1970
DOI: 10.1016/0375-9601(70)90538-4
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Paramagnetic resonance of F-type centres in photochromic sodalites

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Cited by 36 publications
(9 citation statements)
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“…1). Blue, yellow and strong pink colour centres in sodalite are tentatively attributed to sulphur species (McLaughlan and Marshall 1970;Hassib et al 1977) and pale pink colour in AF-07-35 is attributed to an F-centre (Pizani et al 1985). Samples were examined with a commercial mineralogical UV lamp with 'long' (UV-C) and 'short' wave (UV-B) settings.…”
Section: Methodsmentioning
confidence: 99%
“…1). Blue, yellow and strong pink colour centres in sodalite are tentatively attributed to sulphur species (McLaughlan and Marshall 1970;Hassib et al 1977) and pale pink colour in AF-07-35 is attributed to an F-centre (Pizani et al 1985). Samples were examined with a commercial mineralogical UV lamp with 'long' (UV-C) and 'short' wave (UV-B) settings.…”
Section: Methodsmentioning
confidence: 99%
“…This gives rise to a strong exchange coupling between unpaired electrons, which culminates in an antiferromagnetic transition at 48 K. Evidence for this was found in temperature-dependent NMR, EPR, and static susceptibility measurements presented below. We emphasize that unpaired electrons in Na 4 31 centers have predominantly an s character [10], therefore making SES, to the best of our knowledge, the first example of an s-electron antiferromagnet.…”
mentioning
confidence: 87%
“…For localized electrons, paramagnetic shifts may be due to isotropic Fermi contact interaction and/or dipole pseudocontact interaction. The dipolar shift in cubic SES vanishes because s-like electrons associated with tetrahedral Na 4 31 centers have only an isotropic g tensor [10]. This leaves the Fermi contact interaction as the only source of the observed shifts [15] whose magnitude is governed by [16] ͑DB͞B͒ contact 2͑A 0 ͞gm B g N ͒x e ͑T ͒ .…”
mentioning
confidence: 99%
“…In sodalite itself and most other sodalite-type phases with Cs(T16T26024)A2 stoichiometry, the T1,T2 tetrahedral cations are ordered and the symmetry is reduced to P43n. Na~(A16Ge6024)CI z and Nas(Ga6Si6024)CI 2 have been synthesized in powdered form by McLaughlan & Marshall (1970). Here, I report the synthesis and refinement of Nas(AI6Ge6024)Cl z, Nas(AI6Ge6024)Br z, and Nas(A16Ge6024)I z.…”
Section: Department Of Geology University Of Westernmentioning
confidence: 99%