
Ring-Forming Polymerizations Pt B 1
Heterocyclic Rings
- 1st Edition - January 1, 1972
- Imprint: Academic Press
- Author: Robert Cotter
- Language: English
- Hardback ISBN:9 7 8 - 0 - 1 2 - 1 9 1 7 0 2 - 9
- Paperback ISBN:9 7 8 - 0 - 1 2 - 4 3 1 2 0 3 - 6
- eBook ISBN:9 7 8 - 0 - 3 2 3 - 1 5 0 0 1 - 9
Ring-Forming Polymerizations, Part B, 1: Heterocyclic Rings presents a comprehensive review and compilation of ring-forming polymerization reactions that proceed with the formation… Read more

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Request a sales quoteRing-Forming Polymerizations, Part B, 1: Heterocyclic Rings presents a comprehensive review and compilation of ring-forming polymerization reactions that proceed with the formation of heterocyclic rings. Emphasis is placed on polymerizations leading to linear, high molecular weight products. This book is comprised of three chapters and begins with a discussion on polymerizations that result in the formation of a multiple bond containing at least one heteroatom. The condensation of amines with carbonyl compounds to yield poly(Schiff bases) and related polymers is examined, along with other carbon-nitrogen double bond-forming polymerizations. The next chapter is devoted to the polymerization of rings containing two carbon atoms, including the polymerization of polyphenols with diboronic acids and that of diisocyanides with triorganoborons. The last chapter describes the polymerization of rings containing three carbon atoms, with particular reference to polyisoxazoles and related polymers, polythiazoles, polyimidazoles and related polymers, polypyrazoles, and polytriazines. This monograph will be of interest to polymer and organic chemists and others who are concerned with the polymer chemistry of living systems.
Preface
Contents of Part A
Contents of Part B
Introduction
Chapter I. Multiple Bond-Forming Polymerizations
A. Poly(Schiff Bases) and Related Polymers
Method 1. Polymerization of Dicarbonyl Compounds with Diamines
Method 2. Bulk Polymerization of Dicarbonyl Compounds with Diamines
Method 3. Polymerization of Cyclic Oligomeric Schiff Bases Properties of Poly(Schiff Bases)
B. Other Carbon-Nitrogen Double Bond-Forming Polymerizations
Method 1. Polymerization of Monomers Containing Nitrile Groups
Method 2. Dehydrative Polymerization of Nitrile Precursor Monomers
Method 3. Polyrecombination of Nitriles
Method 4. Polymerization of Isonitriles
C. Poly Carbodiimides
Method 1. Polymerization of Diisocyanates
Method 2. Polymerization by Exchange with Monomeric Carbodiimides
Method 3. Pyrolysis of Bis(Urethans)
Method 4. Oxidative Desulfurization of Poly(Thioureas)
Method 5. Polyacylcarbodiimides from Bis(Acylcyanamids) and Diacid Chlorides
Properties of Polycarbodiimides
D. Azo Linkage Formation During Polymerization
Method 1. Oxidative Coupling of Aromatic Diamines
Method 2. Polyrecombination of Diamines
Method 3. Reduction of Bis(Diazonium) Compounds
Method 4. Reactions of Bis(Diazonium) Compounds
Method 5. Thermal Decomposition of Bis(Nitrosoamides)
Method 6. Decomposition of Bis(Chloroimides)
Properties of Azo Polymers
E. Nitrogen-Phosphorus Double Bond-Forming Polymerizations
Method 1. Polymerization of Diphosphines with Bis(Azides)
Table 1.1. Poly(Schiff Bases)
Table 1.2. Polyazines and Other Hydrazine-Derived Polymers
Table 1.3. Carbon-Nitrogen Double-Bond Containing Polymers
Table 1.4. Poly Carbodiimides
Table 1.5. Azo Polymers
References
Chapter II. Rings Containing Two Carbon Atoms
A. Poly(1,3,2-diazaboroles), Poly(1,3,2-oxazaboroles), and Poly(1,3,2-dioxaboroles)
Method 1. Polymerization of Bis(1,2-diamines) with Diboronic Acids
Method 2. Polymerization of Bis(1,2-diamines) with Tetraaminodiborons
Method 3. Miscellaneous Boron-Nitrogen Ring-Containing Polymers Poly(1,3,2-Oxazaboroles)
Method 4. Polymerization of Bis(aminophenols) with Diboronates
Method 5. Polymerization of Bis(aminophenols) with Tetraaminodiborons
Method 6. Miscellaneous Boron-Oxygen-Nitrogen Ring Polymerizations Poly(1,3,2-Dioxaboroles)
Method 7. Polymerization of Polyphenols with Diboronic Acids
Method 8. Polymerization of Tetraphenols with Tetraaminodiborons
Method 9. Miscellaneous 1,3,2-Dioxaboron Ring-Forming Polymerizations
B. Poly(1,3,2-diazaphospholes)
Method 1. Polymerization of Bis(phosphonic Acid Diamides) with Aromatic Tetraamines
Method 2. Polymerization of Aromatic Tetraamines with Phenyl Esters of Phosphorus Acids
C. Poly(1,3-diaza-2-silacyclopentanes)
Method 1. Reaction of Amines with Halo- or Aminosilanes
Method 2. Polymerization of Aromatic Amines with Silicon Tetrafluoride
D. Poly(1,2-oxazetidines)
Poly(1 ,3,4-oxadiazoles)
Method 1. Dehydration of Polyhydrazides
Method 2. Polymerization of Hydrazine and Dihydrazides with Dicarboxylic Acid Derivatives
Method 3. Polymerization of Diacid Chlorides with Bis-(tetrazoles)
Method 4. Polyacylamidrazones as Precursors to Polyoxadiazoles
Poly(l ,2,4-oxadiazoles) and poly(l,2,5-oxadiazoles)
Method 5. Polymerization of Diacid Chlorides with Diamidoximes
Method 6. Polyoxadiazoles from Nitrile Oxides
Properties of Poly(1,3,4-thiadiazoles)
E. Polyoxadiazoles
F. Poly(1,3,4-thiadiazoles)
Method 1. Dehydration of Polyoxathiahydrazides
Method 2. Dihydro-Poly(1,3,4-thiadiazoles) from 1,3-Dipolar Additions
G. Polytriazoles
Method 1. Polymerization of Hydrazine with Dicarboxylic Acid Derivatives
Method 2. Polymerization of Dihydrazides and Bis(amidrazones) with Dicarboxylic Acid Derivatives
Method 3. Polymerization of Bis(imide Chlorides) with Bis-(Tetrazoles)
Method 4. Polytriazoles from Additional Polymeric Precursors
Method 5. Polytriazole Synthesis from Dipolar Addition Reactions
Properties of Polytriazoles
H. Poly(1,2,4,5-tetrazines)
Method 1. Polymerization of Diimino Diesters with Hydrazine
Method 2. Polytetrazines from Dipolar Addition Reactions
I. Poly(2,5-diborapiperazines) and Poly(2,5-dibora-2,5-dihydropyrazines)
Method 1. Polymerization of Diisocyanides with Triorganoborons
Table II. 1. Poly(1,3,2-diazaboroles)
Table II.2. Poly(1,3,2-oxazaboroles)
Table II.3. Poly(1,3,2-dioxaboroles) and Related Polymers
Table II.4. Poly(1,3,2-diazaphospholes)
Table II.5. Poly(1,3-diaza-2-silacyclopentanes)
Table II.6. Poly(1,3,4-oxadiazoles)
Table II.7. Poly(1,2,4-oxadiazoles), Poly(1,2,4-oxadiazolines),and Poly(1,2,5-oxadiazoles)
Table II.8. Poly(1,3,4-thiadiazoles)
Table II.9. Poly(1,2,4-triazoles)
Table 11.10. Poly(1,2,3-triazoles)
Table 11.11. Poly(1,2,4,5-tetrazines)
Table 11.12. Poly(2,5-diborapiperazines) and Poly(2,5-dibora- 2,5-dihydropyrazines)
References
Chapter III. Rings Containing Three Carbon Atoms
A. Polyisoxazoles and Related Polymers Polyisoxazoles
Polyisoxazoles
Method 1. Polyisoxazoles from Dinitrile Di-N-oxides and Diacetylenes
Method 2. Polyisoxazolines from Dinitrile Di-N-oxides and Diolefins
Method 3. Polyisoxazolidines from Bis(nitrones) and Diolefins
Polyoxazoles
Method 4. Polyoxazoles from o-Aminophenols and Carboxylic Acids
Method 5. Polyamides as Precursors to Polyoxazoles
Method 6. Polyesters as Precursors to Polyoxazoles
Method 7. Polyoxazoles from o-Aminophenols and Carboxylic Acid Anhydrides
Method 8. Polyoxazoles from Bis(o-Chloroamines)
Properties of Polyoxazoles
Polyoxazolidones
Method 9. Polyoxazolidones from Diisocyanates and Diepoxides
Method 10. Miscellaneous Additional Syntheses of Polyoxazolidones
Properties of Polyoxazolidones
B. Polythiazoles
Method 1. Polythiazoles from o-Mercaptoamines and Carboxylic Acids
Method 2. Polythiazoles from Bis(thioamides) and Bis(α-Haloketones)
Method 3. Polyamides as Precursors to Polythiazoles
Method 4. Polythiazoles from Sulfur and Toluidines
Properties of Polythiazoles
C. Polyimidazoles and Related Polymers Polyimidazoles
Method 1. Polyimidazoles from Dialdehydes and Bis(α-Diketones)
Method 2. Polyimidazoles from o-Diamines and Carboxylic Acids
Method 3. Polyimidazoles from o-Diamines and Carboxylic Acid Esters
Method 4. Polyimidazoles from o-Diamines and Carboxylic Acid Anhydrides
Method 5. Polymeric Precursors to Polyimidazoles
Method 6. Miscellaneous Syntheses of Polyimidazoles
Properties of Polyimidazoles
Polypyrrones
Method 7. Two-Step Synthesis of Polypyrrones from Tetracarboxylic Acid Derivatives and Tetraamines
Method 8. Direct Synthesis of Polypyrrones in Polyphosphoric Acid
Properties of Polypyrrones
Polyimidazolines
Method 9. Polyimidazolines from o-Diamines and Dicarbonyl Compounds
Method 10. Polyimidazolines from Poly(ethyleneamines) and Cyanogen and Derivates
Method 11. Polyimidazolines from Poly(Amino Amides) Polyimidazolidones
Method 12. Polyimidazolidones from Vic-Diisocyanates Polyimidazolidiones
Method 13. Polyimidazolidiones from Diglycinates and Diisocyanates
Method 14. Polyimidazolidiones from Polymer Precursors
Method 15. Poly(5-iminoimidazolidiones) from Diisocyanates and Hydrogen Cyanide
Properties of Polyimidazolidiones
D. Polypyrazoles
Method 1. Polymerization of Tetracarbonyl Compounds with Dihydrazines or Dihydrazides
Method 2. Polypyrazoles from 1,3-Dipolar Addition Reactions
Method 3. Polymerization of Bis(diazo) Compounds with Diacetylenes
Properties of Polypyrazoles
E. Polytriazines
Method 1. Nitrile Trimerization-Polymerization to Polytriazines
Method 2. Polytriazines via Amidine Intermediates
Method 3. Trimerization of Isocyanates
Method 4. Poly(as-Triazines) from Polymerization of Bis-(Hydrazidines) and Bis(α-Diketones)
Properties of Polytriazines
Table III.1. Polyisoxazoles, Polyisoxazolines, and Polyisoxazolidines
Table III.2. Polyoxazoles
Table III.3. Polyoxazolidones
Table III.4. Polythiazoles
Table III.5. Polyimidazoles and Polybenzimidazoles
Table III.6. Polypyrrones
Table III.7. Polyimidazolines
Table III.8. Polyimidazolidones
Table III.9. Polyimidazolidiones
Table III.10. Polypyrazoles
Table III.11. Polypyrazolines
Table III.12. Polytriazines
References
Supplementary Reference List
Author Index Subject Index
- Edition: 1
- Published: January 1, 1972
- No. of pages (eBook): 446
- Imprint: Academic Press
- Language: English
- Hardback ISBN: 9780121917029
- Paperback ISBN: 9780124312036
- eBook ISBN: 9780323150019
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