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Журнал структурной химии  / №4 2015

A THEORETICAL STUDY OF THE THERMAL CURTIUS REARRANGEMENT OF SOME CINNAMOYL AZIDES USING THE DFT APPROACH (330,00 руб.)

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Первый авторAbu-Eittah
АвторыWalid M.I., Zordok W.
Страниц13
ID359772
АннотацияThe thermal Curtius rearrangement of cinnamoyl azide, 1-azido-3-phenylprop-2-ene-1-one, and the reactions of some of its derivatives is studied theoretically using the DFT (B3LYP631G(d,p) approach. The potential energy surface profiles of the rearrangement are calculated. The transition state was located and confirmed. The Curtius rearrangement of the studied compounds is a one-stage, discrete reaction. A weak effect of substitution on the reaction rate is due to the unique, localized π system of the studied molecules; strong opposing dipoles span the whole molecule.
УДК541.6:547.12
Abu-Eittah, RafieH. A THEORETICAL STUDY OF THE THERMAL CURTIUS REARRANGEMENT OF SOME CINNAMOYL AZIDES USING THE DFT APPROACH / RafieH. Abu-Eittah, M.I. Walid, W. Zordok // Журнал структурной химии .— 2015 .— №4 .— С. 34-46 .— URL: https://rucont.ru/efd/359772 (дата обращения: 03.05.2024)

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Том 56, № 4 UDC 541.6:547.12 A THEORETICAL STUDY OF THE THERMAL CURTIUS REARRANGEMENT OF SOME CINNAMOYL AZIDES USING THE DFT APPROACH Rafie H. Abu-Eittah1, Walid M.I. Hassan1, W. Zordok2 1Department of Chemistry, Faculty of Science, University of Cairo, Giza, Egypt E-mail: aboeittah@yahoo.com 2Department of Chemistry, Faculty of Science, University of Zagazig, Egypt Received September, 26, 2013 The thermal Curtius rearrangement of cinnamoyl azide, 1-azido-3-phenylprop-2-ene-1-one, and the reactions of some of its derivatives is studied theoretically using the DFT (B3LYP631G(d,p) approach. <...> The potential energy surface profiles of the rearrangement are calculated. <...> The transition state was located and confirmed. <...> The Curtius rearrangement of the studied compounds is a one-stage, discrete reaction. <...> A weak effect of substitution on the reaction rate is due to the unique, localized π system of the studied molecules; strong opposing dipoles span the whole molecule. <...> In the first (Scheme 1), the reaction proceeds in one stage with a synchronous formation of isocyanate and N2 evolution (a concerted mechanism). <...> The first stage is the N2 evolution with the formation of acyl nitrene and the second stage is the rearrangement of acyl nitrene into the product (Scheme 2). <...> Т. 56, № 4 677 In the photochemical Curtius rearrangement the formation of acyl nitrene was proved [ 2 ]. <...> Thus, by analogy it was assumed that acyl nitrene participates in the thermal rearrangement of acyl azides. <...> However, the experimental results indicated that acyl nitrenes as well as the by-products of their interaction with specific radical traps did not result from the thermal rearrangements of alkyl and aryl carbonyl azides [ 5 ]. <...> The participation of acyl nitrene was found only in the thermal (and photochemical) decomposition of ethoxycarbonyl azide EtOC(O)N3 [ 6 ] and it was the only case of the thermal reaction in which nitrene was experimentally identified by a chemical method [ 7 ]. <...> The first systematic study of the thermal Curtius reaction of small azides provided by Rauk and Alewood [ 8 ] appointed out two degenerate states of formyl azide, one yielding carbonyl nitrene and another isocyanate. <...> Abu-Eittah et al. [ 9 ] using MP2/6-31G* calculations concluded that while the Curtius rearrangement of formyl azide proceeds in one stage with a simultaneous formation of isocyanate and N2 evolution (concerted mechanism), that <...>