Raman spectrum of 1,5-hexadien-3-yne

  • M. I. Batuev
  • A. P. Meshcheryakov
  • A. D. Matveeva
Brief Communications
  • 18 Downloads

Summary

In the liquid phase, 1,5-hexadien-3-yne apparently exists as a mixture of two isomers, namely cis (I) and trans (II) forms with (I) predominating.

Keywords

Liquid Phase 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literature cited

  1. [1]
    K. Lonsdale, Bull. Soc. chim. France 1949, 476; A. Selwood, Magnetochemistry, Foreign Lit, Press. Moscow, 1958. [Russian translation.]Google Scholar
  2. [2]
    R. S. Rasmussen and R. R. Bratain, J. Chem. Phys. 15, 131 (1947); C. M. Rihhards and J. R. Nielsen, J. Opt. Soc. America 40, 438 (1950).Google Scholar
  3. [3]
    K. Alder and H. Brachel, Liebigs. Ann. Chem. 608, 195 (1957); E. R. Lippincott, C. E. White, and J. P. Sibilia, J. Amer. Chem. Soc. 80, 2926 (1958).Google Scholar
  4. [4]
    K. K. Georgieff, W. T. Cave, and K, G. Blakie, J. Amer. Chem. Soc. 76, 5494 (1954).Google Scholar
  5. [5]
    J. H. Wotiz and F. A. Miller, J. Amer. Chem. Soc. 71, 3441 (1949); N. A. Milas and O. L. Mageli, J. Amer. Chem. Soc. 74, 1471 (1952); R. Filler, M. Harnik, and E. Jensen. Chem. Ind. 1957, 1322.Google Scholar
  6. [6]
    M. I. Batuev, V. A. Ponomarenko, and L. D. Matveeva, Bull. Acad. Sci. USSR, Div. Chem. Sci. 1956, 1420.Google Scholar
  7. [7]
    M. I. Batuev, J. Org. Chem., 28, 3147 (1958).Google Scholar
  8. [8]
    M. I. Batuev and A. D. Matveeva, Bull. Acad. Sci. USSR, Div. Chem. Sci., 1958, 1393.Google Scholar
  9. [9]
    A. D. Walsh, Quart. Rev. 2, 73 (1948).Google Scholar

Copyright information

© Consultants Bureau 1960

Authors and Affiliations

  • M. I. Batuev
    • 1
  • A. P. Meshcheryakov
    • 1
  • A. D. Matveeva
    • 1
  1. 1.Institute of Mineral Fuels and N. D. Zelinskii Institute of Organic ChemistryAcademy of Sciences USSRUSSR

Personalised recommendations