A series of mono and diesters of itaconic acid: Synthesis and structural determination

Summary A series of mono and diesters of itaconic acid containing alkoxy and sulfide side chains of variable lengths has been synthesized. Their structures have been established on the basis of their spectral data.

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Eine Serie von Mono- und Diestern von Itaconsäure: Synthese und Strukturbestimmung

Zusammenfassung Es wurde eine Serie von Mono- und Diestern von Itaconsäure mit Alkoxy- und Sulfidseitenketten variabler Länge synthetisiert. Die Strukturaufklärung erfolgte mittels spektroskopischer Daten.

     

Polarographische Untersuchungen an Solochromviolett RS in Pufferlösungen in Abwesenheit und in Gegenwart oberflächenaktiver Stoffe (SAS)

The polarographic behaviour of solochrome violet RS is investigated in buffer solutions of varying pH in the absence and presence of surfactants (triton 100-X and dodecylbenzene-sulphonate). The reduction proceeds irreversibly along a single wave in acid solutions and two waves in alkaline ones. The electrode reaction corresponds to four electrons in media of pH<2.5 and pH>8.0; in media of pH 4 5.5 two electrons are consumed. In solution of pH 2.5 4 or 5.5–8.0, both reactions contribute in varying magnitudes. The addition ofSAS causes the inhibition of reduction beyond the 2-electrons stage in acid solutions; the polarograms comprise one wave in case ofDBS and two waves of equal height in presence of triton. In alkaline media the polarogram comprises three waves due to the splitting of the main reduction wave. The kinetic parameters of the electrode reaction are also determined.     

Dielectric properties of BaTiO3 modified with ZrO2

The dielectric constant and loss tangent of BaTiO₈ with ZrO₂ additives have been studied. The loss tangent was less ranging between 0.16 for pure BaTiO₃ and 0.05 for samples containing 5% ZrO₂. The dielectric constant at Curie temperature decreased with increasing ZrO₂ concentration up to 0.4%. The volume resistivity measurements illustrate a peak value at a certain range of temperatures for each composition.     

Nitrogen-15 nuclear magnetic resonance spectra of isocyanates,isothiocyanates and N-sulfinylamines

The ¹⁵N NMR spectra of ten isocyanates, four isothiocyanates, and four N-sulfinylamines have been obtained at the natural-abundance level by high-resolution NMR spectroscopy. The results show that isocyanates and isothiocyanates have ¹⁵N chemical shifts over 200 ppm toward higher fields compared to those of N-sulfinylamines. The sensitivity of the ¹⁵N shifts in these substances to substituent and electronic effects are discussed.     

A dynamic nuclear magnetic resonance spectroscopic study of conformational properties of 1,3-dioxepane and 4,4,7,7-tetramethyl-1,3-dioxepane

The 251 MHz ¹H and the natural abundance 63.1 MHz ¹³C NMR spectra of 1,3-dioxepane (1) and 4,4,7,7-tetramethyl-1,3-dioxepane (2) have been investigated over the temperature range of 5 to ?180 °C. While the spectra of 1 show no dynamic NMR effect, compound 2 exists in solution as a 1:1 mixture of a symmetrical (C₂) twist-chair and its mirror image conformation. The free energy barrier for the conformational racemization of 2 is 43 kJ mol^?1 (10.3 kcal mol^?1). Interconversion paths between various conformations of 2 are discussed. Compound 1 is suggested to have a symmetrical (C₂) twist-chair conformation which is rapidly pseudorotating via a chair conformation to achieve a time averaged symmetry of C_2v, even at ?180 °C.     

Preparation and IR-spectroscopic study of charge transfer complexes of naphthalene derivatives with some tri- and di-nitrobenzenes

The charge transfer complexes of naphthalene and some of its derivatives with some trinitro- and dinitrobenzenes are prepared and investigated by irspectroscopy. The shifts in the bands due to functional groups as well as the _CH bands of both donor and acceptor are found to be indicative for the type of bonding in the charge transfer complex.

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Darstellung und IR-spektroskopische Untersuchungen an Charge Transfer Komplexen von Naphthalinderivaten mit Di- und Tri-nitrobenzolen

Zusammenfassung Aus den Verschiebungen der Bandenlagen bei der Komplexierung, bzw. aus der Abhängigkeit der Bandenlagen von den funktionellen Gruppen, wird der Bindungstyp der Charge-Transfer-Komplexe ermittelt.