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N-alkylammonium salt

Palladium clusters [51], solubilized by tetra-n-alkylammonium salts, are effective in the Suzuki coupling of phenylborinic acid with bromoarenes to produce biaryls... [Pg.297]

Materials. The methylammonium Y-zeolites (Table I) were prepared by ion-exchanging NaY (5 grams) with 4 100-ml portions of 1 N alkylammonium salt solution at 80 °C. Monomethylammonium (MMA) chloride, dimethylammonium (DMA) chloride, and tetramethylammonium (TTMA) bromide (Matheson, Coleman, and Bell) and the trimethyl-ammonium (TMA) chloride (Eastman Organic Chemicals) were used as received. [Pg.497]

For ammonium salts, the temperature listed is the isotropization temperature. TA3Br and TA3I decompose immediately after isotropization. All the tetra-n-alkylammonium salts have additional crystal-mesophase transitions. In addition, no heat capacities for the liquid could be measured due to decomposition [67]. [Pg.779]

Stoichiometric triflates [(R4TTF)+ CF3S03 ] are convenient precursors for the conversion depicted. On the addition of alkylammonium salt in acetonitrile solution, either stoichiometric (n = 0) or non-stoichiometric (n A 0) material [(RjTTF +i) X ] can be obtained. These targeted salts precipitate in a very pure state. [Pg.418]

Similarly, N-alkylammonium [28] and alkylphosphonium [29] salts form lamellar phases with smectic bilayer structures. In both cases. X-ray scattering also showed the isotropic liquid not to be completely disordered and still displaying similar features to the mesophase. Buscio et al. [28] showed that in N-alkylammonium chlorides the feature was not only much broader than that observed in the mesophase but increased in width with decreasing chain length. [Pg.137]

Retention of solutes and selectivity can be controlled by adjusting the type and concentration of the ion-pair reagent added and by selection of the type and concentration of the organic solvent in the mobile phase (135,168). The ion pair reagents most commonly used are tetra-alkylammonium salts such as cetrimide (155,156,177) and tetra-n-butylammonium (TBA). The TBA reagent can be used as TBA phosphate (159,184), TBA chloride (221), TBA hydrogen sulfate (188,189), or TBA hydroxide (168,175,183). [Pg.560]

The complex hydrate structure, 1.67 choline hydroxide-tetra-n-propyl-ammonium fluoride 30-33H2O (space group = R-3, a = 12.533, c = 90.525 A) was discovered by Udachin and Ripmeester (1999b). It should be noted that the tetra-n-propylammonium salt will not form a hydrate on its own (Dyadin et al., 1988), even though other tetra-alkylammonium salts will form a variety of hydrate structures. Similar to structures II, H, and IV, this complex structure consists of stacked sequences of layers, CABBCAABCCABBCAAB. That is,... [Pg.68]

Fig. 11. Inhibitory constants of tetra-alkylammonium salts, R4N, as function of n, the number of carbon atoms in the four substituents together (according to Table IV and V). O------O Eel esterase. ------ Human plasma ChE. Fig. 11. Inhibitory constants of tetra-alkylammonium salts, R4N, as function of n, the number of carbon atoms in the four substituents together (according to Table IV and V). O------O Eel esterase. ------ Human plasma ChE.
When alkylammonium salts are recrystallized from water, they often form solids with very low melting points (Fowler et al., 1940). An example is (iso-Am)4N+.F- 40 H20 whose structure (Feil and Jeffrey, 1961) shows that the amyl groups are held in cages of water molecules located tetrahedrally around the N+-charge centre of the onium ion (Fig. 11). Similar structures are observed in tetra-n-butylammonium (McMullan et al., 1963 Bonamico et al., 1962) and tri-n-butylsulphonium salt hydrates (Beurskens and Jeffrey, 1964). [Pg.229]

Quite striking extrema are observed in the dependence of apparent partial molar heat capacities on salt concentration for alkylammonium salts and related compounds, e.g. Bu4N+ octanoate, and these can be understood in terms of long-range hydrophobic interactions (Leduc and Desnoyers, 1973). However, the properties of n-alkylamine hydrobromides have indicated that there are still... [Pg.269]

Capillary electrophoresis Capillary electrophoresis (CE) is used to analyze sodium, potassium, calcium, and magnesium in water samples. The detection is conducted by reverse absorbance measurements. Sufficient separation of the four cations is established with an electrolyte solution of 5 mM imidazole/6.5 mM a-hydroxyisobutyric acid/2 mM 18-crown-6 ether of pEI 4.1 [42]. CE with a contactless conductometric detector is used to determine small anions and cations in water samples from different sources. 2-(N-Morpholino)ethanesulfonic acid/histidine-based (Mes/Elis) electrolytes are used for direct conductivity detection of anions and cations, while ammonium acetate is used for indirect conductivity determination of alkylammonium salts. Eor the simultaneous separation procedure, involving dual-opposite end injection, an electrolyte consisting of 20 mM Mes/EIis, 1.5 mM 18-crown-6 and 20 mM cetyltri-methylammonium bromide provides baseline separation of 13 anions and cations in less than 6 min [43]. Also CE with a capacitively coupled... [Pg.274]

The reaction of the hexachlorozirconate anion as an alkylammonium salt (RH)2ZrClfl, where R = C2H5NH2, (CH3)2NH, (C.Hsl.NH, (CHsljN, and (C2H5)3N, with excess of amine (152), results in no product with tertiary amines, and very slow solvolysis with secondary amines. A product with a Zr N ratio of 1 2.49 with diethylamine was obtained after 8 weeks, and a product with a Zr N ratio of 1 2.86 with dimethyl-... [Pg.20]

P-33 - Efficient co-templating roles of amines and amides admixed with alkylammonium salts for the stabilisation of new AlP04-n topologies... [Pg.194]

The effects of increasing the concentration of initiator (i.e. increased conversion, decreased and broader PDi) and reducing the reaction temperature (i.e. decreased conversion, increased M and narrower PDi) for the polymerizations in ambient-temperature ionic Uquids are the same as observed in conventional solvents. Mays et al. reported similar results and, in addition, used NMR to investigate the stereochemistry of the PMMA produced in (BMIMjlPFej. They found that the stereochemistry is almost identical to that for PMMA produced by free radical polymerization in conventional solvents [28]. The homopolymerization and copolymerization of several other monomers are also reported. Similar to vdiat was found by Noda and Watanabe, in many cases the polymer was not soluble in the ionic liquid and thus phase separated [28,29]. Free radical polymerization of n-butyl methacrylate in ionic liquids based on imidazolium, pyridinium, and alkylammonium salts as solvents was investigated with a systematic variation of the length of the alkyl substituents on the cations, and employing different anions such as tetrafluoroborate, hexafluorophosphate, tosylate, triflate, alkyl sulfates and dimethyl phosphate [31]. [Pg.626]


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See also in sourсe #XX -- [ Pg.188 ]




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