One-dimensional Zn(II) oligo(phenyleneethynylene)dicarboxylate coordination polymers

Synthesis, crystal structures, thermal and photoluminescent properties

verfasst von
Andreas Schaate, Miriam Schulte, Michael Wiebcke, Adelheid Godt, Peter Behrens
Abstract

The rigid, π-conjugated dicarboxylic acid 1,4-bis-[2-(4-carboxyphenyl)ethynyl]-2,5-dihexylbenzene {HO2C[PEP(hexyl)2EP]CO2H} has been used to synthesise the new crystalline coordination polymers {Zn(O2C[PEP(hexyl)2EP]CO2)(DMF)2} (1) and {Zn(O2C[PEP(hexyl)2EP]CO2)(DEF)2} (2) in N,N-dimethylformamide (DMF) and N,N-diethylformamide (DEF), respectively, under mild conditions. Single-crystal X-ray crystallography revealed that 1 and 2 are isostructural and consist of uncharged zigzag coordination chains in which [Zn(formamide)2]2+ fragments are bridged by (O2C[PEP(hexyl)2EP]CO2)2- ligands. The zigzag chains possess different intra-chain Zn⋯Zn⋯Zn angles due to the different volumes of the coordinating formamide molecules and subtle differences in the hydrophobic inter-chain interactions. Upon heating 1 and 2 to 200 °C, removal of the coordinating formamide molecules occurs, yielding the formamide-free compounds 1-DMF and 2-DEF of composition {Zn(O2C[PEP(hexyl)2EP]CO2)}. According to powder X-ray diffraction and FT-IR spectroscopy studies, these materials are not crystalline but still possess partial ordering of intact, yet modified coordination chains in a structural arrangement which appears to be related to the respective parent compounds. Compounds 1, 2, 1-DMF and 2-DEF exhibit blue photoluminescence. The emission maxima of 1-DMF and 2-DEF are red-shifted by ca. 25 nm with respect to λmax of 1 and 2, respectively.

Organisationseinheit(en)
Institut für Anorganische Chemie
ZFM - Zentrum für Festkörperchemie und Neue Materialien
Externe Organisation(en)
Universität Bielefeld
Typ
Artikel
Journal
Inorganica chimica acta
Band
362
Seiten
3600-3606
Anzahl der Seiten
7
ISSN
0020-1693
Publikationsdatum
10.04.2009
Publikationsstatus
Veröffentlicht
Peer-reviewed
Ja
ASJC Scopus Sachgebiete
Physikalische und Theoretische Chemie, Anorganische Chemie, Werkstoffchemie
Elektronische Version(en)
https://doi.org/10.1016/j.ica.2009.04.004 (Zugang: Unbekannt)