Methylene chains

If this electrostatic treatment of the substituent effect of poles is sound, the effect of a pole upon the Gibbs function of activation at a particular position should be inversely proportional to the effective dielectric constant, and the longer the methylene chain the more closely should the effective dielectric constant approach the dielectric constant of the medium. Surprisingly, competitive nitrations of phenpropyl trimethyl ammonium perchlorate and benzene in acetic anhydride and tri-fluoroacetic acid showed the relative rate not to decrease markedly with the dielectric constant of the solvent. It was suggested that the expected decrease in reactivity of the cation was obscured by the faster nitration of ion pairs. [Pg.173]

Composition. Shellac is primarily a mixture of aUphatic polyhydroxy acids in the form of lactones and esters. It has an acid number of ca 70, a saponification number of ca 230, a hydroxyl number of ca 260, and an iodine number of ca 15. Its average molecular weight is ca 1000. Shellac is a complex mixture, but some of its constituents have been identified. Aleuritic acid, an optically inactive 9,10,16-trihydroxypalmitic acid, has been isolated by saponification. Related carboxyflc acids such as 16-hydroxy- and 9,10-dihydroxypalmitic acids, also have been identified after saponification. These acids may not be primary products of hydrolysis, but may have been produced by the treatment. Studies show that shellac contains carboxyflc acids with long methylene chains, unsaturated esters, probably an aliphatic aldehyde, a saturated aliphatic ester, a primary alcohol, and isolated or unconjugated double bonds. [Pg.141]

When the chain between the azirine ring and the alkene end is extended to three carbon atoms, the normal mode of 1,3-intramolecular dipolar cycloaddition occurs. For example, irradiation of azirine (73) gives A -pyrroline (74) in quantitative yield 77JA1871). In this case the methylene chain is sufficiently long to allow the dipole and alkenic portions to approach each other in parallel planes. [Pg.59]

The melting points of open-chain dicarboxylic acids, H20C(CH2)nC02H, alternate with length of the intervening methylene chain. [Pg.156]

When a-tethered nitro ilkenes bearing three or four methylene chains and ester-activated dipolarophiles react with vinyl ethers, splro mode tandem cycloaddidon takes place to give tricyclic splro nitroso acetals In good yield and high diastereoselecdvity CScheme 8.46. ... [Pg.295]

Subsequently it was shown that the P-Pd-P angles were essentially the same as in the corresponding chloride complexes (section 3.8.3) as a result, as the P—Pd—P angle increases, concomitant upon the increase in the length of the methylene chain, steric effects enforce N-bonded thiocyanate, which is less sterically demanding that the non-linear Pd-SCN linkage (favoured on HSAB considerations since Pd2+ is a soft acid and sulphur is a soft base). [Pg.232]

Although these nmr results offer convincing support for the fl-form of 4GT taking the structure proposed by Hall and Pass as their model 7, in the case of the a-form none of the proposed structures were in good agreement with the nmr measurements. This discrepancy highlights the sensitivity of the nmr technique to the exact conformation of the methylene chain, in contrast to the X-ray diffraction technique which is more sensitive to the terephthalolyl residue. [Pg.112]

As might be expected, a complex mixture of lactones corresponding to abstraction of a hydrogen atom from various sites along the methylene chain was obtained from the photolysis. The mixture of lactones was converted by dehydration, ozonolysis, and hydrolysis to a mixture of ketones. It was found that no functionalization occurs with ester side chains of less than nine carbon atoms. This is probably due to the inability of the carbonyl to approach any methylene closely enough to abstract a hydrogen. The data for side chains of nine carbons or greater is presented in Table 3.11. [Pg.62]

According to Steiner et al. [69], who studied the complex of /TCD with 1,4-butanediol, a monomer model of PTHF, the crystal packing in this complex is the cage type and isomorphous to that of the jS-CD hydrate, and the methylene chain vibrates in the cavity. However, in the /J-CD-PTHF complex, the polymer chain lays fixed inside a column formed by linearly bonded CD molecules. In agreement with this picture, CP/MAS NMR spectra showed the PTHF chain in the complex to be much less flexible than that in its mixture with the CD. [Pg.162]

Since the transition moments of the antisymmetric and symmetric CH2 stretching vibrations and the methylene chain axis are mutually perpendicular, the average orientation angle y of the hydrocarbon chain axis around the surface normal is obtained to be 27° by the orthogonal relation... [Pg.164]

Figure 19. Temperature dependence of orientation angle y of the methylene chain axes of the constituent molecules in the alternating S(PS)9-Ba (-) and S(PS)9 films...

Figure 22. Orientation angles yof the methylene chain axes of DOPC-Ba in S(PS)n-Ba...

Figure 13.5 PAMAM dendrimer G1(Cm) (with an aliphatic methylene chain as the central core) and the probe...

After the initial use of pyrene and other excimer-forming molecules in biological applications,(54) it was soon recognized that excimer formation can be strongly enhanced and the probe concentrations therefore strongly reduced if the reaction partners are chemically linked, e.g., by a methylene chain. Thus, intramolecular excimers were developed, some of which are collected in Figure 5.9. [Pg.122]

We Umit this section to a discussion of stereochemical studies that sought to demonstrate discriminating enantiomeric interactions in monolayers of simple surfactants having one hydrophobic chain of methylenes and, generally, a single chiral center. Work in this area includes derivatives of long chain fatty acids, alcohols, or esters whose chiral center is included in the methylene chain. [Pg.221]

Paquette and coworkers (69JOC2866) have demonstrated that H-azepines can be forced into adopting the benzeneimine structure by bridging the 2,7-positions with a trimethylene chain (25). The length of the methylene chain is, however, critical and the tetramethylene derivative (26) exists solely as the bridged azepine. A suggestion that benzeneimines may be involved as intermediates in the formation of 3H-azepines from 2//-azirines and cyclopentadienones (Section 5.16.4.2.1(i)) has been discounted (74JOC3070). [Pg.500]

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