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Hexafluoro-acetylacetonates

Also increasingly common, as CVD precursors, are many halogen-acetylacetonate complexes, such as trifluoro-acetylacetonate thorium, Th(C5H4F302)4, used in the deposition of thoriated tungsten for thermionic emitters, the trifluoro-acetylacetonates of hafnium and zirconium and the hexafluoro-acetylacetonates of calcium, copper, magnesium, palladium, strontium, and yttrium. [Pg.91]

Me2SO solution b Hibbert (1974) Protonated amine salt with magnesium tris(hexafluoro-acetylacetonate) (Truter and Vickery, 1972) 4 CF3COOH solution (Alder et al., 1968) Altman et al. (1978) 1 Protonated amine salt with copper(n) tris(hexafluoroacetylacetonate) (Truter and Vickery, 1972) 9 Hydrobromide salt (Pyzalka et al., 1983) Staab el al. (1983) Staab et al. (1988a) JSaupe et al. (1986) Staab and Saupe (1988) Staab et al. (1988b) Zirnstein and Staab (1987). [Pg.323]

Consequently, Fhb is the difference between the OH barrier calculated in the chelate conformation and the same barrier calculated in a molecule structurally close to the examined compound but hydrogen bond free. In most of our calculations, the reference molecule was attained by substituting the hydrogen bond acceptor fragment with a H atom. When tested on malonaldehyde and acetylacetone the approach worked very well [185]. The method was then applied with discrete success to many other molecules as formazan [186], carbonylamine [187], hexafluoro-acetylacetone [184], glyoxaloxime [188], 2-nitroresorcinol, 4,6-dinitroresorcinol and 2-nitrophenol in vacuum and in solution [189], malonamide and nitromalonamide [158] and ort/zo-halophenols [190]. [Pg.68]

Buemi, G., Ab initio DFT study of hydrogen bridges in hexafluoro-acetylacetone, trifluor-oacetyl-acetone and some 3-substituted derivatives, J. Mol Struct. Theochem, 499, 21-34 (2000). [Pg.101]

Five-membered nitrogen-containing heterocycles may be synthesized from tV,VV-diethylaminomethylene-l,l,l,5,5,5-hexafluoro-acetylacetone (93TL7737) (Scheme 112). [Pg.328]

The major breakthrough that transformed metal chelate GC into a useful analytical technique was the introduction of fluorinated beta-diketone ligands, which formed complexes of greater volatility and thermal stability. Trifluoroacetylacetone (l,l,l-trifluoro-2,4-pentanedione—HTFA) and hexafluoro-acetylacetone (l,l,l,5,5,5-hexafluoro-2,4,-pentanedione—HHFA) are the fluorinated ligands most frequently employed. HTFA extended the range of metals that may be gas chromatographed with little or no evidence of decomposition to include Ga3+, In3+, Sc3+, Rh3+ and V4+. An example of a recent application is the analysis for beryllium in ambient air particulates. After filter sampling and extraction/chelation, packed column GC with electron capture detection allowed ppm level beryllium quantitation in collected particulates which corresponded to levels of 2-20 x 10 5 pg/m3 in the sampled air. [Pg.311]

B4 THE PREPARATION AND PROPERTIES OF RARE EARTH HEXAFLUORO-ACETYLACETONATES, M. Steinberg, J. Masha 11 and A. Glasner... [Pg.467]

The complexes Eu(hfa)3(L), where Hhfa = l,Ll,5,5,5-hexafluoro-acetylacetone, L = mono- or diglyme, give vEu-O bands in the IR spectra near 250 cm. IR bands due to EuFeOs were assigned from the IR spectrum of the Eu203 Fe203 system. "... [Pg.242]

Replacement of the terminal methyl groups of acacH by an electron-withdrawing or aromatic group such as CF3, C4H3S (2-thienyl), and CfiHs shifts the equilibrium in favor of the enol tautomer. Hexafluoro-acetylacetone (hfacH), thenoyltrifluoroacetone (in carbon disulfide), and dibenzoylmethane (dbmH) (in carbon tetrachloride), for example, exist entirely in the enol form. °" ... [Pg.77]


See other pages where Hexafluoro-acetylacetonates is mentioned: [Pg.154]    [Pg.39]    [Pg.400]    [Pg.83]    [Pg.934]    [Pg.13]    [Pg.66]    [Pg.68]    [Pg.68]    [Pg.157]    [Pg.109]    [Pg.400]    [Pg.3854]    [Pg.32]    [Pg.110]    [Pg.340]    [Pg.226]    [Pg.174]    [Pg.931]    [Pg.127]    [Pg.483]    [Pg.163]    [Pg.73]    [Pg.929]    [Pg.161]   
See also in sourсe #XX -- [ Pg.91 ]




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Acetylacetonate

Acetylacetone

Acetylacetones

Hexafluoro

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