Spectral and electrochemical properties of polyaniline-V2O5 composites of the intercalation type

We propose a new approach to obtaining composites of the intercalation type based on polyaniline and V₂O₅. We have determined the characteristics of these composites using x-ray diffraction, IR spectroscopy, and EPR. We show that the compounds obtained exhibit stable redox properties in aqueous and aprotic electrolytes.Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 31, No. 6, pp. 361–364, November–December, 1995.We would like to express our thanks to V. G. II'in for help in carrying out the x-ray phase investigations. This work was made possible with the partial support of the International Science Foundation (grant N U6B000).     

1,4-Phenylen-bis-diphenylderivate der Elemente der 5. Hauptgruppe des Periodensystems

Zusammenfassung Die Darstellung sämtlicher am mittleren Benzolkern p-substitutierten Verbindungen (C₆H₅)₂ MC₆H₄ M(C₆H₅)₂ mitM=N, P, As, Sb und Bi wird beschrieben. Für die bereits bekannte Stickstoff-bzw. Arsen-Verbindung konnte ein neuer Darstellungs-weg mit guten Ausbeuten gefunden werden, während die Antimon-und Wismutverbindung erstmals beschrieben werden. Durch Dipolmomentmessungen, UV- und IR-Aufnahmen ist ein Vergleich mit den einfachen Triphenylderivaten der genannten Elemente möglich.

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The compounds p-(C₆H₅)₂ MC₆H₄ M(C₆H₅)₂,M=N, P, As, Sb, and Bi, were prepared. New methods for the preparation of the N and As compound with good yields were found. The Sb and Bi compound were synthesized for the first time. Dipole moments, IR- and UV-spectra of these compounds were compared with those of the triphenyl derivates.

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Herrn Prof. Dr.F. Wessely zum 70. Geburtstag gewidmet.     

Reaction of 2-chloro-5-methylbenzoquinone with Β-aminocrotonic ester derivatives

The reaction of 2-chloro-5-methylbenzoquinone with -aminocrotonic ester derivatives was studied by PMR spectroscopy in CD₃COOD. The spectra indicate the formation of intermediate hydroquinone and quinone derivatives, which subsequently transform into the corresponding indoles. It was shown that the indolization proceeds unequivocally at the 3-position of the initial benzoquinone, and the rate of formation of the indole derivatives decreases with increase in the size of the substituent at the nitrogen atom of the -aminocrotonic ester. The starting, intermediate compounds and the end products observed in the PMR spectra were identified by comparison with specially synthesized compounds.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 324–328, March, 1990.     

Reaction of 2,3-epoxypropyl alkyl sulfides with carboxylic acids and phenol

Russian Chemical Bulletin -