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Syntheses and Crystal Structures of the Bromide-derivatized Lanthanoid(III) Ortho-Oxomolybdates(VI) LnBr[MoO4] (Ln = Pr, Nd, Sm, Gd– Lu)
Ist Teil von
Zeitschrift für Naturforschung. B, A journal of chemical sciences, 2013-06, Vol.68 (5), p.616-624
Ort / Verlag
Verlag der Zeitschrift für Naturforschung
Erscheinungsjahr
2013
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
The lanthanoid(III) bromide ortho-oxomolybdates(VI) LnBr[MoO
] (Ln = Pr, Nd, Sm, Gd - Lu) crystallize triclinically in the space group P1 (a=686 - 689, b=713 - 741, c=1066 - 1121 pm, a =103 - 106, b =107 - 108, g = 92 - 95°) with Z =4. The crystal structure contains two crystallographically distinguishable Ln
cations, each one with a coordination number of seven plus one. (Ln1)
is surrounded by three bromide and four plus one oxide anions, while for (Ln2)
just one bromide and six plus one oxide anions belong to the coordination sphere. Considering the smallest lanthanoids, however, the distances to the farthest anions increase so much that their contribution to the coordination spheres becomes negligible in both cases. The polyhedra around (Ln1)
are connected to each other via common edges, which consist of two crystallographically identical Br
anions (Br1). Furthermore, the common structure of the LnBr[MoO
] series contains two crystallographically different, discrete [MoO
ortho-oxomolybdate(VI) tetrahedra. Two plus one oxygen atoms of each [(Mo1)O
unit are used to interconnect the polyhedra around (Ln1)
and (Ln2)
together with one Br
anion (Br2). The connection between two polyhedra around (Ln2)
is generated exclusively by two plus one oxygen atoms of two [(Mo2)O
anions. The complete structural arrangement can be considered as a bundle of primitively packed
{LnBr[MoO
]} chains with two alternating motifs of linkage, which are running parallel along [012].