Chromatography nomenclature

Peracid Classification. Peracids can be broadly classified into organic and inorganic peracids, based on standard nomenclature. The limited number of inorganic peracids has required no subclassification scheme (4). However, the tremendous number of new organic peracids developed (85) has resulted in proposals for classification. Eor example, a classification scheme based on Hquid chromatography retention times and critical miceUization constants (CMC) of the parent acids has been proposed (89). The parent acids are used because of the instabiHty of the peracids under chromatographic and miceUization measurement conditions. This classification scheme is shown in Table 1. 

The evolution of media covering aqueous and nonaqueous systems on the one hand and analytical as well as microscale and macroscale preparative applications on the other hand has resulted in an arbitrarily nomenclature within the field. Thus the current practice is to refer to the separation principle based on solute size as size exclusion chromatography (SEC) whereas the application in aqueous systems is traditionally referred to as gel filtration (GF) and the application in nonaqueous systems is designated gel-permeation... 

Figure 5.65 LC-UV and LC-MS-MS (multiple-reaction monitoring (MRM)) traces from the analysis of a enzymatically digested solution of 100 p,g salmon testes DNA (for nomenclature, see text). Reprinted by permission of Elsevier Science from Comparison of negative- and positive-ion electrospray tandem mass spectrometry for the liquid chromatography-tandem mass spectrometry analysis of oxidized deoxynucleosides , by Hua, Y., Wainhaus, S. B., Yang, Y., Shen, L., Xiong, Y., Xu, X., Zhang, F., Bolton, J. L. and van Breemen, R. B., Journal of the American Society for Mass Spectrometry, Vol. 12, pp. 80-87, Copyright 2000 by the American Society for Mass Spectrometry.

Since many of the developments in modern liquid chromatography are of recent origin the nomenclature commonly used is less standardized than that of gas chromatography [188]. Wc have Mde an arbitrary selection of the terms we prefer to use in this book along with some other common alternatives in Table 1.13. 

Other reviews of multidimensional separations have been published. These include a book on polymer characterization by hyphenated and multidimensional techniques (Provder et al., 1995), a review on polymer analysis by 2DLC (van der Horst and Schoenmakers, 2003), and two reviews on two-dimensional techniques in peptide and protein separations (Issaq et al., 2005 Stroink et al., 2005). Reviews on multidimensional separations in biomedical and pharmaceutical analysis (Dixon et al. 2006) and multidimensional column selectivity (Jandera, 2006) were recently published. Suggested nomenclature and conventions for comprehensive multidimensional chromatography were published in 2003 (Schoenmakers et al., 2003), and a book chapter in the Advances in Chromatography series on MDLC was published in 2006 (Shalliker and Gray 2006). 

Schoenmakers, P.J., Marriott, P., Beens, J. (2003). Nomenclature and Conventions in Comprehensive Multidimensional Chromatography. LC-GC Europe, June 2003, l t. 

Nomenclature for chromatography. IUPAC recommendations (1993) J Pure Appl Chem... 

We first confirmed the formation of these macrocycles in the polymerization of THF by using coupled gas chromatography/mass spectrometry ( 2). Macrocyclic ethers containing up to 8 THF units could be separated and identified by this method (23). The two predominant macrocyclic species found in THF polymerization mixtures are a cyclic tetramer and a cyclic pentamer. In analogy to the "crown ether" nomenclature, we proposed the name 20-crown-4 for the cyclic tetramer and 25-crown-5 for the cyclic pentamer (22). 

Figure 27. Epoxide hydrolase catalyzed kinetic resolution of c/.v-2-ethyl-3-methyloxirane and formation of 2i ,3f -2,3-pentanediol as monitored by complexation gas chromatography on 0.08 M nickel(II) bis[3-(heptafluorobutanoyl)-(1 / )-camphorate] in methylpolysiloxane [25 m x 0.25 mm (i.d.) glass capillary column. 95CC, 1.1 bar nitrogen]191 2,3-pentanediol as acetonides 0.14 M nickel(ll) bis[3-(heptafluo-robutanoyl)-(l /t,2S)-pinan-4-onatc]151 in SE-30. Note that there is a change in the numbering of the chiral carbon atoms of the oxiranc vs. the diol due to nomenclature requirements.

Recommendations on Nomenclature for Chromatography, Appendices on Tentative Nomenclature, Symbols, Units and Standards — No. 15, Information Bulletin, International Union of Pure and Applied Chemistry, February 1972. 

---