Classical nomenclature system

Porphyrins are formally derived from the porphin (1) nucleus by substitution of some or all peripheral positions with various side chains. In the classical system of nomenclature T, introduced by H. Fischer,Sc the peripheral /5-pyrrolic positions are numbered front 1 to 8 and the methine positions (also named meso positions) between the pyrrole rings are designated a, //, y, and 5. The rings are lettered clockwise A, B, C, and D. The classical nomenclature was in the past more and more displaced by a nomenclature which numbers all the carbon... 

In the IUPAC system, the four methine positions are conveniently numbered 5, 10, 15 and 20, and the eight remaining peripheral positions fall at 2, 3, 7, 8, 12, 13, 17 and 18. The nitrogen atoms are numbered 21 through 24. Owing to the continued use of trivial names, both in the IUPAC and classical systems of nomenclature, certain other features of porphyrin notation and isomerism need to be explained. If the eight peripheral substituents are made up of two sets of four (for example, four methyls and four ethyls), and if there is one of each on the individual pyrrole subunits (a situation which usually occurs in biologically derived porphyrins), then there are four possible so-called primary type isomers. These four isomers for the methyl/ethyl series, trivially named etioporphyrins, are shown in Scheme 1 the compounds are named etioporphyrin-I (14), etioporphyrin-II (15), etioporphyrin-III (16), and etioporphyrin-IV (17). 

The Schmidt number is the ratio of kinematic viscosity to molecular diffusivity. Considering liquids in general and dissolution media in particular, the values for the kinematic viscosity usually exceed those for diffusion coefficients by a factor of 103 to 104. Thus, Prandtl or Schmidt numbers of about 103 are usually obtained. Subsequently, and in contrast to the classical concept of the boundary layer, Re numbers of magnitude of about Re > 0.01 are sufficient to generate Peclet numbers greater than 1 and to justify the hydrodynamic boundary layer concept for particle-liquid dissolution systems (Re Pr = Pe). It can be shown that [(9), term 10.15, nomenclature adapted]... 

Classical and Modem Nomenclature Systems of Bicentric Configurations... 

Nomenclature for coupled systems in 1H NMR. The interpretation of a spectrum of a molecule with many hydrogen atoms is simplified when signals that fall into classical cases can be observed. These particular cases are usually classified with a nomenclature that uses the letters of the alphabet, chosen in relation to the chemical shift (Fig. 9.18). Protons with identical or similar chemical shifts are designated by identical letters or neighbouring letters in the alphabet (AB, ABC, A2B2, etc.), while protons with very different chemical shifts are designated by letters such as A, M and X. 

During the nineteenth and early twentieth centuries, separation of the proteins was limited to casein and the classical lactalbumin and lacto-globulin fractions of the whey proteins. Subsequent work has resulted in the identification and characterization of numerous proteins from each of these fractions. A classification system of the known proteins in milk developed by the American Dairy Science Association s (ADSA) Committee on Milk Protein Nomenclature, Classification, and Methodology (Eigel et al 1984) is summarized and enlarged to include the minor proteins and enzymes in Table 3.1. 

Nomenclature for coupled systems in NMR. Spectral interpretation for a molecule with many hydrogen atoms is easier when sub-groups of signals correspond to classic situations. These particular cases are classified by means of a nomenclature using the letters of the alphabet, selected with respect to the chemical shift (Figure 15.20). Protons with the same chemical environment or chemical shift are caiied equivalent. If the chemical shifts are too little different, the protons are... 

It is virtually impossible to name carbon nanotubes correctly according to lUPAC nomenclature for two reasons. Firstly, the number of carbon atoms constituting the nanotube is enormous-it might be tens or hundreds of thousands. Secondly, it would be extremely difficult to apply the classical nomenclature of organic compounds. A whole new system has consequently been estabhshed to classify carbon nanotubes. It is perfectly apt to distinguish different structures, and it even permits to infer certain properties of the species at hand from the components of its name. There are three classes of carbon nanotubes differing in the way the basic graphene sheet is rolled up ... 

The BBB model is a means of macroscopic approximation to the system on an exclusively electrostatic basis it describes the solvation effects with the aid of classical field theories, primarily electrostatics and hydrodynamics. The nomenclature BBB, an abbreviation of the expression Brass Balls in a Bathtub , originates from Frank [Fr 65]. The more important classical theories included in this group have led to a result only for dilute solutions nevertheless, their refinement has continued up to the present [Ab 79, Be 78, Kr 79, Li 79]. 

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