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Rare Metal Technology 2020 [[electronic resource] /] / edited by Gisele Azimi, Kerstin Forsberg, Takanari Ouchi, Hojong Kim, Shafiq Alam, Alafara Abdullahi Baba
| Rare Metal Technology 2020 [[electronic resource] /] / edited by Gisele Azimi, Kerstin Forsberg, Takanari Ouchi, Hojong Kim, Shafiq Alam, Alafara Abdullahi Baba |
| Edizione | [1st ed. 2020.] |
| Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2020 |
| Descrizione fisica | 1 online resource (XV, 384 p. 178 illus., 121 illus. in color.) |
| Disciplina | 660.284248 |
| Collana | The Minerals, Metals & Materials Series |
| Soggetto topico |
Metals
Materials science Organometallic chemistry Engineering—Materials Metallic Materials Characterization and Evaluation of Materials Organometallic Chemistry Materials Engineering Metalls de terres rares Extracció (Química) |
| Soggetto genere / forma |
Congressos
Llibres electrònics |
| ISBN | 3-030-36758-4 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910373892203321 |
| Cham : , : Springer International Publishing : , : Imprint : Springer, , 2020 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Rare-Earth Metal Recovery for Green Technologies [[electronic resource] ] : Methods and Applications / / edited by Rajesh Kumar Jyothi
| Rare-Earth Metal Recovery for Green Technologies [[electronic resource] ] : Methods and Applications / / edited by Rajesh Kumar Jyothi |
| Edizione | [1st ed. 2020.] |
| Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2020 |
| Descrizione fisica | 1 online resource (XIII, 166 p. 43 illus., 22 illus. in color.) |
| Disciplina | 546.41 |
| Soggetto topico |
Metals
Materials science Organometallic chemistry Environmental sciences Manufactures Metallic Materials Characterization and Evaluation of Materials Organometallic Chemistry Environmental Science and Engineering Manufacturing, Machines, Tools, Processes |
| ISBN | 3-030-38106-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Chapter 1. Introduction of Rare-Earth Metal Recovery for Green and Clean Energy Technologies -- Chapter 2. Mineral processing of the rare earth ores -- Chapter 3. Thermodynamic aspects for rare earth metal production -- Chapter 4. Fundamental principle and practices of solvent extraction (SX) and supported liquid membrane (SLM) process for extraction and separation of rare earth metal (s) -- Chapter 5. Recent strategies on adsorptive removal of rare earths and precious metals using low-cost natural adsorbents -- Chapter 6. Investigation on extraction and recovery of rare earth elements from secondary solid wastes -- Chapter 7. Fabrication of nanostructured materials with rare-earth elements for bioanalytical applications -- Chapter 8. Rare earths based magnetic materials: Progresses in the fabrication technologies and magnetic properties. |
| Record Nr. | UNINA-9910410049203321 |
| Cham : , : Springer International Publishing : , : Imprint : Springer, , 2020 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Rhodium Catalysis [[electronic resource] /] / edited by Carmen Claver
| Rhodium Catalysis [[electronic resource] /] / edited by Carmen Claver |
| Edizione | [1st ed. 2018.] |
| Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2018 |
| Descrizione fisica | 1 online resource (VII, 288 p.) |
| Disciplina | 541.395 |
| Collana | Topics in Organometallic Chemistry |
| Soggetto topico |
Organometallic chemistry
Catalysis Physical chemistry Organometallic Chemistry Physical Chemistry |
| ISBN | 3-319-66665-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Rhodium catalyzed C-B bond formation -- Rhodium catalyzed tandem reactions -- Rhodium catalyzed hydroformylation -- Rh catalyzed thiolation of olefins -- Rh-catalyzed decarbonylation reactions -- Enantioselective catalysis with Rhodium / Phosphoramidite catalysts -- CO2 reduction reactions by rhodium-based catalysts -- Rh catalyzed Pauson-Khand. |
| Record Nr. | UNINA-9910767501903321 |
| Cham : , : Springer International Publishing : , : Imprint : Springer, , 2018 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Ruthenium in Catalysis [[electronic resource] /] / edited by Pierre H. Dixneuf, Christian Bruneau
| Ruthenium in Catalysis [[electronic resource] /] / edited by Pierre H. Dixneuf, Christian Bruneau |
| Edizione | [1st ed. 2014.] |
| Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2014 |
| Descrizione fisica | 1 online resource (VIII, 401 p. 511 illus., 27 illus. in color.) : online resource |
| Disciplina | 547.05 |
| Collana | Topics in Organometallic Chemistry |
| Soggetto topico |
Organometallic chemistry
Catalysis Chemical engineering Organometallic Chemistry Industrial Chemistry/Chemical Engineering |
| ISBN | 3-319-08482-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | From the contents: Hydrogenation of polar bonds catalyzed by Ruthenium-Pincer complexes -- Ruthenium-catalyzed amide-bond formation -- Hydrogen generation from alcohols and formic acid, with ruthenium catalysts including pincer-type Ru complexes. |
| Record Nr. | UNINA-9910768445703321 |
| Cham : , : Springer International Publishing : , : Imprint : Springer, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Silicon Containing Copolymers [[electronic resource] /] / by Sahar Amiri, Mohammad Ali Semsarzadeh, Sanam Amiri
| Silicon Containing Copolymers [[electronic resource] /] / by Sahar Amiri, Mohammad Ali Semsarzadeh, Sanam Amiri |
| Autore | Amiri Sahar |
| Edizione | [1st ed. 2014.] |
| Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2014 |
| Descrizione fisica | 1 online resource (60 p.) |
| Disciplina | 541.394 |
| Collana | SpringerBriefs in Molecular Science |
| Soggetto topico |
Polymers
Organometallic chemistry Catalysis Nanotechnology Polymer Sciences Organometallic Chemistry |
| ISBN | 3-319-09225-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Introduction -- Polyrotaxane based on inclusion complexes of OH-PDMS-OH and Br-PDMS-Br with γ-cyclodextrin without utilizing sonic energy -- Synthesis and Characterization of PDMS based triblock and pentablock Copolymers -- Cobalt mediated radical polymerization of 4-bromo-2,6-dimethyl phenol and its copolymerization with poly(dimethyl siloxane) in the presence of Co(acac)2: DMF catalyst -- Novel Thermoreversible Block Copolymers: Silicone Macroinitiator in Atom Transfer Radical Polymerization. |
| Record Nr. | UNINA-9910298648603321 |
Amiri Sahar
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| Cham : , : Springer International Publishing : , : Imprint : Springer, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Specific Intermolecular Interactions of Element-Organic Compounds [[electronic resource] /] / by Alexei K. Baev
| Specific Intermolecular Interactions of Element-Organic Compounds [[electronic resource] /] / by Alexei K. Baev |
| Autore | Baev Alexei K |
| Edizione | [1st ed. 2015.] |
| Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015 |
| Descrizione fisica | 1 online resource (300 p.) |
| Disciplina |
536.7
54 541 541.2 |
| Soggetto topico |
Chemistry, Physical and theoretical
Inorganic chemistry Organometallic chemistry Physical chemistry Thermodynamics Theoretical and Computational Chemistry Inorganic Chemistry Organometallic Chemistry Physical Chemistry |
| ISBN | 3-319-08563-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Hydrogen Bonds of Hydrides and Specific Intermolecular Interactions of Alkyl Compounds of Main Group Elements -- Specific Intermolecular Interactions of Silanes and their Derivatives -- Specific Interactions of Element-Organic Compounds of Germanium Subgroup Elements -- Specific Intermolecular Interactions of Sulphurgenated Organic Compounds -- Specific Intermolecular Interactions of Sulphur, Oxygen and Nitrogenated Organic Compounds. |
| Record Nr. | UNINA-9910298618703321 |
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Baev Alexei K
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| Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Stereoselective Heterocycle Synthesis via Alkene Difunctionalization [[electronic resource] ] : Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation / / by David A. Petrone
| Stereoselective Heterocycle Synthesis via Alkene Difunctionalization [[electronic resource] ] : Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation / / by David A. Petrone |
| Autore | Petrone David A |
| Edizione | [1st ed. 2018.] |
| Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2018 |
| Descrizione fisica | 1 online resource (392 pages) |
| Disciplina | 547.2 |
| Collana | Springer Theses, Recognizing Outstanding Ph.D. Research |
| Soggetto topico |
Organometallic chemistry
Catalysis Medicinal chemistry Organometallic Chemistry Medicinal Chemistry |
| ISBN | 3-319-77507-3 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Diastereoselective Synthesis of Heterocycles via Intramolecular Pd-Catalyzed Alkene Aryliodination -- Pd-Catalyzed Diastereoselective Carbocyanation Reactions of Chiral N-Allyl Carboxamides and Indoles -- Development of a Pd-Catalyzed Dearomative 1,2-Diarylation of Indoles using Aryl Boron Reagents -- Harnessing Reversible Oxidative Addition: Application of Diiodinated Aromatic Compounds in Aryliodination. |
| Record Nr. | UNINA-9910298594303321 |
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Petrone David A
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| Cham : , : Springer International Publishing : , : Imprint : Springer, , 2018 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Sulfur Dioxide Insertion Reactions for Organic Synthesis [[electronic resource] /] / by Danqing Zheng, Jie Wu
| Sulfur Dioxide Insertion Reactions for Organic Synthesis [[electronic resource] /] / by Danqing Zheng, Jie Wu |
| Autore | Zheng Danqing |
| Edizione | [1st ed. 2017.] |
| Pubbl/distr/stampa | Singapore : , : Springer Singapore : , : Imprint : Springer, , 2017 |
| Descrizione fisica | 1 online resource (V, 80 p. 73 illus., 5 illus. in color.) |
| Disciplina | 547.2 |
| Collana | SpringerBriefs in Molecular Science |
| Soggetto topico |
Organometallic chemistry
Medicinal chemistry Chemical engineering Organometallic Chemistry Medicinal Chemistry Industrial Chemistry/Chemical Engineering |
| ISBN | 981-10-4202-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Introduction -- Sulfur Dioxide Surrogates -- Sulfur Dioxide Insertion Reactions -- Conclusions and Outlook. |
| Record Nr. | UNINA-9910254140603321 |
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Zheng Danqing
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| Singapore : , : Springer Singapore : , : Imprint : Springer, , 2017 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Sustainable C(sp3)-H Bond Functionalization [[electronic resource] /] / by Jin Xie, Chengjian Zhu
| Sustainable C(sp3)-H Bond Functionalization [[electronic resource] /] / by Jin Xie, Chengjian Zhu |
| Autore | Xie Jin |
| Edizione | [1st ed. 2016.] |
| Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2016 |
| Descrizione fisica | 1 online resource (91 p.) |
| Disciplina | 547.01 |
| Collana | SpringerBriefs in Green Chemistry for Sustainability |
| Soggetto topico |
Organometallic chemistry
Catalysis Chemical engineering Organometallic Chemistry Industrial Chemistry/Chemical Engineering |
| ISBN | 3-662-49496-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Transition-Metal-Catalyzed, Directing Group Assisted C(sp3)-H Bond Functionalization -- Recent Advances in Non-Directed C(sp3)-H Bond Functionalization -- Functionalization of C(sp3)-H Bond by Visible-Light Photoredox Catalysis. |
| Record Nr. | UNINA-9910254023503321 |
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Xie Jin
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| Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2016 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Synthesis and Application of Organoboron Compounds [[electronic resource] /] / edited by Elena Fernández, Andrew Whiting
| Synthesis and Application of Organoboron Compounds [[electronic resource] /] / edited by Elena Fernández, Andrew Whiting |
| Edizione | [1st ed. 2015.] |
| Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015 |
| Descrizione fisica | 1 online resource (VII, 331 p. 492 illus., 14 illus. in color.) |
| Disciplina | 547.05671 |
| Collana | Topics in Organometallic Chemistry |
| Soggetto topico |
Organometallic chemistry
Catalysis Chemical engineering Organometallic Chemistry Industrial Chemistry/Chemical Engineering |
| ISBN | 3-319-13054-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Intro -- Preface -- Contents -- Boryl Anions -- 1 Introduction: History of Boryl Anions Before 2006 -- 2 Chemistry of Boryl Anions -- 2.1 Base-Stabilized Boryl Anions -- 2.2 N-Heterocyclic Boryl Anions -- 2.3 Boryl Anion Derivatives as a Counterpart of Carboanions -- 2.4 Base-Coordinated Diborane(4) as Boryl Anion Equivalents -- 3 Chemistry of Boryl-Transition Metal Complexes Derived from Boryl Anion -- 3.1 Boryl Complexes of Late Transition Metals (Groups 11-12) -- 3.2 Boryl Complexes of Early Transition Metals (Groups 3-5) -- 4 Chemistry of Boryl-Substituted Main Group Element Compounds Derived from Boryl Anions -- 4.1 Boryl-Substituted Group 13 Element Compounds -- 4.2 Boryl-Substituted Group 14 Element Compounds -- 4.3 Boryl-Substituted Group 15 Element Compounds -- 5 Summary and Outlook -- References -- Fundamental and Applied Properties of Borocations -- 1 Introduction -- 2 Fundamentals -- 2.1 Select Synthetic Considerations -- 2.2 Electrophilicity of Borocations -- 2.3 General Reactivity Pathways of Borocations with Nucleophiles -- 3 Borocations in Dehydroboration -- 3.1 Intramolecular Electrophilic Aromatic Borylation -- 3.2 Intramolecular Electrophilic Aliphatic Borylation -- 3.3 Intermolecular Electrophilic Aromatic Borylation -- 4 Borocations in Elemento-Boration -- 4.1 Hydroboration -- 4.2 Other Elemento-Boration Reactions -- 5 Borocations in Catalysis -- 6 Miscellaneous Applications of Borocations -- 6.1 Materials Applications -- 6.2 Borocations as Precursors to Borylenes and Boryl Radicals -- 6.3 Structural Rearrangement of Borocations -- 7 Conclusions and Future Outlook -- References -- Asymmetric Catalytic Borylation of α,beta-Unsaturated Acceptors -- 1 Introduction -- 2 Asymmetric beta-Borylation with Transition Metal Catalysts -- 2.1 Cu-Catalyzed beta-Borylation -- 2.1.1 beta-Monosubstituted Acyclic Substrates.
2.1.2 beta,beta-Disubstituted Acyclic Substrates: Formation of Organoboronates with a Quaternary Carbon -- 2.1.3 Cyclic Compounds -- 2.1.4 α,beta-Unsaturated C=N Compounds and N-Containing Compounds -- 2.1.5 Extended Michael Acceptors -- 2.2 Rh-Catalyzed beta-Borylation -- 2.3 Ni- and Pd-Catalyzed beta-Borylation -- 3 Asymmetric beta-Borylation with Organocatalysts -- 4 Asymmetric beta-Borylation in Water -- 5 Conclusions -- References -- Reactions of Alkynylboron Compounds -- 1 Introduction -- 2 Alkynylboronates (Esters of Alkynylboronic Acids) -- 2.1 Preparations -- 2.2 Insertion Reactions -- 2.3 Cycloaddition Reactions -- 2.4 Miscellaneous -- 3 Alkynylborates (Ate-Complexes) -- 3.1 Preparations -- 3.2 Uncatalyzed Reactions -- 3.3 Transition Metal-Catalyzed Reactions -- 3.4 Reactions Through Intermediacy of Alkynyl(Triorganyl)Borates -- 4 Conclusions -- References -- Improving Transformations Through Organotrifluoroborates -- 1 Introduction -- 2 Improvements Toward Organotrifluoroborate Synthesis -- 3 Recent Advances in C-C Bond Formation with Organotrifluoroborates -- 3.1 Cross-Coupling of Novel Organotrifluoroborates -- 3.2 Improved Incorporation of Important Scaffolds -- 3.3 C-H Functionalization with Organotrifluoroborates -- 3.4 Enantioselective C-C Bond Formation -- 3.5 Radical Reactions with Organotrifluoroborates -- 4 C-Y Bond Formation from Organotrifluoroborates -- 4.1 C-O Bond Formation -- 4.2 C-N Bond Formation -- 4.3 C-X Bond Formation -- 5 Using Organotrifluoroborates to Construct Novel Scaffolds -- 6 Conclusions and Outlook -- References -- The Catalytic Dehydrocoupling of Amine-Boranes and Phosphine-Boranes -- 1 Introduction -- 2 Transition-Metal-Catalysed Dehydrocoupling of Amine-Boranes -- 2.1 General Considerations -- 2.2 Aminoboranes: Observation and Trapping -- 2.3 Linear Diborazanes. 2.4 Early Examples of Metal-Catalysed Dehydrocoupling -- 2.5 Heterogeneous Catalysts for the Dehydrocoupling of Amine-Boranes -- 2.6 Transition-Metal-Catalysed Dehydrocoupling of H3BNH3 Promoted by Ionic Liquids -- 2.7 Homogeneous Dehydrocoupling of Amine-Boranes -- 2.7.1 Sigma Complexes of Amine-Boranes -- 2.8 Mechanistic Studies on Homogeneous Dehydrocoupling Systems -- 2.8.1 Early Transition Metals -- 2.8.2 Mid-Transition Metals -- 2.8.3 Late Transition Metals -- 2.8.4 Dehydrocoupling of Amine-Boranes Involving Ligand Cooperativity -- 2.8.5 The Role of Solvent in Dehydrocoupling Using Late Transition Metals -- 2.9 Generic Mechanisms for Dehydrocoupling of H3BNMe2H Using Transition Metals -- 2.10 Main-Group Element-Catalysed Dehydrocoupling of Amine-Boranes -- 2.10.1 Main-Group Amidoboranes: Stoichiometric Studies -- 2.10.2 Group 2 Metal-Catalysed Dehydrocoupling of Amine-Boranes -- 2.10.3 Group 3 Metal-Catalysed Dehydrocoupling of Amine-Boranes -- 2.10.4 P-Block-Catalysed Dehydrocoupling of Amine-Boranes -- 2.10.5 Frustrated Lewis Pair Dehydrogenation of Amine-Boranes -- 3 Dehydrocoupling of Phosphine-Boranes -- 3.1 Transition-Metal-Catalysed Dehydrocoupling of Phosphine-Boranes -- 3.2 Determination of the Active Catalytic Species: Hetero- or Homogeneous -- 3.3 Sigma Complexes and B-Agostic Interactions of Phosphine-Boranes -- 3.4 Stabilised Phosphinoboranes -- 3.5 Group 8 Metal-Catalysed Dehydrocoupling of Phosphine-Boranes -- 3.6 Mechanistic Investigations into the Rhodium-Catalysed Dehydrocoupling of Secondary Phosphine-Boranes -- 3.7 Mechanistic Investigation into the Rhodium-Catalysed Dehydrocoupling of Primary Phosphine-Boranes -- 3.8 Lewis Acid-Catalysed Dehydrocoupling of Phosphine-Boranes -- 4 Future Prospects -- References -- At the Forefront of the Suzuki-Miyaura Reaction: Advances in Stereoselective Cross-Couplings -- 1 Introduction. 2 Applications to the Synthesis of Enantioenriched Atropisomers -- 3 Mechanistic Considerations in the Suzuki-Miyaura Cross-Coupling of sp3 Centres -- 3.1 Challenges Associated with the Coupling of Saturated Carbon Centres -- 3.2 Stereochemistry of Various Steps in the Suzuki-Miyaura Cross-Coupling Mechanism -- 4 Stereoselective C(sp3)-C(sp2) Suzuki-Miyaura Cross-Coupling Reactions -- 4.1 Stereoselective Couplings of Alkyl Boronates with Aryl or Alkenyl Halides -- 4.2 Stereoselective Couplings of Alkyl Halides and Pseudohalides with Aryl or Alkenyl Boronates -- 5 Stereoselective C(sp3)-C(sp3) Suzuki-Miyaura Cross-Coupling Reactions -- 5.1 Stereoselective Couplings of Alkyl Boranes with Alkyl Halides -- 6 Summary and Outlook -- References -- Boronic Acid-Catalyzed Reactions of Carboxylic Acids -- 1 Introduction -- 2 B(III)-Catalyzed Reactions of α,beta-Unsaturated Carboxylic Acids -- 3 B(III)-Catalyzed Dehydrative Condensation to Carboxamides -- 4 B(III)-Catalyzed Dehydrative Condensation to Carboxylic Acid Esters -- 5 B(III)-Catalyzed Dehydrative Condensation to Carboxylic Anhydrides -- 6 Other B(III)-Catalyzed Reactions -- 7 Conclusions -- References -- Reagent-Controlled Lithiation-Borylation -- 1 Introduction -- 2 Mechanism of Lithiation-Borylation Processes -- 3 α-Chloro-Stabilized Lithium Carbenoids -- 4 α-O-Stabilized Organolithiums -- 4.1 Primary Carbamates/Benzoates -- 4.2 Secondary Benzylic Carbamates -- 4.3 Secondary Allylic/Propargylic Carbamates -- 4.4 Secondary Benzoates -- 5 α-N-Stabilized Organolithiums -- 6 Conclusions and Outlook -- References -- Recent Advances in the Synthesis and Applications of Organoborane Polymers -- 1 Introduction -- 2 Synthesis of Organoborane Polymers -- 2.1 Polymer Modification Reactions on Polyolefins -- 2.2 Direct Polymerization of Borane Monomers by Chain Growth Methods. 2.3 Side-Chain Functionalization of Conjugated Polymers -- 2.4 Boron Incorporation into the Main Chain of Conjugated Polymers -- 3 Selected Examples of Polymers and Their Applications -- 3.1 Borane Polymers as Lewis Acids and Anion Sensors -- 3.2 Luminescent Polymers Based on Boron Chelate Complexes -- 3.2.1 Boron Quinolate-Functionalized Polymers -- 3.2.2 BODIPY-Functionalized Polymers -- 3.2.3 Boron Diketonate-Functionalized Polymers -- 3.3 Boronic and Borinic Acid-Functionalized Polymers for Biomedical Applications and as Smart Materials -- 3.4 Borate and Boronium-Functionalized Polymers as Polyelectrolytes and Polymeric Ligand -- 4 Conclusions -- References -- Index. |
| Record Nr. | UNINA-9910768440103321 |
| Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Soggetto topico
-
Organometallic Chemistry
(95)
- Organometallic chemistry (90)
- Catalysis (56)
- Inorganic Chemistry (26)
- Inorganic chemistry (25)