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Oxidation of organic compounds by dioxiranes
Oxidation of organic compounds by dioxiranes
Pubbl/distr/stampa [Place of publication not identified], : John Wiley & Sons Inc, 2009
Disciplina 547.23
Soggetto topico Organic compounds
Oxidation
Chemistry
Physical Sciences & Mathematics
Organic Chemistry
ISBN 0-470-46675-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910830525303321
[Place of publication not identified], : John Wiley & Sons Inc, 2009
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Oxidation of organic compounds by dioxiranes
Oxidation of organic compounds by dioxiranes
Pubbl/distr/stampa [Place of publication not identified], : John Wiley & Sons Inc, 2009
Disciplina 547.23
Soggetto topico Organic compounds
Oxidation
Chemistry
Physical Sciences & Mathematics
Organic Chemistry
ISBN 0-470-46675-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910840842703321
[Place of publication not identified], : John Wiley & Sons Inc, 2009
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The oxidation of oxygen and related chemistry [[electronic resource] ] : selected papers of Neil Bartlett / / edited with introductory essays by Neil Bartlett
The oxidation of oxygen and related chemistry [[electronic resource] ] : selected papers of Neil Bartlett / / edited with introductory essays by Neil Bartlett
Autore Bartlett Neil <1932->
Pubbl/distr/stampa Singapore ; ; River Edge, NJ, : World Scientific, c2001
Descrizione fisica 1 online resource (626 p.)
Disciplina 541.393
546.7312
Collana World Scientific series in 20th century chemistry
Soggetto topico Fluorine compounds
Gases, Rare
Oxidation
Soggetto genere / forma Electronic books.
ISBN 1-281-96087-X
9786611960872
981-281-198-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Contents ; Acknowledgments ; Introduction ; 1. The Discovery of O2PtF6 and some O+2 Chemistry ; 2. XePtF6 and other Xenon Chemistry ; 3. The Xenon Fluorides and their Complexes ; 4. The Xenon Fluorosulfates and Related Compounds
5. Oxidation-State Limits and Range in the Noble-Metal Fluorides 6. Structural Features of Binary Transition-Element Fluorides ; 7. Thermodynamically Unstable Transition-Element Fluorides ; 8. Chemistry in Liquid Anhydrous Hydrogen Fluoride (aHF) ; 9. Some Thermodynamic Considerations
10. Graphite Intercalation and Evidence for a Thermodynamic Barrier References ; Review-type Papers ; Research Papers
Record Nr. UNINA-9910453546003321
Bartlett Neil <1932->  
Singapore ; ; River Edge, NJ, : World Scientific, c2001
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The oxidation of oxygen and related chemistry [[electronic resource] ] : selected papers of Neil Bartlett / / edited with introductory essays by Neil Bartlett
The oxidation of oxygen and related chemistry [[electronic resource] ] : selected papers of Neil Bartlett / / edited with introductory essays by Neil Bartlett
Autore Bartlett Neil <1932->
Pubbl/distr/stampa Singapore ; ; River Edge, NJ, : World Scientific, c2001
Descrizione fisica 1 online resource (626 p.)
Disciplina 541.393
546.7312
Collana World Scientific series in 20th century chemistry
Soggetto topico Fluorine compounds
Gases, Rare
Oxidation
ISBN 1-281-96087-X
9786611960872
981-281-198-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Contents ; Acknowledgments ; Introduction ; 1. The Discovery of O2PtF6 and some O+2 Chemistry ; 2. XePtF6 and other Xenon Chemistry ; 3. The Xenon Fluorides and their Complexes ; 4. The Xenon Fluorosulfates and Related Compounds
5. Oxidation-State Limits and Range in the Noble-Metal Fluorides 6. Structural Features of Binary Transition-Element Fluorides ; 7. Thermodynamically Unstable Transition-Element Fluorides ; 8. Chemistry in Liquid Anhydrous Hydrogen Fluoride (aHF) ; 9. Some Thermodynamic Considerations
10. Graphite Intercalation and Evidence for a Thermodynamic Barrier References ; Review-type Papers ; Research Papers
Record Nr. UNINA-9910782274203321
Bartlett Neil <1932->  
Singapore ; ; River Edge, NJ, : World Scientific, c2001
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The oxidation of oxygen and related chemistry [[electronic resource] ] : selected papers of Neil Bartlett / / edited with introductory essays by Neil Bartlett
The oxidation of oxygen and related chemistry [[electronic resource] ] : selected papers of Neil Bartlett / / edited with introductory essays by Neil Bartlett
Autore Bartlett Neil <1932->
Pubbl/distr/stampa Singapore ; ; River Edge, NJ, : World Scientific, c2001
Descrizione fisica 1 online resource (626 p.)
Disciplina 541.393
546.7312
Collana World Scientific series in 20th century chemistry
Soggetto topico Fluorine compounds
Gases, Rare
Oxidation
ISBN 1-281-96087-X
9786611960872
981-281-198-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Contents ; Acknowledgments ; Introduction ; 1. The Discovery of O2PtF6 and some O+2 Chemistry ; 2. XePtF6 and other Xenon Chemistry ; 3. The Xenon Fluorides and their Complexes ; 4. The Xenon Fluorosulfates and Related Compounds
5. Oxidation-State Limits and Range in the Noble-Metal Fluorides 6. Structural Features of Binary Transition-Element Fluorides ; 7. Thermodynamically Unstable Transition-Element Fluorides ; 8. Chemistry in Liquid Anhydrous Hydrogen Fluoride (aHF) ; 9. Some Thermodynamic Considerations
10. Graphite Intercalation and Evidence for a Thermodynamic Barrier References ; Review-type Papers ; Research Papers
Record Nr. UNINA-9910826711903321
Bartlett Neil <1932->  
Singapore ; ; River Edge, NJ, : World Scientific, c2001
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Oxidation of polyethylene [[electronic resource] ] : a comparison of plasma and ultraviolet ozone processing techniques / / by Nicole Zander, Daphne Pappas, and Ben Stein
Oxidation of polyethylene [[electronic resource] ] : a comparison of plasma and ultraviolet ozone processing techniques / / by Nicole Zander, Daphne Pappas, and Ben Stein
Autore Zander Nicole
Pubbl/distr/stampa Aberdeen Proving Ground, MD : , : Army Research Laboratory, , [2009]
Descrizione fisica iv, 16 pages : digital, PDF file
Altri autori (Persone) PappasDaphne
SteinBen
Collana ARL-TR
Soggetto topico Polyethylene
X-ray photoelectron spectroscopy
Ultraviolet radiation
Oxidation
Surface energy
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Oxidation of polyethylene
Record Nr. UNINA-9910698753103321
Zander Nicole  
Aberdeen Proving Ground, MD : , : Army Research Laboratory, , [2009]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Oxidative cross-coupling reactions / / Aiwen Lei [and five others]
Oxidative cross-coupling reactions / / Aiwen Lei [and five others]
Pubbl/distr/stampa Weinheim, Germany : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2017
Descrizione fisica 1 online resource (243 p.)
Disciplina 541.39
Soggetto topico Chemical reactions
Nucleophilic reactions
Oxidation
ISBN 3-527-68101-9
3-527-68098-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Title Page; Copyright; Contents; Chapter 1 Oxidative Coupling-Bonding between Two Nucleophiles; 1.1 Introduction/General; 1.1.1 What is Oxidative Cross-Coupling?; 1.1.2 Why Oxidative Cross-Coupling?; 1.1.3 How Does Oxidative Cross-Coupling Work?; 1.1.4 Development and Outlook; References; Chapter 2 Organometals as Nucleophiles; 2.1 Classification and Applications of Organometallic Reagents; 2.2 Csp-M and Csp-M as Nucleophiles; 2.2.1 Alkyne-Alkyne Oxidative Coupling; 2.2.1.1 Alkynyl-Si; 2.2.1.2 Alkynyl-Sn; 2.2.1.3 Alkynyl-B; 2.2.1.4 Alkynyl-Mg; 2.2.1.5 Alkynyl-Te
2.2.2 Alkyne-Cyano Oxidative Coupling2.3 Csp-M and Csp2-M as Nucleophiles; 2.4 Csp-M and Csp3-M as Nucleophiles; 2.5 Csp2-M and Csp2-M as Nucleophiles; 2.5.1 Homocoupling of Csp2-M; 2.5.2 Cross-Coupling between Different Species of Csp2-M; 2.6 Csp2-M and Csp3-M as Nucleophiles; 2.7 Csp3-M and Csp3-M as Nucleophiles; 2.8 Conclusions; References; Chapter 3 Oxidative Couplings Involving the Cleavage of C-H Bonds; 3.1 Theoretical Understandings and Methods in C-H Bond Functionalization; 3.1.1 Introduction; 3.1.2 Mechanisms of C-H Cleavage by Transition Metals; 3.1.2.1 Oxidative Addition
3.1.2.2 Electrophilic Substitution3.1.2.3 -Bond Metathesis; 3.1.2.4 Concerted Metalation Deprotonation (CMD); 3.1.2.5 1,2-Addition; 3.1.2.6 Biomimetic C-H Oxidation; 3.1.2.7 Carbenoid/Nitrenoid C-H Insertion; 3.1.3 Methods for Selective C-H Bond Functionalization; 3.1.3.1 Directed C-H Functionalization; 3.1.3.2 Sterically Controlled C-H Functionalization; 3.1.3.3 C-H Functionalization via Ionic Intermediates; 3.1.3.4 C-H Functionalization via Radical Intermediates; 3.2 Oxidative Couplings between Organometals and Hydrocarbons; 3.2.1 C(sp)-H and Organometals as Nucleophiles
3.2.2 Csp2-H and Organometals as Nucleophiles3.2.3 Csp3-H and Organometals as Nucleophiles; 3.3 Oxidative Couplings between Two Hydrocarbons; 3.3.1 C(sp)-H and C(sp)-H as Nucleophiles; 3.3.2 C(sp)-H and C(sp2)-H as Nucleophiles; 3.3.3 C(sp)-H and C(sp3)-H as Nucleophiles; 3.3.4 Csp2-H and Csp2-H as Nucleophiles; 3.3.4.1 Oxidative Coupling between Directing-Group-Containing Arenes and Unactivated Arenes; 3.3.4.2 Oxidative Coupling of Arenes without Directing Groups; 3.3.4.3 Intramolecular Oxidative Coupling of Unactivated Arenes; 3.3.4.4 Oxidative Heck-Type Cross-Coupling
3.3.5 Csp2-H and Csp3-H as Nucleophiles3.3.5.1 Intramolecular Oxidative Coupling between Aromatic Csp2-H and Csp3-H; 3.3.5.2 Intramolecular Oxidative Coupling between Alkene Csp2-H and Csp3-H; 3.3.5.3 Intermolecular Oxidative Coupling between Csp2-H and Csp3-H; 3.3.6 C(sp3)-H and C(sp3)-H as Nucleophiles; 3.4 Conclusions; References; Chapter 4 Bonding Including Heteroatoms via Oxidative Coupling; 4.1 Introduction; 4.2 Oxidative C-O Bond Formation; 4.2.1 C-H and O-M as Nucleophiles; 4.2.2 C-H and O-H as Nucleophiles; 4.2.2.1 C(sp2, Aryl)-O Bond Formation
4.2.2.2 C(sp2, Heteroaryl, Alkenyl)-O Bond Formation
Record Nr. UNINA-9910134857303321
Weinheim, Germany : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2017
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Oxidative cross-coupling reactions / / Aiwen Lei [and five others]
Oxidative cross-coupling reactions / / Aiwen Lei [and five others]
Pubbl/distr/stampa Weinheim, Germany : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2017
Descrizione fisica 1 online resource (243 p.)
Disciplina 541.39
Soggetto topico Chemical reactions
Nucleophilic reactions
Oxidation
ISBN 3-527-68101-9
3-527-68098-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Title Page; Copyright; Contents; Chapter 1 Oxidative Coupling-Bonding between Two Nucleophiles; 1.1 Introduction/General; 1.1.1 What is Oxidative Cross-Coupling?; 1.1.2 Why Oxidative Cross-Coupling?; 1.1.3 How Does Oxidative Cross-Coupling Work?; 1.1.4 Development and Outlook; References; Chapter 2 Organometals as Nucleophiles; 2.1 Classification and Applications of Organometallic Reagents; 2.2 Csp-M and Csp-M as Nucleophiles; 2.2.1 Alkyne-Alkyne Oxidative Coupling; 2.2.1.1 Alkynyl-Si; 2.2.1.2 Alkynyl-Sn; 2.2.1.3 Alkynyl-B; 2.2.1.4 Alkynyl-Mg; 2.2.1.5 Alkynyl-Te
2.2.2 Alkyne-Cyano Oxidative Coupling2.3 Csp-M and Csp2-M as Nucleophiles; 2.4 Csp-M and Csp3-M as Nucleophiles; 2.5 Csp2-M and Csp2-M as Nucleophiles; 2.5.1 Homocoupling of Csp2-M; 2.5.2 Cross-Coupling between Different Species of Csp2-M; 2.6 Csp2-M and Csp3-M as Nucleophiles; 2.7 Csp3-M and Csp3-M as Nucleophiles; 2.8 Conclusions; References; Chapter 3 Oxidative Couplings Involving the Cleavage of C-H Bonds; 3.1 Theoretical Understandings and Methods in C-H Bond Functionalization; 3.1.1 Introduction; 3.1.2 Mechanisms of C-H Cleavage by Transition Metals; 3.1.2.1 Oxidative Addition
3.1.2.2 Electrophilic Substitution3.1.2.3 -Bond Metathesis; 3.1.2.4 Concerted Metalation Deprotonation (CMD); 3.1.2.5 1,2-Addition; 3.1.2.6 Biomimetic C-H Oxidation; 3.1.2.7 Carbenoid/Nitrenoid C-H Insertion; 3.1.3 Methods for Selective C-H Bond Functionalization; 3.1.3.1 Directed C-H Functionalization; 3.1.3.2 Sterically Controlled C-H Functionalization; 3.1.3.3 C-H Functionalization via Ionic Intermediates; 3.1.3.4 C-H Functionalization via Radical Intermediates; 3.2 Oxidative Couplings between Organometals and Hydrocarbons; 3.2.1 C(sp)-H and Organometals as Nucleophiles
3.2.2 Csp2-H and Organometals as Nucleophiles3.2.3 Csp3-H and Organometals as Nucleophiles; 3.3 Oxidative Couplings between Two Hydrocarbons; 3.3.1 C(sp)-H and C(sp)-H as Nucleophiles; 3.3.2 C(sp)-H and C(sp2)-H as Nucleophiles; 3.3.3 C(sp)-H and C(sp3)-H as Nucleophiles; 3.3.4 Csp2-H and Csp2-H as Nucleophiles; 3.3.4.1 Oxidative Coupling between Directing-Group-Containing Arenes and Unactivated Arenes; 3.3.4.2 Oxidative Coupling of Arenes without Directing Groups; 3.3.4.3 Intramolecular Oxidative Coupling of Unactivated Arenes; 3.3.4.4 Oxidative Heck-Type Cross-Coupling
3.3.5 Csp2-H and Csp3-H as Nucleophiles3.3.5.1 Intramolecular Oxidative Coupling between Aromatic Csp2-H and Csp3-H; 3.3.5.2 Intramolecular Oxidative Coupling between Alkene Csp2-H and Csp3-H; 3.3.5.3 Intermolecular Oxidative Coupling between Csp2-H and Csp3-H; 3.3.6 C(sp3)-H and C(sp3)-H as Nucleophiles; 3.4 Conclusions; References; Chapter 4 Bonding Including Heteroatoms via Oxidative Coupling; 4.1 Introduction; 4.2 Oxidative C-O Bond Formation; 4.2.1 C-H and O-M as Nucleophiles; 4.2.2 C-H and O-H as Nucleophiles; 4.2.2.1 C(sp2, Aryl)-O Bond Formation
4.2.2.2 C(sp2, Heteroaryl, Alkenyl)-O Bond Formation
Record Nr. UNINA-9910830160403321
Weinheim, Germany : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2017
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Oxidative stress : molecular mechanisms and biological effects / / edited by Volodymyr Lushchak and Halyna Semchyshyn
Oxidative stress : molecular mechanisms and biological effects / / edited by Volodymyr Lushchak and Halyna Semchyshyn
Pubbl/distr/stampa Rijeka, Croatia : , : Intech, , [2012]
Descrizione fisica 1 online resource (376 pages) : illustrations
Disciplina 616.39
Soggetto topico Oxidative stress
Oxidation
ISBN 953-51-5285-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Oxidative Stress
Oxidate stress
Record Nr. UNINA-9910137716003321
Rijeka, Croatia : , : Intech, , [2012]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Oxide scales formed on NiTi and NiPtTi shape memory alloys [[electronic resource] /] / James L. Smialek ... [and others]
Oxide scales formed on NiTi and NiPtTi shape memory alloys [[electronic resource] /] / James L. Smialek ... [and others]
Pubbl/distr/stampa Cleveland, Ohio : , : National Aeronautics and Space Administration, Glenn Research Center, , [2011]
Descrizione fisica 1 online resource (30 pages) : illustrations (some color)
Altri autori (Persone) SmialekJames L
Collana NASA/TM
Soggetto topico Nickel alloys
Metallography
Shape memory alloys
Reaction kinetics
Porosity
Oxidation
Isothermal processes
Titanium alloys
Titanium oxides
Crystal morphology
Binary alloys
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910701467203321
Cleveland, Ohio : , : National Aeronautics and Space Administration, Glenn Research Center, , [2011]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui