4.6 Article

Dioxidomolybdenum(VI) complexes with isoniazid-related hydrazones: solution-based, mechanochemical and UV-light assisted deprotonation

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NEW JOURNAL OF CHEMISTRY
卷 39, 期 9, 页码 7322-7332

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c5nj01567g

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  1. Ministry of Science and Technology of the Republic of Croatia

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Synthesis of the dioxidomolybdenum(vi) complexes [MoO2(HLR)(MeOH)10 (1-3) was carried out by using MoO2Cl2 and the corresponding ONO aroylhydrazone ligand H2LR (ligand H2LR is salicylaldehyde isonicotinoyhydrazone (H2LSIH), 2-hydroxy-naphthaldehyde isonicotinoyhydrazone (H2LNIH), or p-(N,N'-diethylamino)salicylaldehyde isonicotinoylhydrazone (H2LEt2NSIH) in methanol. Compounds [MoO2(HLR)(H2O)]Cl (1a-3a) were obtained upon exposure of the corresponding mononuclear complexes 1-3 to moisture. Deprotonation of the mononuclear complexes 1-3 was performed by using Et3N as a base (by the conventional solution based-method and by the mechanochemical approach) as well as by UV-light assisted reactions yielding [MoO2(L-SIH)(MeOH)] (4), [MoO2(L-NIH)(MeOH)] (5) and [MoO2(L-Et2NSIH)](n) (p) respectively. Crystal and molecular structures of all complexes were determined by the single crystal X-ray diffraction method. The complexes were further characterized by elemental analysis, IR spectroscopy, TG analysis, one- and two-dimensional NMR spectroscopy and powder X-ray diffraction.

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