Partition chromatography theory and practice was introduced through the work and publications of Archer Martin and Richard Laurence Millington Synge during the 1940s.[1] They would later receive the 1952 Nobel Prize in Chemistry "for their invention of partition chromatography".[2]

Synopsis

The process of separating mixtures of chemical compounds by passing them through a column that contains a solid stationary phase that was eluted with a mobile phase (column chromatography) was well known at that time.[3] Chromatographic separation was considered to occur by an adsorption process whereby compounds adhered to a solid media and were washed off the column with a solvent, mixture of solvents, or solvent gradient. In contrast, Martin and Synge developed and described a chromatographic separation process whereby compounds were partitioned between two liquid phases similar to the separatory funnel liquid-liquid separation dynamic. This was an important departure, both in theory and inder equilibrium conditions.[4] Martin and Synge initially attempted to devise a method of performing a sequential liquid-liquid extraction with serially connected glass vessels that functioned as separatory funnels.[1] The seminal article presenting their early studies described a rather complicated instrument that allowed partitioning of amino acids between water and chloroform phases. The process was termed "counter-current liquid-liquid extraction."[5] Martin and Synge described the theory of this technique in reference to continuous fractional distillation described by Randall and Longtin.[6] This approach was deemed too cumbersome, so they developed a method of absorbing water onto silica gel as the stationary phase and using a solvent, such as chloroform, as the mobile phase.[7] This work was published in 1941 as "a new form of chromatogram employing two liquid phases."[8] The article describes both the theory in terms of the partition coefficient of a compound, and the application of the process to the separation of amino acids on a water-impregnated silica column eluted with a water:chloroform:n-butanol solvent mixture.

Impact on separation methodology

The previously described work of Martin and Synge impacted the development of the previously known column chromatography and inspired new forms of chromatography such as countercurrent distribution,[9] paper chromatography,[10] and gas-liquid chromatography which is more commonly known as gas chromatography. The modification of silica gel stationary phase led to many creative ways of modifying stationary phases in order to influence the separation characteristics. The most notable modification was the chemical bonding of alkane functional groups to silica gel to produce reversed-phase media.[11] The original problem that Martin and Synge encountered with devising an instrument that would employ two free-flowing liquid phases was solved by Lyman C. Craig in 1944, and commercial counter-current distribution instruments were used for many important discoveries.[12] The introduction of paper chromatography was an important analytical technique which gave rise to thin-layer chromatography.[13] Finally, gas-liquid chromatography, a fundamental technique in modern analytical chemistry, was described by Martin with coauthors A. T. James and G. Howard Smith in 1952.[14]

References

  1. ^ a b Ettre, Leslie S. (2001). "The Birth of Partition Chromatography". LCGC. 19 (5): 506–512. INIST 990422.
  2. ^ "The Nobel Prize in Chemistry 1952". Nobel Media AB. Retrieved 4 February 2021.
  3. ^ Pakhomov, V. P. (2003). "Chromatography in Pharmaceutical Chemistry (100 Years of the Discovery of Chromatography by M. S. Tswett)". Pharmaceutical Chemistry Journal. 37 (8): 451–452. doi:10.1023/A:1027324501053. S2CID 22507057.
  4. ^ Schindler, Hans (November 1957). "Notes on the history of the separatory funnel". Journal of Chemical Education. 34 (11): 528. Bibcode:1957JChEd..34..528S. doi:10.1021/ed034p528.
  5. ^ Martin, A. J. P.; Synge, R. L. M. (1 January 1941). "Separation of the higher monoamino-acids by counter-current liquid-liquid extraction: the amino-acid composition of wool". Biochemical Journal. 35 (1–2): 91–121. doi:10.1042/bj0350091. PMC 1265473. PMID 16747393.
  6. ^ Randall, Merle; Longtin, Bruce (September 1938). "Separation Processes: General Method of Analysis". Industrial & Engineering Chemistry. 30 (9): 1063–1067. doi:10.1021/ie50345a028.
  7. ^ Whelan, William J. (1 May 2001). "Partition Chromatography Revisited". IUBMB Life. 51 (5): 329–330. doi:10.1080/152165401317190851. PMID 11699880.
  8. ^ Martin, A. J. P.; Synge, R. L. M. (1 December 1941). "A new form of chromatogram employing two liquid phases. A theory of chromatography. 2. Application to the micro-determination of the higher monoamino-acids in proteins". Biochemical Journal. 35 (12): 1358–1368. doi:10.1042/bj0351358. PMC 1265645. PMID 16747422.
  9. ^ Craig, Lyman C. (October 1944). "Identification of small amounts of organic compounds by distribution studies: II. Separation by counter-current distribution". Journal of Biological Chemistry. 155 (2): 519–534. doi:10.1016/S0021-9258(18)51183-2.
  10. ^ Consden, R.; Gordon, A. H.; Martin, A. J. P. (1944). "Qualitative analysis of proteins: A partition chromatographic method using paper". Biochemical Journal. 38 (3): 224–232. doi:10.1042/bj0380224. PMC 1258072. PMID 16747784.
  11. ^ Horvath, C.; Melander, W. (1 September 1977). "Liquid Chromatography with Hydrocarbonaceous Bonded Phases; Theory and Practice of Reversed Phase Chromatography". Journal of Chromatographic Science. 15 (9): 393–404. doi:10.1093/chromsci/15.9.393.
  12. ^ Moore, Stanford (1978). "Lyman Creighton Craig 1906-1974". National Academy of Sciences Biographical Memoirs: 49–77. Retrieved 2016-02-26.
  13. ^ Martin, A J P (June 1950). "Partition Chromatography". Annual Review of Biochemistry. 19 (1): 517–542. doi:10.1146/annurev.bi.19.070150.002505. PMID 14771840.
  14. ^ James, A. T.; Martin, A. J. P.; Smith, G. Howard (1 October 1952). "Gas-liquid partition chromatography: the separation and micro-estimation of ammonia and the methylamines". Biochemical Journal. 52 (2): 238–242. doi:10.1042/bj0520238. PMC 1197975. PMID 13018213.