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Diamine hydrate

Common solvents Dimethyl sulfoxide, ethylene-diamine (hydrate and anhydrate), chloral (2)... [Pg.15]

Polyquinoxalines are prepared by the solution polymerisation of aromatic bis((9-diamines) such as 3,3, 4,4 -tetraminobiphenyl and aromatic bis(glyoxal hydrates) such as 4,4 -oxybis(phenylglyoxalhydrate) ... [Pg.536]

X-ray, 4, 160 (79AX(B)2228> lH-Pyrrole-2,4-diamine, 1-t-butyl-JV, JV -dimethyl-3-phenyl-JV -phenylsulfonyl-X-ray, 4, 160 (78BSB893) lH-Pyrrole-3-methanol, 4-acetyl-X-ray, 4, 160 (78AX(B)1248> lH-Pyrrole-3-methanol, 4-acetyl-, hydrate X-ray, 4, 160 (78AX(B)1248> lH-Pyrrole-3-propanoic acid, ester C NMR, 4, 172 (74JCS(P2)1004>... [Pg.55]

Silylation-amination of 4(lH)-quinohnone 255 with a twofold excess of dopamine hydrochloride 256 as amine and an acidic catalyst affords, on heating with excess HMDS 2 for 21 h at 145 °C and subsequent transsilylation in excess boihng methanol, 75% of the crystalline hydrate of 257 (Scheme 4.28). The silylation-amination of 2-thio-6-azauracil 258 with homoveratrylamine 259, HMDS 2, and SnCLj as catalyst for 48 h at 145 °C furnishes 63% of the diamine 260, and MesSiOSiMes 7 and Me3SiSH or Me3SiSSiMe3 601 as leaving groups. [Pg.61]

Diamine chelate complexes are more stable than the monodentate amine heterocycles and, therefore, can be studied under physiological conditions. The imidazole complexes are unstable in aqueous solution and decompose rapidly to technetium oxide hydrate. Six-membered ring chelates are significantly less stable than five-membered ones. Lesser flexibility of the ligand, such as 1.2-diamino-cyclohexane, parallels somewhat lower stability of the complex [53] ... [Pg.91]

Vikram L, Sivasankar BN (2008) New nine coordinated hydrated heavier lanthanide ethyl-diamine tetraacetates containing hydrazinium cation Crystal structure of N2H5[Dy(EDTA) (H20)3(H20)5. Ind J Chem 47A 25-31... [Pg.335]

First, we examine the sequential hydration of a doubly protonated diamine, H3N(CH2)12NH2+. The sequential enthalpies, Atf n, free energies AG , and entropies obtained from van t Hoff plots of the hydration equilibria,62 are... [Pg.291]

The course of the condensation of ethylene glycol with secondary amines (Me2NH, Et2NH, pyrrolidine or morpholine) depends on the catalyst used. Triphenylphosphine complexes of ruthenium, e.g. RuCl2(PPh3)3, give hydroxyalkylamines while hydrated ruthenium(III) chloride yields diamines (equation 24)62. [Pg.543]

X-edge spectra of cobalt compounds appear quite similar to those of manganese compounds. The ionic cobaltous salts and hydrates produce t3q>e I spectra. In Fig. 9 and 10 the spectra of the salts (except for CoBrj) have their principal maximum at 18-20 ev. Spectra of the cobaltic salts stabilized with a coordination sphere of ammonia or of ethylene diamine, shown in Figs. 11 and 12, are all very similar, are of typo I, and have their... [Pg.163]

Frankel and Klager have reported using the Mannich reaction for the condensation of 2,2-dinitroalkanols with ammonia and hydrazine. This method was used to synthesize 2,2,6,6-tetranitro-4-azaheptane (100%) and bis(2,2-dinitropropyl)hydrazine (162) (73%) from the reaction of 2,2-dinitropropanol (25) with ammonia and hydrazine hydrate respectively. This work was later extended to using polynitroaliphatic amines and diamines. " ... [Pg.44]


See other pages where Diamine hydrate is mentioned: [Pg.1505]    [Pg.349]    [Pg.104]    [Pg.129]    [Pg.104]    [Pg.104]    [Pg.268]    [Pg.977]    [Pg.1505]    [Pg.1757]    [Pg.1505]    [Pg.83]    [Pg.2384]    [Pg.3394]    [Pg.1505]    [Pg.349]    [Pg.104]    [Pg.129]    [Pg.104]    [Pg.104]    [Pg.268]    [Pg.977]    [Pg.1505]    [Pg.1757]    [Pg.1505]    [Pg.83]    [Pg.2384]    [Pg.3394]    [Pg.536]    [Pg.86]    [Pg.99]    [Pg.103]    [Pg.22]    [Pg.17]    [Pg.604]    [Pg.489]    [Pg.486]    [Pg.419]    [Pg.104]    [Pg.120]    [Pg.419]    [Pg.931]    [Pg.277]    [Pg.293]    [Pg.299]    [Pg.299]    [Pg.48]    [Pg.80]    [Pg.6]    [Pg.346]    [Pg.243]   
See also in sourсe #XX -- [ Pg.8 , Pg.349 ]




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