The acid-catalyzed and neutral solvolysis of benzoylphenyldiazomethane in water,aqueous t-butanol,and aqueous salt solutions

The acid-catalyzed and water-catalyzed solvolysis ofbenzoylphenyldiazomethane (1) have been studied in water and in t-butanol-water mixtures, the mole fraction of water (n_H2O) being varied from 0·75-1·00. Increasing t-butanol concentrations produce a pronounced decrease in both k_H⊕ and k_H2O. In the “water reaction” mutually compensatory changes of AH

and AS

are associated with the rate variations, with minima in AH

and AS

at about n_H2O = 0·95. In addition it was found that the magnitude of the salt effect of (n-Bu)₄NCl on the rate of hydrolysis of 1 in water at 25° is much larger than that of LiCl, NaCl and NaBr. Assuming that the rate of the “water reaction” is largely determined by water acidity, the data are suggestive for the existence of a relation between water acidity and solvent structural integrity in highly aqueous t-butanol-water solutions.     

Application of the flory-mandelkern equation to individual unfractionated polymer samples

A method is developed for the application of the Flory-Mandelkern equation to the determination of the weight-average molecular weights of individual, broad, unfractionated polymer samples. The method includes appropriate averaging of the sedimentation constants and of the intrinsic viscosity of an unfractionated polymer sample in a θ solution from the velocity sedimentation data. By means of the method, individual samples of polystyrene, poly(isooctyl methacrylate) and of the copolymer of styrene with 20% isooctyl methacrylate prepared under the same emulsion polymerization conditions from commercial monomers have been investigated. Appropriate θ solvents have been found by the Elias method. Equations for the dependence of the sedimentation constants and of the intrinsic viscosities in the θ solvents on the molecular weights have been established for the polymers without fractionation. Osmometric and light-scattering measurements as well as Archibald experiments have shown that by the proposed method the molecular weight cut-off effect is eliminated in the above equations and in the polydispersity parameter M _w/M _n. Molecular weight distributions have been determined for the polymer samples.     

On distribution of molecular weight in anionic polymerizates of caprolactam

Measurement has been made of the dependence of the molecular weight distribution on the ratio of the catalytic system components and on the polymerization time for polycaprolactam obtained by anionic polymerization. A bimodal character of the curves was observed for products made using molar ratios of activator (N-benzoylcaprolactam) to initiator (sodium dihydro-bis(methoxyethoxy)aluminate) of 1:1 and 1:3, when the polymerization times were less than 1 hr. This course is explained by the influence of fast side-reactions, mainly condensations. For a ratio of 3:1 of the components of the catalytic system, smooth integral distribution curves are obtained, accounting for a very fast decrease in the strong base concentration in the initial stages of the polymerization.     

Semi-classical calculations of rotational/vibrational transitions in Li+ − H2

Some semi-classical calculations of rot/vib transitions in Li⁺ ? H₂ at 0.869, 1.469 and 3.919 eV total energy are presented. Comparison with recent quantum mechanical and classical S-matrix calculations is made.     

Spin-adapted wave functions of the serber type and time reversal

A procedure is proposed for generating Serber-type spin eigenfunctions withM _s = 0. The procedure uses the time-reversal invariance of these functions to increase the efficiency and to reduce the storage requirements. Simplifications in calculating the matrix elements of an observable operator which follow from the use of the time-reversal symmetry are briefly discussed.     

Zur Theorie der Bildung von Gelen

Colloid and Polymer Science -     

Stroboskopisehe Untersuchungen über den zeitlichen Aufbau,die optische Absorption und das Nachleuchten gesteuerter Funkenentladungen

Zusammenfassung In elektrischen Funkenentladungen lassen sich Zündphase, Bogenphase und Abklingphase unterscheiden, die besondere charakteristische Eigenschaften aufweisen. Ihre Untersuchung wird durch ein neu entwickeltes Stroboskop ermöglicht, dessen Phasenlage beliebig gegenüber der periodischen Funkenfolge verstellt werden kann. Durch optische Absorption kann im abklingenden Funken nicht nur der atomare Metalldampf durch seine Grundlinien nachgewiesen werden, sondern auch seine molekularen Reaktionsprodukte mit der umgebenden Atmosphäre lassen sich durch Bandenabsorption feststellen. Das Nachleuchten abklingender Funkenentladungen wird im wesentlichen durch das Nachleuchten des aktiven Stickstoffs getragen, wenn der Metalldampfgehalt der Funkenstrecke gering gehalten wird. Gegen Ende der Nachleuchtphase lassen sich Sprüherscheinungen an den Elektroden feststellen, bei denen kleine Partikelchen mit unterschiedlichen, zum Teil spiralig verlaufenden Bahnkurven ausgeschleudert werden. Die Flugbahnen der Teilchen weisen auf starke Gasströmungen in der Funkenstrecke hin.

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Summary In electrical spark discharges it is possible to distinguish ignition phase, arc phase, and decay phase. These display special characteristic properties. It is possible to study them by means of a newly developed stroboscope, whose phase position can be adjusted at will against the periodic succession of sparks. Through optical absorption, not only the atomic metal vapor can be detected, through its ground lines, in the decaying sparks but also its molecular reaction products with the surrounding atmosphere can be established through the band spectrum. The phosphorescence of decaying spark discharges is essentially due to the afterglow of the active nitrogen, if the metal vapor of the spark gap is kept low. Toward the end of the phosphorescence phase, spray phenomena may be observed at the electrodes, in which tiny particles with distinctive, in part spiral, orbital curves are ejected. The flight paths of these particles indicate strong gas currents in the spark gap.

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Résumé On peut distinguer dans la décharge par étincelles, la phase d'ignition, la phase d'arc et la phase de décroissance. On explique ainsi certaines propriétés caractéristiques. On peut étudier ces diverses phases à l'aide d'un dispositif stroboscopique nouveau réglable à volonté pour observer la même phase d'étincelles qui se succèdent périodiquement. Grâce a l'absorption optique on peut détecter soit une vapeur atomique métallique par ses raies caractéristiques pendant la période de décroissance des étincelles, soit les réactions moléculaires qui se produisent dans les gaz environnants grâce aux spectres de bandes. La phosphorescence pendant la décroissance de l'étincelle est due essentiellement à la postluminescence de l'azote actif, si la tension de vapeur du métal entre les électrodes est suffisamment basse. Pendant la fin de la période de phosphorescence on observe sur les électrodes des phénomènes de pulvérisation avec formation de très petites particules qui sont éjectées en décrivant des trajectoires en spirales. Les trajectoires aériennes de ces particules révèlent l'existence de forts courants gazeux entre les électrodes.

     

1-Aryl-6-azauracile, 7. Mitt.: Herstellung einiger funktioneller Derivate der 1-Phenyl-6-azauracil-5-carbonsäure

Zusammenfassung In der vorliegenden Arbeit wird die Herstellung des Chlorids (1), von Estern (2a, 2b), Amiden (3a-3g), des N-Hydroxyamids (3h) und Hydrazids (3i) der 1-Phenyl-6-azauracil-5-carbonsäure beschrieben.