Skip to main content
Log in

Chromatographic Identification of Cyclohexane Chlorination Products by an Additive Scheme for the Prediction of Retention Indices

  • Original
  • Published:
Chromatographia Aims and scope Submit manuscript

Abstract

Identification of the products of free-radical chlorination of cyclohexane seems to be a complex analytical problem due to the following principal reasons: (1) the available reference information (both standard mass spectra and gas chromatographic retention indices, RI) is strongly restricted to the data for only few simplest congeners, (2) mass spectra of isomeric chlorinated derivatives are practically indistinguishable, and (3) the number of isomers increases with the growing number of chlorine atoms in the molecule until six. To solve this problem, the modified additive scheme for precalculation of the RIs of chlorinated cyclohexanes on standard non-polar polydimethyl siloxane stationary phases was proposed and used. This approach is based on the data for congeners with fewer number of chlorine atoms in the molecule; the principal feature is its applicability to a diastereomers. The final set of both experimental and precalculated RI values permits us to identify unambiguously more than 20 products of cyclohexane chlorination in reaction mixtures. Different modes of the quality control of evaluated retention indices are discussed.

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.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  1. Analytical method for residual compositional substances of agricultural chemicals, feed additives, and veterinary drugs in food (2006) Dept. of Food Safety, Ministry of Health, Labour and Welfare, Japan, 52 p; http://www.mhlw.go.jp/english/topics/foodsafety/positivelist060228/de/060526-1a.pdf (Accessed on October 2008)

  2. The Pesticide Manual (2000) Tomlin CDS (ed) British Crop Protection Council, Farnham, p 1250

  3. Muur D, Stern G, Tomy G (2000) Chlorinated paraffins. In: Paasivirta J (ed) The Handbook of Environmental Chemistry, Ch. 8, Vol. 3, Part K, New types of Persistent Halogenated Compounds. Springer, Berlin, pp 203–236

  4. Coelhan M, Saraci M, Parlar H (2000) Chemosphere 40:685–689. doi:10.1016/S0045-6535(99)00444-0

    Article  CAS  Google Scholar 

  5. Zencak Z, Oehme M (2006) Trends Analyt Chem 25:310–317. doi:10.1016/j.trac.2005.10.005

    Article  CAS  Google Scholar 

  6. Eljarrat E, Barcelo D (2006) Trends Analyt Chem 25:421–434. doi:10.1016/j.trac.2006.01.007

    Article  CAS  Google Scholar 

  7. Bayen S, Obbard JP, Thomas GO (2006) Environ Int 32:915–929. doi:10.1016/j.envint.2006.05.009

    Article  CAS  Google Scholar 

  8. Santos FJ, Parera J, Galceran MT (2006) Anal Bioanal Chem 386:837–857. doi:10.1007/s00216-006-0685-x

    Article  CAS  Google Scholar 

  9. Bauer S, Wolff I, Werner N, Schmidt R, Blume R, Pelzing M (1995) Toxicol Ind Health 11:523–541

    CAS  Google Scholar 

  10. Schmidt R, Scheufler H, Bauer S, Wolff I, Pelzing M, Herzschuh R (1995) Toxicol Ind Health 11:49–61

    CAS  Google Scholar 

  11. de Geus HJ, Besselink H, Brouwer A, Klungsoyr J, McHugh B, Nixon E, Rimkus GG, Wester PG, de Boer J (1999) Environ Health Perspect 107(Suppl 1):115–144. doi:10.2307/3434478

    Article  Google Scholar 

  12. Koivisto J, Kolehmainen E, Nikiforov VA, Nissinen M, Linnanto J, Lahtipera M, Miltsov SA, Karavan VS (2001) Chemosphere 44:671–679. doi:10.1016/S0045-6535(00)00336-2

    Article  CAS  Google Scholar 

  13. Nikiforov V, Trukhin A, Kruchkov F, Kiprianova A, Miltsov S, Kalenborn R (2004) Organohalogen Compd 66:467–472

    Google Scholar 

  14. Nikiforov VA, Karavan VS, Miltsov SA (2000) Chemosphere 41:467–472. doi:10.1016/S0045-6535(99)00477-4

    Article  CAS  Google Scholar 

  15. Smalling K, Maruya KA (2001) J Sep Sci 24:104–108. doi:10.1002/1615-9314(20010201)24:2<104::AID-JSSC104>3.0.CO;2-C

    Article  CAS  Google Scholar 

  16. Zenkevich IG, Moeder M, Koeller G, Schrader S (2004) J Chromatogr A 1025:227–236. doi:10.1016/j.chroma.2003.10.106

    Article  CAS  Google Scholar 

  17. Zenkevich IG (2001) Russ J Org Chem 37:283–293. doi:10.1023/A:1012343416008

    Article  Google Scholar 

  18. Zenkevich IG, Makarov AA (2007) Russ J Gen Chem 77:653–662. doi:10.1134/S1070363207040196

    Article  Google Scholar 

  19. Zenkevich IG, Makarov AA, Schrader S, Moeder M (2009) J Chromatogr A 1216:4097–4106. doi:10.1016/j.chroma.2009.03.021

    Article  CAS  Google Scholar 

  20. Zenkevich IG (1998) J High Res Chromatogr 21:565–568. doi:10.1002/(SICI)1521-4168(19981001)21:10<565::AID-JHRC565>3.0.CO;2-6

    Article  CAS  Google Scholar 

  21. NIST/EPA/NIH Mass Spectral Library (2005) Software/Binary Version. National Institute of Standards and Technology, Gaithersburg, MD 20899; NIST Standard Reference Database, Number 69, June 2005. National Institute of Standards and Technology, Gaithersburg. MD 20899; http://webbook.nist.gov. (Accessed March 2009)

  22. Carroll B, Kubler DG, Davis HW, Whaley AM (1951) J Am Chem Soc 73:5382–5383. doi:10.1021/ja01155a107

    Article  CAS  Google Scholar 

  23. Brown AB, Chronister CW, Watkins DM, Mazzaccaro RJ, Rajski SR, Fontain MG, Mckay SE, Gibson TL (1995) Synth Commun 25:485–501. doi:10.1080/00397919508011382

    Article  CAS  Google Scholar 

  24. Raner KD, Lusztyk J, Ingold KU (1988) J Am Chem Soc 110:3519–3524. doi:10.1021/ja00219a028

    Article  CAS  Google Scholar 

  25. Tordeux M, Boumizane K, Nakselman C (1993) J Org Chem 58:1939–1940. doi:10.1021/jo00059a057

    Article  CAS  Google Scholar 

  26. Zenkevich IG (1984) Russ J Anal Chem 39:1286–1307

    Google Scholar 

  27. Zenkevich IG, Ioffe BV (1988) J Chromatogr A 439:185–194. doi:10.1016/S0021-9673(01)83833-4

    Article  CAS  Google Scholar 

  28. Buchman O, Cao GY, Peng CT (1984) J Chromatogr A 312:75–90. doi:10.1016/S0021-9673(01)92765-7

    Article  CAS  Google Scholar 

  29. White CM, Hackett J, Anderson RR, Kail S, Spock PS (1992) J. High Res Chromatogr 15:102–120. doi:10.1002/jhrc.1240150211

    Article  Google Scholar 

  30. Eisenlohr F (1912) Spektrochemie Organischer Verbindungen. Molekularrefraktion und -Dispersion. Verlag von F. Enke, Stuttgart, Germany, p 223

  31. Zenkevich IG, Kochetova MV, Larionov OG, Revina AA, Kosman VM (2005) J Liquid Chromatogr Relat Technol 28:2141–2162. doi:10.1081/JLC-200064000

    Article  CAS  Google Scholar 

Download references

Acknowledgments

This work was supported by the Russian Foundation of Basic Researches (RFBR), grant no. 08-03-00980.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Igor G. Zenkevich.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zenkevich, I.G., Eliseenkov, E.V. & Kasatochkin, A.N. Chromatographic Identification of Cyclohexane Chlorination Products by an Additive Scheme for the Prediction of Retention Indices. Chroma 70, 839–849 (2009). https://doi.org/10.1365/s10337-009-1213-x

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1365/s10337-009-1213-x

Keywords

Navigation