ChemInform Abstract: Solvothermal Syntheses, and Characterization of [Ln(en)4(SbSe4)] (Ln: Ce, Pr) and [Ln(en)4]SbSe4×0.5en (Ln: Eu, Gd, Er, Tm, Tb): The Effect of Lanthanide Contraction of the Crystal Structures of Lanthanide Selenidoantimonates(V).

ChemInform ◽  
2008 ◽  
Vol 39 (52) ◽  
Author(s):  
Dingxian Jia ◽  
Aimei Zhu ◽  
Qinyan Jin ◽  
Yong Zhang ◽  
Wenqing Jiang
2003 ◽  
Vol 18 (2) ◽  
pp. 128-134 ◽  
Author(s):  
A. Le Bail ◽  
A.-M. Mercier

The crystal structures of the chiolite-related room temperature phases α-Na5M3F14 (MIII=Cr,Fe,Ga) are determined. For all of them, the space group is P21/n, Z=2; a=10.5096(3) Å, b=7.2253(2) Å, c=7.2713(2) Å, β=90.6753(7)° (M=Cr); a=10.4342(7) Å, b=7.3418(6) Å, c=7.4023(6) Å, β=90.799(5)° (M=Fe), and a=10.4052(1) Å, b=7.2251(1) Å, c=7.2689(1), β=90.6640(4)° (M=Ga). Rietveld refinements produce final RF factors 0.036, 0.033, and 0.035, and RWP factors, 0.125, 0.116, and 0.096, for MIII=Cr, Fe, and Ga, respectively. The MF6 polyhedra in the defective isolated perovskite-like layers deviate very few from perfect octahedra. Subtle octahedra tiltings lead to the symmetry decrease from the P4/mnc space group adopted by the Na5Al3F14 chiolite aristotype to the P21/n space group adopted by the title series. Facile twinning precluded till now the precise characterization of these compounds.


CrystEngComm ◽  
2009 ◽  
Vol 11 (11) ◽  
pp. 2431 ◽  
Author(s):  
Jonna Jokiniemi ◽  
Jouko Vepsäläinen ◽  
Harri Nätkinniemi ◽  
Sirpa Peräniemi ◽  
Markku Ahlgrén

2009 ◽  
Vol 182 (4) ◽  
pp. 913-919 ◽  
Author(s):  
Xin Wang ◽  
Tian-Lu Sheng ◽  
Sheng-Min Hu ◽  
Rui-Biao Fu ◽  
Jian-Shan Chen ◽  
...  
Keyword(s):  

2010 ◽  
Vol 40 (6) ◽  
pp. 496-500 ◽  
Author(s):  
Yong Zhang ◽  
Jian Zhou ◽  
Ai-Bin Tang ◽  
Guo-Qing Bian ◽  
Jie Dai

2013 ◽  
Vol 68 (2) ◽  
pp. 133-137 ◽  
Author(s):  
Jian Zhou ◽  
Xing Liu ◽  
Feilong Hu

Three new lanthanide thioantimonates(V) [Ln(en)(teta)(SbS4)] {Ln=Sm (1), Eu (2), Gd (3); en=ethylenediamine; teta=triethylenetetramine} have been solvothermally synthesized and structurally characterized. Compounds 1 - 3 are isostructural. The [SbS4]3- anion acting as bichelating ligand is bound to the [Ln(en)(teta)]3+ ion, resulting in a neutral complex [Ln(en)(teta)(SbS4)]. The central Ln3+ ion lies within an eight-coordinate environment forming a distorted bicapped trigonal prism LnN6S2. Although a few lanthanide thioantimonates have been reported to date, they only contain one type of ethylene polyamine. Compounds 1 - 3 are rare examples of lanthanide thioantimonates with mixed ethylene polyamine ligands. The absorption edges of 1:75 eV for 1 and 2:27 eV for 3 have been derived from optical absorption spectra.


2014 ◽  
Vol 43 (46) ◽  
pp. 17352-17357 ◽  
Author(s):  
Xihong He ◽  
Guoxin Tian ◽  
Jing Chen ◽  
Linfeng Rao

Dialkyldithiophosphinate forms different extracted Ln(iii) complexes across the lanthanide series not following the trend of lanthanide contraction.


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