Alkali metal-containing complexes with 2,2,6,6-tetramethyl-3,5-heptane
dione (thd) and trifluoroacetylacetone (tfa) as ligands were studied b
y TG, DTA, DSC and MS methods. Of the complexes studied, Na(thd) and K
(thd) sublimed completely, and NaPr(tfa)(4) and KPr(tfa)(4) sublimed a
lmost completely in vacuum, but in an inert atmosphere the weight rema
ining was up to approximate to 20%. Surprisingly, KPr(tfa)(4) had high
er volatility than the corresponding sodium complex. The strongest pea
ks in the mass spectra of the double complexes were due to NaPr(tfa)(3
) and KPr(tfa)(3). The mass spectra of Na(thd) and K(thd) showed sever
al different species. One thd ligand was always bonded to one or sever
al alkali metal ions. The strongest peaks in both spectra were those d
ue to M(3)thd(2) and M(2)thd.