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Bio-Inspired Nanotechnology [[electronic resource] ] : From Surface Analysis to Applications / / edited by Marc R. Knecht, Tiffany R. Walsh
| Bio-Inspired Nanotechnology [[electronic resource] ] : From Surface Analysis to Applications / / edited by Marc R. Knecht, Tiffany R. Walsh |
| Edizione | [1st ed. 2014.] |
| Pubbl/distr/stampa | New York, NY : , : Springer New York : , : Imprint : Springer, , 2014 |
| Descrizione fisica | 1 online resource (317 p.) |
| Disciplina |
541.395
541395 620 620.11 |
| Soggetto topico |
Nanotechnology
Biomaterials Catalysis Nanoscale science Nanoscience Nanostructures Renewable energy resources Nanotechnology and Microengineering Nanoscale Science and Technology Renewable and Green Energy |
| ISBN | 1-4614-9446-X |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Peptide-Nano particle Strategies, Interactions and Challenges -- Fundamentals of Peptide-Materials Interfaces -- Experimental Characterization of Peptide-Surface Interactions -- Interfacial Structure Determination -- Understanding Bio mineral Growth and Assembly for Engineering Novel Green Nanomaterials -- Understanding Molecular Recognition on Metallic and Oxidic Nanostructures from a Perspective of Computer Simulation and Theory -- Bio-Inspired Nano catalysis -- Addressable Biological Functionalization of Inorganics: Materials-Selective Fusion Proteins in Bio-Nanotechnology -- Environmental Interactions of Geo and Bio-Macromolecules with Nanomaterials -- Mimicking Bio mineral Systems: What Have We Achieved and Where Do We Go From Here?. |
| Record Nr. | UNINA-9910299730103321 |
| New York, NY : , : Springer New York : , : Imprint : Springer, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Bioactivity of Engineered Nanoparticles / Bing Yan, Hongyu Zhou, Jorge L. Gardea-Torresdey editors
| Bioactivity of Engineered Nanoparticles / Bing Yan, Hongyu Zhou, Jorge L. Gardea-Torresdey editors |
| Pubbl/distr/stampa | Singapore, : Springer, 2017 |
| Descrizione fisica | XIV, 376 p. : ill. ; 24 cm |
| Disciplina |
615.1(Farmacologia. Farmaci. Farmacia)
615.19(Chimica farmaceutica. Tecnologia farmaceutica. Chimica medica) 615.902(Tossicologia industriale) 610.28(Ingegneria biomedica) 620.5(Nanotecnologia) 620.1(Scienze dei materiali) 541.395(Catalisi) |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNICAMPANIA-VAN0123642 |
| Singapore, : Springer, 2017 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Vanvitelli | ||
| ||
Bioactivity of Engineered Nanoparticles / Bing Yan, Hongyu Zhou, Jorge L. Gardea-Torresdey editors
| Bioactivity of Engineered Nanoparticles / Bing Yan, Hongyu Zhou, Jorge L. Gardea-Torresdey editors |
| Edizione | [Singapore : Springer, 2017] |
| Pubbl/distr/stampa | XIV, 376 p., : ill. ; 24 cm |
| Descrizione fisica | Pubblicazione in formato elettronico |
| Disciplina |
615.1(Farmacologia. Farmaci. Farmacia)
615.19(Chimica farmaceutica. Tecnologia farmaceutica) 615.902(Tossicologia industriale) 610.28(Ingegneria biomedica) 620.5(Nanotecnologia) 620.1(Scienza dei materiali) 541.395(Catalisi) |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNICAMPANIA-SUN0123642 |
| XIV, 376 p., : ill. ; 24 cm | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Vanvitelli | ||
| ||
Biomass processing over gold catalysts / / Olga A. Simakova, Robert J. Davis, Dmitry Yu. Murzin
| Biomass processing over gold catalysts / / Olga A. Simakova, Robert J. Davis, Dmitry Yu. Murzin |
| Autore | Simakova Olga A |
| Edizione | [1st ed. 2013.] |
| Pubbl/distr/stampa | Cham, Switzerland : , : Springer, , 2013 |
| Descrizione fisica | 1 online resource (viii, 54 pages) : illustrations (some color) |
| Disciplina | 541.395 |
| Collana | SpringerBriefs in Molecular Science |
| Soggetto topico |
Metal catalysts
Biomass conversion Biomass energy |
| ISBN | 3-319-00906-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Introduction -- Selective Oxidation/Dehydrogenation Reactions -- Acetalization -- N-alkylation -- Selective Hydrogenation Reactions -- Double Bond Oxidation Reactions -- Isomerization Reactions -- Gold Catalysts Stability -- Summary. |
| Record Nr. | UNINA-9910741139003321 |
Simakova Olga A
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| Cham, Switzerland : , : Springer, , 2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Bridging heterogeneous and homogeneous catalysis : concepts, strategies, and applications / / edited by Can Li and Yan Liu
| Bridging heterogeneous and homogeneous catalysis : concepts, strategies, and applications / / edited by Can Li and Yan Liu |
| Pubbl/distr/stampa | Weinheim an der Bergstrasse, Germany : , : Wiley-VCH, , 2014 |
| Descrizione fisica | 1 online resource (651 p.) |
| Disciplina | 541.395 |
| Soggetto topico |
Heterogeneous catalysis - Data processing
Catalysis - Industrial applications |
| ISBN |
3-527-67592-2
3-527-67590-6 3-527-67593-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Bridging Heterogeneous and Homogeneous Catalysis; Contents; Preface; List of Contributors; Chapter 1 Acid-Base Cooperative Catalysis for Organic Reactions by Designed Solid Surfaces with Organofunctional Groups; 1.1 Introduction; 1.2 Bifunctional Catalysts Possessing Both Acidic and Basic Organic Groups; 1.2.1 Urea-Amine Bifunctional Catalyst; 1.2.2 Sulfonic or Carboxylic Acid-Amine Bifunctional Catalyst; 1.3 Bifunctional Catalysts Possessing Basic Organic Groups and Acid Sites Derived from Their Support Surface; 1.3.1 Organic Base-Catalyzed Reactions Enhanced by SiO2
1.3.2 Amine-Catalyzed Reactions Enhanced by Acid Site on Silica-Alumina1.3.3 Control of Acid-Base Interaction on Solid Surface; 1.3.4 Cooperative Catalysis of Acid Site, Primary Amine, and Tertiary Amine; 1.4 Prospect; References; Chapter 2 Catalytic Reactions in or by Room-Temperature Ionic Liquids: Bridging the Gap between Homogeneous and Heterogeneous Catalysis; 2.1 Introduction and Background; 2.2 Catalysis with IL-Supported or Mediated Metal Nanoparticles; 2.2.1 Preparation of MNPs in ILs; 2.2.1.1 IL Itself as the Reducing Agent; 2.2.1.2 Molecular Hydrogen as Reducing Agent 2.2.1.3 NaBH4 as the Reducing Agent2.2.1.4 Other Reducing Agents; 2.2.2 Characterization of IL-Supported or Mediated MNPs; 2.2.2.1 XPS and NMR; 2.2.2.2 SEM and TEM; 2.2.2.3 Molecular Dynamics Simulations; 2.2.3 Hydrogenation Reactions; 2.2.4 IL-Supported Pd NPs; 2.2.5 IL-Supported Pt and Ir NPs; 2.2.6 IL-Supported Ru NPs; 2.2.6.1 IL-Supported Rh NPs; 2.2.7 C-C Coupling Reactions; 2.2.7.1 Suzuki Reaction; 2.2.7.2 Mizoroki-Heck Reaction; 2.2.7.3 Stille Reaction; 2.2.7.4 Sonogashira Reaction; 2.2.7.5 Ullmann Reaction; 2.2.8 Brief Summary 2.3 Reactions Catalyzed by Solid-Supported IL: Heterogeneous Catalysis with Homogeneous Performance2.3.1 Introduction; 2.3.1.1 Design, Preparation, and Properties of Supported IL-Phase Catalysis; 2.3.2 Design, Preparation, and Properties of Silica Gel-Confined IL Catalysts; 2.3.2.1 Design, Preparation, and Properties of Covalently Supported IL Catalysts; 2.3.3 Catalytic Reaction with Supported IL Catalysts; 2.3.3.1 Catalytic Hydrogenation; 2.3.3.2 Selective Oxidation; 2.3.3.3 Catalytic Carbonylation Reaction; 2.3.3.4 Water-Gas Shift Reaction; 2.3.3.5 Isomerization and Oligomerization 2.3.3.6 Alkylation and Esterification Reactions2.3.3.7 Asymmetric Catalysis; 2.3.3.8 Enzyme Catalysis; 2.3.4 Brief Summary; 2.4 Outlook; References; Chapter 3 Heterogeneous Catalysis with Organic-Inorganic Hybrid Materials; 3.1 Introduction; 3.1.1 Ordered Mesoporous Silica; 3.1.2 Organic-Inorganic Hybrid Materials; 3.1.3 Heterogeneous Catalysis; 3.2 Organic-Inorganic Hybrid Materials; 3.2.1 General Advantages of Organic-Inorganic Hybrid Materials; 3.2.2 Grafting and Co-Condensation; 3.2.2.1 Amine Groups; 3.2.2.2 Ionic Liquids (ILs); 3.2.2.3 Others 3.2.3 Periodic Mesoporous Organosilicas (PMOs) |
| Record Nr. | UNINA-9910132214703321 |
| Weinheim an der Bergstrasse, Germany : , : Wiley-VCH, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Bridging heterogeneous and homogeneous catalysis : concepts, strategies, and applications / / edited by Can Li and Yan Liu
| Bridging heterogeneous and homogeneous catalysis : concepts, strategies, and applications / / edited by Can Li and Yan Liu |
| Pubbl/distr/stampa | Weinheim an der Bergstrasse, Germany : , : Wiley-VCH, , 2014 |
| Descrizione fisica | 1 online resource (651 p.) |
| Disciplina | 541.395 |
| Soggetto topico |
Heterogeneous catalysis - Data processing
Catalysis - Industrial applications |
| ISBN |
3-527-67592-2
3-527-67590-6 3-527-67593-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Bridging Heterogeneous and Homogeneous Catalysis; Contents; Preface; List of Contributors; Chapter 1 Acid-Base Cooperative Catalysis for Organic Reactions by Designed Solid Surfaces with Organofunctional Groups; 1.1 Introduction; 1.2 Bifunctional Catalysts Possessing Both Acidic and Basic Organic Groups; 1.2.1 Urea-Amine Bifunctional Catalyst; 1.2.2 Sulfonic or Carboxylic Acid-Amine Bifunctional Catalyst; 1.3 Bifunctional Catalysts Possessing Basic Organic Groups and Acid Sites Derived from Their Support Surface; 1.3.1 Organic Base-Catalyzed Reactions Enhanced by SiO2
1.3.2 Amine-Catalyzed Reactions Enhanced by Acid Site on Silica-Alumina1.3.3 Control of Acid-Base Interaction on Solid Surface; 1.3.4 Cooperative Catalysis of Acid Site, Primary Amine, and Tertiary Amine; 1.4 Prospect; References; Chapter 2 Catalytic Reactions in or by Room-Temperature Ionic Liquids: Bridging the Gap between Homogeneous and Heterogeneous Catalysis; 2.1 Introduction and Background; 2.2 Catalysis with IL-Supported or Mediated Metal Nanoparticles; 2.2.1 Preparation of MNPs in ILs; 2.2.1.1 IL Itself as the Reducing Agent; 2.2.1.2 Molecular Hydrogen as Reducing Agent 2.2.1.3 NaBH4 as the Reducing Agent2.2.1.4 Other Reducing Agents; 2.2.2 Characterization of IL-Supported or Mediated MNPs; 2.2.2.1 XPS and NMR; 2.2.2.2 SEM and TEM; 2.2.2.3 Molecular Dynamics Simulations; 2.2.3 Hydrogenation Reactions; 2.2.4 IL-Supported Pd NPs; 2.2.5 IL-Supported Pt and Ir NPs; 2.2.6 IL-Supported Ru NPs; 2.2.6.1 IL-Supported Rh NPs; 2.2.7 C-C Coupling Reactions; 2.2.7.1 Suzuki Reaction; 2.2.7.2 Mizoroki-Heck Reaction; 2.2.7.3 Stille Reaction; 2.2.7.4 Sonogashira Reaction; 2.2.7.5 Ullmann Reaction; 2.2.8 Brief Summary 2.3 Reactions Catalyzed by Solid-Supported IL: Heterogeneous Catalysis with Homogeneous Performance2.3.1 Introduction; 2.3.1.1 Design, Preparation, and Properties of Supported IL-Phase Catalysis; 2.3.2 Design, Preparation, and Properties of Silica Gel-Confined IL Catalysts; 2.3.2.1 Design, Preparation, and Properties of Covalently Supported IL Catalysts; 2.3.3 Catalytic Reaction with Supported IL Catalysts; 2.3.3.1 Catalytic Hydrogenation; 2.3.3.2 Selective Oxidation; 2.3.3.3 Catalytic Carbonylation Reaction; 2.3.3.4 Water-Gas Shift Reaction; 2.3.3.5 Isomerization and Oligomerization 2.3.3.6 Alkylation and Esterification Reactions2.3.3.7 Asymmetric Catalysis; 2.3.3.8 Enzyme Catalysis; 2.3.4 Brief Summary; 2.4 Outlook; References; Chapter 3 Heterogeneous Catalysis with Organic-Inorganic Hybrid Materials; 3.1 Introduction; 3.1.1 Ordered Mesoporous Silica; 3.1.2 Organic-Inorganic Hybrid Materials; 3.1.3 Heterogeneous Catalysis; 3.2 Organic-Inorganic Hybrid Materials; 3.2.1 General Advantages of Organic-Inorganic Hybrid Materials; 3.2.2 Grafting and Co-Condensation; 3.2.2.1 Amine Groups; 3.2.2.2 Ionic Liquids (ILs); 3.2.2.3 Others 3.2.3 Periodic Mesoporous Organosilicas (PMOs) |
| Record Nr. | UNINA-9910819201203321 |
| Weinheim an der Bergstrasse, Germany : , : Wiley-VCH, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
C-C Bond Activation [[electronic resource] /] / edited by Guangbin Dong
| C-C Bond Activation [[electronic resource] /] / edited by Guangbin Dong |
| Edizione | [1st ed. 2014.] |
| Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2014 |
| Descrizione fisica | 1 online resource (VII, 262 p. 352 illus., 13 illus. in color.) : online resource |
| Disciplina | 541.395 |
| Collana | Topics in Current Chemistry |
| Soggetto topico |
Organic chemistry
Organic Chemistry |
| ISBN | 3-642-55055-X |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Intro -- Preface -- Contents -- Mechanistic Studies of Transition Metal-Mediated C-C Bond Activation -- 1 Introduction -- 2 C-C Cleavage of Biphenylene -- 3 C-C Cleavage of C-CN Bonds -- 4 C-C Cleavage of C-CC Bonds -- 5 C-C Cleavage of Aryl-CH3 Bonds -- 6 Conclusion -- References -- Catalytic C-CN Bond Activation -- 1 Introduction -- 2 Coupling Reactions via C-CN Bond Activation -- 2.1 Hydrodecyanation Reactions -- 2.2 Cross-Coupling Reactions -- 2.3 Silylation and Borylation Reactions -- 2.4 Cycloaddition Reactions -- 3 Cyanation Reactions via C-CN Bond Activation -- 3.1 Cyanation of Aryl Halides and Arenes -- 3.2 Carbocyanation of Unsaturated Bonds -- 4 Summary, Conclusions, Outlook -- References -- Metal-Organic Cooperative Catalysis in C-C Bond Activation -- 1 Introduction -- 1.1 Strategies for C-C Bond Cleavage -- 1.2 Metal-Organic Cooperative Strategy for C-H Bond Cleavage -- 2 Main Text -- 2.1 Metal-Organic Cooperative C-C Single Bond Cleavage -- 2.2 Metal-Organic Cooperative C-C Double Bond Cleavage -- 2.3 Metal-Organic Cooperative C-C Triple Bond Cleavage -- 3 Summary, Conclusions, Outlook -- References -- Carbon-Carbon Bond Activation with 8-Acylquinolines -- 1 Introduction -- 2 Stoichiometric Carbon-Carbon Bond Activation Reactions -- 2.1 Directed Cleavage of sp2-sp Carbon-Carbon Bonds -- 2.2 Directed Cleavage of sp2-sp3 Carbon-Carbon Bonds -- 2.2.1 Substrates Without beta-Hydrogens -- 2.2.2 Substrates with beta-Hydrogens -- 3 Catalytic Carbon-Carbon Bond Activation: Fragmentations -- 3.1 Sp2-sp3 Carbon-Carbon Bonds: Hydroacylation -- 3.2 Sp2-sp2 Carbon-Carbon Bonds: Hydroacylation -- 3.3 Cross-Coupling Reactions -- 4 Catalytic C-C Bond Activation Reactions: Carboacylation -- 4.1 Intermolecular Carboacylation -- 4.2 Intramolecular Carboacylation -- 4.3 Mechanistic Considerations -- 4.3.1 Investigations with RhCl(PPh3)3.
4.3.2 Investigations with [RhCl(C2H4)2]2 -- 5 Conclusion -- References -- Catalysis of Diazoalkane-Carbonyl Homologation. How New Developments in Hydrazone Oxidation Enable the Carbon Insertion Strate... -- 1 Introduction -- 2 History of Diazoalkane Ring Expansion and Chain Extension Reactions -- 2.1 Protic Solvent-Promoted Reactions -- 2.2 Lewis Acid-Promoted Reactions -- 2.3 Lewis Acid-Catalyzed Reactions -- 3 Modern Methods in Non-stabilized Diazoalkane Synthesis -- 3.1 Base-Mediated Hydrolysis of N-Nitrosylamides, -Carbamates, and -Ureas -- 3.2 Diazotization of Alkylamines -- 3.3 Bamford-Stevens Reaction and the Rise of In Situ Methodologies -- 3.3.1 Reactions that Consume Aryldiazomethanes Without Isolation -- 3.3.2 Examples in Total Synthesis -- 3.4 Dehydrogenation of Hydrazones and Diazoalkane Stock Solutions -- 3.4.1 Lead(IV) Oxidation of Hydrazones -- 3.4.2 Azidotris(diethylamino)phosphonium Bromide with Lithium Hydrazinides -- 3.4.3 Oxidation by Peracids and Catalytic Iodine -- 3.4.4 Oxidation of N-(tert-Butyldimethylsilyl)hydrazones with Hypervalent Iodine -- 3.4.5 Oxidation of Hydrazones by ``Activated´´ DMSO -- 3.4.6 Hybrid Protocols and Modern Titration Methods -- 3.4.7 Examples in Total Synthesis -- 4 Modern Catalytic Diazoalkyl Carbon Insertion Methodology -- 4.1 Diazoacetate Homologation of Aldehydes (Roskamp Reactions) -- 4.2 Stereoselective Additions of α-Aryl Diazoacetates to Aldehydes -- 4.3 Diazocarbonyl Homologation of Ketones -- 4.4 Ketone α-Arylation by Ring Expansion with Aryldiazomethanes -- 5 Applications of Single Carbon Insertion in Total Synthesis -- 6 Conclusions -- References -- Asymmetric Transformations via C-C Bond Cleavage -- 1 Introduction -- 2 Cyclobutanones in C-C Cleavage Processes -- 3 C-C Bond Cleavages by beta-Carbon Eliminations of tert-Alcoholates. 3.1 Metal tert-Cyclobutanolates by 1,2-Additions of Cyclobutanones -- 3.2 Metal tert-Cyclobutanolates by Ligand Exchange -- 3.3 Retro-Allylations of Tertiary Homoallyl Alcohols -- 3.4 beta-Carbon Eliminations from Unstrained tert-Alcohols -- 4 Ring Expansions via 1,2-Carbon Shift Reactions -- 5 Vinylcyclopropanes in C-C Bond Cleavage Processes -- 6 Alkylidenecyclopropanes in C-C Bond Cleavage Processes -- 7 Metal-Catalyzed Cleavages of C-CN Bonds -- 8 Conclusions and Outlook -- References -- Transition Metal-Catalyzed Cycloadditions of Cyclopropanes for the Synthesis of Carbocycles: C-C Activation in Cyclopropanes -- 1 Introduction -- 2 VCP Chemistry in Transition Metal-Catalyzed Cycloadditions -- 2.1 VCP as a Five-Carbon Synthon in Transition Metal-Catalyzed Cycloadditions -- 2.1.1 [5+1] Cycloadditions -- 2.1.2 [5+2] Cycloadditions -- Rhodium-Catalyzed [5+2] Cycloadditions -- Ruthenium-Catalyzed [5+2] Cycloadditions -- Iron- and Nickel-Catalyzed [5+2] Cycloadditions -- 2.1.3 [5+2+1] and [5+1+2+1] Cycloadditions -- 2.2 VCP as a Three-Carbon Synthon in Transition Metal-Catalyzed Cycloaddition -- 2.2.1 [3+2] Cycloadditions -- 2.2.2 Higher Order Cycloadditions -- 3 MCP Chemistry in Transition Metal-Catalyzed Cycloadditions -- 3.1 [3+2] Cycloadditions -- 3.2 Other Types of Cycloadditions -- 4 Other Types of Cyclopropanes -- 5 Applications in Natural Products Synthesis -- 6 Conclusion -- References -- Transition Metal-Catalyzed C-C Bond Activation of Four-Membered Cyclic Ketones -- 1 Introduction -- 2 C-C Bond Activation of Cyclobutanones -- 2.1 Rh-Catalyzed C-C Bond Activation via Oxidative Addition -- 2.2 Rh-Catalyzed C-C Bond Activation via beta-C Elimination -- 2.3 Ni-Catalyzed C-C Bond Activation via beta-C Elimination -- 3 C-C Bond Activation of Cyclobutenones -- 3.1 Stoichiometric C-C Bond Activation. 3.2 Rh-Catalyzed C-C Bond Activation of Cyclobutenones -- 4 C-C Bond Activation of Cyclobutenediones -- 4.1 Stoichiometric C-C Bond Activation of Cyclobutenediones -- 4.2 Catalytic C-C Bond Activation of Cyclobutenediones -- 5 Conclusion -- References -- Index. |
| Record Nr. | UNINA-9910298645203321 |
| Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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C-H Bond Activation and Catalytic Functionalization 1 / editors Pierre H. Dixneuf, Henri Doucet
| C-H Bond Activation and Catalytic Functionalization 1 / editors Pierre H. Dixneuf, Henri Doucet |
| Pubbl/distr/stampa | Cham, : Springer, 2016 |
| Descrizione fisica | VIII, 264 p. : ill. ; 24 cm |
| Disciplina |
540(Chimica generale)
541.395(Catalisi) 661(Chimica organica applicata) 547.782(Chimica organica. Macromolecole e composti connessi. Carboidrati. Polisaccaridi) |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNICAMPANIA-VAN0243634 |
| Cham, : Springer, 2016 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Vanvitelli | ||
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C-H Bond Activation and Catalytic Functionalization 2/ editors Pierre H. Dixneuf, Henri Doucet
| C-H Bond Activation and Catalytic Functionalization 2/ editors Pierre H. Dixneuf, Henri Doucet |
| Pubbl/distr/stampa | Cham, : Springer, 2016 |
| Descrizione fisica | VII, 212 p. : ill. ; 24 cm |
| Disciplina |
540(Chimica generale)
541.395(Catalisi) 661(Chimica organica applicata) 547.782(Chimica organica. Macromolecole e composti connessi. Carboidrati. Polisaccaridi) |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNICAMPANIA-VAN0243093 |
| Cham, : Springer, 2016 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Vanvitelli | ||
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Cage Metal Complexes : Clathrochelates Revisited / Yan Voloshin, Irina Belaya, Roland Krämer
| Cage Metal Complexes : Clathrochelates Revisited / Yan Voloshin, Irina Belaya, Roland Krämer |
| Autore | Voloshin, Yan |
| Pubbl/distr/stampa | Cham, : Springer, 2017 |
| Descrizione fisica | XI, 467 p. : ill. ; 24 cm |
| Disciplina |
540(Chimica generale)
547(Chimica organica) 546(Chimica inorganica) 615.19(Chimica farmaceutica. Tecnologia farmaceutica. Chimica medica) 620.5(Nanotecnologia) 541.395(Catalisi) |
| Altri autori (Persone) |
Belaya, Irina
Krämer, Roland |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNICAMPANIA-VAN0123762 |
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Voloshin, Yan
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| Cham, : Springer, 2017 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Vanvitelli | ||
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