Skip to main content
Log in

Adamant-1,3,5-triyl super dodecahedranes

  • Brief Communications
  • Published:
Journal of Structural Chemistry Aims and scope Submit manuscript

Abstract

By quantum chemical DFT M06-2X/6-31G(d,p) method, the equilibrium parameters of rigid and stable hydrocarbon clusters of icosahedral symmetry with a dodecahedron structure whose sites are occupied by 20 adamant-1,3,5-triyl moieties linked with each other either directly or through bridges containing two or four carbon atoms are determined. The radius of the smallest studied quasispherical molecules is 1.05 nm and that of the largest one is 1.76 nm. The radius of the inner cavity in them varies from 0.37 nm (C200H260) to 1.06 nm (C320H260). Perfluorination increases the outer and decreases the inner radius of super dodecahedrane.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  1. W. A. Smit, A. F. Bochkov, and R. Caple, Organic Synthesis: The Science Behind the Art, The Royal Society of Chemistry, London (1998).

    Google Scholar 

  2. Y. Zhao and D. G. Truhlar, Acc. Chem. Res., 41, No. 2, 157–167 (2008).

    Article  CAS  Google Scholar 

  3. M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, G. Scalmani, V. Barone, B. Mennucci, G. A. Petersson, H. Nakatsuji, M. Caricato, X. Li, H. P. Hratchian, A. F. Izmaylov, J. Bloino, G. Zheng, J. L. Sonnenberg, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, J. A. Montgomery Jr., J. E. Peralta, F. Ogliaro, M. Bearpark, J. J. Heyd, E. Brothers, K. N. Kudin, V. N. Staroverov, R. Kobayashi, J. Normand, K. Raghavachari, A. Rendell, J. C. Burant, S. S. Iyengar, J. Tomasi, M. Cossi, N. Rega, J. M. Millam, M. Klene, J. E. Knox, J. B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann, O. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. Ochterski, R. L. Martin, K. Morokuma, V. G. Zakrzewski, G. A. Voth, P. Salvador, J. J. Dannenberg, S. Dapprich, A. D. Daniels, O. Farkas, J. B. Foresman, J. V. Ortiz, J. Cioslowski, and D. J. Fox, GAUSSIAN-09, Revision A.02, Gaussian, Inc., Wallingford CT (2009).

    Google Scholar 

  4. L. V. Vilkov, V. S. Mastryukov, and N. I. Sadova, Determination of the Geometrical Structure of Free Molecules, Mir Publishers, Moscow (1983).

    Google Scholar 

  5. P. E. Eaton, E. Galopini, and R. Gilardi, J. Am. Chem. Soc., 116, No. 17, 7588–7596 (1994).

    Article  CAS  Google Scholar 

  6. A. de Meijere, S. Kozhushkov, T. Haumann, et al., Chem. Eur. J., 1, No. 1, 124–131 (1995).

    Article  Google Scholar 

  7. A. de Meijere (ed.), in: Modern Problems of Organic Chemistry, Vol. 12, 3–20 (1998).

    Google Scholar 

  8. S. G. Semenov and Yu. F. Sigolaev, Zh. Obsch. Khim., 76, No. 6, 1006–1009 (2006).

    Google Scholar 

  9. L. N. Sidorov, M. A. Yurovskaya, and A. Ya. Borshchevskii et al., Fullerenes [in Russian]. Examen, Moscow (2005).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Yu. F. Sigolaev.

Additional information

Original Russian Text Copyright © 2013 by S. G. Semenov, Yu. F. Sigolaev, A. V. Belyakov

__________

Translated from Zhurnal Strukturnoi Khimii, Vol. 54, No. 5, pp. 923–925, September–October, 2013.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Semenov, S.G., Sigolaev, Y.F. & Belyakov, A.V. Adamant-1,3,5-triyl super dodecahedranes. J Struct Chem 54, 960–962 (2013). https://doi.org/10.1134/S002247661305017X

Download citation

  • Received:

  • Revised:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S002247661305017X

Keywords

Navigation