Weil Matthias
Institute for Chemical Technologies and Analytics, Division of Structural Chemistry, Vienna University of Technology, Getreidemarkt 9/164-SC, A-1060 Vienna, Austria.
Acta Crystallogr E Crystallogr Commun. 2017 May 16;73(Pt 6):853-855. doi: 10.1107/S2056989017006995. eCollection 2017 Jun 1.
Reaction of chromium(III) precursors with TeO in PbF/PbO melts in air led to oxidation of chromium(III) to chromium(VI), whereas tellurium remained its oxidation state of IV. In the resulting title compound, Pb(CrO)(TeO), the two types of anions are isolated from each other, hence a double salt is formed. The two independent Pb cations exhibit coordination number nine under formation of very distorted coordination polyhedra [bond-length range = 2.363 (6)-3.276 (7) Å]. The oxochromate(VI) and oxotellurate(IV) anions have tetra-hedral and trigonal-pyramidal configurations, respectively. In the crystal structure, (001) layers of metal cations alternate with layers of TeO and CrO anions along [001], forming a three-dimensional framework structure. Pb(CrO)(TeO) is isotypic with its sulfate analogue Pb(SO)(TeO) and is comparatively discussed.
在空气中,铬(III)前体与TeO在PbF/PbO熔体中反应,导致铬(III)氧化为铬(VI),而碲保持其IV价氧化态。在所得的标题化合物Pb(CrO)(TeO)中,两种类型的阴离子彼此分离,因此形成了复盐。两个独立的Pb阳离子在形成非常扭曲的配位多面体时表现出配位数为9 [键长范围 = 2.363 (6)-3.276 (7) Å]。铬酸根(VI)和碲酸根(IV)阴离子分别具有四面体和三角锥构型。在晶体结构中,金属阳离子的(001)层沿[001]与TeO和CrO阴离子层交替,形成三维骨架结构。Pb(CrO)(TeO)与其硫酸盐类似物Pb(SO)(TeO)同型,并进行了比较讨论。