Mass spectrometric studies of alkyl-, phenyl- and chloropyrimidines

The mass spectra of alkyl- and chloropyrimidines are recorded. A generalised fragmentation mechanism for the derivatives of pyrimidine is proposed. The principle of α-cleavage for heterocyclic compounds as proposed in the previous paper is shown to be valid for pyrimidine derivatives. Electronic structures of some molecular and intermediate ions are calculated by the openshell CNDO/2 and INDO methods.     

Synthesis of polystyrene latex with amphoteric surfactant and its characterization

An emulsion polymerization of styrene in the presence of an amphoteric surfactant; N,N-dimethyl-n-laurylbetaine (LNB) was carried out at pH 7.0. The polymerization rate and the concentration of the latex particle were proportional to the LNB concentration of 0.6 power. The latex particle sizes became smaller with increasing concentrations of LNB. The molecular weights of polystyrene latices increased with the concentration of LNB. The zeta-potentials of latex particles were significantly dependent on the pH, and showed the existence of an isoelectric point.     

Semidifferential electroanalysis with a solid working electrode

Semidifferential electroanalysis is described for hexacyanoferrate(III), dichromate, copper(II), p-aminophenol, p-benzoquinone, m-dinitrobenzene, guanine, guanosine, adenine, and adenosine at a stationary solid working electrode. Nearly symmetrical, peaked curves are obtained for the electrode processes of all the samples investigated. The predicted dependence of peak height and peak potential on concentration, electrode area, and potential scan rate are confirmed-experimentally for the glassy carbon disk electrode. It is demonstrated that the technique with the solid working electrode provides higher sensitivity and better resolution than ordinary linear sweep voltammetry. The sensitivity is somewhat worse than in differential pulse voltammetry, but the technique has the advantage of Speed.     

A SENSITIVE METHOD FOR DETERMINING CHLOROPHYLL b IN PLANT EXTRACTS

Abstract— A new method of using hydroxylamine as the reagent was developed to determine the concentrations of chlorophylls a and b in plant extracts accurately and sensitively. The method is based on the principle that hydroxylamine reacts in a short time with the aldehyde group of chlorophyll b in 95 per cent methanol at pH 5.8 to afford a derivative having a red band similar in position to the red band of chlorophyll a , while the spectrum of chlorophyll a is unaffected by the treatment with hydroxylamine. The method includes the measurements of absorbanlce for the mixture of a plant extract with hydroxylamine and for the reagent blank at a single wavelength, 666 mμ, and the concentrations of chlorophylls a and b are calculated from the absorbance value for the reagent blank and the increment of absorbance due to the reaction. By measuring this increment directly by difference photometry, one can determine a low concentration of chlorophyll b relative to chlorophyll a . The contents of chlorophylls in matured and etiolated leaves were determined by the method, and the errors included in this method were shown to be smaller than those in a commonly used technique including the measurements at two different wavelengths.     

Synthesis of pyrimidinopurinophanes

Synthesis and structures of the title compounds 2a–d are described. In spite of non-parallel orientation of the two base rings, fairly large hypochromism was observed for 2a–d.