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A structure-based nomenclature for linear polymers. Macromolecules. 1:1968;193-198.
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CAS, CA Index Guide, Appendix IV (© 1999). Chemical Abstracts Service, 2540 Olentangy River Road, P.O. Box 3012, Columbus, OH 43210: (a) Section 222 - Description of CAS Polymer Indexing Rules; (b) Section 138 - Description of Ring Seniority; (c) Section 215 - Coordination Compounds; (d) Section 106 - Order of Precedence of Compound Classes
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CAS, CA Index Guide, Appendix IV (© 1999). Chemical Abstracts Service, 2540 Olentangy River Road, P.O. Box 3012, Columbus, OH 43210: (a) Section 222 - Description of CAS Polymer Indexing Rules; (b) Section 138 - Description of Ring Seniority; (c) Section 215 - Coordination Compounds; (d) Section 106 - Order of Precedence of Compound Classes.
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Metanomski W.V. Macromolecular Nomenclature Note No. 3, Source-Based vs. Structure-Based Nomenclature. Polym Prepr. 33:(2):1992;6-7. (Paragraphs reprinted with permission).
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IUPAC, Nomenclature of regular single-strand organic polymers. Pure Appl Chem 1976;48:373-385. Reprinted in: Metanomski WV, editor. Compendium of macromolecular nomenclature (The Purple Book). Oxford: Blackwell Scientific Publications, 1991 (Chapter 5).
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The Purple Book
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This document contains a summary of the major documents, in the formats of both position papers and articles in books and encyclopedias, on polymer nomenclature that have been published by CAS and IUPAC from 1952 to 1999. (a) The planned IUPAC document Source-Based Nomenclature For Modified Polymer Molecules, listed in Table 3 of this reference as Feasibility Study F-19, is now known as Project No. 410/33/99
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Wilks ES. Macromolecular Nomenclature Note No. 17, Whither Nomenclature? Polym Prepr;40(2):6-11. This document contains a summary of the major documents, in the formats of both position papers and articles in books and encyclopedias, on polymer nomenclature that have been published by CAS and IUPAC from 1952 to 1999. (a) The planned IUPAC document Source-Based Nomenclature For Modified Polymer Molecules, listed in Table 3 of this reference as Feasibility Study F-19, is now known as Project No. 410/33/99.
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IUPAC
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IUPAC, Source-based nomenclature for copolymers (Recommendations 1985). Pure Appl Chem 1985;57:1427-1440. Reprinted in: Metanomski WV, editor. Compendium of macromolecular nomenclature (The Purple Book). Oxford: Blackwell Scientific Publications, 1991 (Chapter 7).
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14
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0344521884
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Compendium of macromolecular nomenclature
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Reprinted in editor Oxford: Blackwell Scientific Publications (Chapter 7)
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IUPAC, Source-based nomenclature for copolymers (Recommendations 1985). Pure Appl Chem 1985;57:1427-1440. Reprinted in: Metanomski WV, editor. Compendium of macromolecular nomenclature (The Purple Book). Oxford: Blackwell Scientific Publications, 1991 (Chapter 7).
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The Purple Book
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Metanomski, W.V.1
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0004491655
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Graphic representations (chemical formulae) of macromolecules (Recommendations 1994)
-
IUPAC Examples of violations of the rules and recommendations laid down by the documents cited in Refs. [1,4] are: (a) example 2-E1 - poly(2-phenylethylene) is an acceptable alternative to poly(1-phenylethylene); (b) example 2-E4 - trans-1,4-polyisoprene is drawn out of phase (double bond not assigned lowest locant); (c) example 4.2-E1 - 1,3-butadiene SRU is drawn out of phase (double bond not assigned lowest locant); (d) example 4.2-E7 - both SRUs are drawn left-to-right reversed
-
IUPAC, Graphic representations (chemical formulae) of macromolecules (Recommendations 1994). Pure Appl Chem 1994;66:2469-2482. Examples of violations of the rules and recommendations laid down by the documents cited in Refs. [1,4] are: (a) example 2-E1 - poly(2-phenylethylene) is an acceptable alternative to poly(1-phenylethylene); (b) example 2-E4 - trans-1,4-polyisoprene is drawn out of phase (double bond not assigned lowest locant); (c) example 4.2-E1 - 1,3-butadiene SRU is drawn out of phase (double bond not assigned lowest locant); (d) example 4.2-E7 - both SRUs are drawn left-to-right reversed.
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Pure Appl Chem
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16
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IUPAC
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IUPAC, Nomenclature for regular single-strand and quasi single-strand inorganic and coordination polymers (recommendations 1984). Pure Appl Chem 1985;57:149-168. Reprinted in: Metanomski WV, editor. Compendium of macromolecular nomenclature (The Purple Book). Oxford: Blackwell Scientific Publications, 1991 (Chapter 6).
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IUPAC, Nomenclature for regular single-strand and quasi single-strand inorganic and coordination polymers (recommendations 1984). Pure Appl Chem 1985;57:149-168. Reprinted in: Metanomski WV, editor. Compendium of macromolecular nomenclature (The Purple Book). Oxford: Blackwell Scientific Publications, 1991 (Chapter 6).
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A list of valid IUPAC and other recommendations on macromolecular terminology and nomenclature is published twice yearly in Polymer Preprints; see, for example The list is also available at the web site Most of these references are also available at: http://www.chem.umr.edu/~poly/nomenclature.html#rec
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A list of valid IUPAC and other recommendations on macromolecular terminology and nomenclature is published twice yearly in Polymer Preprints; see, for example, Polym Prepr 1999;40(2):1314-1315. The list is also available at the web site: http://www.iupac.org/divisions/IV/IV.1/index.html. Most of these references are also available at: http://www.chem.umr.edu/~poly/nomenclature.html#rec.
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editor Oxford: Blackwell Scientific Publications Rule 2.2.2 (Chapter 5, p. 99) states: consistent with the fixed numbering of the heterocyclic rings, the points of attachment to the main chain of the CRU should have the lowest permissible locants. When there is a choice, the point of attachment at the left side of the ring should have the lowest permissible number. This rule is also covered by Ref. [5a], which states: Each multivalent radical retains its own numbering and is oriented, if possible, so that the point of attachment written on the left end of the repeating unit is assigned the lowest possible number. This permits the naming of the SRU in a directional manner, reading from left to right
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Metanomski WV, editor. Compendium of macromolecular nomenclature (The Purple Book). Oxford: Blackwell Scientific Publications, 1991. Rule 2.2.2 (Chapter 5, p. 99) states: consistent with the fixed numbering of the heterocyclic rings, the points of attachment to the main chain of the CRU should have the lowest permissible locants. When there is a choice, the point of attachment at the left side of the ring should have the lowest permissible number. This rule is also covered by Ref. [5a], which states: Each multivalent radical retains its own numbering and is oriented, if possible, so that the point of attachment written on the left end of the repeating unit is assigned the lowest possible number. This permits the naming of the SRU in a directional manner, reading from left to right.
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Hedrick JL, Twieg R, Matray T. Poly(aryl ether benzimidazoles). Polym Prepr 1995;36(1):763-764. It is respectfully pointed out that the SRUs, as drawn by the authors, are incomplete (two subunits are inadvertently omitted) and incorrectly oriented per CAS rules [7a]; the corrected SRUs are presented in Fig. 16.
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