Anmerkung: Intro -- Preface -- Contents -- 1 Hydrogen Bonding-Controlled Photoinduced Electron and Energy Transfer -- Abstract -- 1.1 Introduction -- 1.2 Basic Theories for Photoinduced Electron and Energy Transfer -- 1.2.1 Photoinduced Electron Transfer (PET) Processes -- 1.2.2 Photoinduced Energy Transfer Processes -- 1.3 Hydrogen Bonding-Controlled Photoinduced Electron Transfer -- 1.3.1 Mechanistic Studies -- 1.3.2 Electron Transfer Based on Double and Triple Hydrogen Bonding -- 1.3.3 Photoinduced Electron Transfer Based on Quadruply and Multiple Hydrogen Bonding -- 1.3.4 Applications of Hydrogen Bonding-Based Photoinduced Electron Transfer -- 1.4 Hydrogen Bonding-Controlled Photoinduced Energy Transfer -- 1.4.1 Photoinduced Energy Transfer Based on Triple Hydrogen Bonding -- 1.4.2 Energy Transfer Based on Quadruply Hydrogen Bonding and Its Applications -- 1.5 Summary and Outlook -- Acknowledgments -- References -- 2 Hydrogen Bonding in Supramolecular Nanoporous Materials -- Abstract -- 2.1 Introduction -- 2.2 Supramolecular Hydrogen Bonded Nanoporous Frameworks -- 2.2.1 Two-dimensional Hydrogen Bonded Nanoporous Networks -- 2.2.2 Three-dimensional Hydrogen Bonded Molecular Nanoporous Networks -- 2.3 Hydrogen Bonding in Block Copolymers as Nanoporous Networks -- 2.4 Hydrogen Bonding in Liquid Crystals as Nanoporous Networks -- 2.5 Conclusions and Outlook -- Ackowledgement -- References -- 3 Hydrogen Bonding for the Self-assembly of Organogels and Hydrogels -- Abstract -- 3.1 Introduction -- 3.2 Type of Organogels and Hydrogels Relevant to Hydrogen Bonding -- 3.2.1 Amino Acid and Amide Based Gels -- 3.2.2 Urea-Based Gels -- 3.2.3 Sugar-Based Organogels -- 3.2.4 Two Component Gels Based on Amino Acid Interaction -- 3.2.5 Multiple Hydrogen Bonding Interactions in Organogels -- 3.3 The Adjustment of the Hydrogen Bonding. , 3.3.1 Hydrogen Bonding Tuned by the Alkane Chain -- 3.3.2 Gelation Tuned by the Number and Position of the Hydrogen Bonding Sites -- 3.3.3 Hydrogen Bonding Tuned by Anions -- 3.3.4 Hydrogen Bonding Gelation Tuned by Enzymes and Proteins -- 3.3.5 Hydrogen Bonding Tuned by Sonication -- 3.4 Conclusions and Outlook -- Acknowledgments -- References -- 4 Designing Charge-Assisted Hydrogen Bonded Supramolecular Gelators -- Abstract -- 4.1 Introduction -- 4.2 Designing LMWGs -- 4.2.1 Molecular Engineering Approach -- 4.2.2 Supramolecular Synthon Approach in the Context of Crystal Engineering -- 4.2.2.1 Secondary Ammonium Monocarboxylate (SAM) Synthon -- 4.2.2.2 Secondary Ammonium Dicarboxylate (SAD) Synthon -- 4.2.2.3 Primary Ammonium Monocarboxylate (PAM) Synthon -- 4.2.2.4 Primary Ammonium Dicarboxylate (PAD) Synthon -- 4.2.2.5 Diprimary Ammonium Monocarboxyate (DPAM) Synthon -- 4.2.2.6 Diprimary Ammonium Dicarboxylate (DPAD) Synthon -- 4.2.2.7 Organic Salt-Based Supramolecular Synthons Versus Gelation -- 4.3 Conclusion -- Acknowledgments -- References -- 5 Hydrogen Bonding for Supramolecular Liquid Crystals -- Abstract -- 5.1 Introduction -- 5.2 Supramolecular Rodlike LCs -- 5.3 Supramolecular Columnar LCs from Hydrogen Bonded Discotic or Non-discotic Complex -- 5.3.1 Supramolecular Columnar LCs Containing Close-Type Hydrogen Bonds -- 5.3.2 One or Two-Dimensional Open-Type Assembly -- 5.3.3 Columnar Phase from Hydrogen Bonded Non-discotic Shape -- 5.4 Nonconventional Liquid Crystal with Open-Type Network of Hydrogen Bonds -- 5.4.1 Polyhydroxy Amphiphiles -- 5.4.2 Star-Shaped Block Molecules -- 5.4.3 Bolaamphiphiles -- 5.4.4 Imidazolium-Based Rodlike Ionic Liquid Crystals -- 5.4.5 Complicated 3D Cubic Phases from Triazol-Based Triblock Polyphiles and 2-Thienyl-4,6-diamino-1,3,5-triazines -- 5.4.5.1 Triazol-Based Triblock Polyphiles. , 5.4.5.2 2-Thienyl-4,6-diamino-1,3,5-triazines -- 5.5 Summary and Conclusion -- References -- 6 Hydrogen Bonding for Molecular, Macromolecular, and Supramolecular Materials -- Abstract -- 6.1 Introduction -- 6.2 Molecular Conformational Switching -- 6.3 Self-Healing Organic Materials -- 6.4 Artificial Antenna and Photosynthetic Systems -- 6.5 Dye-Sensitized Solar Cells -- 6.6 Organic Photovoltaic Materials -- 6.7 Organic Light-Emitting Diodes -- 6.8 Organic Field-Effect Transistor -- 6.9 Conclusion and Perspectives -- References.

Anmerkung: Intro -- Preface -- Contents -- 1 Hydrogen Bonding Motifs: New Progresses -- Abstract -- 1.1 Hydrogen Bonding: The Basic Aspects -- 1.1.1 Definition -- 1.1.2 Hydrogen Bonding Donors and Acceptors -- 1.1.3 The Strength of the Hydrogen Bond -- 1.1.4 Hydrogen Bonding Formed by a Single Functional Group -- 1.2 Intramolecular Hydrogen Bonding -- 1.2.1 The O--H00B700B700B7X Hydrogen Bonding -- 1.2.2 The N--H00B700B700B7X Hydrogen Bonding -- 1.3 Intermolecular Hydrogen Bonding -- 1.3.1 Double Hydrogen Bonding -- 1.3.2 Triple Hydrogen Bonding -- 1.3.3 Quadruple Hydrogen Bonding -- 1.4 Conclusion -- Acknowledgments -- References -- 2 Understanding of Noncovalent Interactions Involving Organic Fluorine -- Abstract -- 2.1 Introduction -- 2.1.1 Why Fluorine Is So Special? -- 2.2 Debate on Participation of Fluorine as a Hydrogen Bond Donor: Overview of the Weak X--H00B700B700B7F--C -- X = N, O, C Hydrogen Bond -- 2.3 Inputs from Other Interactions Involving Organic Fluorine -- 2.3.1 Insight into Halogen--Halogen Interactions Involving Fluorine -- 2.3.2 Insights into Halogen Bond Formation Involving Fluorine (C--F00B700B700B7X -- X = Halogen, N, O, S) -- 2.4 Conclusions -- Acknowledgments -- References -- 3 Hydrogen Bonding in Supramolecular Crystal Engineering -- Abstract -- 3.1 Introduction -- 3.2 Crystal Engineering Strategies -- 3.2.1 Supramolecular Synthons and Retrosynthesis -- 3.2.2 Reticular Synthesis -- 3.3 Hydrogen Bonding -- 3.3.1 Definition and Scopes -- 3.3.2 Description of Hydrogen Bonding Motifs: The Graph Sets -- 3.3.3 Hydrogen Bonding Rules -- 3.4 Interpenetration -- 3.5 Hydrogen Bonding Structures -- 3.5.1 Discrete Hydrogen Bonding Capsules -- 3.5.1.1 Dimeric Capsules -- 3.5.1.2 Hexameric Capsules -- 3.5.1.3 A Quasi-truncated Octahedron -- 3.5.2 1D Infinite Hydrogen Bonding Nanotubes -- 3.5.2.1 Tubes Constructed from Flat Macrocycles. , 3.5.2.2 Tubes Constructed from Calixarenes -- 3.5.2.3 Tubes Constructed from Acyclic Molecules -- 3.5.3 2D and 3D Borromean Arrayed Organic Crystals -- 3.5.4 2D 2192 3D Parallel Polycatenated Structures -- 3.5.5 3D Interpenetrated dia and pcu Frameworks -- 3.5.6 Unusual Aggregation Phase of Water Molecules -- 3.6 Applications -- 3.6.1 Crystal Engineering of Solid State Photochemical Reactions -- 3.6.1.1 Self-complementary Reactants -- 3.6.1.2 Auxiliary Templates -- 3.6.1.3 Confined Environments of Cavities -- 3.6.2 Gas Adsorption and Separation -- 3.6.3 Crystal Engineering of Pharmaceutical Cocrystals -- References -- 4 Hydrogen Bonding-Mediated Self-assembly of Aromatic Supramolecular Duplexes -- Abstract -- 4.1 Introduction -- 4.2 Oligoamide-Based Molecular Duplex Strands -- 4.2.1 Oligoamide-Based Molecular Duplex Strands -- 4.2.2 Applications -- 4.3 Oligohydrazide-Based Molecular Duplex Strands -- 4.3.1 From Supramolecular Zipper to Quadruple Hydrogen-Bonded Heterodimer -- 4.3.2 Strict Self-complementary Oligohydrazide-Based Duplexes -- 4.3.3 Shuttle Movement -- 4.3.4 Mutual Responsive Low Molecular Mass Organic Gelators -- 4.3.5 Supramolecular Substitution -- 4.3.6 Amide-Urea-Based Molecular Duplexes -- 4.3.7 ``Hao'' Templated Molecular Duplex -- 4.4 ``Covalent Casting'' Strategy-Based Molecular Duplexes -- 4.5 Other Molecular Duplex Strands -- 4.6 Conclusions and Outlook -- References -- 5 Hydrogen Bonding-Driven Anion Recognition -- Abstract -- 5.1 Introduction -- 5.2 Amide-Based Anion Recognition -- 5.3 Urea-Based Anion Recognition -- 5.4 Pyrrole-Based Anion Recognition -- 5.5 CH Donor-Based Anion Recognition -- 5.6 OH-Based Anion Recognition -- 5.7 Conclusion -- References -- 6 Formation of Hydrogen-Bonded Self-assembled Structures in Polar Solvents -- Abstract -- 6.1 Introduction -- 6.2 Nucleobase Pairing and Nanostructure Formation in Water. , 6.3 Self-sorting/Orthogonal Self-assembly -- 6.4 Supramolecular Polymers -- 6.5 Supramolecular Gels in Aqueous and Polar Organic Media -- 6.6 Vesicles, Bilayers, Micelles Through H-Bonding -- References -- 7 Hydrogen Bonded Capsules: Chemistry in Small Spaces -- Abstract -- 7.1 Why Study Encapsulated Molecules? -- 7.2 The Capsules and Their Contents -- 7.2.1 The Tennis Ball -- 7.2.2 The Softball -- 7.2.3 A Cylindrical Capsule -- 7.2.4 The Volleyball -- 7.3 What's It Like Inside the Capsules? -- 7.4 How Do Molecules Get In and Out of the Capsules? -- 7.5 Amplified Intermolecular Forces -- 7.6 Arrangements in Encapsulation Space: New Stereochemistry -- 7.6.1 Social Isomers -- 7.6.2 Single Molecule Solvation -- 7.6.3 Isotope Effects -- 7.6.4 Constellations -- 7.6.5 Diastereomers -- 7.7 Chiral Spaces -- 7.8 Reactivity -- 7.9 Conclusion -- Acknowledgments -- References -- 8 Hydrogen Bonded Organic Nanotubes -- Abstract -- 8.1 Introduction -- 8.2 Strategies for the Construction of Hydrogen Bonding-Driven Organic Nanotubes -- 8.3 Nanotubes from Hydrogen Bonding-Induced Helical Structures -- 8.4 Nanotubes from Tubular Molecules -- 8.5 Nanotubes from Hydrogen Bonded Rod-like Molecular Units -- 8.6 Nanotubes from Hydrogen Bonded Cyclic Molecules -- 8.6.1 Nanotubes from Hydrogen Bonded Cyclic Peptides -- 8.6.2 Nanotubes from Hydrogen Bonded Cyclic Ureas -- 8.7 Nanotubes from Hydrogen Bonded Wedge- or Sector-like Molecules -- 8.8 Conclusions and Outlooks -- References -- 9 H-Bonding-Assisted One-Pot Macrocyclization for Rapid Construction of H-Bonded Macrocyclic Aromatic Foldamers -- Abstract -- 9.1 Introduction -- 9.2 Concept Formulation -- 9.3 Aryl Amide Macrocycles -- 9.3.1 Non-fivefold Symmetric Aryl Amide Macrocycles -- 9.3.2 Fivefold Symmetric Aryl Amide Macrocycles -- 9.3.2.1 Evolution of Fivefold Symmetric Macrocycles. , 9.3.2.2 Fivefold Symmetric Macrocyclic Alkoxybenzene Pentamers -- 9.3.2.3 Fivefold Symmetric Macrocyclic Pyridone Pentamers -- 9.3.3 Highly Selective Production of Strained Aromatic Hexamers -- 9.3.4 Chemo- and Regio-Selective Demethylations -- 9.4 Macrocycles Containing Non-amide Linkages -- 9.5 Mechanism of One-Pot Macrocyclization -- 9.5.1 Variable Functionalizations Around the Pentameric Periphery -- 9.5.2 A Chain-Growth Mechanism Underlying the Formation of Aromatic Pentamers -- 9.5.3 A Non-chain Growth Mechanism Underlying the Formation of Strained Aromatic Hexamers and Heptamers -- 9.6 Conclusion -- References -- 10 Hydrogen-Bonded Supramolecular Polymers -- Abstract -- 10.1 Introduction -- 10.2 Hydrogen-Bonding Building Blocks -- 10.3 Hydrogen-Bonded Main-Chain Supramolecular Polymers Constructed by Low-Molecular-Weight Monomers -- 10.4 Hydrogen-Bonded Supramolecular Polymers Constructed by High-Molecular-Weight Conventional Polymers that Are Functionalized by Hydrogen-Bonded Motifs -- 10.4.1 Telechelic Supramolecular Polymers -- 10.4.2 ``Side-Chain'' Supramolecular Polymer Networks -- 10.5 Supramolecular Polymers Constructed by Orthogonal Hydrogen Bonding-Driven Self-assembly and Other Non-covalent Interactions -- 10.6 Conclusions -- References.