Synthesis and crystal structure of a novel double 1:11 series arsenotungstate: [Cu^I(phen)2]5H6[Sm(AsW11O39)2]·6H2O

A novel double 1:11 series arsenotungstate, [Cu^I(phen)2]5H6[Sm(AsW11O39)2]·6H2O (phen=1, 10-phenanthroline) was synthesized by the hydrothermal method and characterized by elemental analysis, 1R spectra, and single-crystal X-ray diffraction. The title compound was monoclinic, space group P2 1/c, a=...

Full description

Saved in:
Bibliographic Details
Published inJournal of rare earths Vol. 26; no. 5; pp. 638 - 642
Main Author 王敬平 王伟 燕庆霞 牛景杨
Format Journal Article
LanguageEnglish
Published Institute of Molecalar and Crystal Engineering,School of Chemistry and Chemical Engineering,Henan University,Kaifeng 475004,China 01.10.2008
Subjects
Online AccessGet full text
ISSN1002-0721
2509-4963
DOI10.1016/S1002-0721(08)60152-0

Cover

More Information
Summary:A novel double 1:11 series arsenotungstate, [Cu^I(phen)2]5H6[Sm(AsW11O39)2]·6H2O (phen=1, 10-phenanthroline) was synthesized by the hydrothermal method and characterized by elemental analysis, 1R spectra, and single-crystal X-ray diffraction. The title compound was monoclinic, space group P2 1/c, a=3.75710(2) nm, b=1.39776(8) nm, c=-3.33735(18) nm, β=96.967(10)°, V=17.3969(17) nm^3, Z=4. Single crystal X-ray structural analyses revealed that the dimeric polyanion, [SmAs2W22O78]^1-, consisted of one central Sm^3+ ion and two tetradentate heteropoly ligands [ASW11O39]^7-. The Sm^3+ ion and two tetradentate defective [AsW11O39]^7- anions were joined together by the sharing of four oxygen atoms from each heteropoly ligand. The bond valence sum (BVS) calculations of the title compound suggested that all four Cu atoms were in the +1 oxidation sate.
Bibliography:11-2788/TF
hydrothermal synthesis
double 1:11 series
crystal structure
O616
hydrothermal synthesis; crystal structure; arsenotungstate; double 1:11 series; rare earths
arsenotungstate
rare earths
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:1002-0721
2509-4963
DOI:10.1016/S1002-0721(08)60152-0