Your browser doesn't support javascript.
loading
Several (4,4)- and (5,6,8)-connected lanthanide-organic frameworks: structures, luminescence and magnetic properties.
Zhao, Xiao-Qing; Liu, Xu-Hui; Zhao, Bin.
Afiliación
  • Zhao XQ; College of Life and Basic Sciences, Sichuan Agricultural University, Ya'an 625014, China.
Dalton Trans ; 42(41): 14786-93, 2013 Oct 01.
Article en En | MEDLINE | ID: mdl-23985990
A series of lanthanide-based organic frameworks with formulas of {[PrL(H2O)2]·2H2O}n () and {[Ln3L3(H2O)2]·2H2O}n (Ln = Eu (), Gd (), Tb (), Dy (), Ho (), Er (); H3L = 4-(carboxymethoxy)isophthalic acid), were hydrothermally synthesized and structurally characterized. It is the first time that 4-(carboxymethoxy)isophthalic acid is employed in producing lanthanide compounds. The seven compounds exhibit two types of structures with the decreasing radius of the lanthanide ions, representing the lanthanide contraction effect. Compound with the large Pr(3+) ion displays a 2D layered structure with a binodal (4,4)-connected topology with the Schläfli symbol of (3(3)6(3))2, whereas compounds with small Ln(3+) ions feature a 3D framework constructed from carboxyl groups with a (5,6,8)-connected topology with the Schläfli symbol of (3(2)4(4)5(4))·(3(4)4(4)5(4)6(3))·(3(4)4(8)5(6)6(9)8). The luminescence and magnetic properties were investigated, and the results indicate that the H3L ligand can sensitize the lanthanide luminescence in compounds , and and makes a contribution to the antiferromagnetic interactions in compound or the uncertain magnetic interactions in compounds . Additionally, the thermal analyses suggest the high thermal stability of compounds .

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Dalton Trans Asunto de la revista: QUIMICA Año: 2013 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Dalton Trans Asunto de la revista: QUIMICA Año: 2013 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido