α-Diimines as monodentate or bridging ligands; synthesis and characterization of palladium(II) and rhodium(I) di(t-butyl)diimine complexes

Complexes of di(t-butyl)diimine with PdCl₂(PhCN)₂ and with (CO)₂RhCl dimer have been synthesized and characterized. The diimine ligand is monodentate bonded in PdCl₂(t-butyldiimine)₂, while in (t-butyldiimine)-[Rh(CO)₂Cl]₂ it bridges two Cl(CO)₂Rh units.     

Energy-dispersive x-ray fluorescence analysis for sulphur,chlorine, potassium and calcium in aerosols

Problems in the use of x-ray spectrometry for the fast multi-element analysis of environmental samples such as aerosols collected on filters arise from absorption of the fluorescence intensity in the filter and in the collected matter. A procedure is described for the determination of the elements sulphur to calcium in aerosols collected on Whatman 41 filters. Two methods are compared for deconvolution of the spectra. These are based on counting in fixed energy channels or on non-linear least-squares analysis. Corrections for absorption effects have been calculated. Calibration is done with thin film standard deposits. The accuracy of the method is better than 15%. Difficulties in ascertaining the chlorine content of the filter are discussed. The evaporation of the chlorine fraction from the filter was studied in detail.     

Activation analysis of geological material using ruthenium as a multiisotopic comparator

The isotopes⁹⁷Ru,¹⁰³Ru and¹⁰⁵Ru, produced by reactor irradiation of elemental ruthenium, were applied as triple comparators in the activation analysis of rock FU-41, a basanitoid from Fuerteventura, Canary Island. The concentrations of the following elements were determined: Sm, Sc, Fe, Co, Na, La, Hf, Eu, Th and Cr. The aim of this work was the experimental control of the error theory of the multiple comparator method as well as the experimental check of the accuracy. Presented at the 3rd Symposium on the Recent Developments in Neutron Activation Analysis, Cambridge (U.K.), 2–4 July 1973.     

Sequential injection spectrophotometric determination of phenylephrine hydrochloride in pharmaceutical preparations

A fully automated sequential injection spectrophotometric method for the determination of phenylephrine hydrochloride in pharmaceutical preparations is reported. The method is based on the condensation reaction of the analyte with 4-aminoantipyrine in the presence of potassium ferricyanide. The absorbance of the condensation product was monitored at 503 nm. A linear relationship between the relative peak height and concentration was obtained in the range 0.5-17.5 mg l⁻¹. The detection limit (as 3σ value) was 0.09 mg l⁻¹ and repeatability was 0.8 and 0.6% at 2.5 and 5 mg l⁻¹, respectively. Results obtained by this method agreed very well with those obtained by the AOAC official method.     

Oxidation of polypropylene in benzene solution

The oxidation of both amorphous and crystalline polypropylene in benzene solution was studied at 100–130°C. tert-Butyl peroxide was used as an initiator. The kinetic behavior of the amorphous and crystalline forms differs slightly; the oxidation rate of the amorphous type is slower for a given polymer and initiator concentration. The oxidation rate of solutions of the crystalline form can be simply described by the expression: R₀ = 1.87 × 10¹³ exp {?29,000/RT} [t-Bu₂O₂]^0.58[polypropylene]^0.73, mole/l.-min. Product analyses of the oxidized solutions are incomplete, but the results do show that only ～40% of the absorbed oxygen is present as hydroperoxide. Further, much of the hydroperoxide is present in low molecular weight polar fragments which are acetone-soluble. These results show that oxidized polypropylene cannot be regarded simply as “polypropylene hydroperoxide” with repeating hydroperoxide groups attached to the polymer chain in 1,3,5… (tertiary) positions.     

HPLC–MS determination of the oxidation products of the reaction between α- and β-pinene and OH radicals

Biogenic non-methane hydrocarbons such as isoprene, alpha-pinene, and beta-pinene, are emitted by forests in very large quantities. To evaluate the role of alpha- and beta-pinene and their contribution to the global production of trace gases and especially aerosol precursors, a study of the oxidation mechanism of alpha- and beta-pinene with hydroxyl radicals must be conducted.The degradation products of both monoterpenes with hydroxyl radicals were identified and quantified in a fast-flow reactor. The products were collected on a liquid-nitrogen trap coated with a 2,4-DNPH solution to which two internal standards (benzaldehyde-2,4-DNPH and tolualdehyde-2,4-DNPH) had been added. The collection method was based on the in situ conversion of aldehyde and/or ketone compounds to their 2,4-dinitrophenylhydrazone derivatives. The derivatives were analyzed by HPLC-MS using APCI(-). TIC chromatograms and mass spectral data for the various oxidation products are presented.For alpha-pinene, pinonaldehyde is the most important degradation product, with smaller amounts of acetone, formaldehyde, campholenealdehyde, and acetaldehyde. For beta-pinene, nopinone and formaldehyde are the most abundant products, of almost equal importance, whereas acetone and acetaldehyde are minor compounds.     

Benzo- and indoloquinolizine derivatives. III. Synthesis and structural assignments of 4b,5,6,7,8,8a,10,11-octahydro-15bH-tribenzo-[a,c,h]quinolizine (4b,5,6,7,8,8a,10,11–octahydro-15bH-isoquino[2,1-f] phenanthridine)

Starting from either trans-2-phenylcyclohexylamine or the cis isomer, two epimers of 4b,5,6,7,8,8a,10,11-Octahydro-15bH-tribenzo[a,c,h]quinolizine have been synthesized. The four possible diastereoisomers of this compound were obtained by reduction of the enamine 5,6,7,8,10,11-hexahydro-15bH-tribenzo[a,c,h]quinolizine. Configuration and conformation are discussed by use of ir, 67.88 MHz cmr and 270 MHz pmr spectroscopy.     

Exploiting C3-symmetry in the dynamic coordination of a chiral trisoxazoline to copper(II): improved enantioselectivity, and catalyst stability in asymmetric lewis acid catalysis

Chiral C3-symmetric trisoxazolines are highly efficient stereodirecting ligands in enantioselective Cu(II) Lewis acid catalysis which is based on the concept of a stereoelectronic hemilability of the divalent copper; in direct comparison with the analogous bisoxazoline systems they are more efficient in the enantioselective alpha-amination as well as the enantioselective Mannich reaction of prochiral beta-ketoesters.     

Flash photolysis studies of the reaction of NH2 radicals with NO

The kinetics of the reaction NH₂ + NO → N₂ + H₂O were studied, using a conventional flash photolysis system. A value of k₁ = (1.1 ± 0.2) × 10¹⁰ & mole^?1 s^?1 was obtained at room temperature and in the pressure range 2–700 torr in the presence of nitrogen. A slight negative temperature coefficient was observed between 300 and 500 K, equivalent to a negative activation energy of 1.05 ± 0.2 kcal mole^?1.     

INDUCTION OF FREE RADICALS IN DNA BY PROFLAVINE AND VISIBLE LIGHT: INFLUENCE OF OXYGEN AND IONIC STRENGTH

Abstract —The photosensitization of native DNA is observed as an induction of free radicals in the DNA moiety of proflavine-DNA complexes. The intensity of the electron paramagnetic resonance spectra (at 77 K) is a measure of the number of free radicals present in frozen solutions of DNA-proflavine complexes after irradiation with visible light (Λ > 320 nm). In the absence of O₂, the photosensitization is significant but very low; it increases slightly with increasing NaCl ionic strength; it appears to be due to intercalated dye molecules and the qualitative analysis of the spectra obtained shows that mainly thymidine is involved. The reaction measured after saturation with O₂ is the same as the reaction in air but is quantitatively higher; the free radicals observed are peroxides. This induction of free radicals appears to be due to the intercalated dye molecules, each molecule acting independently. The important observation is a very sharp and large (around a hundred-fold) increase in the photosensitizing efficiency of the bound dye molecules occurring in NaCl between μ, # 0–25 and μ= 0–5 and in MgCl₂ between μ# 0–01 and μ=0–1.