phases of the main group metals remain largely unex-The first Sn(II)-organophosphonate solid phases have been plored. Consequently, while molecular clusters of the tinprepared and structurally characterized by single crystal X-ray organophosphonate system have been described (12) as diffraction. The
Room Temperature Synthesis and Structural Characterization of Sn(O3PCH2CH3): A Layered Phase of the Sn(II)-Organophosphonate System
β Scribed by Pamela J. Zapf; David J. Rose; Robert C. Haushalter; Jon Zubieta
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 300 KB
- Volume
- 132
- Category
- Article
- ISSN
- 0022-4596
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β¦ Synopsis
The title compound, Sn(O 3 PCH 2 CH 3 ), (1), was synthesized from a mixture of SnF 2 , CH 3 CH 2 PO 3 H 2 , and H 2 O in the mole ratio 1:0.85:1741 at 25Β°C for 1 h. Phosphonate (1) crystallizes in the orthorhombic space group Pbca with a β«Ψβ¬ 7.785(2), b β«Ψβ¬ 7.450(1), c β«Ψβ¬ 20.026(4) A s , V β«Ψβ¬ 1161.5(6) A s 3 , Z β«Ψβ¬ 8, and R β«Ψβ¬ 0.0797. The two-dimensional structure of ( 1) is composed of corner sharing {SnO 3 } pyramids and {O 3 PC} tetrahedra that alternate to form four-and eight-member polyhedral rings within the layers. The ethyl groups of the phosphonate tetrahedra are directed outward from both faces of the layer, effectively forming inorganic layers alternating with organic bilayers.
π SIMILAR VOLUMES
The title compound Cs[(VO) 2 (OH)(O 3 PCH 2 CH 2 PO 3 )] 1 was synthesized hydrothermally from a mixture of CsVO 3 , H 2 O 3 PCH 2 CH 2 PO 3 H 2 , and H 2 O in the mole ratio 1 : 1.22 : 535 and heated to 200Β°C for 48 hr. Phosphonate 1 is formed in 45% yield and crystallizes in the monoclinic space g
A new tin(II) phosphate, [NH 3 CH 2 CH(NH 3 )CH 3 ] 0.5 [Sn 4 P 3 O 12 ] ' H 2 O, was synthesized by hydrothermal technique. It crystallizes in monoclinic space group P2 1 /c (No. 14) with lattice parameters a β«Ψβ¬ 7.326(1) A s , b β«Ψβ¬ 23.614(3) A s , c β«Ψβ¬ 9.081(1) A s , β«Ψβ¬ 102.8(1)3, V β«Ψβ¬ 1532.1(
A new layered tin(II) phosphate [Sn 2 (PO 4 ) 2 ] 2Ψ [C 2 N 2 H 10 ] 2Ψ β’ H 2 O was synthesized by hydrothermal technique. It crystallizes in monoclinic space group P2 1 /c (No. 14) with lattice parameters a β«Ψβ¬ 9.4112(1) A s ; b β«Ψβ¬ 8.5998(1) A s ; c β«Ψβ¬ 15.9921(2) A s ; β«Ψβ¬ 100.009(1)Β°; V β«Ψβ¬ 12