1978
DOI: 10.1021/ic50184a005
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Magnetic and structural characterization of dibromo- and dichlorobis(thiazole)copper(II)

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Cited by 377 publications
(230 citation statements)
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“…2͑C͒. In both orientations one finds a behavior typical of one-dimensional systems showing a broad maximum around T Ϸ 28 K that can be nicely described by the Bonner-Fisher model as documented by a corresponding fit 30 depicted as solid black and grey lines for H ʈ b and H Ќ b, respectively. The deduced exchange coupling constants J NMR / k B are given in Table I and again confirm the values from the bulk susceptibility.…”
Section: Amentioning
confidence: 61%
See 1 more Smart Citation
“…2͑C͒. In both orientations one finds a behavior typical of one-dimensional systems showing a broad maximum around T Ϸ 28 K that can be nicely described by the Bonner-Fisher model as documented by a corresponding fit 30 depicted as solid black and grey lines for H ʈ b and H Ќ b, respectively. The deduced exchange coupling constants J NMR / k B are given in Table I and again confirm the values from the bulk susceptibility.…”
Section: Amentioning
confidence: 61%
“…For both orientations the lineshift K͑T͒ nicely follows the Bonner-Fisher-type behavior 29 for the bulk susceptibility bulk ͑T͒ of an antiferromagnetic spin chain as indicated by the solid line. This line is a fit using the rational function given by Estes et al 30 The coupling constants J NMR / k B deduced from these fits are summarized in Table I for 7 Li NMR for comparison with the respective values of the bulk susceptibility. We note that the strong anisotropy of the 7 Li lineshift seems to be intimately connected with the crystallographic arrangement of the Li + ions on nonmagnetic chains.…”
Section: Amentioning
confidence: 99%
“…The closed-form solution to the BF model, eq 2, is given by Estes et al 46 where x=|ℑ|/k B T, and g=2.000…”
Section: Cp* 2 Yb(dad(h)-t-bu)mentioning
confidence: 99%
“…accordance with the fact that chelation increases the activity. e chelation reduces the polarity [24,25] of the metal ion, mainly, because of the partial sharing of its positive charge with the donor groups and possibly the -electron delocalization within the whole chelate ring [26][27][28]. is process of chelation thus increases the lipophilic nature of the central metal atom, which in turn favours its permeation through the lipid layer of the membrane [29][30][31].…”
Section: 3mentioning
confidence: 99%