1.0-2.0 ppm due to the methylene and methine protons, and B singlet at 3.14 ppm due to the methoxy group. Heating of ethoxybenzene with HGeCI3 for 0.5 h at 110 to 1 3 0 ' C and subsequent methylation lead to t h e ethoxy derivatives corresponding to (3). I t is remarkable that the reaction of alkoxy
CsUV3O11, a New Uranyl Vanadate with a Layered Structure
β Scribed by I. Duribreux; C. Dion; F. Abraham; M. Saadi
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 227 KB
- Volume
- 146
- Category
- Article
- ISSN
- 0022-4596
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β¦ Synopsis
A new cesium uranyl vanadate CsUV 3 O 11 has been synthesized by solid state reaction. Its crystal structure has been determined from single-crystal X-ray di4raction data. It crystallizes in the monoclinic system with space group P2 1 /a and unit cell parameters a β«Ψβ¬ 11.904(2) A s , b β«Ψβ¬ 6.8321(6) A s , c β«Ψβ¬ 12.095(2) A s , β«Ψβ¬ 106.989(5)3, Z β«Ψβ¬ 4, and D exp β«Ψβ¬ 4.89(2) g/cm 3 . A full-matrix least squares re5nement yielded R β«Ψβ¬ 0.046 and R w β«Ψβ¬ 0.045 for 1831 independent re6ections with I > 3 (I) collected on a Nonius CAD4 di4ractometer (MoK radiation). The structure of CsUV 3 O 11 is characterized by [UV 3 O 11 ] layers parallel to the (001) plane. The layers, very similar to those found in UV 3 O 10 , are built up from VO 5 square pyramids sharing corners of their equatorial bases and UO 8 hexagonal bipyramids, the U atoms occupying the hexagonal holes created by the VO 5 array. The Cs Ψ ions are located between two successive layers and hold them together; the Cs Ψ ions and two layers constitute a neutral 99sandwich::
In this unusual structure, the neutral sandwiches are stacked one above another along the [104] direction with no formal chemical bonds between the neutral sandwiches. The Cs mobilities in CsUV 3 O 11 and Cs carnotite are compared.
π SIMILAR VOLUMES
Two new alkali uranyl vanadates, M 6 (UO 2 ) 5 (VO 4 ) 2 O 5 with M β«Ψβ¬ Na, K, have been synthesized by solid state reactions and their structures determined from single-crystal X-ray di4raction data. They crystallize in the monoclinic system with space group P2 1 /c. Unit cell b, c, and parameters
## Abstract The title compound is synthesized by calcination of an equimolar mixture of FeVO~4~ and Pb~2~V~2~O~7~ and characterized by magnetization measurements and EPR spectroscopy.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
A new layered cuprate Pb 2 Sr 2 Cu 2 TaO 8 Cl has been successfully synthesized and identified by X-ray diffraction analysis. The compound crystallizes in the hematophanite structure with the space group P4/mmm. The lattice parameters of a β«Ψβ¬ 3.8921(1) A s s and c β«Ψβ¬ 15.3835(4) A s s were obtained