Conclusions
From the example of 1,1-di(tert-butylperoxy)cyclohexane it was shown that not only intramolecular steric interactions (the type of substituent at the O-O bond) but also the influence of crystal field forces have a substantial effect on the conformation of the peroxide group in the crystals of peroxyketals of cyclanes.
Similar content being viewed by others
Literature cited
V. L. Antonovskii, Chemical Sources of Free Radicals [in Russian], Znanie, Moscow (1980).
Modern Plastica,57, 50 (1980).
P. Groth, Acta Chem. Scand.,23, 2277 (1969).
A. Yu. Kosnikov, V. L. Antonovskii, S. V. Lindeman, et al., Kristallografiya,31, 97 (1986).
Yu. L. Slovokhotov, T. V. Timofeeva, M. Yu. Antipina, and Yu. T. Struchkov, J. Mol. Struct.,112, 127 (1984).
S. Patai (ed.), The Chemistry of Functional Groups. Peroxides, John Wiley and Sons, New York-London (1983), p. 378.
M. A. Kravers, M. Yu. Antipin, V. I. Kulishov, and Yu. T. Struchkov, Kristallografiya,22, 1118 (1977).
R. G. Gerr, A. L. Yanovskii, and Yu. T. Struchkov, Kristallografiya,28, 1029 (1983).
V. G. Dashevskii, Conformation of Organic Molecules [in Russian], Khimiya, Moscow (1974).
M. I. Dakhis, A. A. Lugovskoi, and V. G. Dashevskii, Opt. Spektrosk.,33, 243 (1972).
Author information
Authors and Affiliations
Additional information
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 2, pp. 294–297, February, 1989.
Rights and permissions
About this article
Cite this article
Kosnikov, A.Y., Antonovskii, V.L., Lindeman, S.V. et al. Structure of 1,1-di(tert-butylperoxy)cyclohexane. Russ Chem Bull 38, 247–249 (1989). https://doi.org/10.1007/BF00953606
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00953606