Some considerations of the steady-state and transient behaviour of membrane-covered dissolved oxygen detectors

The behaviour of commercial, membrane-covered dissolved oxygen detectors is considerably more complicated than the orginal model of Mancy et al. would suggest. For example, the steady-state current is dependent both on the thickness and nature of the electrolyte behind the membrane. And transient currents obtained for switch-on of the detector are not completely described by the simple diffusional model. This paper examines these examples of more complicated behaviour. An analysis of the transient current for a step change in dissolved oxygen concentration is also given.     

Alkylation and silylation of directed enolates from diethylketene and organometallic reagents

Diethylketene and organometallic reagents form enolates capturable by methyl iodide or trimethylsilyl chloride with greater than 95% positional selectivity.     

Mixed ligand complexes of ruthenium(III), rhodium(III) and iridium(III) with dipicolinic acid and some monobasic bidentate nitrogen,oxygen donor ligands

The trivalent ruthenium, rhodium and iridium complexes of dipicolinic acid and its mixed ligand complexes with several nitrogen, oxygen donor molecules, of types: Na[M(dipic)₂]·2H₂O and [M(dipic)(N-O)]·nH₂O (where M = Ru(III), Rh(III) or Ir(III); dipicH₂ = dipicolinic acid; NOH represents different nitrogen, oxygen donor molecules, viz., picolinic acid, nicotinic acid, isonicotinic acid, glycine, aminophenol, o- or p-aminobenzoic acid), have been synthesized and characterised on the basis of elemental analyses, electrical conductance, magnetic susceptibility measurements and spectral (electronic and infrared) data. The parent dipicolinic acid complexes are found to have a six-coordinate pseudooctahedral structure, whereas for mixed ligand complexes, a polymeric six-coordinate structure has been assigned. Various ligand field and nephelauxetic parameters have also been evaluated.     

Peptides—XXXV: Synthesis of the 17–26 fragment of a lysozyme analogue

The fully protected 17–26 fragment of a lysozyme analogue has been synthesised. A fragment condensation approach has been employed using the protected subfragments 17–19, 20–22 and 23–26. In the synthesis of the subfragments the use of the diphenylphosphinyl mixed anhydride method has been demonstrated.     

Endor frequencies of randomly oriented triplets by electron spin echo spectroscopy

ENDOR frequencies of randomly oriented triplets have been measured from the fast Fourier transform of electron spin echo envelope modulation. Important experimental conditions are low temperatures, high microwave power and long phase memory time in a proper form of solvent. The technique is exemplified by using diphenylmethylenes in rigid glasses, polycrystalline forms and single crystals of benzophenones.     

The noncumulative effect of methyl substituents on the rate of addition of benzeneselenenyl chloride to olefins1

The rates and products of addition of benzeneselenenyl chloride to ethylene and its six Me substituted derivatives have been determined in methylene chloride at 25°. Unlike the addition of 4-chlorobenzenesulfenyl chloride to this same series of compounds, the effect of Me groups on the rates of addition is not cumulative. Also the regiochemistry of the product is different. For arenesulfenyl chloride additions, products of anti-Markownikoff orientation are formed preferentially under conditions of kinetic control. Under similar conditions regiospecific formation of the Markownikoff adduct is observed for the addition of benzeneselenenyl chloride to methylpropene and 2-methyl-2-butene. These data indicate a difference in both rate and product determining transition states between additions of arenesulfenyl and selenenyl chlorides to alkenes.     

A re-investigation of the far-infrared spectrum of isotactic polystyrene in the 7–2400 cm−1 region at ambient temperature

Fourier-transformed interferometric techniques have been utilized to obtain new data for the far-infrared spectrum of isotactic polystyrene. The region in which rotational and translational crystalline bands are observed has been investigated and 21 absorptions associated with infrared active crystal lattice modes have been observed in the 7–400 cm^?1 region. Possible assignments of these bands have been attempted, and a comparison with the previously reported data for polypropylene has been made.