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3-(4-Pyridyl)-acetylacetone - a fully featured substituted pyridine and a flexible linker for complex materials.

Authors :
Merkens, Carina
Truong, Khai-Nghi
Englert, Ulli
Source :
Acta Crystallographica Section B: Structural Science, Crystal Engineering & Materials. Aug2014, Vol. 70 Issue 4, p705-713. 9p.
Publication Year :
2014

Abstract

3-(4-Pyridyl)-acetylacetone (HacacPy) acts as a pyridine-type ligand towards Cd X2 ( X = Cl, Br, I). Chain polymers with six-coordinated metal cations are obtained from CdCl2 and with alternating five- and six-coordinated Cd centers from CdBr2. In either case, the formation of these compounds does not depend on the precise stoichiometry. In contrast, two different reaction products form with the heavier congener CdI2, namely a ligand-rich molecular complex CdI2(HacacPy)2 and a ligand-deficient one-dimensional polymer [CdI2(HacacPy)]1∞. Interconversion between these two iodo derivatives is possible via thermal degradation and mechanochemical synthesis. The acetylacetone moiety in HacacPy may be deprotonated and chelated to FeIII, and the resulting complex Fe(acacPy)3 reacts analogously to a bridging polypyridine ligand towards the same Cd halides as the molecule HacacPy itself. With CdCl2 and CdBr2, isomorphous chain polymers are obtained in which the Cd cations adopt distorted octahedral coordination and one of the peripheric pyridyl groups remains uncoordinated. With CdI2, the iron complex acts as a -Fe(acacPy)3 bridge between tetrahedral Cd centers and gives rise to a ladder structure. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20525192
Volume :
70
Issue :
4
Database :
Academic Search Index
Journal :
Acta Crystallographica Section B: Structural Science, Crystal Engineering & Materials
Publication Type :
Academic Journal
Accession number :
97320401
Full Text :
https://doi.org/10.1107/S2052520614006210