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Dimethyl propylene-urea

In contrast, dipolar aprotic solvents possess large relative permittivities (sr > 15), sizeable dipole moments p > 8.3 10 ° Cm = 2.5 D), and average C.f values of 0.3 to 0.5. These solvents do not act as hydrogen-bond donors since their C—H bonds are not sufficiently polarized. However, they are usually good EPD solvents and hence cation sol-vators due to the presence of lone electron pairs. Among the most important dipolar aprotic solvents are acetone, acetonitrile [75], benzonitrile, A,A-dimethylacetamide [76, 77], A,A-dimethylformamide [76-78], dimethylsulfone [79], dimethyl sulfoxide [80-84], hex-amethylphosphoric triamide [85], 1-methylpyrrolidin-2-one [86], nitrobenzene, nitro-methane [87], cyclic carbonates such as propylene carbonate (4-methyl-l,3-dioxol-2-one) [88], sulfolane (tetrahydrothiophene-1,1-dioxide) [89, 90, 90a], 1,1,3,3-tetramethylurea [91, 91a] and tetrasubstituted cyclic ureas such as 3,4,5,6-tetrahydro-l,3-dimethyl-pyr-imidin-2-(l//)-one (dimethyl propylene urea, DMPU) [133]. The latter is a suitable substitute for the carcinogenic hexamethylphosphoric triamide cf. Table A-14) [134]. [Pg.82]

Hexahydro-l,3-dimethyl-2-oxopyrimidine, Dimethyl propylene urea, DMPU 42.1 0.352... [Pg.423]

DMPU 1,3-dimethyl-3,4,5,6-tetrahydro-2(1 /-/)-pyrimidone (A/,A/-dimethyl propylene urea) I... [Pg.784]

Some studies have examined the effect of solvent on the structure of EB films cast from solutions. For example, Ou and Samuels193 found that EB films cast from NMP solution were partially crystalline, as evidenced by shoulders appearing above the amorphous band in x-ray diffraction (XRD) studies. However, when the EB was cast from a solution in A, A-dimethyl propylene urea (DMPU), no evidence of crystallinity was observed. Whereas the NMP solutions were unstable (undergoing gelation owing to the formation of H-bonded networks between the PAn chains), the... [Pg.161]

Tzou, K.T., and R.V. Gregory. 1995. Improved solution stability and spinnability of concentrated polyaniline solutions using N,N -dimethyl propylene urea as the spin bath solvent. Synth Met 69 109. [Pg.1187]

The precondition is that solvent si is polar and almost immiscible with the nonpolar solvent s2. Solvent s3 is characterized by a semipolar nature and serves as the extracting agent. The miscibility gap is dependent on the properties of the participating solvents and the temperature. Commonly, solvent si dissolves the catalyst and solvent s2 extracts the products. Typical solvent mixtures are ATjAf-dimethylformamide (DMF)/Af,Af -dimethyl propylene urea/ -decane, DMF/NMP/ -decane, and propylene carbonate/n-dodecane/ethyl lactate. [Pg.655]

Good solvent DMAC, DMF, DMSO, NMP (emeraldine base) DMPU (N.N -dimethyl propylene urea) ... [Pg.278]

The chemical structure of polyaniline in various oxidation states is shown in Figure 3. The fully reduced form is referred to as leucoemeraldine base (LEB) while the fully oxidized form is called pemigraniline (PNB). Both LEB and PNB will shift towards the EB form upon exposure to an oxidizing environment.[2] Although it is well known that the oxidation state of polyaniline is an important characteristic of this polymer, there are few reports of its influence on the development of morphology in fibers and films. Previous work has shown that both films and fibers produced from solutions of leucoemeraldine base in N,N -dimethyl propylene urea (DMPU) exhibit crystallinity and a melting transition.[12]... [Pg.54]

Scheme 5-170. Silylation of aryl bromides. DMPU MA -dimethyl propylene urea (i. e., 1,3-dimethy ltetrahydropyrimidin-2( 1 //)-one). ... Scheme 5-170. Silylation of aryl bromides. DMPU MA -dimethyl propylene urea (i. e., 1,3-dimethy ltetrahydropyrimidin-2( 1 //)-one). ...
One area of interest concerns the assignment of the metal ligand vibrations in simple complexes through a comparison of the spectra of similar compounds. Often the observed data can be used to predict the geometrical structures of isomers although in the absence of supporting Raman data, the structures must be considered tentative. As an example of the FT-IR spectra of coordination compounds, we will consider the 1 1 addition compounds formed by triphenyltin(IV) bromide and iodide (Ph3SnX, X = Br, I) with dimethyl-propylene-urea (DMPU) [3]. The bromo complex exhibits three characteristic... [Pg.83]


See other pages where Dimethyl propylene-urea is mentioned: [Pg.32]    [Pg.226]    [Pg.272]    [Pg.643]    [Pg.272]    [Pg.237]    [Pg.50]    [Pg.51]    [Pg.156]    [Pg.751]    [Pg.1308]    [Pg.1796]    [Pg.1830]   
See also in sourсe #XX -- [ Pg.83 ]




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