Biologically active natural products from Asia and Africa : a selection of topics / / edited by Anna Capasso |
Pubbl/distr/stampa | Singapore : , : Bentham Science Publishers, , [2021] |
Descrizione fisica | 1 online resource (141 pages) |
Disciplina | 547.7 |
Soggetto topico | Natural products |
ISBN | 981-14-8974-2 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910794587903321 |
Singapore : , : Bentham Science Publishers, , [2021] | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Biologically active natural products from Asia and Africa : a selection of topics / / edited by Anna Capasso |
Pubbl/distr/stampa | Singapore : , : Bentham Science Publishers, , [2021] |
Descrizione fisica | 1 online resource (141 pages) |
Disciplina | 547.7 |
Soggetto topico | Natural products |
ISBN | 981-14-8974-2 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910812227603321 |
Singapore : , : Bentham Science Publishers, , [2021] | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Biomedical applications [[electronic resource] /] / edited by Alaa S. Abd-El-Aziz ... [et al.] |
Pubbl/distr/stampa | Hoboken, NJ, : Wiley-Interscience, c2004 |
Descrizione fisica | 1 online resource (234 p.) |
Disciplina |
547.7
610/.28 |
Altri autori (Persone) | Abd-El-AzizAlaa S |
Collana | Macromolecules containing metal and metal-like elements |
Soggetto topico |
Polymers in medicine
Macromolecules Organometallic compounds |
Soggetto genere / forma | Electronic books. |
ISBN |
1-280-54216-0
9786610542161 0-471-68375-2 0-471-68377-9 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Macromolecules Containing Metal and Metal-Like Elements Volume 3; Contributors; Contents; Preface; Series Preface; 1. Organometallic Compounds in Biomedical Applications; I. Introduction; II. Case for Metal-Containing Bioactive Agents; A. Tin-Containing Biocidal Polymers; B. Ferrocene: A Therapeutic Role in Polymeric Systems?; C. Polymeric Moderation of OsO(4) Toxicity; III. Miscellaneous Polymers; A. Metal Chelation Polymers; B. Condensation Polymers; IV. Small-Molecule Analogs; V. Summary; VI. References; 2. Metal-Labeled DNA on Surfaces; I. Introduction; II. Ferrocene Nucleotides
III. Ferrocene-DNA ConjugatesIV. Other Metal-DNA Conjugates; V. Metallated DNA; A. Cu-DNA; B. M-DNA; VI. Summary; VII. Acknowledgments; VIII. References; 3. Artificial DNA through Metal-Mediated Base Pairing: Structural Control and Discrete Metal Assembly; I. Introduction; II. Alternative Hydrogen-Bonding Schemes for DNA Base Pairing; III. Non-Hydrogen-Bonding Basepairs in DNA; IV. Metal-Mediated Base Pairing in DNA; A. Basic Concept; B. Artificial Nucleosides Designed for Metal-Mediated Base Pairs; C. Incorporation of a Metallo-Base Pair in DNA and Its Effect on Thermal Stability D. Discrete Self-Assembled Metal Arrays in DNAV. Future Prospects for Artificial Metallo-DNA; VI. Summary; VII. References; 4. Organotin Macromolecules as Anticancer Drugs; I. General; II. Anticancer Activity of Small Organotin Compounds; III. Molecule-Level Studies on Monomeric Organotin Compounds; IV. Anticancer Activity of Organotin Polymers; V. Future Work; VI. References; 5. Organotin Oligomeric Drugs Containing the Antivirial Agent Acyclovir; I. Early History of Organotin Compounds; II. Mechanisms and Reactions; III. General Structures; IV. Acyclovir; V. Bioactivity of Related Compounds VI. Experimental WorkVII. Results and Discussion; VIII. References; 6. Polymeric Ferrocene Conjugates as Antiproliferative Agents; I. Introduction; II. The Ferrocene-Ferricenium System in the Biological Environment; III. Polymer-Drug Conjugation as a Pharmaceutical Tool for Drug Delivery; IV. Polymer-Ferrocene Conjugates: Synthesis and Structure; A. The Carrier Component: Structural Considerations; B. Conjugates of Amide-Linked Ferrocene; C. Conjugates of Ester-Linked Ferrocene; V. Bioactivity Screening; VI. Summary and Conclusions; VII. Acknowledgments; VIII. References 7. Polymeric Platinum-Containing Drugs in the Treatment of CancerI. Introduction; II. Basic Mechanisms of Pt(II) Complex Formation; III. Nomenclature; IV. Currently Approved Platinum-Containing Compounds; V. Properties of Cisplatin; VI. Structure-Activity Relationships; VII. Polymer-Drug Conjugation Strategy and Possible Benefits; A. Polymers as Carriers; B. Polymers as Drugs; C. General; VIII. Mainchain-Incorporated cis-Diamine-Coordinated Platinum; A. Simple Amine Derivatives; B. Amino Acid Derivatives; C. Other Nitrogen-Platinum Products; D. Solution Stability; E. Thermal Stability F. Antiviral Activity |
Record Nr. | UNINA-9910146071703321 |
Hoboken, NJ, : Wiley-Interscience, c2004 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Biomedical applications [[electronic resource] /] / edited by Alaa S. Abd-El-Aziz ... [et al.] |
Pubbl/distr/stampa | Hoboken, NJ, : Wiley-Interscience, c2004 |
Descrizione fisica | 1 online resource (234 p.) |
Disciplina |
547.7
610/.28 |
Altri autori (Persone) | Abd-El-AzizAlaa S |
Collana | Macromolecules containing metal and metal-like elements |
Soggetto topico |
Polymers in medicine
Macromolecules Organometallic compounds |
ISBN |
1-280-54216-0
9786610542161 0-471-68375-2 0-471-68377-9 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Macromolecules Containing Metal and Metal-Like Elements Volume 3; Contributors; Contents; Preface; Series Preface; 1. Organometallic Compounds in Biomedical Applications; I. Introduction; II. Case for Metal-Containing Bioactive Agents; A. Tin-Containing Biocidal Polymers; B. Ferrocene: A Therapeutic Role in Polymeric Systems?; C. Polymeric Moderation of OsO(4) Toxicity; III. Miscellaneous Polymers; A. Metal Chelation Polymers; B. Condensation Polymers; IV. Small-Molecule Analogs; V. Summary; VI. References; 2. Metal-Labeled DNA on Surfaces; I. Introduction; II. Ferrocene Nucleotides
III. Ferrocene-DNA ConjugatesIV. Other Metal-DNA Conjugates; V. Metallated DNA; A. Cu-DNA; B. M-DNA; VI. Summary; VII. Acknowledgments; VIII. References; 3. Artificial DNA through Metal-Mediated Base Pairing: Structural Control and Discrete Metal Assembly; I. Introduction; II. Alternative Hydrogen-Bonding Schemes for DNA Base Pairing; III. Non-Hydrogen-Bonding Basepairs in DNA; IV. Metal-Mediated Base Pairing in DNA; A. Basic Concept; B. Artificial Nucleosides Designed for Metal-Mediated Base Pairs; C. Incorporation of a Metallo-Base Pair in DNA and Its Effect on Thermal Stability D. Discrete Self-Assembled Metal Arrays in DNAV. Future Prospects for Artificial Metallo-DNA; VI. Summary; VII. References; 4. Organotin Macromolecules as Anticancer Drugs; I. General; II. Anticancer Activity of Small Organotin Compounds; III. Molecule-Level Studies on Monomeric Organotin Compounds; IV. Anticancer Activity of Organotin Polymers; V. Future Work; VI. References; 5. Organotin Oligomeric Drugs Containing the Antivirial Agent Acyclovir; I. Early History of Organotin Compounds; II. Mechanisms and Reactions; III. General Structures; IV. Acyclovir; V. Bioactivity of Related Compounds VI. Experimental WorkVII. Results and Discussion; VIII. References; 6. Polymeric Ferrocene Conjugates as Antiproliferative Agents; I. Introduction; II. The Ferrocene-Ferricenium System in the Biological Environment; III. Polymer-Drug Conjugation as a Pharmaceutical Tool for Drug Delivery; IV. Polymer-Ferrocene Conjugates: Synthesis and Structure; A. The Carrier Component: Structural Considerations; B. Conjugates of Amide-Linked Ferrocene; C. Conjugates of Ester-Linked Ferrocene; V. Bioactivity Screening; VI. Summary and Conclusions; VII. Acknowledgments; VIII. References 7. Polymeric Platinum-Containing Drugs in the Treatment of CancerI. Introduction; II. Basic Mechanisms of Pt(II) Complex Formation; III. Nomenclature; IV. Currently Approved Platinum-Containing Compounds; V. Properties of Cisplatin; VI. Structure-Activity Relationships; VII. Polymer-Drug Conjugation Strategy and Possible Benefits; A. Polymers as Carriers; B. Polymers as Drugs; C. General; VIII. Mainchain-Incorporated cis-Diamine-Coordinated Platinum; A. Simple Amine Derivatives; B. Amino Acid Derivatives; C. Other Nitrogen-Platinum Products; D. Solution Stability; E. Thermal Stability F. Antiviral Activity |
Record Nr. | UNINA-9910830634203321 |
Hoboken, NJ, : Wiley-Interscience, c2004 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Biomedical applications [[electronic resource] /] / edited by Alaa S. Abd-El-Aziz ... [et al.] |
Pubbl/distr/stampa | Hoboken, NJ, : Wiley-Interscience, c2004 |
Descrizione fisica | 1 online resource (234 p.) |
Disciplina |
547.7
610/.28 |
Altri autori (Persone) | Abd-El-AzizAlaa S |
Collana | Macromolecules containing metal and metal-like elements |
Soggetto topico |
Polymers in medicine
Macromolecules Organometallic compounds |
ISBN |
1-280-54216-0
9786610542161 0-471-68375-2 0-471-68377-9 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Macromolecules Containing Metal and Metal-Like Elements Volume 3; Contributors; Contents; Preface; Series Preface; 1. Organometallic Compounds in Biomedical Applications; I. Introduction; II. Case for Metal-Containing Bioactive Agents; A. Tin-Containing Biocidal Polymers; B. Ferrocene: A Therapeutic Role in Polymeric Systems?; C. Polymeric Moderation of OsO(4) Toxicity; III. Miscellaneous Polymers; A. Metal Chelation Polymers; B. Condensation Polymers; IV. Small-Molecule Analogs; V. Summary; VI. References; 2. Metal-Labeled DNA on Surfaces; I. Introduction; II. Ferrocene Nucleotides
III. Ferrocene-DNA ConjugatesIV. Other Metal-DNA Conjugates; V. Metallated DNA; A. Cu-DNA; B. M-DNA; VI. Summary; VII. Acknowledgments; VIII. References; 3. Artificial DNA through Metal-Mediated Base Pairing: Structural Control and Discrete Metal Assembly; I. Introduction; II. Alternative Hydrogen-Bonding Schemes for DNA Base Pairing; III. Non-Hydrogen-Bonding Basepairs in DNA; IV. Metal-Mediated Base Pairing in DNA; A. Basic Concept; B. Artificial Nucleosides Designed for Metal-Mediated Base Pairs; C. Incorporation of a Metallo-Base Pair in DNA and Its Effect on Thermal Stability D. Discrete Self-Assembled Metal Arrays in DNAV. Future Prospects for Artificial Metallo-DNA; VI. Summary; VII. References; 4. Organotin Macromolecules as Anticancer Drugs; I. General; II. Anticancer Activity of Small Organotin Compounds; III. Molecule-Level Studies on Monomeric Organotin Compounds; IV. Anticancer Activity of Organotin Polymers; V. Future Work; VI. References; 5. Organotin Oligomeric Drugs Containing the Antivirial Agent Acyclovir; I. Early History of Organotin Compounds; II. Mechanisms and Reactions; III. General Structures; IV. Acyclovir; V. Bioactivity of Related Compounds VI. Experimental WorkVII. Results and Discussion; VIII. References; 6. Polymeric Ferrocene Conjugates as Antiproliferative Agents; I. Introduction; II. The Ferrocene-Ferricenium System in the Biological Environment; III. Polymer-Drug Conjugation as a Pharmaceutical Tool for Drug Delivery; IV. Polymer-Ferrocene Conjugates: Synthesis and Structure; A. The Carrier Component: Structural Considerations; B. Conjugates of Amide-Linked Ferrocene; C. Conjugates of Ester-Linked Ferrocene; V. Bioactivity Screening; VI. Summary and Conclusions; VII. Acknowledgments; VIII. References 7. Polymeric Platinum-Containing Drugs in the Treatment of CancerI. Introduction; II. Basic Mechanisms of Pt(II) Complex Formation; III. Nomenclature; IV. Currently Approved Platinum-Containing Compounds; V. Properties of Cisplatin; VI. Structure-Activity Relationships; VII. Polymer-Drug Conjugation Strategy and Possible Benefits; A. Polymers as Carriers; B. Polymers as Drugs; C. General; VIII. Mainchain-Incorporated cis-Diamine-Coordinated Platinum; A. Simple Amine Derivatives; B. Amino Acid Derivatives; C. Other Nitrogen-Platinum Products; D. Solution Stability; E. Thermal Stability F. Antiviral Activity |
Record Nr. | UNINA-9910840948203321 |
Hoboken, NJ, : Wiley-Interscience, c2004 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Biomedicine / / edited by Chao Lin |
Pubbl/distr/stampa | Rijeka, Croatia : , : IntechOpen, , 2012 |
Descrizione fisica | 1 online resource (214 pages) : illustrations |
Disciplina | 547.7 |
Soggetto topico | Proteins |
ISBN | 953-51-6920-3 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910317617203321 |
Rijeka, Croatia : , : IntechOpen, , 2012 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Bioreactor immobilized enzymes and cells : fundamentals and applications / edited by Murray Moo-Young |
Pubbl/distr/stampa | London, : Elsevier, 1988 |
Descrizione fisica | xvi, 327 p. : ill. ; 23 cm. |
Disciplina | 547.7 |
ISBN | 1851661603 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNICAS-RML0282464 |
London, : Elsevier, 1988 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. di Cassino | ||
|
Block copolymers [[electronic resource] ] : synthetic strategies, physical properties, and applications / / Nikos Hadjichristidis, Stergios Pispas, George Floudas |
Autore | Hadjichristidis Nikos <1943-> |
Pubbl/distr/stampa | Hoboken, N.J., : Wiley-Interscience, c2003 |
Descrizione fisica | 1 online resource (445 p.) |
Disciplina |
547
547.7 547.84 |
Altri autori (Persone) |
PispasStergios <1967->
FloudasGeorge <1961-> |
Soggetto topico | Block copolymers |
Soggetto genere / forma | Electronic books. |
ISBN |
1-280-36675-3
9786610366750 0-470-23239-0 0-471-46134-2 0-471-26980-8 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
BLOCK COPOLYMERS; CONTENTS; Preface; Abbreviations and Symbols; I BLOCK COPOLYMER SYNTHESIS; 1 BLOCK COPOLYMERS BY ANIONIC POLYMERIZATION; 1. Synthesis of AB Diblock Copolymers; 2. Synthesis of Triblock Copolymers; 3. Linear Block Copolymers With More Than Three Blocks; 2 BLOCK COPOLYMERS BY CATIONIC POLYMERIZATION; 1. Synthesis of AB Diblock Copolymers; 2. Synthesis of Triblock Copolymers; 3 BLOCK COPOLYMERS BY LIVING FREE RADICAL POLYMERIZATION; 1. Synthesis of AB Diblock Copolymers; 2. Synthesis of ABA Triblock Copolymers
3. Synthesis of ABC Triblock Terpolymers and ABCD Tetrablock Quarterpolymers4 BLOCK COPOLYMERS BY GROUP TRANSFER POLYMERIZATION; 1. Synthesis of AB Diblock Copolymers; 2. Synthesis of ABA Triblock Copolymers; 3. Synthesis of ABC Triblock Terpolymers; 5 BLOCK COPOLYMERS BY RING OPENING METATHESIS POLYMERIZATION; 1. Synthesis of AB Diblock Copolymers; 2. Synthesis of ABA Triblock Copolymers; 6 SYNTHESIS OF BLOCK COPOLYMERS BY A COMBINATION OF DIFFERENT POLYMERIZATION METHODS; 1. Synthesis of Block Copolymers by Anionic to Cationic Mechanism Transformation 2. Synthesis of Block Copolymers by Anionic to Living Free Radical Mechanism Transformation3. Synthesis of Block Copolymers by Cationic to Anionic Mechanism Transformation; 4. Synthesis of Block Copolymers by Cationic to Onium Mechanism Transformation; 5. Synthesis of Block Copolymers by Cationic to Living Free Radical Mechanism Transformation; 6. Synthesis of Block Copolymers by Living Free Radical to Cationic Mechanism Transformation; 7. Synthesis of Block Copolymers by Ring Opening Metathesis to Living Free Radical Mechanism Transformation 8. Synthesis of Block Copolymers by Ring Opening Metathesis to Group Transfer Mechanism Transformation9. Other Combinations; 10. Bifunctional (DUAL) Initiators; 11. Synthesis of Block Copolymers by Direct Coupling of Preformed Living Blocks; 12. Synthesis of Block Copolymers by Coupling of End-functionalized Prepolymers; 7 SYNTHESIS OF BLOCK COPOLYMERS BY CHEMICAL MODIFICATION; 1. Hydrogenation; 2. Hydrolysis; 3. Quaternization; 4. Sulfonation; 5. Hydroboration/Oxidation; 6. Epoxidation; 7. Chloro/BromoMethylation; 8. Hydrosilylation; 8 NONLINEAR BLOCK COPOLYMERS; 1. Star Block Copolymers 2. Graft Copolymers3. Miktoarm Star Copolymers; 4. Other Complex Architectures; II MOLECULAR CHARACTERIZATION OF BLOCK COPOLYMERS; 9 MOLECULAR CHARACTERIZATION OF BLOCK COPOLYMERS; 1. Purification of Block Copolymers by Fractionation; 2. Molecular Characterization; III SOLUTION PROPERTIES OF BLOCK COPOLYMERS; 10 DILUTE SOLUTIONS OF BLOCK COPOLYMERS IN NONSELECTIVE SOLVENTS; 11 DILUTE SOLUTIONS OF BLOCK COPOLYMERS IN SELECTIVE SOLVENTS; 1. Thermodynamics of Micellization; 2. Phenomenology of Block Copolymer Micellar Structure; 3. Experimental Techniques for Studying Micelle Formation 4. Equilibrium Structure of Block Copolymer Micelles |
Record Nr. | UNINA-9910143177103321 |
Hadjichristidis Nikos <1943-> | ||
Hoboken, N.J., : Wiley-Interscience, c2003 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Block copolymers [[electronic resource] ] : synthetic strategies, physical properties, and applications / / Nikos Hadjichristidis, Stergios Pispas, George Floudas |
Autore | Hadjichristidis Nikos <1943-> |
Pubbl/distr/stampa | Hoboken, N.J., : Wiley-Interscience, c2003 |
Descrizione fisica | 1 online resource (445 p.) |
Disciplina |
547
547.7 547.84 |
Altri autori (Persone) |
PispasStergios <1967->
FloudasGeorge <1961-> |
Soggetto topico | Block copolymers |
ISBN |
1-280-36675-3
9786610366750 0-470-23239-0 0-471-46134-2 0-471-26980-8 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
BLOCK COPOLYMERS; CONTENTS; Preface; Abbreviations and Symbols; I BLOCK COPOLYMER SYNTHESIS; 1 BLOCK COPOLYMERS BY ANIONIC POLYMERIZATION; 1. Synthesis of AB Diblock Copolymers; 2. Synthesis of Triblock Copolymers; 3. Linear Block Copolymers With More Than Three Blocks; 2 BLOCK COPOLYMERS BY CATIONIC POLYMERIZATION; 1. Synthesis of AB Diblock Copolymers; 2. Synthesis of Triblock Copolymers; 3 BLOCK COPOLYMERS BY LIVING FREE RADICAL POLYMERIZATION; 1. Synthesis of AB Diblock Copolymers; 2. Synthesis of ABA Triblock Copolymers
3. Synthesis of ABC Triblock Terpolymers and ABCD Tetrablock Quarterpolymers4 BLOCK COPOLYMERS BY GROUP TRANSFER POLYMERIZATION; 1. Synthesis of AB Diblock Copolymers; 2. Synthesis of ABA Triblock Copolymers; 3. Synthesis of ABC Triblock Terpolymers; 5 BLOCK COPOLYMERS BY RING OPENING METATHESIS POLYMERIZATION; 1. Synthesis of AB Diblock Copolymers; 2. Synthesis of ABA Triblock Copolymers; 6 SYNTHESIS OF BLOCK COPOLYMERS BY A COMBINATION OF DIFFERENT POLYMERIZATION METHODS; 1. Synthesis of Block Copolymers by Anionic to Cationic Mechanism Transformation 2. Synthesis of Block Copolymers by Anionic to Living Free Radical Mechanism Transformation3. Synthesis of Block Copolymers by Cationic to Anionic Mechanism Transformation; 4. Synthesis of Block Copolymers by Cationic to Onium Mechanism Transformation; 5. Synthesis of Block Copolymers by Cationic to Living Free Radical Mechanism Transformation; 6. Synthesis of Block Copolymers by Living Free Radical to Cationic Mechanism Transformation; 7. Synthesis of Block Copolymers by Ring Opening Metathesis to Living Free Radical Mechanism Transformation 8. Synthesis of Block Copolymers by Ring Opening Metathesis to Group Transfer Mechanism Transformation9. Other Combinations; 10. Bifunctional (DUAL) Initiators; 11. Synthesis of Block Copolymers by Direct Coupling of Preformed Living Blocks; 12. Synthesis of Block Copolymers by Coupling of End-functionalized Prepolymers; 7 SYNTHESIS OF BLOCK COPOLYMERS BY CHEMICAL MODIFICATION; 1. Hydrogenation; 2. Hydrolysis; 3. Quaternization; 4. Sulfonation; 5. Hydroboration/Oxidation; 6. Epoxidation; 7. Chloro/BromoMethylation; 8. Hydrosilylation; 8 NONLINEAR BLOCK COPOLYMERS; 1. Star Block Copolymers 2. Graft Copolymers3. Miktoarm Star Copolymers; 4. Other Complex Architectures; II MOLECULAR CHARACTERIZATION OF BLOCK COPOLYMERS; 9 MOLECULAR CHARACTERIZATION OF BLOCK COPOLYMERS; 1. Purification of Block Copolymers by Fractionation; 2. Molecular Characterization; III SOLUTION PROPERTIES OF BLOCK COPOLYMERS; 10 DILUTE SOLUTIONS OF BLOCK COPOLYMERS IN NONSELECTIVE SOLVENTS; 11 DILUTE SOLUTIONS OF BLOCK COPOLYMERS IN SELECTIVE SOLVENTS; 1. Thermodynamics of Micellization; 2. Phenomenology of Block Copolymer Micellar Structure; 3. Experimental Techniques for Studying Micelle Formation 4. Equilibrium Structure of Block Copolymer Micelles |
Record Nr. | UNINA-9910830358303321 |
Hadjichristidis Nikos <1943-> | ||
Hoboken, N.J., : Wiley-Interscience, c2003 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Block copolymers [[electronic resource] ] : synthetic strategies, physical properties, and applications / / Nikos Hadjichristidis, Stergios Pispas, George Floudas |
Autore | Hadjichristidis Nikos <1943-> |
Pubbl/distr/stampa | Hoboken, N.J., : Wiley-Interscience, c2003 |
Descrizione fisica | 1 online resource (445 p.) |
Disciplina |
547
547.7 547.84 |
Altri autori (Persone) |
PispasStergios <1967->
FloudasGeorge <1961-> |
Soggetto topico | Block copolymers |
ISBN |
1-280-36675-3
9786610366750 0-470-23239-0 0-471-46134-2 0-471-26980-8 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
BLOCK COPOLYMERS; CONTENTS; Preface; Abbreviations and Symbols; I BLOCK COPOLYMER SYNTHESIS; 1 BLOCK COPOLYMERS BY ANIONIC POLYMERIZATION; 1. Synthesis of AB Diblock Copolymers; 2. Synthesis of Triblock Copolymers; 3. Linear Block Copolymers With More Than Three Blocks; 2 BLOCK COPOLYMERS BY CATIONIC POLYMERIZATION; 1. Synthesis of AB Diblock Copolymers; 2. Synthesis of Triblock Copolymers; 3 BLOCK COPOLYMERS BY LIVING FREE RADICAL POLYMERIZATION; 1. Synthesis of AB Diblock Copolymers; 2. Synthesis of ABA Triblock Copolymers
3. Synthesis of ABC Triblock Terpolymers and ABCD Tetrablock Quarterpolymers4 BLOCK COPOLYMERS BY GROUP TRANSFER POLYMERIZATION; 1. Synthesis of AB Diblock Copolymers; 2. Synthesis of ABA Triblock Copolymers; 3. Synthesis of ABC Triblock Terpolymers; 5 BLOCK COPOLYMERS BY RING OPENING METATHESIS POLYMERIZATION; 1. Synthesis of AB Diblock Copolymers; 2. Synthesis of ABA Triblock Copolymers; 6 SYNTHESIS OF BLOCK COPOLYMERS BY A COMBINATION OF DIFFERENT POLYMERIZATION METHODS; 1. Synthesis of Block Copolymers by Anionic to Cationic Mechanism Transformation 2. Synthesis of Block Copolymers by Anionic to Living Free Radical Mechanism Transformation3. Synthesis of Block Copolymers by Cationic to Anionic Mechanism Transformation; 4. Synthesis of Block Copolymers by Cationic to Onium Mechanism Transformation; 5. Synthesis of Block Copolymers by Cationic to Living Free Radical Mechanism Transformation; 6. Synthesis of Block Copolymers by Living Free Radical to Cationic Mechanism Transformation; 7. Synthesis of Block Copolymers by Ring Opening Metathesis to Living Free Radical Mechanism Transformation 8. Synthesis of Block Copolymers by Ring Opening Metathesis to Group Transfer Mechanism Transformation9. Other Combinations; 10. Bifunctional (DUAL) Initiators; 11. Synthesis of Block Copolymers by Direct Coupling of Preformed Living Blocks; 12. Synthesis of Block Copolymers by Coupling of End-functionalized Prepolymers; 7 SYNTHESIS OF BLOCK COPOLYMERS BY CHEMICAL MODIFICATION; 1. Hydrogenation; 2. Hydrolysis; 3. Quaternization; 4. Sulfonation; 5. Hydroboration/Oxidation; 6. Epoxidation; 7. Chloro/BromoMethylation; 8. Hydrosilylation; 8 NONLINEAR BLOCK COPOLYMERS; 1. Star Block Copolymers 2. Graft Copolymers3. Miktoarm Star Copolymers; 4. Other Complex Architectures; II MOLECULAR CHARACTERIZATION OF BLOCK COPOLYMERS; 9 MOLECULAR CHARACTERIZATION OF BLOCK COPOLYMERS; 1. Purification of Block Copolymers by Fractionation; 2. Molecular Characterization; III SOLUTION PROPERTIES OF BLOCK COPOLYMERS; 10 DILUTE SOLUTIONS OF BLOCK COPOLYMERS IN NONSELECTIVE SOLVENTS; 11 DILUTE SOLUTIONS OF BLOCK COPOLYMERS IN SELECTIVE SOLVENTS; 1. Thermodynamics of Micellization; 2. Phenomenology of Block Copolymer Micellar Structure; 3. Experimental Techniques for Studying Micelle Formation 4. Equilibrium Structure of Block Copolymer Micelles |
Record Nr. | UNINA-9910840767003321 |
Hadjichristidis Nikos <1943-> | ||
Hoboken, N.J., : Wiley-Interscience, c2003 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|