Cobalt(iii) complexes with tridentate hydrazone ligands: protonation state and hydrogen bond competitionElectronic supplementary information (ESI) available: (1) DSC thermograms, (2) PXRD patterns, (3) TG curves, (4) figures for compounds (6) tables of selected bond distances and angles and of hydrogen bonds parameters and (7) 1H NMR spectra. CCDC [1432533-1432539 & crystallographic data sets for the structures H2L3, H2L5, H2L6, 1, 2, 2·0.7MeOH and 6·MeOH]. For ESI and crystallographic data in C

• Main Authors: Vrdoljak, Višnja, Pavlovi, Gordana, Hrenar, Tomica, Rub i, Mirta, Siega, Patrizia, Dreos, Renata, Cindri, Marina
• Format: Article
• ISSN: 2046-2069
• DOI: 10.1039/c5ra22068h

Cobalt( iii ) complexes of the type [Co(HL)(L)] were synthesized under solvothermal conditions staring from [Co(C 5 H 7 O 2 ) 3 ] and the corresponding ligand H 2 L (salicylaldehyde 4-hydroxybenzhydrazone, 3-methoxysalicylaldehyde 4-hydroxybenzhydrazone, 4-methoxysalicylaldehyde 4-hydroxybenzhydrazone, salicylaldehyde benzhydrazone, 3-methoxysalicylaldehyde benzhydrazone, 4-methoxysalicylaldehyde benzhydrazone). The presence of differently protonated forms of the same ligand in the complexes was supported by IR and NMR spectroscopy as well as by the single crystal X-ray diffraction method. The effects of weak interactions on the supramolecular architecture and their role on the ligand form stabilization have been analysed. Molecular interactions within the unit cells were investigated and quantified by extensive quantum chemical analysis on models built from crystal structures using density functional theory and empirical dispersion. Ligands used in this study were prepared under environmentally friendly conditions by mechanochemical synthesis. Their thermal behaviour and phase transitions were investigated using TG and DSC analysis and the powder X-ray diffraction method. Differently protonated ligands in [Co(HL)(L)] are stabilized via supramolecular assembling through O-H O/N and N-H N/O hydrogen bonding. Channels spreading either in each space dimension or predominantly in one direction are formed.