Molecular Nanographenes
portes grátis
Molecular Nanographenes
Synthesis, Properties, and Applications
Martin, Nazario; Nuckolls, Colin
Wiley-VCH Verlag GmbH
04/2025
426
Dura
9783527353224
Pré-lançamento - envio 15 a 20 dias após a sua edição
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FUNDAMENTAL CONCEPTS IN NANOGRAPHENES
1. Aromaticity and Antiaromaticity: An Overview
2. Nanographenes by Top-Down Approach
3. Nanographenes by Bottom-up Approach: The Scholl Reaction
4. Chiral Molecular Nanographenes: the critical value of the racemization barrier
SYNTHESIS OF MOLECULAR NANOGRAPHENES
5. Synthesis of Helicenes
6. Synthesis of Nanographenes: The Annulative p-Extension (APEX) Approach
7. An Organic Chemistry Approach to Precise Synthesis of Curved Nanocarbons
8. Highly-strained Cyclophanes and other Nanographenes
9. Pi-Conjugated Molecular Nanorings: Synthesis and Properties
10. Chiral Bilayer Nanographenes: Synthesis and Properties
11. Large p-Extended Carbon Nanorings: From Synthesis to Properties
12. Synthesis of Some Challenging Molecular Carbons
13. Monkey Saddles and other Contorted Polycyclic Aromatic Compounds
14. Conjugated Nanohoops: Synthesis and Properties
15. Heteronanogrpahenes
16. On-surface Synthesis of 1D Nanographenes
17. Tailored Synthesis of Nanographenes
PROPERTIES AND APPLICATIONS OF MOLECULAR NANOGRAPHENES
18. Chiral Materials from Perylene Diimide Building Blocks: Twistacenes and Helicenes
19. Circularly Polarized Luminescence (CPL) in Nanographenes
20. Open-shell Nanographenes
21. Non-Kekule and Kekule Hydrocarbons
22. Redox Properties of Nanographenes
23. Supramolecular Assembly of Curved Carbon-Rich Molecules
1. Aromaticity and Antiaromaticity: An Overview
2. Nanographenes by Top-Down Approach
3. Nanographenes by Bottom-up Approach: The Scholl Reaction
4. Chiral Molecular Nanographenes: the critical value of the racemization barrier
SYNTHESIS OF MOLECULAR NANOGRAPHENES
5. Synthesis of Helicenes
6. Synthesis of Nanographenes: The Annulative p-Extension (APEX) Approach
7. An Organic Chemistry Approach to Precise Synthesis of Curved Nanocarbons
8. Highly-strained Cyclophanes and other Nanographenes
9. Pi-Conjugated Molecular Nanorings: Synthesis and Properties
10. Chiral Bilayer Nanographenes: Synthesis and Properties
11. Large p-Extended Carbon Nanorings: From Synthesis to Properties
12. Synthesis of Some Challenging Molecular Carbons
13. Monkey Saddles and other Contorted Polycyclic Aromatic Compounds
14. Conjugated Nanohoops: Synthesis and Properties
15. Heteronanogrpahenes
16. On-surface Synthesis of 1D Nanographenes
17. Tailored Synthesis of Nanographenes
PROPERTIES AND APPLICATIONS OF MOLECULAR NANOGRAPHENES
18. Chiral Materials from Perylene Diimide Building Blocks: Twistacenes and Helicenes
19. Circularly Polarized Luminescence (CPL) in Nanographenes
20. Open-shell Nanographenes
21. Non-Kekule and Kekule Hydrocarbons
22. Redox Properties of Nanographenes
23. Supramolecular Assembly of Curved Carbon-Rich Molecules
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Graphene; chiroptics; optoelectronics; non-homogenous nanographenes; planar geometry; bilayer geometry; nanoribbon geometry; nanobelt geometry; bandgap; lattice nanostructure; graphite; photophysical analysis; discrete molecules
FUNDAMENTAL CONCEPTS IN NANOGRAPHENES
1. Aromaticity and Antiaromaticity: An Overview
2. Nanographenes by Top-Down Approach
3. Nanographenes by Bottom-up Approach: The Scholl Reaction
4. Chiral Molecular Nanographenes: the critical value of the racemization barrier
SYNTHESIS OF MOLECULAR NANOGRAPHENES
5. Synthesis of Helicenes
6. Synthesis of Nanographenes: The Annulative p-Extension (APEX) Approach
7. An Organic Chemistry Approach to Precise Synthesis of Curved Nanocarbons
8. Highly-strained Cyclophanes and other Nanographenes
9. Pi-Conjugated Molecular Nanorings: Synthesis and Properties
10. Chiral Bilayer Nanographenes: Synthesis and Properties
11. Large p-Extended Carbon Nanorings: From Synthesis to Properties
12. Synthesis of Some Challenging Molecular Carbons
13. Monkey Saddles and other Contorted Polycyclic Aromatic Compounds
14. Conjugated Nanohoops: Synthesis and Properties
15. Heteronanogrpahenes
16. On-surface Synthesis of 1D Nanographenes
17. Tailored Synthesis of Nanographenes
PROPERTIES AND APPLICATIONS OF MOLECULAR NANOGRAPHENES
18. Chiral Materials from Perylene Diimide Building Blocks: Twistacenes and Helicenes
19. Circularly Polarized Luminescence (CPL) in Nanographenes
20. Open-shell Nanographenes
21. Non-Kekule and Kekule Hydrocarbons
22. Redox Properties of Nanographenes
23. Supramolecular Assembly of Curved Carbon-Rich Molecules
1. Aromaticity and Antiaromaticity: An Overview
2. Nanographenes by Top-Down Approach
3. Nanographenes by Bottom-up Approach: The Scholl Reaction
4. Chiral Molecular Nanographenes: the critical value of the racemization barrier
SYNTHESIS OF MOLECULAR NANOGRAPHENES
5. Synthesis of Helicenes
6. Synthesis of Nanographenes: The Annulative p-Extension (APEX) Approach
7. An Organic Chemistry Approach to Precise Synthesis of Curved Nanocarbons
8. Highly-strained Cyclophanes and other Nanographenes
9. Pi-Conjugated Molecular Nanorings: Synthesis and Properties
10. Chiral Bilayer Nanographenes: Synthesis and Properties
11. Large p-Extended Carbon Nanorings: From Synthesis to Properties
12. Synthesis of Some Challenging Molecular Carbons
13. Monkey Saddles and other Contorted Polycyclic Aromatic Compounds
14. Conjugated Nanohoops: Synthesis and Properties
15. Heteronanogrpahenes
16. On-surface Synthesis of 1D Nanographenes
17. Tailored Synthesis of Nanographenes
PROPERTIES AND APPLICATIONS OF MOLECULAR NANOGRAPHENES
18. Chiral Materials from Perylene Diimide Building Blocks: Twistacenes and Helicenes
19. Circularly Polarized Luminescence (CPL) in Nanographenes
20. Open-shell Nanographenes
21. Non-Kekule and Kekule Hydrocarbons
22. Redox Properties of Nanographenes
23. Supramolecular Assembly of Curved Carbon-Rich Molecules
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
