Structural characterization of the {3[BPMTU]+• 3[X] -• nH2O} salts (BPMTU = 1,3-bis(3-pyridylmethyl)-2- thiourea and X = Cl, Br, I). A polychlorine network based on O⋯Cl - and OH⋯Cl- interactions
Date
2011Author
Ozturk, I. I.![ORCID logo](https://orcid.org/sites/default/files/images/orcid_16x16.png)
Tsipis, Athanassios C.
Malandrinos, G.
Kourkoumelis, Nikolaos
Manos, Manolis J.
![ORCID logo](https://orcid.org/sites/default/files/images/orcid_16x16.png)
Light, M. E.
Hursthouse, M.
Bocanegra, P. E.
Butler, I. S.
Hadjiliadis, Nick
Source
Journal of Coordination ChemistryVolume
64Issue
2Pages
202-221Google Scholar check
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Ionic salts with the formulae {3[BPMTU]+ 3[X]- nH2O} (BPMTU = 1,3-bis(3-pyridylmethyl)-2-thiourea, X = Cl - and n = 1.5 (1), X = Br-and n = 1 (2), X = I- and n = 1 (3)) were synthesized. The compounds have been characterized by elemental anaylses, TG-DTA, FT-IR, far-IR, Raman, ESI-MS and 1H, 13C-NMR spectroscopic methods, and X-ray powder diffraction techniques. The crystal structures of 1 and 2 have also been determined by X-ray diffraction at 120(2) and 100(2) K, respectively. In 1, weak lp(Cl-) → σ*(O-H) hyperconjugative interactions and OH⋯Cl- hydrogen-bonding interactions lead to the formation of 1-D zigzag tetrameric complexes consisting of four chlorides bridged by four waters. Two oxygens of the bridging waters are also coordinated to Cl- of the complex forming a parallelogram-shaped ring. Two chlorides are also anchored by NH⋯Cl - hydrogen bonds in the free space between four tetrameric complexes. Heating 1 at 100C for 4 h does not remove lattice water and the framework structure is retained. In 2, NH⋯Br- hydrogen-bonding interactions stabilize the supramolecular architecture. In this case, however, only two bromides are bridged by one water through OH⋯Br- hydrogen bonds. The supramolecular interactions existing in the crystal packing of the ionic salts have been analyzed at the density functional theories and ab initio CCSD(T) levels of the theory. © 2011 Taylor & Francis.