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2015-10-19 11:18:00

International Workshop in Organic Electronics of Highly Correlated Molecular Systems at ZIOC RAS

On October 8-10 2015, the Third Joint Workshop in Organic Electronics of Highly Correlated Molecular Systems was held at the Institute. It was organized by Zelinsky Institute of Organic Chemistry RAS in cooperation with Vorozhtsov Novosibirsk Institute of Organic Chemistry.

46 eminent experts in the design and synthesis of organic molecular materials for microelectronics and functional devices on their basis from Russia, Japan and the UK participated in the workshop.

It is an annual conference held under the auspices of the Japan Japanese Society for the Promotion of Science (Core-to Core program) and the British Liverhulme Trust. This workshop was supported by the Russian Foundation for Basic Research, Russian division of Chemical Abstracts Service, Japan Japanese Society for the Promotion of Science, and British Liverhulme Trust. for details go to link.

The scientific program included 24 presentations, for details see link.

Important events:

The European Academy of Sciences (Academia Europaea) was founded in 1988. It unites about four thousand globally acknowledged experts in mathematics, medicine, natural sciences, humanities, law, economy, and social and political sciences from many countries of Europe. Among its members are also European scientists who live in other regions of the world. Currently, it includes seventy two Nobel laureates and it should be highlighted that many of them were elected to the Academy before winning the Prize.
Prof Mario Pagliaro (Palermo Italy) gave two talks on June 8th and 9th.
Alexey Sukhorukov, N. D. Zelinsky Institute of Organic Chemistry, Moscow, Russia, and colleagues studied the selective reactions of in-situ generated metal azides on N,N-bis(oxy)enamines. By combining readily generated bis(oxy)enamine substrates with sodium azide and one of a variety of metal salts (including Mg, Cu, Zn, Co, and Ni), the researchers showed that the metal cation selectively alters the mechanism to favor the formation of specific organoazide products.
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