Coordination Chemistry of the Calixarenes. II. Europium(III) and p-t-Butyl Calix[6]arene

Autor: Faye R. Wilner, Lutz M. Engelhardt, DL Kepert, A. H. White, John M. Harrowfield, B. M. Furphy
Rok vydání: 1988
Předmět:
Zdroj: Australian Journal of Chemistry. 41:1465
ISSN: 0004-9425
DOI: 10.1071/ch9881465
Popis: The possible nature of p-t-butyl-calix [6] arene complexes of lanthanide elements has been explored by determination of the single-crystal X-ray structure of a complex with a 1:2 europium/ ligand ratio, obtained from dimethylformamide (dmf ≡ Me2NCHO) solution. This complex is formulated as [ Eu (LH4)(Me2NCHO)6(OH)].LH6.~4Me2NCHO (LH6 = p-t-butyl-calix [6] arene) on the basis of the structure determination. Crystals are monoclinic, P21/n, a 36.11(3), b 23.35(2), c 21.85(2)Ǻ, β 97.46(6)°, Z = 4 formula units; R was 0.11 for 8488 'observed' reflections. The complex is remarkable in that the only interaction of either of the two calixarene ligands (one presumably doubly or triply deprotonated ) with the eight-coordinate europium atom is by way of one behaving as monodentate, the other having no interaction. Eu -O( calix ) is 2.35(1) Ǻ; Eu -O( dmf )6 range from 2.38(2) to 2.49(2)Ǻ, and Eu -O(H ½?) is 2.49(2)Ǻ.
Databáze: OpenAIRE