| Description |
1 online resource (xv, 313 pages) : illustrations (1 color) |
| Series |
Monographs in supramolecular chemistry ; number 2 |
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Monographs in supramolecular chemistry ; no. 2.
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| Contents |
Cover -- Preface -- Contents -- Chapter 1 -- 1.1 The Origins of Cyclophane Chemistry -- 1.2 Molecular Shape: An Experimental Calibration of the Space Occupancy of Atoms and FunctionalGroups -- 1.3 Probing Weak Non-covalent Interactions Between Chromophores in Rigid, GeometricallyDefined Cyclophane Frames -- 1.3.1 Transannular Interactions in Cyclophanes -- 1.3.2 Models for Intermolecular Excimers and Exciplexes -- 1.3.3 Donor-Acceptor Cyclophanes as Models forIntermolecular Charge-transfer Complexes |
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2.4 Aggregation Behavior of Cyclophanes in Aqueous Solution -- 2.5 Complexes of Polycyclic Aromatic Hydrocarbons -- 2.6 Complexes of Naphthalene Derivatives -- 2.6.1 Determination of Stoichiometry and Stability of Solution Complexes -- 2.6.2 Complexation of Neutral Naphthalene Derivatives -- 2.7 Complexes of Benzene Derivatives -- 2.7.1 Complexation of Flat Benzene Derivatives -- 2.7.2 Complexes of [m.n]Paracyclophanes -- 2.8 Complexes of Heteroaromatic Substrates -- 2.9 Complexes of Aliphatic Substrates -- Chapter 3 -- 3.1 Introduction -- 3.2 Complexation of Polycyclic Arenes |
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3.2.1 Structural Factors Determining the Complexation Strength -- 3.2.2 The Strength of Molecular Complexation of Arenes in Water and in Organic Solvents is Predictable by Linear Free Energy Relationships -- 3.3 Electron Donor-Acceptor Interactions Stabilize Inclusion Complexes of Aromatic Guests -- 3.4. The Cryptophanes: Shape-selective Inclusion Complexation of Methane Derivatives -- 3.5 From Cavitands to Hemicarcerands to Carcerands: Increasing the Barriers for Escape of Encapsulated Organic Molecules -- 3.5.1 Cavitands for Small Linear Guests |
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3.5.2 Strong Dimer Formation between Kite-type Molecules inOrganic Solvents -- 3.5.3 Carcerands: Closed-surface Hosts that Imprison Guests behind Covalent Bars -- 3.5.4 Hemicarcerands: Guest Exchange with High Structural Recognition and Activation Free Energies -- 3.6 Apolar Complexation Strength in Binary Solvent Mixtures -- Chapter 4 -- 4.1 Introduction -- 4.2 High Guest Selectivity in the Inclusion Complexation of Charged Aromatic Compounds -- 4.3 Ion-Dipole Effect as a Force for Molecular Recognition |
| Summary |
Cyclophanes are bridged aromatic compounds and represent the central class of synthetic receptors in molecular recognition. All types of substrates, from inorganic and organic cations and anions, to neutral molecules have been complexed by tailor-made cyclophanes. This monograph focuses on the principles of supramolecular complexation and catalysis. It provides a state-of-the-art review of the intermolecular forces that hold together the supramolecular complexes of cyclophanes with neutral and charged organic molecules in the liquid phase. Cyclophanes also demonstrates the characteristics and advantages of bridged aromatic compounds as receptors. The book has great clarity, is very readable and will be extremely useful in both teaching and research |
| Bibliography |
Includes bibliographical references and indexes |
| Notes |
Print version record |
| Subject |
Cyclophanes.
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Polycyclic aromatic compounds.
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Cyclophanes.
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Polycyclic aromatic compounds.
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Cyclophane
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Chimie supramoléculaire.
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Cyclophanes.
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Composés aromatiques.
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| Form |
Electronic book
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| Author |
Royal Society of Chemistry (Great Britain)
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| ISBN |
9781788010924 |
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1788010922 |
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0851869661 |
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9780851869667 |
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