Structure-Based Nomenclature for Cyclic Organic Macromolecules (IUPAC Recommendations 2008)
Structure-Based Nomenclature for Cyclic Organic Macromolecules (IUPAC Recommendations 2008)
W. Mormann and K.-H. Hellwich
Pure and Applied Chemistry, 2008
Vol. 80, No. 2, pp. 201–232
doi:10.1351/pac200880020201
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Example 39 | |
Name: | [B1],[B4]- [poly(sulfanediylethylene)]- [B2],[B3]- [poly(sulfanediylethylene)]- cyclo[poly(oxyethylene)- [1:B1][2:B2]ethylene- poly(oxyethylene)- [1:B3][2:B4]ethylene] |
or | [B1],[B4]:[B2],[B3]- bis[poly(sulfanediylethylene)]- cyclo[poly(oxyethylene)- [1:B1][2:B2]ethylene- poly(oxyethylene)- [1:B3][2:B4]ethylene] |
A structure-based nomenclature system for monocyclic and polycyclic organic macromolecules is presented. Single-strand mono- and polycyclic macromolecules, as well as spiro macrocyclic compounds, are covered. However, rotaxanes and catenanes, which contain interlocked rings, and rings or ring systems formed by noncovalent bonds are excluded. Also, polypeptides and carbohydrate polymers are not included. The nomenclature of cyclic macromolecules is based on the existing nomenclature of regular and irregular macromolecules, which in turn is based on the nomenclature of organic chemistry, also published by IUPAC.
The procedure for naming a cyclic macromolecule consists of transforming it to an open-chain regular or irregular macromolecule in such a way that naming of units proceeds in descending order of seniority but otherwise follows the rules established for these types of macromolecules. For polycyclic macromolecules, the same principles are followed after the main ring, bridges, and branch units are identified and locants for branch units as well as bridges are assigned. The complete names are assembled by citing the component names and locants in the appropriate order according to the rules in this document. Wherever possible, examples for illustration of the naming procedure have been chosen from the literature.
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Articles in the same Issue
- Masthead
- Contents
- Adding a Stone to the IUPAC Edifice
- Spain Celebrates Its Year of Science Honoring Mendeleev
- Where Does IUPAC Stand with Regard to this Discipline?
- Triads, Triads, Everywhere
- Chemistry in the Information and Communications Technology Age
- Analytical Terminology and the Orange Book–The Resources at the End of the Rainbow
- Peter Mahaffy Awarded 3M Canada Teaching Fellowship
- Pieter S. Steyn Receives Science for Society Gold Medal
- Chemical Heritage Foundation Produces Distillations, a Weekly Podcast
- Mechanistic Aspects of Chemical Vapor Generation of Volatile Hydrides for Trace Element Determination
- Assessment of Theoretical Methods for the Study of Reactions Involving Global Warming Gas Species Degradation and Byproduct Formation
- Analysis of the Usage of Nanoscience and Technology in Chemistry
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- Provisional Recommendations
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- Transport of Pesticides via Macropores (IUPAC Technical Report)
- Performance Evaluation Criteria for Preparation and Measurement of Macro- and Microfabricated Ion-Selective Electrodes (IUPAC Technical Report)
- Chemists and “The Public”: IUPAC’s Role in Achieving Mutual Understanding (IUPAC Technical Report)
- DE STERS!
- Glossary of Terms Related to Solubility (IUPAC Recommendations 2008)
- Structure-Based Nomenclature for Cyclic Organic Macromolecules (IUPAC Recommendations 2008)
- Impact of Scientific Developments on the Chemical Weapons Convention (IUPAC Technical Report)
- Graphical Representation Standards for Chemical Structure Diagrams (IUPAC Recommendations 2008)
- The Periodic Table: Database or XML?
- The Investigation of Organic Reactions and their Mechanisms
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- Malta III–Research and Education in the Middle East
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- Nano-Bio & Clean Tech
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- Mark Your Calendar