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The chemistry of explosives / / Jacqueline Akhavan
| The chemistry of explosives / / Jacqueline Akhavan |
| Autore | Akhavan Jacqueline |
| Edizione | [Fourth edition.] |
| Pubbl/distr/stampa | London, UK : , : The Royal Society of Chemistry, , [2022] |
| Descrizione fisica | 1 online resource (194 p.) : ill |
| Disciplina | 662/.201547 |
| Soggetto topico | Explosives |
| ISBN |
9781839168802
1839168803 9781839166181 1839166185 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910955483403321 |
Akhavan Jacqueline
|
||
| London, UK : , : The Royal Society of Chemistry, , [2022] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Organic chemistry of explosives [[electronic resource] /] / Jai Prakash Agrawal, Robert Dale Hodgson
| Organic chemistry of explosives [[electronic resource] /] / Jai Prakash Agrawal, Robert Dale Hodgson |
| Autore | Agrawal J. P (Jai Prakash) |
| Pubbl/distr/stampa | Chichester, England ; ; Hoboken, NJ, : John Wiley & Sons Ltd, c2007 |
| Descrizione fisica | 1 online resource (416 p.) |
| Disciplina |
662.201547
662/.201547 |
| Altri autori (Persone) | HodgsonR. D |
| Soggetto topico | Explosives |
| ISBN |
1-280-73999-1
9786610739998 0-470-05936-2 0-470-05935-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Organic Chemistry of Explosives; Contents; Foreword; Preface; Abbreviations; Acknowledgements; Background; 1 Synthetic Routes to Aliphatic C-Nitro Functionality; 1.1 Introduction; 1.2 Aliphatic C-Nitro Compounds as Explosives; 1.3 Direct Nitration of Alkanes; 1.4 Addition of Nitric Acid, Nitrogen Oxides and Related Compounds to Unsaturated Bonds; 1.4.1 Nitric Acid and its Mixtures; 1.4.2 Nitrogen Dioxide; 1.4.3 Dinitrogen Pentoxide; 1.4.4 Nitrous Oxide and Dinitrogen Trioxide; 1.4.5 Other Nitrating Agents; 1.5 Halide Displacement; 1.5.1 Victor Meyer Reaction
1.5.2 Modified Victor Meyer Reaction1.5.3 Ter Meer Reaction; 1.5.4 Displacements Using Nitronate Salts as Nucleophiles; 1.6 Oxidation and Nitration of C-N Bonds; 1.6.1 Oxidation and Nitration of Oximes; 1.6.2 Oxidation of Amines; 1.6.3 Nitration of Nitronate Salts; 1.6.4 Oxidation of Pseudonitroles; 1.6.5 Oxidation of Isocyanates; 1.6.6 Oxidation of Nitrosoalkanes; 1.7 Kaplan-Shechter Reaction; 1.8 Nitration of Compounds Containing Acidic Hydrogen; 1.8.1 Alkaline Nitration; 1.8.2 Acidic Nitration; 1.9 Oxidative Dimerization; 1.10 Addition and Condensation Reactions 1.10.1 1,2-Addition Reactions1.10.2 1,4-Addition Reactions; 1.10.3 Mannich Reaction; 1.10.4 Henry Reaction; 1.11 Derivatives of Polynitroaliphatic Alcohols; 1.12 Miscellaneous; 1.12.1 1,1-Diamino-2,2-Dinitroethylenes; 1.12.2 Other Routes to Aliphatic Nitro Compounds; 1.12.3 Selective Reductions; 1.13 Chemical Stability of Polynitroaliphatic Compounds; 1.13.1 Reactions with Mineral Acids; 1.13.2 Reactions with Base and Nucleophiles; References; 2 Energetic Compounds 1: Polynitropolycycloalkanes; 2.1 Caged Structures as Energetic Materials; 2.2 Cyclopropanes and Spirocyclopropanes 2.3 Cyclobutanes and Their Derivatives2.4 Cubanes; 2.5 Homocubanes; 2.6 Prismanes; 2.7 Adamantanes; 2.8 Polynitrobicycloalkanes; 2.8.1 Norbornanes; 2.8.2 Bicyclo[3.3.0]octane; 2.8.3 Bicyclo[3.3.1]nonane; References; 3 Synthetic Routes to Nitrate Esters; 3.1 Nitrate Esters as Explosives; 3.2 Nitration of the Parent Alcohol; 3.2.1 O-Nitration with Nitric Acid and Its Mixtures; 3.2.2 O-Nitration with Dinitrogen Tetroxide; 3.2.3 O-Nitration with Dinitrogen Pentoxide; 3.2.4 O-Nitration with Nitronium Salts; 3.2.5 Transfer Nitration; 3.2.6 Other O-Nitrating Agents 3.3 Nucleophilic Displacement with Nitrate Anion3.3.1 Metathesis between Alkyl halides and Silver Nitrate; 3.3.2 Decomposition of Nitratocarbonates; 3.3.3 Displacement of Sulfonate Esters with Nitrate Anion; 3.3.4 Displacement with Mercury (I) Nitrate; 3.4 Nitrate Esters from the Ring-Opening of Strained Oxygen Heterocycles; 3.4.1 Ring-Opening Nitration of Epoxides; 3.4.2 1,3-Dinitrate Esters from the Ring-Opening Nitration of Oxetanes with Dinitrogen Pentoxide; 3.4.3 Other Oxygen Heterocycles; 3.5 Nitrodesilylation; 3.6 Additions to Alkenes; 3.6.1 Nitric Acid and its Mixtures 3.6.2 Nitrogen Oxides |
| Record Nr. | UNINA-9910143588703321 |
|
Agrawal J. P (Jai Prakash)
|
||
| Chichester, England ; ; Hoboken, NJ, : John Wiley & Sons Ltd, c2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Organic chemistry of explosives [[electronic resource] /] / Jai Prakash Agrawal, Robert Dale Hodgson
| Organic chemistry of explosives [[electronic resource] /] / Jai Prakash Agrawal, Robert Dale Hodgson |
| Autore | Agrawal J. P (Jai Prakash) |
| Pubbl/distr/stampa | Chichester, England ; ; Hoboken, NJ, : John Wiley & Sons Ltd, c2007 |
| Descrizione fisica | 1 online resource (416 p.) |
| Disciplina |
662.201547
662/.201547 |
| Altri autori (Persone) | HodgsonR. D |
| Soggetto topico | Explosives |
| ISBN |
1-280-73999-1
9786610739998 0-470-05936-2 0-470-05935-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Organic Chemistry of Explosives; Contents; Foreword; Preface; Abbreviations; Acknowledgements; Background; 1 Synthetic Routes to Aliphatic C-Nitro Functionality; 1.1 Introduction; 1.2 Aliphatic C-Nitro Compounds as Explosives; 1.3 Direct Nitration of Alkanes; 1.4 Addition of Nitric Acid, Nitrogen Oxides and Related Compounds to Unsaturated Bonds; 1.4.1 Nitric Acid and its Mixtures; 1.4.2 Nitrogen Dioxide; 1.4.3 Dinitrogen Pentoxide; 1.4.4 Nitrous Oxide and Dinitrogen Trioxide; 1.4.5 Other Nitrating Agents; 1.5 Halide Displacement; 1.5.1 Victor Meyer Reaction
1.5.2 Modified Victor Meyer Reaction1.5.3 Ter Meer Reaction; 1.5.4 Displacements Using Nitronate Salts as Nucleophiles; 1.6 Oxidation and Nitration of C-N Bonds; 1.6.1 Oxidation and Nitration of Oximes; 1.6.2 Oxidation of Amines; 1.6.3 Nitration of Nitronate Salts; 1.6.4 Oxidation of Pseudonitroles; 1.6.5 Oxidation of Isocyanates; 1.6.6 Oxidation of Nitrosoalkanes; 1.7 Kaplan-Shechter Reaction; 1.8 Nitration of Compounds Containing Acidic Hydrogen; 1.8.1 Alkaline Nitration; 1.8.2 Acidic Nitration; 1.9 Oxidative Dimerization; 1.10 Addition and Condensation Reactions 1.10.1 1,2-Addition Reactions1.10.2 1,4-Addition Reactions; 1.10.3 Mannich Reaction; 1.10.4 Henry Reaction; 1.11 Derivatives of Polynitroaliphatic Alcohols; 1.12 Miscellaneous; 1.12.1 1,1-Diamino-2,2-Dinitroethylenes; 1.12.2 Other Routes to Aliphatic Nitro Compounds; 1.12.3 Selective Reductions; 1.13 Chemical Stability of Polynitroaliphatic Compounds; 1.13.1 Reactions with Mineral Acids; 1.13.2 Reactions with Base and Nucleophiles; References; 2 Energetic Compounds 1: Polynitropolycycloalkanes; 2.1 Caged Structures as Energetic Materials; 2.2 Cyclopropanes and Spirocyclopropanes 2.3 Cyclobutanes and Their Derivatives2.4 Cubanes; 2.5 Homocubanes; 2.6 Prismanes; 2.7 Adamantanes; 2.8 Polynitrobicycloalkanes; 2.8.1 Norbornanes; 2.8.2 Bicyclo[3.3.0]octane; 2.8.3 Bicyclo[3.3.1]nonane; References; 3 Synthetic Routes to Nitrate Esters; 3.1 Nitrate Esters as Explosives; 3.2 Nitration of the Parent Alcohol; 3.2.1 O-Nitration with Nitric Acid and Its Mixtures; 3.2.2 O-Nitration with Dinitrogen Tetroxide; 3.2.3 O-Nitration with Dinitrogen Pentoxide; 3.2.4 O-Nitration with Nitronium Salts; 3.2.5 Transfer Nitration; 3.2.6 Other O-Nitrating Agents 3.3 Nucleophilic Displacement with Nitrate Anion3.3.1 Metathesis between Alkyl halides and Silver Nitrate; 3.3.2 Decomposition of Nitratocarbonates; 3.3.3 Displacement of Sulfonate Esters with Nitrate Anion; 3.3.4 Displacement with Mercury (I) Nitrate; 3.4 Nitrate Esters from the Ring-Opening of Strained Oxygen Heterocycles; 3.4.1 Ring-Opening Nitration of Epoxides; 3.4.2 1,3-Dinitrate Esters from the Ring-Opening Nitration of Oxetanes with Dinitrogen Pentoxide; 3.4.3 Other Oxygen Heterocycles; 3.5 Nitrodesilylation; 3.6 Additions to Alkenes; 3.6.1 Nitric Acid and its Mixtures 3.6.2 Nitrogen Oxides |
| Record Nr. | UNINA-9910830626203321 |
|
Agrawal J. P (Jai Prakash)
|
||
| Chichester, England ; ; Hoboken, NJ, : John Wiley & Sons Ltd, c2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Organic chemistry of explosives / / Jai Prakash Agrawal, Robert Dale Hodgson
| Organic chemistry of explosives / / Jai Prakash Agrawal, Robert Dale Hodgson |
| Autore | Agrawal J. P (Jai Prakash) |
| Pubbl/distr/stampa | Chichester, England ; ; Hoboken, NJ, : John Wiley & Sons Ltd, c2007 |
| Descrizione fisica | 1 online resource (416 p.) |
| Disciplina | 662/.201547 |
| Altri autori (Persone) | HodgsonR. D |
| Soggetto topico | Explosives |
| ISBN |
9786610739998
9781280739996 1280739991 9780470059364 0470059362 9780470059357 0470059354 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Organic Chemistry of Explosives; Contents; Foreword; Preface; Abbreviations; Acknowledgements; Background; 1 Synthetic Routes to Aliphatic C-Nitro Functionality; 1.1 Introduction; 1.2 Aliphatic C-Nitro Compounds as Explosives; 1.3 Direct Nitration of Alkanes; 1.4 Addition of Nitric Acid, Nitrogen Oxides and Related Compounds to Unsaturated Bonds; 1.4.1 Nitric Acid and its Mixtures; 1.4.2 Nitrogen Dioxide; 1.4.3 Dinitrogen Pentoxide; 1.4.4 Nitrous Oxide and Dinitrogen Trioxide; 1.4.5 Other Nitrating Agents; 1.5 Halide Displacement; 1.5.1 Victor Meyer Reaction
1.5.2 Modified Victor Meyer Reaction1.5.3 Ter Meer Reaction; 1.5.4 Displacements Using Nitronate Salts as Nucleophiles; 1.6 Oxidation and Nitration of C-N Bonds; 1.6.1 Oxidation and Nitration of Oximes; 1.6.2 Oxidation of Amines; 1.6.3 Nitration of Nitronate Salts; 1.6.4 Oxidation of Pseudonitroles; 1.6.5 Oxidation of Isocyanates; 1.6.6 Oxidation of Nitrosoalkanes; 1.7 Kaplan-Shechter Reaction; 1.8 Nitration of Compounds Containing Acidic Hydrogen; 1.8.1 Alkaline Nitration; 1.8.2 Acidic Nitration; 1.9 Oxidative Dimerization; 1.10 Addition and Condensation Reactions 1.10.1 1,2-Addition Reactions1.10.2 1,4-Addition Reactions; 1.10.3 Mannich Reaction; 1.10.4 Henry Reaction; 1.11 Derivatives of Polynitroaliphatic Alcohols; 1.12 Miscellaneous; 1.12.1 1,1-Diamino-2,2-Dinitroethylenes; 1.12.2 Other Routes to Aliphatic Nitro Compounds; 1.12.3 Selective Reductions; 1.13 Chemical Stability of Polynitroaliphatic Compounds; 1.13.1 Reactions with Mineral Acids; 1.13.2 Reactions with Base and Nucleophiles; References; 2 Energetic Compounds 1: Polynitropolycycloalkanes; 2.1 Caged Structures as Energetic Materials; 2.2 Cyclopropanes and Spirocyclopropanes 2.3 Cyclobutanes and Their Derivatives2.4 Cubanes; 2.5 Homocubanes; 2.6 Prismanes; 2.7 Adamantanes; 2.8 Polynitrobicycloalkanes; 2.8.1 Norbornanes; 2.8.2 Bicyclo[3.3.0]octane; 2.8.3 Bicyclo[3.3.1]nonane; References; 3 Synthetic Routes to Nitrate Esters; 3.1 Nitrate Esters as Explosives; 3.2 Nitration of the Parent Alcohol; 3.2.1 O-Nitration with Nitric Acid and Its Mixtures; 3.2.2 O-Nitration with Dinitrogen Tetroxide; 3.2.3 O-Nitration with Dinitrogen Pentoxide; 3.2.4 O-Nitration with Nitronium Salts; 3.2.5 Transfer Nitration; 3.2.6 Other O-Nitrating Agents 3.3 Nucleophilic Displacement with Nitrate Anion3.3.1 Metathesis between Alkyl halides and Silver Nitrate; 3.3.2 Decomposition of Nitratocarbonates; 3.3.3 Displacement of Sulfonate Esters with Nitrate Anion; 3.3.4 Displacement with Mercury (I) Nitrate; 3.4 Nitrate Esters from the Ring-Opening of Strained Oxygen Heterocycles; 3.4.1 Ring-Opening Nitration of Epoxides; 3.4.2 1,3-Dinitrate Esters from the Ring-Opening Nitration of Oxetanes with Dinitrogen Pentoxide; 3.4.3 Other Oxygen Heterocycles; 3.5 Nitrodesilylation; 3.6 Additions to Alkenes; 3.6.1 Nitric Acid and its Mixtures 3.6.2 Nitrogen Oxides |
| Record Nr. | UNINA-9911019954303321 |
|
Agrawal J. P (Jai Prakash)
|
||
| Chichester, England ; ; Hoboken, NJ, : John Wiley & Sons Ltd, c2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||