abstract
The crystalline compounds (Hbipy)(2)[Ge(C(2)O(4))(3)] (1) and (Hphen)(2)[Ge(C(2)O(4))(3)] center dot 2(H(2)O) (2) [Hbipy(+) is the 2,2'-bipyridinium cation (C(10)H(9)N(2)), and Hphen(+) is the 1,10'-phenathrolinium cation (C(12)H(9)N(2))] were isolated from mild hydrothermal syntheses and their structures were elucidated from single-crystal X-ray diffraction. The two compounds were further characterised by vibrational spectroscopy (FT-IR and FT-Raman), thermogravimetric analysis (TGA) and CHN elemental composition. Compounds 1 and 2 comprise the tris(oxalato-O,O')germanate dianion complex, [Ge(C(2)O(4))(3)](2-), which co-crystallises with Hbipy(+) (in 1), or Hphen(+) and water molecules (in 2). In 1, the germanium oxalate anionic complex, [Ge(C(2)O(4))(3)](2-), and the Hbipy(+) organic residues interact mutually via N-H center dot center dot center dot O hydrogen bonding interactions, leading to supramolecular discrete hydrogen-bonded units which are further interconnected via pi-pi stacking. Compound 2, on the other hand, exhibits a more complex hydrogen bonding network due to the presence of the water molecules of crystallisation which, along with pi-pi stacking between neighbouring Hphen(+) residues, mediate the crystal packing. (c) 2008 Elsevier B.V. All rights reserved.
keywords
X-RAY-DIFFRACTION; CAMBRIDGE STRUCTURAL DATABASE; METAL-ORGANIC FRAMEWORK; COORDINATION POLYMERS; SOLID-STATE; CRYSTAL-STRUCTURE; DESIGN; DERIVATIVES; STORAGE
subject category
Chemistry
authors
Cunha-Silva, L; Shi, FN; Paz, FAA; Hardie, MJ; Klinowski, J; Trindade, T; Rocha, J
our authors
acknowledgements
We are grateful to FEDER, POCI (Portugal) and to the Portuguese Foundation for Science and Technology (FCT, MCTES) for their general financial support (POCI-PPCDT/ QUI/58377/2004) and also for the postdoctoral grants SFRH/BPD/14410/2003 (to L.C.-S.) and SFRH/ BPD/9309/2002 (to F.-N.S.). We also wish to thank the EPSRC (UK) and the University of Leeds for equipment funding.