Comparative studies of reactions of commercial polymers with molecular oxygen,singlet oxygen,atomic oxygen and ozone—II. Reactions with 1,2-polybutadiene

The oxidations of 1,2-polybutadiene by molecular oxygen, singlet oxygen, atomic oxygen and ozone have been studied using u.v. and i.r. spectroscopic methods. Some possible implications of the results of oxidation in the presence of singlet oxygen (parallel free radical oxidation) and atomic oxygen (formation of NO₂ and its reaction with polymer) are discussed. Crosslinking was observed during all types of oxidation. A new mechanism involving formation of free radicals has been considered in detail. During ozonization of 1,2-polybutadiene, formation of formaldehyde and formic acid were detected. An ozonization mechanism has been proposed.     

Polychlorinated polyamides. II. Synthesis and characterization of polyamides derived from 2, 5-dichloroterephthaloyl dichloride and perchloroterephthaloyl dichloride

New thermally stable polyamides were prepared by interfacial polymerization of the title compounds and various aliphatic and aromatic diamines. The polymers were characterized by infrared spectrometry, elemental analysis, and differential scanning calorimetry. The molecular weights of the polymers were estimated by viscosity measurements. The influence of the halogen content on the thermal properties and degree of polymerization of the polymers was studied. One of the polyamides was fractionated to determine the degree of polydispersity.     

Energy levels of iodine monochloride near the first dissociation limit

Absorption transitions to vibrational levels close to the A state dissociation limit of ICI have been examined using a two-photon sequential absorption technique. The discrete rotational structures of I³⁷ Cl bands to within 0.7 cm^?1 of the limit have been selectively excited and analysed. A value of 17557.514 ± 0.030 cm^?1 has been obtained for the I(²P^o_{$\text{3}\text{2}$}) + Cl(²P^o_{$\text{3}\text{2}$}) dissociation energy D_e, relative to the minimum of the ICI ground state potential well. The two-photon technique can be used to excite and display separately the high resolution absorption spectra of different isotopic species of a molecule which are contained in a mixture.     

Transitions between disordered phases in supercooled liquid silicon

We have investigated the transitions between disordered phases in supercooled liquid silicon using computer simulations. The thermodynamic properties were directly obtained from the free energy, which was computed using the recently proposed reversible scaling method. The calculated free energies of the crystalline and liquid phases of silicon at zero pressure, obtained using the environment dependent interatomic potential, are in excellent agreement with the available experimental data. The results show that, at zero pressure, a weak first-order liquid-liquid transition occurs at 1135 K and a continuous liquid-amorphous transition takes place at 843 K. These results are consistent with the existence of a second critical point for the liquid-liquid transition at a negative pressure.     

A low-cost non instrumental method for semiquantitative determination of mercury in fish

A non instrumental method for the semiquantitative determination of mercury in fish is described. The sample is acid digested and the mercury vapor released after chemical reduction with SnCl2. The mercury vapor is then collected on a detecting paper covered with an emulsion of Cu2I2, 3% carboxymethylcellulose and MgCl2 as moistener agent. The colored Cu2[HgI4] complex is formed and the color intensity is proportional to the mercury concentration in the original sample. Parameters such as sample mass/digestion solution volume ratio, emulsion composition, paper covering technique, carrier gas flow were investigated. Comparative studies using CVAAS and digital color analysis after scanning the papers confirmed the applicability of the method to real samples.     

Novel routes to 1-aryl-1,4-dihydro-3(2H)-isoquinolinones and 2-substituted or 2,3-disubstituted benzofurans by intramolecular cyclizations

N-(α-Benzotriazolylalkyl)arylacetamides, readily available from an arylacetamide, an aldehyde and benzotriazole, undergo intramolecular cyclization under acidic conditions to give 1-aryl-1,4-dihydro-3(2H)-isoquinolinones in good to excellent yields. Similarly, 2-(benzotriazol-1-yl)-2-(o-hydroxyphenyl)ethanols, obtained by lithiation of 2-(benzotriazol-1-ylmethyl)phenols followed by quenching with aldehydes or ketones, eliminate a molecule of water and a molecule of benzotriazole yielding 2-substituted and 2,3-disubstituted benzofurans.     

A comparative potentiostatic study of the electrocrystallization of PbO2 on platinum and glassy carbon electrodes

The deposition of PbO₂ on platinum and glassy carbon electrodes was investigated experimentally. The comparison of the different behaviour on the two types of electrodes is presented. The effects of variation of temperature, potential, nucleation order and induction time-lags on the electrocrystallisation process are discussed.The present investigations have confirmed that electrocrystallisation of PbO₂ occurs through 3-D nucleation and growth on glassy carbon and most probably also on platinum. The data on platinum contains considerable noise from simultaneous chemical processes and is not amenable for analysis in a simple way. The steady state behaviour is unusual because it has generally been assumed that charge transfer is rate determining under most conditions. However, as shown here, if lattice incorporation is slow even at the steady state, it provides a method for separating the activation energies associated with the nucleation and growth rate constants. Finally, the dissolution of PbO₂ into the platinum substrate and its implication on transient rates merits more attention. In this context the Pt-PbO₂ system is probably not a good choice because of the large contribution of substrate oxidation to the measured transient rates.     

Studies in sesquiterpenes—LVI: Isolongifolene (part 7): mechanism of rearrangement of longifolene to isolongifolene—II

The question of possible neutral intermediates which may lie on the reaction pathway in going from longifolene to isolongifolene has been investigated using BF₃·Et₂O-AcOD and D₃PO₄-dioxane, as reagents. It has been found that longicyclene is not an obligatory intermediate. The mode of cleavage of cyclopropane ring in longicyclene has been investigated.     

PHOTOCHEMISTRY OF DNA CONTAINING IODINATED CYTOSINE*

Abstract— –Irradiation at 313 nm of compounds containing iodinated cytosine moieties results in the photolysis of iodine. Photolysis occurs with a quantum yield of 0·0224·024 for 5-iododeoxycytidine and 5-iododeoxycytidine monophosphate, and 0·004–0·008 for iodinated DNA as well as for iodinated polycytidylate. Photodegradation of the cytosine moiety occurs when air is present during irradiation, presumably due to the reaction of oxygen with the cytosyl radical formed when iodine is lost. This oxygen promoted photodegradation destroys the cytosine chromophore and is complete in the monomers but occurs to only a limited extent in the polymers. In the absence of oxygen or in the presence of ethanol, photodegradation is prevented and the loss of iodine leads exclusively to the formation of the cytosine chromophore. In DNA, the loss of iodine is accompanied by the formation of sugar damage and/or chain breaks. As measured by sedimentation in alkaline sucrose gradients, approximately one break is made for every six iodinqs lost in denatured DNA. The frequency of chain breakage per iodine photolyzed is reduced 2-fold in renatured DNA. Analysis in neutral gradients suggests that half of the breaks observed in alkali are alkali-labile bonds. Both ethanol and cysteamine reduce the number of chain breaks observed in alkali by ˜ 3-fold.     

On the formation of artefact peaks in linked scans of the magnet and electric sector fields in a mass spectrometer

The apperrance of peaks at non-integral masses in linked scans, where the ratio B/E is kept constant, is shown to be caused by fragmentations of metastable ions occuring in the region between the magnetic and electric sectors. A formula is given for calculating the mass of the parent metastable ion and that of its daughter ion.