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Chemical Science of π-Electron Systems

This book presents the most advanced review available of all aspects of π-electron systems, including novel structures, new synthetic protocols, chemical and physical properties, spectroscopic and computational insights, molecular engineering, device properties, and physiological properties. π-Elect...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor Corporativo: SpringerLink (Online service)
Otros Autores: Akasaka, Takeshi (Editor ), Osuka, Atsuhiro (Editor ), Fukuzumi, Shunichi (Editor ), Kandori, Hideki (Editor ), Aso, Yoshio (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Tokyo : Springer Japan : Imprint: Springer, 2015.
Edición:1st ed. 2015.
Temas:
Acceso en línea:Texto Completo
Tabla de Contenidos:
  • Dibenzopentalenes and Related Compounds
  • Synthesis of a Porphyrin-fused π-Electron System
  • Higher-order π-Electron Systems Based on Helicene Molecules
  • Planar Cyclooctatetraenes and Related Ring Systems: Antiaromaticity and Applications
  • Synthesis, Crystal Structures, and Solid-state Optical Properties of Substituted Tetracenes
  • Chiral Sumanene, Triazasumanene, and Related Buckybowls
  • Heteroatom-containing Sumanenes
  • Open-cage Fullerene Derivatives: Synthesis, Reactions and Encapsulation of a Small Molecule
  • Endohedral Metallofullerenes: From Chemical Reactivity to Material Performance
  • Tuning Physical Properties and Structures of π-Electron System formed by Single-Wall Carbon Nanotubes with Selected Chiralities
  • Recent Progress on the Chemical Reactions of Single-Walled Carbon Nanotubes
  • Novel π-Conjugated Systems Based on N-Confused Porphyrinoids
  • Heteroatom-modified Porphyrinoids
  • Synthesis of Novel Porphyrinoids from Dipyrrins
  • Möbius Aromatic and Antiaromatic Expanded Porphyrins
  • Recent Advances in the Chemistry of Phthalocyanines as Functional Chromophores
  • Localized Singlet 1,3-Diradicals
  • Unique Orbital Interactions in the Ground and Electronically Excited States of Biradicals Brought About by the Existence of "Twisted π -Space"
  • Recent Progress in Stable High-Spin Molecules Based on Nitroxide Radicals
  • Organic Chemistry of Graphene Framework
  • Boron-Containing π-Electron Systems
  • Doubly-Bonded Silicon Compounds Showing Intramolecular Charge Transfer Transitions
  • π-Conjugated Disilenes and Tetrasilacyclobutadiene
  • Tin-containing π-Electron Systems
  • Supramolecular Structures and Photoelectronic Properties of π-Complexes Composed of Self-Assembling Cyclic Porphyrin Dimers and Fullerenes
  • Sequence Control of π-Electron Systems
  • Integrated π-Electron System on Artificial Cell Membranes
  • Supramolecular Porphyrin Nanorods for Light Energy Conversion
  • Metal Nano-particle/Porphyrinoid Hybrids
  • Control of Chiral π-Space in Highly-Organized π-Conjugated Polymer Nanotube Composites and Their Functions
  • Photoinduced Electron-Transfer Functions of π-Electron Donor-Acceptor Supramolecular Complexes
  • Fused π-Electron Systems Containing Group 15 Elements and Their Application to Organic Electronics
  • Fullerene Derivatives for Organic Solar Cells
  • Efficient Organic Devices Based on π-Electron systems: Comparative Study of Fullerene Derivatives Blended with a High Efficiency Naphthobisthiadiazole-Based Polymer for Organic Photovoltaic Applications
  • Solution-processed Organic Thin-film Transistors
  • Unveiling Charge Carrier Transport in π-Conjugated Molecular Wire on Micro and Macroscopic Scales
  • STM Characterization of π-Electron Systems
  • Light Amplification in Low-Dimensional Crystals of Thiophene/Phenylene Co-Oligomer Derivatives
  • Electron Transfer Pathway Analysis in Bacterial Photosynthetic Reaction Center
  • Spectroscopic Analysis of the Redox Reactions of π-Conjugated Cofactors in Photosynthetic Reaction Center
  • Protein-controlled Isomerization in Rhodopsins
  • β-Diketiminates as Redox Non-innocent Supporting Ligands in Coordination Chemistry
  • Novel Functions of π-Electron Systems in a Heme-DNA Complex
  • Increasing the Hole Transfer Rate through DNA by Chemical Modification
  • Theoretical Calculations of Excitation-Energy Transfer.