89 research outputs found
Laser-induced splittings in the nuclear magnetic resonance spectra of the rare gases
Circularly polarized laser field causes a shift in the nuclear magnetic
resonance (NMR) spectra of all substances. The shift is proportional to the
intensity of the laser beam and yields oppositely signed values for left- and
right-circularly polarized light, CPL -/+, respectively. Rapid switching -- in
the NMR time scale -- between CPL+ and CPL- gives rise to a splitting of the
NMR resonance lines. We present uncorrelated and correlated quadratic response
calculations of the splitting per unit of beam intensity in the NMR spectra of
Ne, Kr, and Xe. We study both the regions far away from
and near to optical resonance and predict off-resonance shifts of the order
0.01, 0.1, and Hz for Ne, Kr, and Xe,
respectively, for a beam intensity of 10 W/cm. Enhancement by several
orders of magnitude is predicted as the beam frequency approaches resonance.
Only then can the effect on guest Xe atoms be potentially useful as a
probe of the properties of the host material.Comment: 5 pages, 1 figur
SynthÚse et caractérisation de nouveaux catalyseurs mésoporeux structurés mono et bifonctionnels : Ti-SBA15 et Ti-AISBA15 (application à l'époxydation des oléfines et à la synthÚse directe de l'acide adipique)
PARIS-BIUSJ-ThĂšses (751052125) / SudocPARIS-BIUSJ-Physique recherche (751052113) / SudocSudocFranceF
Les empreintes sectorielles en prothĂšse conjointe (description des techniques actuelles)
CLERMONT FD-BCIU Odontol. (631132226) / SudocCLERMONT FD-BCIU-Santé (631132104) / SudocPARIS-BIUM (751062103) / SudocSudocFranceF
NMR chemical shifts of molecules physisorbed on two distinct sites
We propose methods for determining the chemical shifts of molecules physically adsorbed on two fairly different sites when these species are in fast exchange. As example we study the adsorption of xenon on Na36 Ni10Y zeolite
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1ST LOW-TEMPERATURE N-15 NUCLEAR-MAGNETIC-RESONANCE STUDY OF NITROGEN PHYSISORPTION CONDENSATION IN MICROPOROUS SOLIDS
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