1966
DOI: 10.1002/anie.196601342
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Tri(cyclopentadienyl)americium(III)

Abstract: inclined towards [loo] at 138 + 5 ' . The calculation shows a very small deviation from the plane (010) (about 5 O in the direction [OlO]) and an inclination towards [loo] of 140 3~ 5 '.With ro = 0.98 A, (XYZ)H = 0.75, 0.18, 0.61. Results for a-KNH2 agree with the assumptions of Juza and collaborators 191. It thus appears that a direct relation exists for crystalline hydroxo compounds between the course of the electrostatic equipotential lines near the proton-carrying particles and the positions of the proton… Show more

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Cited by 30 publications
(14 citation statements)
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“…Synthesis and chemical properties 243 Am(III) triscyclopentadienide was prepared using the procedure described by BAUMGÄRTNER et al [3] for the synthesis of the 241 3 do not exhibit any difference in sensitivity to air and oxygen or in their decomposition by water or dilute acid, which is accompanied by gas evolution and the formation of pink Am 3+ solutions.…”
Section: Methodsmentioning
confidence: 99%
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“…Synthesis and chemical properties 243 Am(III) triscyclopentadienide was prepared using the procedure described by BAUMGÄRTNER et al [3] for the synthesis of the 241 3 do not exhibit any difference in sensitivity to air and oxygen or in their decomposition by water or dilute acid, which is accompanied by gas evolution and the formation of pink Am 3+ solutions.…”
Section: Methodsmentioning
confidence: 99%
“…2 mark the averaged molar susceptibility directly determined on powder samples with masses from 80 to 100 mg at a given temperature and corrected only for diamagnetic contribution [18] of the ligands and of the central ion(x diam for Am(C s Hs) 3 : 235 · 10" 6 e. m. u. / mole).…”
Section: Physical Chemical Propertiesmentioning
confidence: 99%
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“…Dropwise addition of aqueous Am 3þ (pH 4.5) to warm, slightly less than stoichiometric amounts of ammonium benzoylacetone yields pale-rose Am(C 10 H 6 F 3 O 2 ) 3 · 3H 2 O. Both compounds decompose in air at [1] (Asprey et al, , 1951(Asprey et al, , 1954b; [2] (Keller and Schreck, 1969); [3] (Karraker, 1975(Karraker, , 1977; [4] (Baumgärtner et al, 1966a(Baumgärtner et al, , 1977Kanellakopoulos et al, 1970Kanellakopoulos et al, , 1978Seaborg, 1972); [5] (Danford et al, 1970;Moore, 1970;Sakanoue and Amano, 1975); [6] (Lebedev et al, 1960b(Lebedev et al, , 1962); [7] (Burns and Danford, 1969;Danford et al, 1970;Bagnall, 1972;Sakanoue and Amano, 1975); [8] (Davydov et al, 1975); [9] (Keller et al, 1965a(Keller et al, , 1966; [10] (Eyring et al, 1952;Yakovlev and Kosyakov, 1958b;Lebedev et al, 1960a;Weigel et al, 1966;…”
Section: (D) Acetone Derivate Compoundsmentioning
confidence: 99%