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Modern cyclophane chemistry [[electronic resource] /] / Rolf Gleiter, Henning Hopf, eds
| Modern cyclophane chemistry [[electronic resource] /] / Rolf Gleiter, Henning Hopf, eds |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH |
| Descrizione fisica | 1 online resource (588 p.) |
| Disciplina |
547.59
547/.59 |
| Altri autori (Persone) |
GleiterRolf <1936->
HopfHenning <1940-> |
| Soggetto topico | Cyclophanes |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-51992-4
9786610519927 3-527-60396-4 3-527-60463-4 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Modern Cyclophane Chemistry; Contents; Preface; List of Contributors; 1 Cyclophynes; 1.1 Introduction; 1.2 Orthocyclophynes and Related Systems; 1.2.1 Planar Dehydrobenzoannulenes; 1.2.2 Nonplanar Orthocyclophynes; 1.3 Metacyclophynes and Related Systems; 1.4 Paracyclophynes and 1,3,5-Bridged Cyclophynes; 1.5 Concluding Remarks; 1.6 Acknowledgement; 1.7 References; 2 Hetera (Cyclo-)phanes; 2.1 Introduction; 2.1.1 Selection of Topics Presented; 2.1.2 Definitions; 2.1.3 Why Conduct a Survey on Heteraphanes?; 2.2 Heteraphanes; 2.2.1 Planar Chiral and Helical Chiral Phanes
2.2.1.1 Design of Phanes with Planar and Helical Chirality2.2.1.2 Hetera [2.2]Metacyclophanes; 2.2.1.3 Planar Chiral [2.2]Metacyclophanes; 2.2.1.4 Planar Chiral Hetera [n]Para- and Hetera [n]Metacyclophanes; 2.2.1.5 Dioxa [2.2]Phanes and Oxaza [2.2]Phanes; 2.2.1.6 Enantiomer Separations; 2.2.1.7 Strongly Helical Heteraphanes; 2.2.2 Catenanes, Rotaxanes, and Knotanes of the Heteraphane Type; 2.2.2.1 Template Synthesis of Rotaxanes Using Cyclophane Wheels; 2.2.2.2 Higher Order [n]Rotaxanes via Non-ionic Template Effect; 2.2.2.3 Combination of Anionic and Non-ionic Template 2.2.2.4 Molecular Knots and Similar Macrocycles of the Heteraphane Type2.2.3 Further Heteraphanes, Metallaphanes and Supramolecular Phanes; 2.3 Conclusions; 2.4 Acknowledgement; 2.5 References; 3 Highly Strained Cyclophanes; 3.1 Introduction; 3.2 [n]Metacyclophanes; 3.2.1 Synthesis; 3.2.2 Structures and Physical Properties; 3.2.3 Reactions of Strained [n]Metacyclophanes; 3.2.3.1 Thermal and Photochemical Reactions; 3.2.3.2 Addition Reactions; 3.2.3.3 Reactions with Electrophiles; 3.2.3.4 Reactions with Nucleophiles; 3.3 [n]Paracyclophanes; 3.3.1 Synthesis 3.3.2 Structures and Physical Properties3.3.3 Reactions of Strained [n]Paracyclophanes; 3.3.3.1 Thermal and Photochemical Reactions; 3.3.3.2 Reactions with Electrophiles; 3.3.3.3 Diels-Alder and Other Reactions; 3.3.3.4 Kinetic Stabilization of [4]Paracyclophane Systems; 3.4 Aromaticity of Bent Benzene Rings; 3.5 Cyclophanes containing Polycyclic Aromatic Rings: (2,7)Pyrenophanes; 3.6 [1.1]Paracyclophanes; 3.6.1 Synthesis; 3.6.2 Kinetic Stabilization of [1.1]Paracyclophane Systems; 3.6.3 Structures and Physical Properties; 3.7 References and Notes; 4 Superphanes; 4.1 Introduction 4.2 [n(2)]Cyclopropenonophanes4.2.1 Synthesis; 4.3 Superbridged Cyclopropenyliophanes; 4.4 C(4)-Superphanes; 4.4.1 Properties of Cyclobutadieno Superphanes; 4.4.2 Oxidative Demetallations; 4.5 C(5)-Superphanes; 4.6 Superbridged Benzene Rings; 4.7 Concluding Remarks; 4.8 Acknowledgement; 4.9 References; 5 Carbon-Bridged Ferrocenophanes; 5.1 Introduction; 5.2 Nomenclature; 5.3 Mononuclear Carbon-Bridged Ferrocenophanes; 5.3.1 [1]Ferrocenophanes; 5.3.2 [2]Ferrocenophanes; 5.3.3 [3]Ferrocenophanes; 5.3.4 [4]Ferrocenophanes; 5.3.5 [5]Ferrocenophanes; 5.3.6 [m]Ferrocenophanes (m>5) 5.3.7 Multiply-Bridged Mononuclear Ferrocenophanes ([m](n)Ferrocenophanes) |
| Record Nr. | UNINA-9910144297003321 |
| Weinheim, : Wiley-VCH | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Modern cyclophane chemistry [[electronic resource] /] / Rolf Gleiter, Henning Hopf, eds
| Modern cyclophane chemistry [[electronic resource] /] / Rolf Gleiter, Henning Hopf, eds |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH |
| Descrizione fisica | 1 online resource (588 p.) |
| Disciplina |
547.59
547/.59 |
| Altri autori (Persone) |
GleiterRolf <1936->
HopfHenning <1940-> |
| Soggetto topico | Cyclophanes |
| ISBN |
1-280-51992-4
9786610519927 3-527-60396-4 3-527-60463-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Modern Cyclophane Chemistry; Contents; Preface; List of Contributors; 1 Cyclophynes; 1.1 Introduction; 1.2 Orthocyclophynes and Related Systems; 1.2.1 Planar Dehydrobenzoannulenes; 1.2.2 Nonplanar Orthocyclophynes; 1.3 Metacyclophynes and Related Systems; 1.4 Paracyclophynes and 1,3,5-Bridged Cyclophynes; 1.5 Concluding Remarks; 1.6 Acknowledgement; 1.7 References; 2 Hetera (Cyclo-)phanes; 2.1 Introduction; 2.1.1 Selection of Topics Presented; 2.1.2 Definitions; 2.1.3 Why Conduct a Survey on Heteraphanes?; 2.2 Heteraphanes; 2.2.1 Planar Chiral and Helical Chiral Phanes
2.2.1.1 Design of Phanes with Planar and Helical Chirality2.2.1.2 Hetera [2.2]Metacyclophanes; 2.2.1.3 Planar Chiral [2.2]Metacyclophanes; 2.2.1.4 Planar Chiral Hetera [n]Para- and Hetera [n]Metacyclophanes; 2.2.1.5 Dioxa [2.2]Phanes and Oxaza [2.2]Phanes; 2.2.1.6 Enantiomer Separations; 2.2.1.7 Strongly Helical Heteraphanes; 2.2.2 Catenanes, Rotaxanes, and Knotanes of the Heteraphane Type; 2.2.2.1 Template Synthesis of Rotaxanes Using Cyclophane Wheels; 2.2.2.2 Higher Order [n]Rotaxanes via Non-ionic Template Effect; 2.2.2.3 Combination of Anionic and Non-ionic Template 2.2.2.4 Molecular Knots and Similar Macrocycles of the Heteraphane Type2.2.3 Further Heteraphanes, Metallaphanes and Supramolecular Phanes; 2.3 Conclusions; 2.4 Acknowledgement; 2.5 References; 3 Highly Strained Cyclophanes; 3.1 Introduction; 3.2 [n]Metacyclophanes; 3.2.1 Synthesis; 3.2.2 Structures and Physical Properties; 3.2.3 Reactions of Strained [n]Metacyclophanes; 3.2.3.1 Thermal and Photochemical Reactions; 3.2.3.2 Addition Reactions; 3.2.3.3 Reactions with Electrophiles; 3.2.3.4 Reactions with Nucleophiles; 3.3 [n]Paracyclophanes; 3.3.1 Synthesis 3.3.2 Structures and Physical Properties3.3.3 Reactions of Strained [n]Paracyclophanes; 3.3.3.1 Thermal and Photochemical Reactions; 3.3.3.2 Reactions with Electrophiles; 3.3.3.3 Diels-Alder and Other Reactions; 3.3.3.4 Kinetic Stabilization of [4]Paracyclophane Systems; 3.4 Aromaticity of Bent Benzene Rings; 3.5 Cyclophanes containing Polycyclic Aromatic Rings: (2,7)Pyrenophanes; 3.6 [1.1]Paracyclophanes; 3.6.1 Synthesis; 3.6.2 Kinetic Stabilization of [1.1]Paracyclophane Systems; 3.6.3 Structures and Physical Properties; 3.7 References and Notes; 4 Superphanes; 4.1 Introduction 4.2 [n(2)]Cyclopropenonophanes4.2.1 Synthesis; 4.3 Superbridged Cyclopropenyliophanes; 4.4 C(4)-Superphanes; 4.4.1 Properties of Cyclobutadieno Superphanes; 4.4.2 Oxidative Demetallations; 4.5 C(5)-Superphanes; 4.6 Superbridged Benzene Rings; 4.7 Concluding Remarks; 4.8 Acknowledgement; 4.9 References; 5 Carbon-Bridged Ferrocenophanes; 5.1 Introduction; 5.2 Nomenclature; 5.3 Mononuclear Carbon-Bridged Ferrocenophanes; 5.3.1 [1]Ferrocenophanes; 5.3.2 [2]Ferrocenophanes; 5.3.3 [3]Ferrocenophanes; 5.3.4 [4]Ferrocenophanes; 5.3.5 [5]Ferrocenophanes; 5.3.6 [m]Ferrocenophanes (m>5) 5.3.7 Multiply-Bridged Mononuclear Ferrocenophanes ([m](n)Ferrocenophanes) |
| Record Nr. | UNISA-996211953003316 |
| Weinheim, : Wiley-VCH | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
| ||
Modern cyclophane chemistry [[electronic resource] /] / Rolf Gleiter, Henning Hopf, eds
| Modern cyclophane chemistry [[electronic resource] /] / Rolf Gleiter, Henning Hopf, eds |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH |
| Descrizione fisica | 1 online resource (588 p.) |
| Disciplina |
547.59
547/.59 |
| Altri autori (Persone) |
GleiterRolf <1936->
HopfHenning <1940-> |
| Soggetto topico | Cyclophanes |
| ISBN |
1-280-51992-4
9786610519927 3-527-60396-4 3-527-60463-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Modern Cyclophane Chemistry; Contents; Preface; List of Contributors; 1 Cyclophynes; 1.1 Introduction; 1.2 Orthocyclophynes and Related Systems; 1.2.1 Planar Dehydrobenzoannulenes; 1.2.2 Nonplanar Orthocyclophynes; 1.3 Metacyclophynes and Related Systems; 1.4 Paracyclophynes and 1,3,5-Bridged Cyclophynes; 1.5 Concluding Remarks; 1.6 Acknowledgement; 1.7 References; 2 Hetera (Cyclo-)phanes; 2.1 Introduction; 2.1.1 Selection of Topics Presented; 2.1.2 Definitions; 2.1.3 Why Conduct a Survey on Heteraphanes?; 2.2 Heteraphanes; 2.2.1 Planar Chiral and Helical Chiral Phanes
2.2.1.1 Design of Phanes with Planar and Helical Chirality2.2.1.2 Hetera [2.2]Metacyclophanes; 2.2.1.3 Planar Chiral [2.2]Metacyclophanes; 2.2.1.4 Planar Chiral Hetera [n]Para- and Hetera [n]Metacyclophanes; 2.2.1.5 Dioxa [2.2]Phanes and Oxaza [2.2]Phanes; 2.2.1.6 Enantiomer Separations; 2.2.1.7 Strongly Helical Heteraphanes; 2.2.2 Catenanes, Rotaxanes, and Knotanes of the Heteraphane Type; 2.2.2.1 Template Synthesis of Rotaxanes Using Cyclophane Wheels; 2.2.2.2 Higher Order [n]Rotaxanes via Non-ionic Template Effect; 2.2.2.3 Combination of Anionic and Non-ionic Template 2.2.2.4 Molecular Knots and Similar Macrocycles of the Heteraphane Type2.2.3 Further Heteraphanes, Metallaphanes and Supramolecular Phanes; 2.3 Conclusions; 2.4 Acknowledgement; 2.5 References; 3 Highly Strained Cyclophanes; 3.1 Introduction; 3.2 [n]Metacyclophanes; 3.2.1 Synthesis; 3.2.2 Structures and Physical Properties; 3.2.3 Reactions of Strained [n]Metacyclophanes; 3.2.3.1 Thermal and Photochemical Reactions; 3.2.3.2 Addition Reactions; 3.2.3.3 Reactions with Electrophiles; 3.2.3.4 Reactions with Nucleophiles; 3.3 [n]Paracyclophanes; 3.3.1 Synthesis 3.3.2 Structures and Physical Properties3.3.3 Reactions of Strained [n]Paracyclophanes; 3.3.3.1 Thermal and Photochemical Reactions; 3.3.3.2 Reactions with Electrophiles; 3.3.3.3 Diels-Alder and Other Reactions; 3.3.3.4 Kinetic Stabilization of [4]Paracyclophane Systems; 3.4 Aromaticity of Bent Benzene Rings; 3.5 Cyclophanes containing Polycyclic Aromatic Rings: (2,7)Pyrenophanes; 3.6 [1.1]Paracyclophanes; 3.6.1 Synthesis; 3.6.2 Kinetic Stabilization of [1.1]Paracyclophane Systems; 3.6.3 Structures and Physical Properties; 3.7 References and Notes; 4 Superphanes; 4.1 Introduction 4.2 [n(2)]Cyclopropenonophanes4.2.1 Synthesis; 4.3 Superbridged Cyclopropenyliophanes; 4.4 C(4)-Superphanes; 4.4.1 Properties of Cyclobutadieno Superphanes; 4.4.2 Oxidative Demetallations; 4.5 C(5)-Superphanes; 4.6 Superbridged Benzene Rings; 4.7 Concluding Remarks; 4.8 Acknowledgement; 4.9 References; 5 Carbon-Bridged Ferrocenophanes; 5.1 Introduction; 5.2 Nomenclature; 5.3 Mononuclear Carbon-Bridged Ferrocenophanes; 5.3.1 [1]Ferrocenophanes; 5.3.2 [2]Ferrocenophanes; 5.3.3 [3]Ferrocenophanes; 5.3.4 [4]Ferrocenophanes; 5.3.5 [5]Ferrocenophanes; 5.3.6 [m]Ferrocenophanes (m>5) 5.3.7 Multiply-Bridged Mononuclear Ferrocenophanes ([m](n)Ferrocenophanes) |
| Record Nr. | UNINA-9910830909803321 |
| Weinheim, : Wiley-VCH | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Modern cyclophane chemistry / / Rolf Gleiter, Henning Hopf, eds
| Modern cyclophane chemistry / / Rolf Gleiter, Henning Hopf, eds |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH |
| Descrizione fisica | 1 online resource (588 p.) |
| Disciplina | 547/.59 |
| Altri autori (Persone) |
GleiterRolf <1936->
HopfHenning <1940-> |
| Soggetto topico | Cyclophanes |
| ISBN |
1-280-51992-4
9786610519927 3-527-60396-4 3-527-60463-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Modern Cyclophane Chemistry; Contents; Preface; List of Contributors; 1 Cyclophynes; 1.1 Introduction; 1.2 Orthocyclophynes and Related Systems; 1.2.1 Planar Dehydrobenzoannulenes; 1.2.2 Nonplanar Orthocyclophynes; 1.3 Metacyclophynes and Related Systems; 1.4 Paracyclophynes and 1,3,5-Bridged Cyclophynes; 1.5 Concluding Remarks; 1.6 Acknowledgement; 1.7 References; 2 Hetera (Cyclo-)phanes; 2.1 Introduction; 2.1.1 Selection of Topics Presented; 2.1.2 Definitions; 2.1.3 Why Conduct a Survey on Heteraphanes?; 2.2 Heteraphanes; 2.2.1 Planar Chiral and Helical Chiral Phanes
2.2.1.1 Design of Phanes with Planar and Helical Chirality2.2.1.2 Hetera [2.2]Metacyclophanes; 2.2.1.3 Planar Chiral [2.2]Metacyclophanes; 2.2.1.4 Planar Chiral Hetera [n]Para- and Hetera [n]Metacyclophanes; 2.2.1.5 Dioxa [2.2]Phanes and Oxaza [2.2]Phanes; 2.2.1.6 Enantiomer Separations; 2.2.1.7 Strongly Helical Heteraphanes; 2.2.2 Catenanes, Rotaxanes, and Knotanes of the Heteraphane Type; 2.2.2.1 Template Synthesis of Rotaxanes Using Cyclophane Wheels; 2.2.2.2 Higher Order [n]Rotaxanes via Non-ionic Template Effect; 2.2.2.3 Combination of Anionic and Non-ionic Template 2.2.2.4 Molecular Knots and Similar Macrocycles of the Heteraphane Type2.2.3 Further Heteraphanes, Metallaphanes and Supramolecular Phanes; 2.3 Conclusions; 2.4 Acknowledgement; 2.5 References; 3 Highly Strained Cyclophanes; 3.1 Introduction; 3.2 [n]Metacyclophanes; 3.2.1 Synthesis; 3.2.2 Structures and Physical Properties; 3.2.3 Reactions of Strained [n]Metacyclophanes; 3.2.3.1 Thermal and Photochemical Reactions; 3.2.3.2 Addition Reactions; 3.2.3.3 Reactions with Electrophiles; 3.2.3.4 Reactions with Nucleophiles; 3.3 [n]Paracyclophanes; 3.3.1 Synthesis 3.3.2 Structures and Physical Properties3.3.3 Reactions of Strained [n]Paracyclophanes; 3.3.3.1 Thermal and Photochemical Reactions; 3.3.3.2 Reactions with Electrophiles; 3.3.3.3 Diels-Alder and Other Reactions; 3.3.3.4 Kinetic Stabilization of [4]Paracyclophane Systems; 3.4 Aromaticity of Bent Benzene Rings; 3.5 Cyclophanes containing Polycyclic Aromatic Rings: (2,7)Pyrenophanes; 3.6 [1.1]Paracyclophanes; 3.6.1 Synthesis; 3.6.2 Kinetic Stabilization of [1.1]Paracyclophane Systems; 3.6.3 Structures and Physical Properties; 3.7 References and Notes; 4 Superphanes; 4.1 Introduction 4.2 [n(2)]Cyclopropenonophanes4.2.1 Synthesis; 4.3 Superbridged Cyclopropenyliophanes; 4.4 C(4)-Superphanes; 4.4.1 Properties of Cyclobutadieno Superphanes; 4.4.2 Oxidative Demetallations; 4.5 C(5)-Superphanes; 4.6 Superbridged Benzene Rings; 4.7 Concluding Remarks; 4.8 Acknowledgement; 4.9 References; 5 Carbon-Bridged Ferrocenophanes; 5.1 Introduction; 5.2 Nomenclature; 5.3 Mononuclear Carbon-Bridged Ferrocenophanes; 5.3.1 [1]Ferrocenophanes; 5.3.2 [2]Ferrocenophanes; 5.3.3 [3]Ferrocenophanes; 5.3.4 [4]Ferrocenophanes; 5.3.5 [5]Ferrocenophanes; 5.3.6 [m]Ferrocenophanes (m>5) 5.3.7 Multiply-Bridged Mononuclear Ferrocenophanes ([m](n)Ferrocenophanes) |
| Record Nr. | UNINA-9910877745703321 |
| Weinheim, : Wiley-VCH | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||