Structural studies and physico-chemical properties of new oxodiperoxomolybdenum complexes with nicotinic acid

Three new oxodiperoxomolybdenum complexes with nicotinic acid have been synthesized and characterized with the use of single-crystal analysis, XRPD versus temperature, TG/DSC, SEM and IR spectroscopy. The investigated compounds are: 1 – (NH4)2·[MoO(O2)2.N-nicO]2, 2 – (nicH)2·[MoO(O2)2.N-nicO]2·2(H2O), 3 – MoO(O2)2(H2O)nicH; (N-nicO, nicH − denote nicotinic acid N-oxide and protonated nicotinic acid, respectively). Compounds 1, 2 are salts of the same acid with cyclic dinuclear anions, whereas compound 3 can be regarded as an inner salt. Compounds 1–3 are stable in ambient conditions, the respective percentages of oxygen in peroxo groups are 19.21%, 14.06% and 20.19%, respectively. Above 125 °C peroxo compounds 1–3 decompose, forming nanometric MoO2 and MoO3. TG/DSC curves reveal clear effects connected with the release of oxygen and strong exothermic effects connected with final loss of organic components. All the investigated complexes were found to be active in the oxidation of cyclooctane to cyclooctanone and cyclooctanol with molecular oxygen.

Graphical abstractThree new oxodiperoxomolybdenum complexes with nicotinic acid have been synthesized and characterized with the use of single-crystal analysis, XRPD versus temperature, TG/DSC, SEM and IR spectroscopy. Compounds 1, 2 are salts of the same acid with cyclic dimeric anions, whereas compound 3 can be regarded as an inner salt. Compounds 1–3 are stable in ambient conditions, above 125 °C decompose forming nanometric MoO2 and MoO3. All the investigated complexes are active in the oxidation of cyclooctane to cyclooctanone and cyclooctanol with molecular oxygen.Figure optionsDownload full-size imageDownload as PowerPoint slide