On the mechanism of the photocyclization of azadienes

  1. Marazzi, M. 2
  2. Blanco-Lomas, M. 1
  3. Rodríguez, M.A. 1
  4. Campos, P.J. 1
  5. Castaño, O. 2
  6. Sampedro, D. 1
  7. Frutos, L.M. 2
  1. 1 Universidad de La Rioja
    info

    Universidad de La Rioja

    Logroño, España

    ROR https://ror.org/0553yr311

  2. 2 Universidad de Alcalá
    info

    Universidad de Alcalá

    Alcalá de Henares, España

    ROR https://ror.org/04pmn0e78

Aldizkaria:
Tetrahedron

ISSN: 0040-4020

Argitalpen urtea: 2012

Alea: 68

Zenbakia: 2

Orrialdeak: 730-736

Mota: Artikulua

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DOI: 10.1016/J.TET.2011.10.101 SCOPUS: 2-s2.0-82955198387 WoS: WOS:000299443900042 GOOGLE SCHOLAR

Beste argitalpen batzuk: Tetrahedron

Lotura duten proiektuak

Procesos fotoquímicos de sistemas con enlaces C=N. Reacciones radicalarias, cicloadicionales 2+2 y nuevos motores moleculares biomiméticos

2007/00077/001

Laburpena

The photocyclization of azadienes to yield quinolines has been studied by means of CASPT2//CASSCF calculations. In order to study this extensive family of compounds, a minimal model system keeping the fundamental key features of this kind of compounds have been analyzed with the aim of explaining the general behavior of azadienes found experimentally. We show that, although several conformers of the reacting molecule are populated on the ground-state at room temperature, there is only one capable of successfully yield the products. It is shown that photocyclization takes place with fast relaxation in both S 2 and S 1 excited states, in agreement with the experimental lack of fluorescence. This fact, together with the presence of reaction paths that allow effective recovery of the starting molecule, explains not only the experimental photocyclization of azadienes under UV radiation, but also accounts for the low efficiency of the process. The mechanistic information obtained allows to provide an explanation of the found reaction outcome and to suggest some modifications to improve the synthetic utility of these reactions. © 2011 Elsevier Ltd. All rights reserved.