Designed molecular space in material science and catalysis /
General Material Designation
[Book]
First Statement of Responsibility
Seiji Shirakawa, editor.
.PUBLICATION, DISTRIBUTION, ETC
Place of Publication, Distribution, etc.
Singapore :
Name of Publisher, Distributor, etc.
Springer,
Date of Publication, Distribution, etc.
2018.
PHYSICAL DESCRIPTION
Specific Material Designation and Extent of Item
1 online resource :
Other Physical Details
illustrations (some color)
INTERNAL BIBLIOGRAPHIES/INDEXES NOTE
Text of Note
Includes bibliographical references.
CONTENTS NOTE
Text of Note
?-Electronic Ion-Pairing Supramolecular Assemblies -- Molecular Space Chemistry Based on Pillar[n]arenes -- Inherently Chiral Calix[4]arenes as Supramolecular Catalysts -- Synthesis of the Longest Carbohelicene by Multiple Oxidative Photocyclizations of Arylene-Vinylene Oligomers -- Design of the Chiral Environment for Asymmetric Acid-Base Catalysis -- Biaryl Amino Acids and Their Surrogates: A Unique Class of Unnatural Amino Acid -- Interplay of Diamides and Rare Earth Metals: Specific Molecular Spaces and Catalytic Activity -- Control of Chiral Molecular Space Using Helical Polymers -- Functional Supramolecular Materials Formed by Non-covalent Bond -- Photo-responsive Dynamic Molecular Catalyst for Spatiotemporal Control of Chemical Reactions -- Mimicking Integrated Functions of "Molecular Space" in Biological Systems by Using Crystalline Cavities Consisting of Short Peptides.
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4.3 Helicene Synthesis by Oxidative Photocyclization4.4 Synthetic Guideline for Precursor Stilbenes Toward Longer Helicenes; 4.5 [9]Helicene; 4.6 [16]Helicene; 4.6.1 TIPSO-[2]+[1]+[1]+[2]+[1]+[1]+[2]-OTIPS Precursor; 4.6.2 Sextuple Photocyclization; 4.6.3 X-Ray Crystal Structure; 4.6.4 Conversion to Unsubstituted [16]Helicene; 4.7 Conclusion; References; Chapter 5: Design of the Chiral Environment for Asymmetric Acid-Base Catalysis; 5.1 Introduction; 5.2 Conformationally Flexible Guanidine/Bisthiourea Organocatalysts; 5.2.1 Enantiodivergent Mannich-Type Reactions.
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Chapter 3: Inherently Chiral Calix[4]arenes as Supramolecular Catalysts3.1 Introduction; 3.2 Inherently Chiral Calix[4]arenes with ABCC Substitution Pattern; 3.2.1 Aminophenol-Type Inherently Chiral Calix[4]arenes; 3.2.2 Inherently Chiral Calix[4]arene Amino Acid and its Derivatives; 3.3 Inherently Chiral Calix[4]arenes with ABCD Substitution Pattern; 3.4 Conclusions; References; Chapter 4: Synthesis of the Longest Carbohelicene by Multiple Oxidative Photocyclizations of Arylene-Vinylene Oligomers; 4.1 Introduction; 4.2 History of Longer Carbohelicenes.
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SUMMARY OR ABSTRACT
Text of Note
This book focuses on molecular space chemistry, which is recognized as an important concept for the design of novel functional materials and catalysts. A wide variety of topics and ideas included in this book are based on that concept. The book showcases recent representative examples of molecular space design to create functional materials and catalysts possessing unique properties. This unique volume will be of great interest to chemists in a wide variety of research fields, including organic, inorganic, biological, polymer, and supramolecular chemistry. Readers will obtain new ideas and directions to create novel functional molecules, and those ideas will lead to innovative views of science.
ACQUISITION INFORMATION NOTE
Source for Acquisition/Subscription Address
Springer Nature
Stock Number
com.springer.onix.9789811312564
OTHER EDITION IN ANOTHER MEDIUM
Title
Designed molecular space in material science and catalysis.