Maximal Convex Subgroups of the Automorphism Group of a Doubly Transitive Chain

We characterise all maximal convex l-subgroups of A(), the automorphismgroup of a doubly transitive chain of countable coterminality.We then determine, up to isomorphism, all doubly transitiveactions of the l-group A(). Finally, assuming the ContinuumHypothesis, we show that there exists an unbounded chain ofproper prime subgroups of A().     

Reversibly-formed ion pairs are not involved during the solvolysis of N,O-diacetyl-N-arylhydroxylamines

Appropriate oxygen-18 labeling experiments demonstrate that N,O-diarylhydroxylamines do not undergo solvolysis $\text{via}$ the reversible formation of ion pairs. This is in total conflict with the conclusions from previous indirect kinetic studies of these ultimate carcinogen models.     

Shearing of oriented polyethylene and polypropylene

To learn more about the out-of-plane deformation of polymer lamellae during drawing, we have measured the resistance to shear along various planes in uniaxially oriented polyethylene and polypropylene. Fissures parallel to the orientation axis in oriented materials always cause too small an experimental value for the resistance of crystal glide parallel to the chain axes, but a rough estimate for the resistance to crystal glide is obtained using the elastic anisotropy. Also, the results suggest that kinking can be easier than glide when glide is inhibited by tie molecules.     

Surface photochemistry: The photo-chlorination of aromatic hydrocarbons with ferric chloride on alumina

Irradiation of a number of aromatic hydrocarbons adsorbed on alumina in the presence of ferric chloride leads to monochlorination.     

Structure elucidation with lanthanide-induced shifts. 4—Bound shifts vs relative shifts

The use of lanthanide shift reagents (LSR's) to obtain additional structural information from nuclear magnetic resonance studies has gained widespread acceptance. However, there has not been general agreement with regard to the most appropriate methodology for analysis of the shifted NMR spectra. We present arguments that only the bound shifts (Δ₁) corresponding to the LS complex should be used for correlation of lanthanide-induced shifts with molecular structure by means of the pseudocontact equation. Several examples are discussed of compounds for which the relative induced shifts are dependent on the concentration of LSR. For such cases it is not possible for both Δ₁ and Δ₂ (the bound shift corresponding to the LS₂ complex) to correlate successfully with the correct structure. Alternative methods of obtaining bound shifts are critically evaluated.     

When electron exchange is chemical exchange-assignment of 1H NMR spectra of paramagnetic cobalt(II)-2,2':6'2''-terpyridine complexes

Electron exchange between [Co(terpy)2]3+ and [Co(terpy)2]2+ can be monitored by 1H NMR exchange spectroscopy and allows the cobalt(II) spectra to be fully assigned.