Conformational Analysis of 2-Formylselenophene by Means of 13C–1H, 13C–13C, and 77Se–1H Spin–Spin Coupling Constants
Yury Yu. Rusakov A , Leonid B. Krivdin A B , Natalia V. Istomina A , Ekaterina P. Levanova A and Galina G. Levkovskaya AA A. E. Favorsky Institute of Chemistry, Irkutsk, Siberian Branch of the Russian Academy of Sciences, Favorsky Street 1, 664033 Irkutsk, Russia.
B Corresponding author. Email: krivdin_office@irioch.irk.ru
Australian Journal of Chemistry 62(7) 734-738 https://doi.org/10.1071/CH09010
Submitted: 7 January 2009 Accepted: 4 February 2009 Published: 13 July 2009
Abstract
Theoretical energy-based conformational analysis of 2-formylselenophene performed at the MP2/6–311G** level together with experimental measurements and SOPPA/aug-cc-pVTZ-J calculations of its 13C–1H, 13C–13C, and 77Se–1H spin–spin coupling constants showed that this compound predominantly adopts the s-cis conformation. Most of the spin–spin coupling constants under study, especially vicinal 77Se–1H couplings, demonstrate remarkable stereochemical behaviour with respect to the internal rotation of the formyl group, which is of major importance in stereochemical studies of the related selenium-containing compounds.
Acknowledgements
Financial support from the Russian Foundation for Basic Research (Grant no. 08–03–00021) is acknowledged. L.B.K. thanks Professor Sauer for providing him with the extended aug-cc-pVTZ-J basis set including selenium.
[1]
Yu. Yu. Rusakov,
L. B. Krivdin,
N. V. Istomina,
V. A. Potapov,
S. V. Amosova,
Magn. Reson. Chem. 2008, 46, 979.
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