Fundamentals of Porphyrin Chemistry
John Wiley & Sons Inc (Verlag)
978-1-119-12928-8 (ISBN)
In Fundamentals of Porphyrin Chemistry: A 21st Century Approach, a team of distinguished researchers delivers a compact and accessible introduction to the broad field of porphyrin chemistry. It discusses the basics of porphyrin synthesis and structure, as well as that of related molecules, and the current and future roles that porphyrins play in chemical transformations, materials design and synthesis, energy capture and transduction, human health, and the environment.
This edited volume is a self-contained tutorial on concepts of critical importance to porphyrin chemistry and serves as the foundation for discussions about the applications of porphyrin-related compounds found in the second volume. This book contains:
A thorough introduction to porphyrins, including their structure, nomenclature, naturally occurring porphyrins, synthetic porphyrins, and common families of porphyrin-related compounds
Comprehensive explorations of chemical porphyrin synthesis, including how to synthesize porphyrins from simple, symmetric, and advanced ABCD-substituted porphyrins
Practical discussions of the physical characteristics of porphyrins, including their structural features, electronic structure, spectroscopy, magnetism, electrochemistry, and electron transfer processes
Perfect for experienced academic researchers in the field of porphyrin chemistry seeking a quick reference, Fundamentals of Porphyrin Chemistry: A 21st Century Approach is also an indispensable resource for researchers new to the field who need an overview directing them to literature in more focused areas.
Penelope J. Brothers is Director of the Research School of Chemistry at the Australian National University, and Honorary Professor at the School of Chemical Sciences at the University of Auckland in New Zealand. Mathias O. Senge, is Professor and Chair of Organic Chemistry at Trinity College Dublin and Hans Fischer Senior Fellow at the Institute of Advanced Study of the Technical University Munich.
Volume 1
List of Contributors xiii
1 An Introduction to Porphyrins for the Twenty-First Century 1
Penelope J. Brothers and Mathias O. Senge
1.1 Why Porphyrins? 1
1.2 The Natural World of Porphyrins 3
1.3 Brief History of Porphyrins 4
1.4 Practical Applications 5
1.5 Porphyrins for the Twenty-First Century 7
2 It's All in the Name 9
Mathias O. Senge
2.1 Basic Structure and Nomenclature of Porphyrins 9
2.2 General Classes of Porphyrin Systems 11
2.3 Naturally Occurring Porphyrins 15
2.4 Special Aspects of Porphyrin Nomenclature 24
2.5 Porphyrin Stenography 30
3 Organic Synthesis and Reactivity of Porphyrins 37
Mathias O. Senge and Alina Meindl
3.1 Introduction 37
3.2 Synthesis of meso-Substituted Porphyrins from Pyrrole Building Blocks 39
3.3 Synthesis of Β-Substituted Porphyrins from Pyrrole Building Blocks 52
3.4 Total Synthesis of Other Porphyrin(oid)s 57
3.5 Reactivity of Porphyrins 66
3.6 Transition-Metal-Catalyzed Reactions at the Porphyrin Macrocycle 79
3.7 Peripheral Functionalization 91
3.8 Examples of Classic and Contemporary Target Systems 103
4 Coordination Chemistry 141
Penelope J. Brothers and Abhik Ghosh
4.1 Introduction 142
4.2 Overview of the Coordination Chemistry of Porphyrin and its Analogues 143
4.3 Metallation, Demetallation, and Characterization 152
4.4 Main Group Elements 158
4.5 Transition Metals 170
4.6 Lanthanides and Actinides 197
4.7 Organometallic Porphyrin Complexes 204
5 Phthalocyanines and Porphyrazines 241
Ümit Isci and Fabienne Dumoulin
5.1 Phthalocyanines and Porphyrazines: Structures and Syntheses of Peculiar Members of the Porphyrin Family 241
5.2 Synthetic Methods and Strategies 247
5.3 Preparation and Characterization of Precursors 250
5.4 Formation of Macrocycles with Asymmetric Substitution Patterns 262
5.5 Lanthanide Double- and Multi-Decker Derivatives 272
5.6 Other Double- and Multi-Decker Derivatives 276
5.7 Reactions on Phthalocyanines and Porphyrazines 278
5.8 Conclusion 289
6 Oxidation and Reduction of Porphyrins 303
Christian Brückner and Nisansala Hewage
6.1 Introduction: Scope and Limits of This Chapter 303
6.2 Reductions of Porphyrins 304
6.3 Oxidations of Porphyrins 311
6.4 Metal-Centered and Resonance-Stabilized Π-System Redox Events 330
7 Corroles and Contracted Porphyrins 349
Daniel T. Gryko and Mariusz Tasior
7.1 Introduction 349
7.2 Corroles 349
7.3 Isocorroles 368
7.4 N-Confused Corroles 369
7.5 Heteroanalogues of Corroles 369
7.6 Norcorroles 373
7.7 Outlook 374
8 Heteroporphyrins and Carbaporphyrins 385
Timothy D. Lash
8.1 Introduction 385
8.2 Mono- and Diheteroporphyrins (O, S, Se, Te) 386
8.3 Tetraoxa-, Tetrathia-, and Tetraselenaporphyrin Dications 397
8.4 Phosphaporphyrins 400
8.5 Carbaporphyrinoid Systems 402
8.6 True Carbaporphyrins 405
8.7 Azuliporphyrins 416
8.8 Neo-Confused Porphyrins 427
8.9 Benziporphyrins 427
8.10 Miscellaneous Carbaporphyrinoid Systems 434
8.11 Dicarbaporphyrinoids 439
8.12 Tetracarbaporphyrinoids 445
8.13 Related Porphyrin Analogues 447
8.14 Conclusions 448
9 Expanded Porphyrins 453
Atsuhiro Osuka and Takayuki Tanaka
9.1 Historical Background 453
9.2 One-Pot Synthesis of Expanded Porphyrins 455
9.3 Size-Selective Syntheses of Expanded Porphyrins 461
9.4 Möbius Aromatic Expanded Porphyrins 466
9.5 Giant Expanded Porphyrins 471
References 473
Volume 2
List of Contributors xiii
10 Fundamentals of Porphyrin and Metalloporphyrin Stereochemistry 479
W. Robert Scheidt
11 Porphyrins: Electronic Structure and Ultraviolet/Visible Absorption Spectroscopy 505
M. Cather Simpson and Nina I. Novikova
12 Photoinduced Electron and Energy Transfer 587
Eugeny A. Ermilov and Beate Röder
13 NMR Spectroscopy of Porphyrins 611
Craig J. Medforth
14 Spin States in Iron Porphyrins 631
Mikio Nakamura
15 Electrochemical Properties of Porphyrin-Type Complexes 661
Tebello Nyokong
16 Heme Proteins -- Structure and Function 709
Sk Amanullah, Chandradeep Ghosh, Somdatta Ghosh Dey and Abhishek Dey
17 Chlorophylls 743
Hitoshi Tamiaki
18 Vitamin B12 and Cofactor F430 777
Bernhard Kräutler and Bernhard M. Jaun
Index 815
| Erscheinungsdatum | 25.03.2019 |
|---|---|
| Verlagsort | New York |
| Sprache | englisch |
| Maße | 189 x 246 mm |
| Gewicht | 2098 g |
| Themenwelt | Naturwissenschaften ► Chemie ► Organische Chemie |
| ISBN-10 | 1-119-12928-1 / 1119129281 |
| ISBN-13 | 978-1-119-12928-8 / 9781119129288 |
| Zustand | Neuware |
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