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Tris salts, structural

Cadmium, tris(acetylacetone)-potassium salt structure, 1, 65 structure, 1,65... [Pg.96]

Cadmium, tris(diethyldithiocarbamato)-tetrabutylammonium salt structure, 1, 62... [Pg.96]

Figure 3. The lattice parameter for the family of rock-salt structure actinide-antimonide compounds is shown where the line is for the corresponding lanthanide compounds. The metallic radii for the light actinide elements are plotted. The smooth line simply connects Ac to the heavy actinides. In both cases the smooth line represents the ideal tri-valent behavior. Figure 3. The lattice parameter for the family of rock-salt structure actinide-antimonide compounds is shown where the line is for the corresponding lanthanide compounds. The metallic radii for the light actinide elements are plotted. The smooth line simply connects Ac to the heavy actinides. In both cases the smooth line represents the ideal tri-valent behavior.
The diethylammonium salt of the tris(tetraphenyldisiloxanediolato)zirconate(IV) anion (33) has been obtained in very low yield from the reaction of [Zr(NEt2)4] with diphenylsilanediol in THF. The ligand results, under the basic reaction conditions, from condensation of two Ph2Si(OH)2 molecules. Anion (33) has an octahedral tris-chelate structure with a twist angle (46.9°) that indicates some distortion towards trigonal prismatic geometry.466... [Pg.418]

Frensch and Vdgtle have recently appended three crown ether units to the cyclo-triveratrylene unit . Note that Hyatt had previously prepared the open-chained relatives of this structure (see Sect. 7.3 and Eq. 7.6). Whereas Hyatt prepared the cyclo-triveratrylene skeleton and then appended polyethyleneoxy arms to it, Frensch and Vogtle conducted the condensation reaction (formaldehyde/HCl) on the preformed benzocrown. Thus benzo-15-crown-5 was converted into the corresponding tris-crown (IS) (mp 203.5—205.5°) in 4% yield. The yield was somewhat higher for the condensation of benzo-18-crown-6, but in both cases, yield ranges were observed. These species formed 1 3 (ligand/salt) complexes with sodium and potassium ions. [Pg.37]

The alkynylation of estrone methyl ether with the lithium, sodium and potassium derivatives of propargyl alcohol, 3-butyn-l-ol, and propargyl aldehyde diethyl acetal in pyridine and dioxane has been studied by Miller. Every combination of alkali metal and alkyne tried, but one, gives the 17a-alkylated products (65a), (65c) and (65d). The exception is alkynylation with the potassium derivative of propargyl aldehyde diethyl acetal in pyridine at room temperature, which produces a mixture of epimeric 17-(3, 3 -diethoxy-T-propynyl) derivatives. The rate of alkynylation of estrone methyl ether depends on the structure of the alkyne and proceeds in the order propar-gylaldehyde diethyl acetal > 3-butyn-l-ol > propargyl alcohol. The reactivity of the alkali metal salts is in the order potassium > sodium > lithium. [Pg.68]

Angier and Marsico followed the course of alkylation first. The 7-dimethylamino-5-methylmercapto derivative reacted with dimethyl sulfate in an alkaline medium to yield a mixture of the 2- and 3-methyl derivatives. The reaction of the 7-diraethylamino derivative with ethyl iodide in an alkaline medium led to a mixture of all three possible monoethyl derivatives. The position of the alkyl group in all these substances was defined by comparing the UV spectra with derivatives prepared by a straightforward synthesis. After reacting the mercuric salts with tri-0-benzoylribofuranosyl chloride, they demonstrated the ribose residue to be bound in position 2. The same structure was shown to be valid for the derivative prepared by Andrews and Barber. ... [Pg.249]

Chemical Name 3-pyridinecarboxylic acid aluminum salt Common Name Tris(nicotinato)aluminum Structural Formula ... [Pg.50]


See other pages where Tris salts, structural is mentioned: [Pg.92]    [Pg.224]    [Pg.108]    [Pg.110]    [Pg.225]    [Pg.226]    [Pg.225]    [Pg.226]    [Pg.601]    [Pg.3679]    [Pg.3680]    [Pg.179]    [Pg.278]    [Pg.113]    [Pg.518]    [Pg.1248]    [Pg.36]    [Pg.122]    [Pg.140]    [Pg.177]    [Pg.216]    [Pg.164]    [Pg.166]    [Pg.137]    [Pg.111]    [Pg.14]    [Pg.178]    [Pg.156]    [Pg.114]    [Pg.292]   


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Tri-salts

Tris salts

Tris structure

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