Molecular Nanographenes - Synthesis, Properties, and Applications
Reduzierte Artikel in dieser Kategorie
38,99 €
| Verlag | Wiley-VCH |
| Auflage | 2025 |
| Seiten | 544 |
| Format | 17,8 x 3,2 x 24,4 cm |
| Gewicht | 1148 g |
| Artikeltyp | Englisches Buch |
| EAN | 9783527353224 |
| Bestell-Nr | 52735322A |
This book aims to overview the variety of nanographenes. Their diverse morphologies, mostly stemming from their structural defects, different approaches of synthesis, their singular chiroptical and photophysical properties and potential applications are covered in this book. Includes both top-down approach where nanographenes are obtained from graphite by fragmentation of pristine graphene by chemical methods, leading to non-homogeneous NGs (flakes) without control of their size and shape and bottom down approach is using standard synthetic chemical protocols resulting in homogeneous and well-defined discrete molecules with a full control on their size and shape.
Inhaltsverzeichnis:
Fundamental Concepts in Nanographenes
1. Aromaticity and Antiaromaticity in Nanographenes: An Overview
2. Covalent Patterned Functionalization of Graphene
3. Nanographenes by Bottom-up Approach: The Scholl Reaction
4. Racemization barriers in chiral molecular nanographenes
Synthesis of Molecular Nanographenes
5. Synthesis of Helicenes
6. Carbon Nanobelts
7. Negatively Curved Nanographenes
8. Highly-strained Cyclophanes and other Nanographenes
9. Chiral Bilayer Nanographenes: Synthesis and Properties
10. Large p-Extended Carbon Nanorings: From Synthesis to Properties
11. Nanographenes with Multiple Zigzag Edges
12. Monkey Saddles and other Contorted Polycyclic Aromatic Compounds
13. Conjugated Nanohoops: Synthesis, Properties and Applications
14. Synthesis of Graphene Nanoribbons, Nanographenes and Fused Aromatic Networks Through the Formation of Pyrazine Rings
15. On-surface Synthesis of p-conjugated polymers
16. Merging orga nic chemistry with surface synthesis for the preparation of nanographenes
Properties and Applications of Molecular Nanographenes
17. Chiral Materials from Perylene Diimide Building Blocks: Twistacenes and Helicenes
18. Circularly Polarized Luminescence (CPL) in Nanographenes
19. Open-shell Nanographenes
20. Kekulé and Non-Kekulé Nanographenes: A Magnetic Perspective
21. Redox Properties of Nanographenes
