOND MOMENT IN THE CARBONATE IONen_US
dc.typearticleen_US


Files in this item

Thumbnail

Items in Knowledge Bank are protected by copyright, with all rights reserved, unless otherwise indicated.

This item appears in the following Collection(s)

Show simple item record