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Acetylacetonate complex

The chelated organic titanates also function as adhesion promoters of the ink binder to printed substrates such as plastic films, paper, and aluminum foil (504). The acetylacetone complexes of titanium are the preferred products for promoting adhesion of printing inks to polypropylene films. [Pg.163]

Kaeriyama and Shimura [34] have reported the photoinitiation of polymerization of MMA and styrene by 12 metal acetylacetonate complex. These are Mn(acac)3, Mo02(acac)2, Al(acac)3, Cu(bzac)2, Mg(acac)2, Co(a-cac)2, Co(acac)3, Cr(acac)3, Zn(acac)2, Fe(acac)3, Ni(a-cac)2, and (Ti(acac)2) - TiCU. It was found that Mn(a-cac)3 and Co(acac)3 are the most efficient initiators. The intraredox reaction with production of acac radicals is proposed as a general route for the photodecomposition of these chelates. [Pg.248]

Discussion. Beryllium forms an acetylacetone complex, which is soluble in chloroform, and yields an absorption maximum at 295 nm. The excess of acetylacetone in the chloroform solution may be removed by rapid washing with O.lM-sodium hydroxide solution. It is advisable to treat the solution containing up to 10 g of Be with up to 10 mL of 2 per cent EDTA solution the latter will mask up to 1 mg of Fe, Al, Cr, Zn, Cu, Pb, Ag, Ce, and U. [Pg.175]

Alkene complexes Alkynyl complexes Ammine complexes Aqueous chemistry Arsine complexes Auranofin Auride ion Aurophilicity Binary compounds Bond lengths acetylacetonate complex alkyls and aryls ammine complexes carboxylates cyanide complexes dialkyl sulphide complexes dithiocarbamates to gold... [Pg.363]

Chromium, (ri6-benzene)tricarbonyl-stereochemistry nomenclature, 1,131 Chromium complexes, 3,699-948 acetylacetone complex formation, 2,386 exchange reactions, 2,380 amidines, 2,276 bridging ligands, 2,198 chelating ligands, 2,203 anionic oxo halides, 3,944 applications, 6,1014 azo dyes, 6,41 biological effects, 3,947 carbamic acid, 2,450 paddlewheel structure, 2, 451 carboxylic acids, 2,438 trinuclear, 2, 441 carcinogenicity, 3, 947 corroles, 2, 874 crystal structures, 3, 702 cyanides, 3, 703 1,4-diaza-1,3-butadiene, 2,209 1,3-diketones... [Pg.102]

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]

Komiya, S., and Kochi, J.K. (1977) Reversible linkage isomerisms of p-diketonato ligands. Oxygen-bonded and carbon-bonded stmctures in gold(III) acetylacetonate complexes induced by phosphines. Journal of the American Chemical Society, 99, 3695. [Pg.90]

Another particularly convenient preparative method is the reaction of the corresponding gold(l) acetylacetonate complex with the alkyne, which requires no auxiliary base.42 68-71 This reaction is also useful for the simple acetylides (L)AuC=CH.72 The acetylacetonates can be isolated and introduced as the true reagents, or prepared in situ using the corresponding gold(l) halide complex and Tl(acac) (Equations (16) and (17)).73... [Pg.257]

After our report, many other examples of SIMs based on mononuclear lanthanide complexes have appeared. As relevant examples, we should mention the erbium-organometallic double-decker complexes [11] and the dysprosium-acetylacetonate complexes [12], and the dysprosium-DOTA (H4DOTA, 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid) complexes reported by Sessoli etal. [13]. [Pg.29]

Beryllium Beryllium pre-concentrated as acetylacetone complex onto activated charcoal Charcoal introduced directly into graphite furnace AAS 0.6 ng/1 0.0006 xg/l [79]... [Pg.291]

As shown by Breslow et al. during the mid-1960s, most transition-metal alkox-ide or acetylacetonate complexes catalyze the hydrogenation of alkenes in the presence of an activator (Table 6.19) [5]. Other precursors have been used such as [CpCr(CO)3]2, but it is more difficult to understand how the active species are formed [133]. [Pg.138]

Copper (II) -acetylacetonate complex (Resonating ring compound)... [Pg.399]

These routes rely on vapor phase preparation of catalysts by deposition of metal precursors onto carbon or by direct formation of the catalyst in the vapor phase. Direct vapor deposition of volatile molecular precursors such as acetylacetonate complexes onto carbon has been demonstrated by Sivakumar and Tricoli for PtRu and PtRuIr. ... [Pg.12]

Fig. 4.15 The system La(III) acetylacetone (HA) - IM NaC104/benzene at 25°C as a function of lanthanide atomic number Z. (a) The distribution ratio Hl (stars, right axis) at [A ] = 10 and [HA] rg = 0.1 M, and extraction constants (crosses, left axis) for the reaction Ln + 4HA(org) LnA3HA(org) + 3FE. (b) The formation constants, K , for formation of LnA " lanthanide acetylacetonate complexes (a break at 64Gd is indicated) circles n = 1 crosses n = 2 triangles w = 3 squares w = 4. (c) The self-adduct formation constants, for the reaction of LnA3(org) + HA(org) LnA3HA(org) for org = benzene. (A second adduct, LnA3(HA)2, also seems to form for the lightest Ln ions.) (d) The distribution constant Ajc for hydrated lanthanum triacetylacetonates, LnAs (H20)2 3, between benzene and IM NaC104. (From Ref. 28.)... Fig. 4.15 The system La(III) acetylacetone (HA) - IM NaC104/benzene at 25°C as a function of lanthanide atomic number Z. (a) The distribution ratio Hl (stars, right axis) at [A ] = 10 and [HA] rg = 0.1 M, and extraction constants (crosses, left axis) for the reaction Ln + 4HA(org) LnA3HA(org) + 3FE. (b) The formation constants, K , for formation of LnA " lanthanide acetylacetonate complexes (a break at 64Gd is indicated) circles n = 1 crosses n = 2 triangles w = 3 squares w = 4. (c) The self-adduct formation constants, for the reaction of LnA3(org) + HA(org) LnA3HA(org) for org = benzene. (A second adduct, LnA3(HA)2, also seems to form for the lightest Ln ions.) (d) The distribution constant Ajc for hydrated lanthanum triacetylacetonates, LnAs (H20)2 3, between benzene and IM NaC104. (From Ref. 28.)...
Mn(acac)3 reacts with ethylenediamine (L2) or other primary amines (L) to yield [Mn"(acac)2L2], which can also be prepared by the reaction of the amine or diamine with [Mn(acac)2(H20)2]. Allylamine reacts with [Mn(acac)2-(H20)2] in ether to give a second complex, [Mn(acac)2(H2NCH2==CH2)]2 which is dimeric both in the solid and vapour phases. This is the First example of a dinuclear manganese(ii) acetylacetonate complex. Thermodynamic data have been reported for the manganese(ii)-acetylacetone system in propan-1-ol-water. ... [Pg.190]

Among the chelated species, octacoordination is often encountered. The tetrakis-acetylacetonate complex of U(IV) (a-form) and Ce(IV) are isostructural. A two-dimensional X-ray analysis showed a slightly distorted square antiprismatic geometry [109—111) for Ce(acac)4 belonging to space group P2i/c [Ctn] with an average Ce—O (acac) bond length of 2.40 A and an <0—Ce—0 of 72°. The a-form of Th(acac)4 is found to be isomorphous (770) with Ce(acac)4 (Th—0=2.41 A)... [Pg.98]

Similar to chemical vapor deposition, reactants or precursors for chemical vapor synthesis are volatile metal-organics, carbonyls, hydrides, chlorides, etc. delivered to the hot-wall reactor as a vapor. A typical laboratory reactor consists of a precursor delivery system, a reaction zone, a particle collector, and a pumping system. Modification of the precursor delivery system and the reaction zone allows synthesis of pure oxide, doped oxide, or multi-component nanoparticles. For example, copper nanoparticles can be prepared from copper acetylacetone complexes [70], while europium doped yttiria can be obtained from their organometallic precursors [71]. [Pg.384]

The acetylacetone complex Be(acac)2 is a neutral compound with an organic ligand, and hence is extractable from HOH into immiscible non-aqueous solvents such as benzene, carbon tetrachloride, chloroform, and diethylether. [Pg.133]

The great bulk of studies carried out on the spectra of five-coordinate complexes of oxovanadium(IV) has involved essentially square pyramidal structures. A classic example is the acetylacetonate complex whose structure is shown in Fig. 6 (18). [Pg.58]

The combination of rhodium dicarbonyl acetylacetonate complex (Rh(acac)(CO)2) and a diphosphite ligand, (2,2 -bis[(biphenyl-2,2 -dioxy)phosphinoxy]-3,3 -di-/i t/-butyl-5,5 -dimethoxy-l,T-biphenyl (BIPHEPHOS), is an excellent catalyst system for the linear-selective hydroformylation of a wide range of alkenes. This catalyst system has been successfully applied to the cyclohydrocarbonylation reactions of alkenamides and alkenylamines, which are employed as key steps for the syntheses of piperidine,indolizidine, and pyrrolizidine alkaloids. ... [Pg.516]

Scheme 8. The synthesis of an acetylacetonate complex of rhodium from the peroxo complex. Scheme 8. The synthesis of an acetylacetonate complex of rhodium from the peroxo complex.
The Cotton effects in mixed amino acidate/acetylacetonate complexes [Cr(acac)2L] (L = l-alanine, L-valine or L-phenylalanine) have been studied 774 absolute configurations were assigned by reference to the parent tris(acetylacetonate) complexes. Synthesis was achieved by the photolysis of mixtures of the amino acid and [Cr(acac)3]. The partial photoresolution of both cis- and irans-(l,l,l-trifluoro-2,4-pentanedionato)chromium has been accomplished by irradiation with circularly polarized light (5461 A) in chlorobenzene solution.775 The results indicated that both bond rupture and twist mechanisms were important. A number of other jS-diketonates have also been investigated.776... [Pg.864]

The electrophilic substitutions of acetylacetonate complexes have been taken as suggesting aromatic character in the chelate ring. Results with seventeen different 1,3-diketonatochromium(III) complexes were recently held to support this suggestion (176-178 equation 43).784 The bromination of tris(l,l,l-trifluoro-2,4-pentanedionato)chromium(III), previously claimed to be unreactive,785 has been reported.786... [Pg.864]


See other pages where Acetylacetonate complex is mentioned: [Pg.13]    [Pg.175]    [Pg.857]    [Pg.17]    [Pg.220]    [Pg.141]    [Pg.142]    [Pg.146]    [Pg.81]    [Pg.989]    [Pg.1000]    [Pg.222]    [Pg.160]    [Pg.270]    [Pg.43]    [Pg.142]    [Pg.365]    [Pg.94]    [Pg.1]    [Pg.142]    [Pg.339]    [Pg.115]    [Pg.862]    [Pg.321]   
See also in sourсe #XX -- [ Pg.141 ]

See also in sourсe #XX -- [ Pg.343 , Pg.418 ]




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Acetylacetonate

Acetylacetonate complexes lanthanide

Acetylacetonate complexes scandium

Acetylacetonate complexes, magnetic

Acetylacetone

Acetylacetone alkali metal complexes

Acetylacetone complex structures

Acetylacetone complexes

Acetylacetone complexes with nickel

Acetylacetone complexes, electrophilic

Acetylacetone coordination complexes with

Acetylacetone transition metal complexes

Acetylacetone, cobalt complexes, electron

Acetylacetone, complexing and

Acetylacetones

Alkenes acetylacetone metal complexes

Alkylation acetylacetone metal complexes

Aluminum complexes acetylacetone

Anhydrous tris acetylacetonate complexes

Beryllium complex compounds nonelectrolytes, with acetylacetone, Be(CsH

Beryllium complexes acetylacetone

Bond lengths acetylacetonate complex

Boron complexes acetylacetone

Bromination acetylacetone chromium complexes

Cadmium complexes acetylacetone

Calcium complexes acetylacetone

Chloromethylation acetylacetone metal complexes

Chromium complexes acetylacetonate

Chromium complexes acetylacetonates

Chromium complexes acetylacetone

Cobalt acetylacetonate complexes

Cobalt complexes acetylacetone

Copper complexes acetylacetone

Determination of beryllium as the acetylacetone complex

Electrophilic substitution, acetylacetone complexes

Erbium complexes acetylacetone

Germanium complexes acetylacetone

Halogen-acetylacetonate complexes

Iridium complexes acetylacetone

Iron complexes acetylacetonate

Iron complexes acetylacetone

Lanthanide complexes acetylacetone

Manganese complexes acetylacetonate

Manganese complexes acetylacetonates

Manganese complexes acetylacetone

Molybdenum acetylacetonate complexes

Molybdenum acetylacetonate complexes deoxygenation

Molybdenum acetylacetonate complexes epoxides

Molybdenum complexes acetylacetone

Nickel complexes acetylacetonate

Nickel complexes acetylacetone

Palladium complexes acetylacetone

Platinum acetylacetonate complexes

Platinum complexes acetylacetonate reactions

Platinum complexes acetylacetone

Rare earth complexes acetylacetone

Rhenium complexes acetylacetonates

Rhenium complexes acetylacetone

Rhodium complexes acetylacetonate

Rhodium complexes acetylacetone

Silicon complexes acetylacetone

Silver complexes acetylacetone

Tellurium complexes acetylacetone

Tetrakis acetylacetonate complex

Thorium complex compounds, nonelectrolytes, with acetylacetone

Titanium complexes acetylacetone

Transition metal complexes acetylacetonates

Vanadium complexes acetylacetonates

Vanadium complexes acetylacetone

Ytterbium complexes acetylacetone

Zinc complexes acetylacetone

Zirconium acetylacetonate complexes

Zirconium complex compounds, nonelectrolytes, with acetylacetone

Zirconium complexes acetylacetone

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