davideandClaude Sonnet 5.5
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Co-Authored-By: Claude Sonnet 5.5 <noreply@anthropic.com>
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| 54 | ref-54 | identificata_manualmente | 10.1002/047147875x | https://doi.org/10.1002/047147875x | 2004 | null | null | null | null | null |
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[54] Odian (2004) -
Come è scritta nella tesi
Odian, G. G. Principles of Polymerization. (Wiley-Interscience, Hoboken, N.J, 2004).
Scheda bibliografica
Citazione completa: Odian, G. Principles of Polymerization, 4th ed.; Wiley-Interscience: Hoboken, NJ, 2004.
- ISBN: 9780471274001, 9780471478751
- Edizione: 1
- Data di pubblicazione: 2004-01-09
- Lingua: en
Autori e affiliazioni
- George Odian - John Wiley & Sons (Germany); John Wiley & Sons (United Kingdom); John Wiley & Sons (United States)
Stato della verifica
Identificata con ricerca manuale - fonte dati: ricerca manuale (Crossref, COD, Royal Society, archive.org)
Note e discrepanze
- Anno 2004, editore Wiley e ISBN (9780471274001 stampa, 9780471478751 online) confermati da Crossref. Crossref indica 'edizione 1' (metadato inaffidabile); la dicitura '4th ed.' deriva da una recensione del 2008 (DOI 10.1002/aic.11625). L'imprint 'Wiley-Intersciencè non è stato confermato. Libro: nessun abstract.
Dove trovarla
- DOI: https://doi.org/10.1002/047147875x
- OpenAlex: https://openalex.org/W1495482938
- Accesso: closed - il testo completo richiede un abbonamento dell'editore o l'acquisto
Abstract
Preface. 1. Introduction. 1.1 Types of Polymers and Polymerizations. 1.2 Nomenclature of Polymers. 1.3 Linear, Branched, and Crosslinked Polymers. 1.4 Molecular Weight. 1.5 Physical State. 1.6 Applications of Polymers. 2. Step Polymerization. 2.1 Reactivity of Functional Groups. 2.2 Kinetics of Step Polymerization. 2.3 Accessibility of Functional Groups. 2.4 Equilibrium Considerations. 2.5 Cyclization versus Linear Polymerization. 2.6 Molecular Weight Control in Linear Polymerization. 2.7 Molecular Weight Distribution in Linear Polymerization. 2.8 Process Condition. 2.9 Multichain Polymerization. 2.10 Crosslinking. 2.11 Molecular Weight Distributions in Nonlinear Polymerizations. 2.12 Crosslinking Technology. 2.13 Step Copolymerization. 2.14 High-Performance Polymers. 2.15 Inorganic and Organometallic Polymers. 2.16 Dendric (Highly Branched) Polymers. 3. Radical Chain Polymerization. 3.1 Nature and Radical Chain Polymerization. 3.2 Structural Arrangement of Monomer Units. 3.3 Rate of Radical Chain Polymerization. 3.4 Initiation. 3.5 Molecular Weight. 3.6 Chain Transfer. 3.7 Inhibition and Retardation. 3.8 Determination of Absolute Rate Constants. 3.9 Energetic Characteristics. 3.10 Autoacceleration. 3.11 Molecular Weight Distribution. 3.12 Effect of Pressure. 3.13 Process Conditions. 3.14 Specific Commercial Polymers. 3.15 Living Radical Polymerization. 3.16 Other Polymerizations. 4. Emulsion Polymerization. 4.1 Description of Process. 4.2 Quantitative Aspects. 4.3 Other Characteristics of Emulsion Polymerization. 5. Ionic Chain Polymerization. 5.1 Comparison of Radical and Ionic Polymerization. 5.2 Cationic Polymerization of the Carbon-Carbon Double Bond. 5.3 Anionic Polymerization of the Carbon-Carbon Double. 5.4 Block and Other Polymer Architecture. 5.5 Distinguishing Between Radical, Cationic, and Anionic Polymerizations. 5.6 Carbonyl Polymerization. 5.7 Miscellaneous Polymerizations. 6. Chain Copolymerization. 6.1 General Considerations. 6.2 Copolymer Composition. 6.3 Radical Copolymerization. 6.4 Ionic Copolymerization. 6.5 Deviations from Terminal Copolymerization Model. 6.6 Copolymerizations Involving Dienes. 6.7 Other Copolymerizations. 6.8 Applications of Copolymerizations. 7. Ring-Opening Polymerization. 7.1 General Characteristics. 7.2 Cyclic Ethers. 7.3 Lactams. 7.4 N-Carboxy-alphaAmino Acid Anhydrides. 7.5 Lactones. 7.6 Nitrogen Heterocyclics. 7.7 Sulfur Heterocyclics. 7.8 Cycloalkenes. 7.9 Miscellaneous Oxygen Heterocyclics. 7.10 Other Ring-Opening Polymerizations. 7.11 Inorganic and Partially Inorganic Polymers. 7.12 Copolymerization. 8. Stereochemistry of Polymerizaton. 8.1 Types of Stereoisomerism in Polymers. 8.2 Properties of Stereoregular Polymers. 8.3 Forces of Stereoregulation in Alkene Polymerization. 8.4 Traditional Ziegler-Natta Polymerization of Nonpolar Alkene Monomers. 8.5 Metallocene Polymerization of Nonpolar Alkene Monomers. 8.6 Other Hydrocarbon Monomers. 8.7 Copolymerization. 8.8 Postmetallocene: Chelate Initiators. 8.9 Living Polymerization. 8.10 Polymerization of 1,3-Dienes. 8.11 Commercial Applications. 8.12 Polymerization of Polar Vinyl Monomers. 8.13 Alehydes. 8.14 Optical Activity in Polymers. 8.15 Ring-Opening Polymerization. 8.16 Statistical Models of Propagation. 9. Reactions of Polymers. 9.1 Principles of Polymers Reactivity. 9.2 Crosslinking. 9.3 Reactions of Cellulose. 9.4 Reactions of Poly(vinyl) acetate). 9.5 Halogenation. 9.6 Aromatic Substitution. 9.7 Cyclization. 9.8 Other Reactions. 9.9 Graft Copolymers. 9.10 Block Copolymers. 9.11 Polymers as Carriers or Supports. 9.12 Polymer Reagents. 9.13 Polymer Catalysts. 9.14 Polymer Substrates. Index.
(Fonte: OpenAlex. Non è il testo integrale dell'articolo.)
Argomenti e parole chiave
- Argomenti (OpenAlex): Advanced Polymer Synthesis and Characterization (Organic Chemistry); Polymer Synthesis and Characterization (Polymers and Plastics); biodegradable polymer synthesis and properties (Biomaterials)
- Parole chiave: polymerization, step-growth polymerization, radical chain polymerization, emulsion polymerization, controlled radical polymerization, crosslinking, molecular weight distribution, polymer kinetics, dendrimers, block copolymers
- Concetti: Polymerization
Contenuto in sintesi
Il testo completo non è ad accesso aperto e non è stato consultato: sono disponibili solo i metadati e l'abstract riportati sopra. Per approfondire, aprire la fonte dal DOI (o tramite biblioteca/abbonamento).
Come è citata nella tesi
- Sez. 4.2 Copolimeri coniugati (
tesi.mdr. 942): Nei processi convenzionali, infatti, l'assenza di un rigoroso controllo sulla cinetica di crescita e sulle reazioni di terminazione o trasferimento di catena porta a distribuzioni dei pesi molecolari ampie, con valori teorici e sperimentali di PD che si assestano tipicamente attorno a 2 (distribuzione più probabile di Flory) o superiori.[54]
Bibliografia della fonte
Elenco dei riferimenti non depositato dall'editore su Crossref.
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Metriche
- Citata 7144 volte (OpenAlex)
- Citazioni per anno: 2026: 132, 2025: 187, 2024: 203, 2023: 212, 2022: 210, 2021: 284
Torna alla bibliografia della tesi · Generata dal catalogo bibliografia.json e da Crossref, OpenAlex, Europe PMC.