Designed molecular space in material science and catalysis /
نام عام مواد
[Book]
نام نخستين پديدآور
Seiji Shirakawa, editor.
وضعیت نشر و پخش و غیره
محل نشرو پخش و غیره
Singapore :
نام ناشر، پخش کننده و غيره
Springer,
تاریخ نشرو بخش و غیره
2018.
مشخصات ظاهری
نام خاص و کميت اثر
1 online resource :
ساير جزييات
illustrations (some color)
یادداشتهای مربوط به کتابنامه ، واژه نامه و نمایه های داخل اثر
متن يادداشت
Includes bibliographical references.
یادداشتهای مربوط به مندرجات
متن يادداشت
?-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.
متن يادداشت
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.
متن يادداشت
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.
بدون عنوان
0
بدون عنوان
8
بدون عنوان
8
یادداشتهای مربوط به خلاصه یا چکیده
متن يادداشت
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.
یادداشتهای مربوط به سفارشات
منبع سفارش / آدرس اشتراک
Springer Nature
شماره انبار
com.springer.onix.9789811312564
ویراست دیگر از اثر در قالب دیگر رسانه
عنوان
Designed molecular space in material science and catalysis.