the nanopowders of sno2, casno3 and ca2sno4 in the size rang of 5-70 nm have been prepared using solid-state reaction technique. the technique is convenient and inexpensive in comparison to the conventional routes of compound prepared and processing where, many steps of mixing and annealing are involved. formation of resultant compounds was explained on the basis of reaction taken place between...

The nanopowders of SnO2, CaSnO3 and Ca2SnO4 in the size rang of 5-70 nm have been prepared using solid-state reaction technique. The technique is convenient and inexpensive in comparison to the conventional routes of compound prepared and processing where, many steps of mixing and annealing are i...

The five-coordinate Sn atom in the title mixed organyl stannate compound, (C(12)H(24)N)[Sn(C(5)H(9))(C(6)H(5))(2)(C(2)ClF(2)O(2))], is in a trans-C(3)SnO(2) trigonal-bipyramidal coordination environment. The NH(2) groups of the cations act as hydrogen-bond donors to two symmetry-related anions, resulting in the formation of linear chains. One of the phenyl rings is disordered over two sites wit...

In the title mixed-organyl stannate, (C(12)H(24)N)[Sn(C(6)H(5))(2)(C(6)H(11))(CClF(2)O(2))(2)], there are two cations and two anions in the asymmetric unit. Each five-coordinate Sn atom shows trans-C(3)SnO(2) trigonal bipyramidal coordination. The four Sn-O distances are approximately equal in the two independent anions. Each ammonium cation serves as a hydrogen-bond donor to two stannates, the...

In the title salt, [(CH3CH2CH2)2NH2]4[Sn(C2O4)4]·H2O, the Sn(IV) atom of the stannate anion is located on a special position with -42m symmetry. It is eight-coordinated by four chelating oxalate anions. The di-propyl-ammonium cation possesses mirror symmetry while the lattice water mol-ecule is disordered about a position with -42m symmetry and has an occupancy of 0.25. In the crystal, the anio...

The Sn(IV) atom of the stannate anion in the title salt, (C(7)H(11)N(2))(2)[SnBr(4)(C(6)H(5))(2)], lies on a center of inversion in a tetra-gonally compressed octa-hedron. The two independent Br atoms in the anion are hydrogen-bond acceptors for the same cation.

We report density functional studies of electron rich interfaces between KTaO3 or KNbO3 and CaSnO3 or ZnSnO3 and in particular the nature of the interfacial electron gasses that can be formed. We find that depending on the details these may occur on either the transition metal or stannate sides of the interface and in the later case can be shifted away from the interface by ferroelectricity. We...

The cation and the anion in the title salt, (C(6)H(16)N)[SnCl(4)(C(6)H(4)NO(2))], are linked by an N-H⋯O hydrogen bond. The Sn(IV) atom in the stannate anion is chelated by the pyridine-2-carboxyl-ate group and exists in a cis-SnCl(4)NO octa-hedral geometry. The cation is disordered over two positions in a 0.564 (1):0.436 (1) ratio.

The Sn(IV) atom in the title ammonium stannate, (Et(3)NH)[Sn(C(5)H(3)N(2)O(2))Cl(4)], is chelated by an pyrazine-2-carboxyl-ate ligand and exists in a cis-SnCl(4)NO octa-hedral geometry. The cation and the anion are linked by an N-H⋯N hydrogen bond.