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CHEMIEROHSTOFFE aus Kohle. / Herausgegeben von Jurgen Falbe
CHEMIEROHSTOFFE aus Kohle. / Herausgegeben von Jurgen Falbe
Pubbl/distr/stampa Stuttgart : G. Thieme Verlag, 1977
Descrizione fisica IX,445 p., ill., 25 cm
Disciplina 662
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione ita
Record Nr. UNINA-990000310620403321
Stuttgart : G. Thieme Verlag, 1977
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The chemistry of the fullerenes [[electronic resource] /] / Andreas Hirsch
The chemistry of the fullerenes [[electronic resource] /] / Andreas Hirsch
Autore Hirsch Andreas, Dr. rer. nat.
Pubbl/distr/stampa Stuttgart ; ; New York, : G. Thieme Verlag, 1994
Descrizione fisica 1 online resource (218 p.)
Disciplina 543.0894
546.681
Collana Thieme organic chemistry monograph series
Soggetto topico Fullerenes
ISBN 1-281-84341-5
9786611843410
3-527-61921-6
3-527-61922-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto The Chemistry of the Fullerenes; Contents; Chapter 1. The Parent Fullerenes; 1.1 The Fullerenes: Molecular Allotropes of Carbon; 1.2 The Discovery of the Fullerenes; 1.3 Fullerene Production; 1.3.1 Fullerene Generation by Vaporization of Graphite; 1.3.1.1 Resitive Heating of Graphite; 1.3.1.2 Arc heating of Graphite; 1.3.1.3 Solar Generators; 1.3.1.4 Inductive Heating of Graphite; 1.3.2 Fullerene Synthesis in Combustion; 1.3.3 Formation of Fullerenes by Pyrolysis of Naphthalene; 1.3.4 Endohedrals; 1.3.5 The Formation Process; 1.4 Separation and Purification; 1.5 Properties; 1.5.1 Structures
1.5.2 Physical and Spectroscopic PropertiesReferences; Chapter 2. Reduction; 2.1 Introduction; 2.2 Fulleride Anions; 2.3 Reductive Electrosynthesis; 2.3.1 Electrocrystallization; 2.3.2 Electrophilic Additions to Fulleride Anions; 2.4 Reduction with Metals; 2.4.1 Alkali Metal Fullerides; 2.4.1.1 Generation in Solution and Quenching Experiments; 2.4.1.2 Synthesis and Properties of Alkali Metal Fulleride Solids; 2.4.2 Alkaline Earth Metal Fullerides; 2.4.3 Reduction with Mercury; 2.5 Reduction with Organic Donor Molecules; References; Chapter 3. Nucleophilic Additions; 3.1 Introduction
3.2 Addition of Carbon Nucleophiles3.2.1 Hydroalkylation and Hydroarylation of C60 and C70; 3.2.2 Langmuir - Blodgett Films of C60Ht-Bu; 3.2.3 Addition of Macromolecular Carbanions - Fullerene Polymers; 3.2.4 Cyclopropanation of C60 and C70; 3.3 Addition of Amines; 3.4 Addition of Hydroxide; References; Chapter 4. Cycloadditions; 4.1 Introduction; 4.2 [4+2] Cycloadditions; 4.3 [3+2] Cycloadditions; 4.3.1 Addition of Diazomethanes. Diazoacetates and Diazoamides; 4.3.2 Addition of Azides; 4.3.3 Addition of Trimethylenemethanes; 4.3.4 Addition of Azomethine Ylides
4.3.5 Addition of Nitrile Oxides4.3.6 Addition of Sulfinimides; 4.3.7 Addition of Disiliranes; 4.4 [2+2] Cycloadditions; 4.4.1 Addition of Benzyne; 4.4.2 Addition of Enones; 4.4.3 Addition of Quadricyclane; 4.4.4 Addition of Electron Rich Alkynes; 4.4.5 Photopolymerization of C60; 4.5 [2+1] Cycloadditions; 4.5.1 Addition of Carbenes; 4.5.2 Addition of Silylenes; References; Chapter 5. Hydrogenation; 5.1 Introduction; 5.2 Oligohydrofullerenes C60Hzn and C70H2n (n = 1 - 6); 5.2.1 Hydrogenation via Hydroboration, Hydrozirconation and Zinc/Acid Reduction; 5.2.2 Theoretical Investigations
5.3 Polyhydrofullerenes C60H2n and C70H2n (n = 7 - 70)5.3.1 Birch - Huckel Reduction; 5.3.2 Transfer Hydrogenation of C60 and C70; 5.3.3 Catalytic Hydrogenation; 5.3.4 Theoretical Investigations; References; Chapter 6. Radical Additions; 6.1 Introduction; 6.2 ESR Investigations of Radical Additions; 6.2.1 Addition of Single Radicals; 6.2.2 Multiple Radical Additions; 6.3 Metalation of C60 with Pentacarbonylrhenium Radicals; 6.4 Hydrostannylation of C60; 6.5 Addition of Bis(trifluoromethyl)nitroxide; 6.6 Radical Copolymerization of C60 and Paracyclophane; References
Chapter 7. Transition Metal Complex Formation
Record Nr. UNINA-9910144098003321
Hirsch Andreas, Dr. rer. nat.  
Stuttgart ; ; New York, : G. Thieme Verlag, 1994
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The chemistry of the fullerenes [[electronic resource] /] / Andreas Hirsch
The chemistry of the fullerenes [[electronic resource] /] / Andreas Hirsch
Autore Hirsch Andreas, Dr. rer. nat.
Pubbl/distr/stampa Stuttgart ; ; New York, : G. Thieme Verlag, 1994
Descrizione fisica 1 online resource (218 p.)
Disciplina 543.0894
546.681
Collana Thieme organic chemistry monograph series
Soggetto topico Fullerenes
ISBN 1-281-84341-5
9786611843410
3-527-61921-6
3-527-61922-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto The Chemistry of the Fullerenes; Contents; Chapter 1. The Parent Fullerenes; 1.1 The Fullerenes: Molecular Allotropes of Carbon; 1.2 The Discovery of the Fullerenes; 1.3 Fullerene Production; 1.3.1 Fullerene Generation by Vaporization of Graphite; 1.3.1.1 Resitive Heating of Graphite; 1.3.1.2 Arc heating of Graphite; 1.3.1.3 Solar Generators; 1.3.1.4 Inductive Heating of Graphite; 1.3.2 Fullerene Synthesis in Combustion; 1.3.3 Formation of Fullerenes by Pyrolysis of Naphthalene; 1.3.4 Endohedrals; 1.3.5 The Formation Process; 1.4 Separation and Purification; 1.5 Properties; 1.5.1 Structures
1.5.2 Physical and Spectroscopic PropertiesReferences; Chapter 2. Reduction; 2.1 Introduction; 2.2 Fulleride Anions; 2.3 Reductive Electrosynthesis; 2.3.1 Electrocrystallization; 2.3.2 Electrophilic Additions to Fulleride Anions; 2.4 Reduction with Metals; 2.4.1 Alkali Metal Fullerides; 2.4.1.1 Generation in Solution and Quenching Experiments; 2.4.1.2 Synthesis and Properties of Alkali Metal Fulleride Solids; 2.4.2 Alkaline Earth Metal Fullerides; 2.4.3 Reduction with Mercury; 2.5 Reduction with Organic Donor Molecules; References; Chapter 3. Nucleophilic Additions; 3.1 Introduction
3.2 Addition of Carbon Nucleophiles3.2.1 Hydroalkylation and Hydroarylation of C60 and C70; 3.2.2 Langmuir - Blodgett Films of C60Ht-Bu; 3.2.3 Addition of Macromolecular Carbanions - Fullerene Polymers; 3.2.4 Cyclopropanation of C60 and C70; 3.3 Addition of Amines; 3.4 Addition of Hydroxide; References; Chapter 4. Cycloadditions; 4.1 Introduction; 4.2 [4+2] Cycloadditions; 4.3 [3+2] Cycloadditions; 4.3.1 Addition of Diazomethanes. Diazoacetates and Diazoamides; 4.3.2 Addition of Azides; 4.3.3 Addition of Trimethylenemethanes; 4.3.4 Addition of Azomethine Ylides
4.3.5 Addition of Nitrile Oxides4.3.6 Addition of Sulfinimides; 4.3.7 Addition of Disiliranes; 4.4 [2+2] Cycloadditions; 4.4.1 Addition of Benzyne; 4.4.2 Addition of Enones; 4.4.3 Addition of Quadricyclane; 4.4.4 Addition of Electron Rich Alkynes; 4.4.5 Photopolymerization of C60; 4.5 [2+1] Cycloadditions; 4.5.1 Addition of Carbenes; 4.5.2 Addition of Silylenes; References; Chapter 5. Hydrogenation; 5.1 Introduction; 5.2 Oligohydrofullerenes C60Hzn and C70H2n (n = 1 - 6); 5.2.1 Hydrogenation via Hydroboration, Hydrozirconation and Zinc/Acid Reduction; 5.2.2 Theoretical Investigations
5.3 Polyhydrofullerenes C60H2n and C70H2n (n = 7 - 70)5.3.1 Birch - Huckel Reduction; 5.3.2 Transfer Hydrogenation of C60 and C70; 5.3.3 Catalytic Hydrogenation; 5.3.4 Theoretical Investigations; References; Chapter 6. Radical Additions; 6.1 Introduction; 6.2 ESR Investigations of Radical Additions; 6.2.1 Addition of Single Radicals; 6.2.2 Multiple Radical Additions; 6.3 Metalation of C60 with Pentacarbonylrhenium Radicals; 6.4 Hydrostannylation of C60; 6.5 Addition of Bis(trifluoromethyl)nitroxide; 6.6 Radical Copolymerization of C60 and Paracyclophane; References
Chapter 7. Transition Metal Complex Formation
Record Nr. UNISA-996203742303316
Hirsch Andreas, Dr. rer. nat.  
Stuttgart ; ; New York, : G. Thieme Verlag, 1994
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
The chemistry of the fullerenes [[electronic resource] /] / Andreas Hirsch
The chemistry of the fullerenes [[electronic resource] /] / Andreas Hirsch
Autore Hirsch Andreas, Dr. rer. nat.
Pubbl/distr/stampa Stuttgart ; ; New York, : G. Thieme Verlag, 1994
Descrizione fisica 1 online resource (218 p.)
Disciplina 543.0894
546.681
Collana Thieme organic chemistry monograph series
Soggetto topico Fullerenes
ISBN 1-281-84341-5
9786611843410
3-527-61921-6
3-527-61922-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto The Chemistry of the Fullerenes; Contents; Chapter 1. The Parent Fullerenes; 1.1 The Fullerenes: Molecular Allotropes of Carbon; 1.2 The Discovery of the Fullerenes; 1.3 Fullerene Production; 1.3.1 Fullerene Generation by Vaporization of Graphite; 1.3.1.1 Resitive Heating of Graphite; 1.3.1.2 Arc heating of Graphite; 1.3.1.3 Solar Generators; 1.3.1.4 Inductive Heating of Graphite; 1.3.2 Fullerene Synthesis in Combustion; 1.3.3 Formation of Fullerenes by Pyrolysis of Naphthalene; 1.3.4 Endohedrals; 1.3.5 The Formation Process; 1.4 Separation and Purification; 1.5 Properties; 1.5.1 Structures
1.5.2 Physical and Spectroscopic PropertiesReferences; Chapter 2. Reduction; 2.1 Introduction; 2.2 Fulleride Anions; 2.3 Reductive Electrosynthesis; 2.3.1 Electrocrystallization; 2.3.2 Electrophilic Additions to Fulleride Anions; 2.4 Reduction with Metals; 2.4.1 Alkali Metal Fullerides; 2.4.1.1 Generation in Solution and Quenching Experiments; 2.4.1.2 Synthesis and Properties of Alkali Metal Fulleride Solids; 2.4.2 Alkaline Earth Metal Fullerides; 2.4.3 Reduction with Mercury; 2.5 Reduction with Organic Donor Molecules; References; Chapter 3. Nucleophilic Additions; 3.1 Introduction
3.2 Addition of Carbon Nucleophiles3.2.1 Hydroalkylation and Hydroarylation of C60 and C70; 3.2.2 Langmuir - Blodgett Films of C60Ht-Bu; 3.2.3 Addition of Macromolecular Carbanions - Fullerene Polymers; 3.2.4 Cyclopropanation of C60 and C70; 3.3 Addition of Amines; 3.4 Addition of Hydroxide; References; Chapter 4. Cycloadditions; 4.1 Introduction; 4.2 [4+2] Cycloadditions; 4.3 [3+2] Cycloadditions; 4.3.1 Addition of Diazomethanes. Diazoacetates and Diazoamides; 4.3.2 Addition of Azides; 4.3.3 Addition of Trimethylenemethanes; 4.3.4 Addition of Azomethine Ylides
4.3.5 Addition of Nitrile Oxides4.3.6 Addition of Sulfinimides; 4.3.7 Addition of Disiliranes; 4.4 [2+2] Cycloadditions; 4.4.1 Addition of Benzyne; 4.4.2 Addition of Enones; 4.4.3 Addition of Quadricyclane; 4.4.4 Addition of Electron Rich Alkynes; 4.4.5 Photopolymerization of C60; 4.5 [2+1] Cycloadditions; 4.5.1 Addition of Carbenes; 4.5.2 Addition of Silylenes; References; Chapter 5. Hydrogenation; 5.1 Introduction; 5.2 Oligohydrofullerenes C60Hzn and C70H2n (n = 1 - 6); 5.2.1 Hydrogenation via Hydroboration, Hydrozirconation and Zinc/Acid Reduction; 5.2.2 Theoretical Investigations
5.3 Polyhydrofullerenes C60H2n and C70H2n (n = 7 - 70)5.3.1 Birch - Huckel Reduction; 5.3.2 Transfer Hydrogenation of C60 and C70; 5.3.3 Catalytic Hydrogenation; 5.3.4 Theoretical Investigations; References; Chapter 6. Radical Additions; 6.1 Introduction; 6.2 ESR Investigations of Radical Additions; 6.2.1 Addition of Single Radicals; 6.2.2 Multiple Radical Additions; 6.3 Metalation of C60 with Pentacarbonylrhenium Radicals; 6.4 Hydrostannylation of C60; 6.5 Addition of Bis(trifluoromethyl)nitroxide; 6.6 Radical Copolymerization of C60 and Paracyclophane; References
Chapter 7. Transition Metal Complex Formation
Record Nr. UNINA-9910831094603321
Hirsch Andreas, Dr. rer. nat.  
Stuttgart ; ; New York, : G. Thieme Verlag, 1994
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The chemistry of the fullerenes / / Andreas Hirsch
The chemistry of the fullerenes / / Andreas Hirsch
Autore Hirsch Andreas, Dr. rer. nat.
Pubbl/distr/stampa Stuttgart ; ; New York, : G. Thieme Verlag, 1994
Descrizione fisica 1 online resource (218 p.)
Disciplina 543.0894
546.681
Collana Thieme organic chemistry monograph series
Soggetto topico Fullerenes
ISBN 1-281-84341-5
9786611843410
3-527-61921-6
3-527-61922-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto The Chemistry of the Fullerenes; Contents; Chapter 1. The Parent Fullerenes; 1.1 The Fullerenes: Molecular Allotropes of Carbon; 1.2 The Discovery of the Fullerenes; 1.3 Fullerene Production; 1.3.1 Fullerene Generation by Vaporization of Graphite; 1.3.1.1 Resitive Heating of Graphite; 1.3.1.2 Arc heating of Graphite; 1.3.1.3 Solar Generators; 1.3.1.4 Inductive Heating of Graphite; 1.3.2 Fullerene Synthesis in Combustion; 1.3.3 Formation of Fullerenes by Pyrolysis of Naphthalene; 1.3.4 Endohedrals; 1.3.5 The Formation Process; 1.4 Separation and Purification; 1.5 Properties; 1.5.1 Structures
1.5.2 Physical and Spectroscopic PropertiesReferences; Chapter 2. Reduction; 2.1 Introduction; 2.2 Fulleride Anions; 2.3 Reductive Electrosynthesis; 2.3.1 Electrocrystallization; 2.3.2 Electrophilic Additions to Fulleride Anions; 2.4 Reduction with Metals; 2.4.1 Alkali Metal Fullerides; 2.4.1.1 Generation in Solution and Quenching Experiments; 2.4.1.2 Synthesis and Properties of Alkali Metal Fulleride Solids; 2.4.2 Alkaline Earth Metal Fullerides; 2.4.3 Reduction with Mercury; 2.5 Reduction with Organic Donor Molecules; References; Chapter 3. Nucleophilic Additions; 3.1 Introduction
3.2 Addition of Carbon Nucleophiles3.2.1 Hydroalkylation and Hydroarylation of C60 and C70; 3.2.2 Langmuir - Blodgett Films of C60Ht-Bu; 3.2.3 Addition of Macromolecular Carbanions - Fullerene Polymers; 3.2.4 Cyclopropanation of C60 and C70; 3.3 Addition of Amines; 3.4 Addition of Hydroxide; References; Chapter 4. Cycloadditions; 4.1 Introduction; 4.2 [4+2] Cycloadditions; 4.3 [3+2] Cycloadditions; 4.3.1 Addition of Diazomethanes. Diazoacetates and Diazoamides; 4.3.2 Addition of Azides; 4.3.3 Addition of Trimethylenemethanes; 4.3.4 Addition of Azomethine Ylides
4.3.5 Addition of Nitrile Oxides4.3.6 Addition of Sulfinimides; 4.3.7 Addition of Disiliranes; 4.4 [2+2] Cycloadditions; 4.4.1 Addition of Benzyne; 4.4.2 Addition of Enones; 4.4.3 Addition of Quadricyclane; 4.4.4 Addition of Electron Rich Alkynes; 4.4.5 Photopolymerization of C60; 4.5 [2+1] Cycloadditions; 4.5.1 Addition of Carbenes; 4.5.2 Addition of Silylenes; References; Chapter 5. Hydrogenation; 5.1 Introduction; 5.2 Oligohydrofullerenes C60Hzn and C70H2n (n = 1 - 6); 5.2.1 Hydrogenation via Hydroboration, Hydrozirconation and Zinc/Acid Reduction; 5.2.2 Theoretical Investigations
5.3 Polyhydrofullerenes C60H2n and C70H2n (n = 7 - 70)5.3.1 Birch - Huckel Reduction; 5.3.2 Transfer Hydrogenation of C60 and C70; 5.3.3 Catalytic Hydrogenation; 5.3.4 Theoretical Investigations; References; Chapter 6. Radical Additions; 6.1 Introduction; 6.2 ESR Investigations of Radical Additions; 6.2.1 Addition of Single Radicals; 6.2.2 Multiple Radical Additions; 6.3 Metalation of C60 with Pentacarbonylrhenium Radicals; 6.4 Hydrostannylation of C60; 6.5 Addition of Bis(trifluoromethyl)nitroxide; 6.6 Radical Copolymerization of C60 and Paracyclophane; References
Chapter 7. Transition Metal Complex Formation
Record Nr. UNINA-9910877823703321
Hirsch Andreas, Dr. rer. nat.  
Stuttgart ; ; New York, : G. Thieme Verlag, 1994
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Die fumente und ihre wirkungen. Bnad 1,2,3,4 / Von Carl Oppenheimer
Die fumente und ihre wirkungen. Bnad 1,2,3,4 / Von Carl Oppenheimer
Autore Oppenheimer, Carl <1874-1941>
Edizione [5° ed.]
Pubbl/distr/stampa Leipzig : G. Thieme Verlag, 1925-1929
Descrizione fisica 4 voll., ill., 27 cm
Disciplina 660
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione ita
Record Nr. UNINA-990000315840403321
Oppenheimer, Carl <1874-1941>  
Leipzig : G. Thieme Verlag, 1925-1929
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Planta medica : journal of medicinal plant research
Planta medica : journal of medicinal plant research
Pubbl/distr/stampa Stuttgart : G. Thieme Verlag
Descrizione fisica v. : ill.
Disciplina 615
Soggetto topico Farmacologia - Periodici
ISSN 0032-0943
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Note periodicità Pubbl. 8 n. l'anno
Record Nr. UNISA-990001041700203316
Stuttgart : G. Thieme Verlag
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui