The complex, Mn(hfa) 2 tmeda [(H-hfa ¼ 1, 1,1,5,5,5-hexafluoro-2,4-pentandione, tmeda ¼ N,N,N 0 ,N 0 -tetramethylethylendiamine)], is synthesized in a single-step reaction and characterized by elemental analysis, thermal analysis, and infrared (IR) spectroscopy. The solid-state crystal structure of Mn(hfa) 2 tmeda provides evidence of a mononuclear structure. The thermal analyses show that the complex is thermally stable and can be evaporated to leave less than 2% residue. The complex properties are compared with the first generation, commercially available Mn II and Mn III precursors, Mn(acac) 2 (Hacac ¼ acetylacetone) and Mn(tmhd) 3 (Htmhd ¼ 2,2,6,6-tetramethyl-3,5-heptanedione), respectively. Mn(hfa) 2 tmeda represents the first example of manganese(II) precursor that can be used in the liquid phase without decomposition, thus providing constant evaporation rates, even for long deposition times. It is successfully applied to the reduced-pressure, metal-organic (MO)CVD of the Mn 3 O 4 phase.[**] The authors thank the MIUR for the financial support within the PRIN 2009 N. 20097 Â 44S7_002 (Hybrid materials based on lanthanide complexes for sensing applications) and the FIRB ITALNANONET RBPR05JH2P project.
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