Download A New Unifying Biparametric Nomenclature That Spans All Of by Seymour B. Elk PDF

By Seymour B. Elk

As a byproduct of ancient improvement, there are diversified, unrelated platforms of nomenclature for "inorganic chemistry", "organic chemistry", "polymer chemistry", "natural items chemistry", and so forth. With every one new discovery within the laboratory, in addition to each one new theoretical inspiration for a chemical, the strains that routinely have separated those "distinct" subsets of subject always develop extra blurred. This loss of uniformity in characterizing and naming chemical compounds raises the communique problems among otherwise knowledgeable chemists, in addition to different scientists, and drastically impedes development. With the set of recognized chemical compounds numbering over 42,000,000 (in Chemical Abstracts' information base) and consistently becoming (about 2,000 new additions each day), the desirability for a unified method for naming all chemical compounds at the same time grows. in addition, with the intention to meet the necessities of disparate teams of scientists, and of society as a rule, the identify assigned to a given chemical should still, not just uniquely describe that substance, but additionally may be part of a with no trouble recognizable order for the whole box. For those reasons, a topology-based "bi-parametric" method of nomenclature is herein proposed.- during this booklet, a brand new nomenclature process is proposed- the recent nomenclature is appropriate to a 3 dimensional global, and is internally constant- This nomenclature unifies ALL branches of chemistry, removal the necessity for numerous shortly current units of principles"

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Additional info for A New Unifying Biparametric Nomenclature That Spans All Of Chemistry

Example text

To try to accomplish his intended uniqueness, Patterson added the adjective "free" to emphasize that this is the only union between the rings. 'Unlike molecules that shall be described later in this study, one can assume from the example chosen that Patterson's idea of bridges that crossed each other was more a matter of assigning locant numbers and a canonical name to a wrong projection of a molecule than it was to there being an intrinsic non-planarity to the molecule. In other words, the mind set of planarity is deeply ingrained in IUPAC's rules.

Meanwhile, one should note that, although the GTDs between corresponding atoms is identical, there is a vast MD difference (about 800 nm in the trans conformer vs. 200 nm in the cis conformer), which produces a drastically different environment (Figure 7) in which these two conformers both exist and react. f This gross inadequacy, which is perpetuated in traditional nomenclatures, such as both IUPAC and nodal nomenclature, will be remedied in the proposed new system. (2) Although above there was presented a simple representation technique that one could use for describing, and thus nomenclating, a monocyclic compound as though it were only one-dimensional, the presence of two or more rings in a compound makes such an evasion of the intrinsic planar geometry of "Exotic symbols, such as the Mars sign, were not among those employed; rather one had only various combinations of numbers, letters that were not used as abbreviations of the elements, slashes, etc.

Furthermore, in order to maintain consistency, terminal hydrogen atoms are not incorporated into any abbreviation. In particular, the carbon atom in a terminal methyl group does not have three underscores. Instead it is written as 1C1H, etc. Similarly, use of 10 for the hydroxyl group is precluded. The correct code contains the terminal hydrogen atom: 1O1H, etc. Using these simplifications, (8) can be rewritten as: H1C3(C1C1)2C1C3C1C1H:9[(2C)21H:5(1H)]; 13[2C1H:3(1H)] (9) * An identical simplification could be made in the domain of highly fluorinated [91-92] (or any other similarly selected parameter) molecules.

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