Literature cited
I. N. Strel'tsova and Yu. T. Struchkov. Zh. strukt. khimii.2, 4, 312 (1961).
A. P. Terent'ev, A. N. Kost, A. M. Tsukerman, and V. F. Potapov. Nomenclature of Organic Compounds [in Russian] (Izd. AN SSSR. Moscow. 1955) p. 200.
H. W. W. Ehrlich. Acta crystallogr.,10. 699 (1957).
G. L. Avoyan and Yu. T. Struchkov. Zh. strukt. khimii.2, 1, 67 (1961).
H. Viervoll and O. Ögrim. Acta. crystallogr.,2. 277 (1949).
Yu. T. Struchkov and T. L. Khotsyanova, Izv. AN SSSR. Otd. khim. n.5. 821 (1960).
B. K. Vainshtein. Zh. éksperim. i teor. fiziki.27, 1, 44 (1954).
S. F. Darlow, Acta crystallogr.,13. 687 (1960).
M. A. Davydova and Yu. T. Struchkov Zh. strukt. khimii.2. 1. 69 (1961).
E. Mason and W. Rice. J. Chem. Phys.22. 522 (1954).
T. L. Hill. J. Chem. Phys..16. 399 (1948).
A. D. Crowell J. Chem. Phys.,29. 446 (1958).
L. S. Bartell. J. Chem. Phys..32. 827 (1960).
A. I. Kitaigorodskii. Dokl. AN SSSR.137. 116 (1961).
A. I. Kitaigorodskii and K. V. Mirskaya. Kristallografiya.6. 4. 507 (1961).
A. L. Kitaigorodskii. Organic Crystal Chemistry [in Russian] (Izd. AN SSSR. Moscow. 1955) pp. 116. 121, 128.
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Translated from Zhurnal Strukturnol Khimii. Vol. 2, No. 6. pp. 719–733. November–December, 1961
For communication 5 of this series, see [1].
We adopted a numbering convention for the stoms which differs from the usual chemical convention [2], but is more convenient in the structural seme. The two systems are compared in Fig. 1. In the structural system 5,6-dichloroacenaphibene is called 4,4′-cichloroacenaphthene.
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Avoyan, R.L., Struchkov, Y.T. Steric hindrances and conformation of molecules communication 6. Crystal and molecular structure of 4.4′-dichloroacenaphthene. J Struct Chem 2, 662–675 (1961). https://doi.org/10.1007/BF00747322
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DOI: https://doi.org/10.1007/BF00747322