Skip to main content
Log in

Structure of an Inclusion Compound of 28,28,35,35-Tetramethyl-11-oxo-1,4,18,21-tetraoxa[4,1,4,1,1]paracycloph ane with para-Xylene

  • Published:
Journal of inclusion phenomena and macrocyclic chemistry Aims and scope Submit manuscript

Abstract

The structure of the 2:3 complex between cyclophane 1 and para-xylene has been determined by a single crystal X-ray diffraction study at 143 K. One para-xylene molecule is enclosed within the cavity formed by two molecules of the host cyclophane; this ensemble displays crystallographic inversion symmetry. The other independent para-xylene molecule is located on a general position in the intermolecular cavities of the crystal lattice. The complex crystallizes in the triclinic space group P(-1) with a = 10β = 89.51(3), γ = 87.26(2)°, and Z = 1. Refinement based on 7539 unique reflections led to a final R(F) value of 0.0609.

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.

Similar content being viewed by others

References

  1. K. Krieger and F. Diederich: Chem. Ber. 118, 3620 (1985).

    Google Scholar 

  2. J. Ratilainen, K. Airola, M. Nieger, M. BÖhmer, J. Huuskonen, and K. Rissanen: Chem. Eur. J. 3, 749 (1997).

    Google Scholar 

  3. N. K. Dalley, X. Kou, R. A. Bartsch, B. P. Czech, and P. Kus: J. Incl. Phenom. 29, 323 (1997).

    Google Scholar 

  4. K. Odashima, A. Itai, Y. Iitaka, and K. Koga: J. Am. Chem. Soc. 102, 2504 (1980).

    Google Scholar 

  5. K. Odashima, A. Itai, Y. Iitaka, Y. Arata, and K. Koga: Tetrahedron Lett. 21, 4347 (1980).

    Google Scholar 

  6. I. Tabushi, K. Yamamura, H. Nonoguchi, K. Hirotsu, and T. Higuchi: J. Am. Chem. Soc. 106, 2621 (1984).

    Google Scholar 

  7. H. Nonoguchi, K. Yamamura, I. Tabushi, T. Higuchi, and K. Hirotsu: Bull. Chem. Soc. Jpn. 65, 805 (1992).

    Google Scholar 

  8. T. Takemura, K. Kozawa, T. Uchida, and N. Mori: Chem. Lett. 1984, 1839.

  9. Stoe et Cie., Darmstadt, Germany: Diffractometer control software.

  10. G. M. Sheldrick, Acta Crystallogr. A46, 467 (1990).

    Google Scholar 

  11. G.M. Sheldrick, SHELXL93, a program for refining crystal structures, University of GÖttingen, Germany (1993).

    Google Scholar 

  12. Siemens. XP, molecular graphics program, version 5.03. Siemens Analytical X-ray Instruments, Madison, USA (1994).

  13. We have synthesized other tetraoxaparacyclophanes, and will report on them elsewhere.

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Jones, P.G., Kuś, P. Structure of an Inclusion Compound of 28,28,35,35-Tetramethyl-11-oxo-1,4,18,21-tetraoxa[4,1,4,1,1]paracycloph ane with para-Xylene. Journal of Inclusion Phenomena 34, 267–276 (1999). https://doi.org/10.1023/A:1008085829837

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1008085829837

Navigation