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9780080420929

Expanded, Contracted and Isomeric Porphyrins

by ;
  • ISBN13:

    9780080420929

  • ISBN10:

    0080420923

  • Format: Hardcover
  • Copyright: 1997-09-01
  • Publisher: Elsevier Science Serials
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Summary

The porphyrins are a class of naturally-occurring macrocycles and are ubiquitous in our world. As such, they have been called the Pigments of Life. This auspicious designation reflects their importance in numerous biological functions. Indeed, life as we understand it relies on the full range of biological processes that are either performed by or catalyzed by porphyrin-containing proteins. Chlorophyll-containing photosynthetic reaction centers in plants, for instance, convert light energy into chemical energy while producing oxygen along the way. It is this oxygen, evolved from photosynthesis, that is transported, stored, and reduced by heme-containing proteins in many organisms, including mammals. Not surprisingly, therefore, these molecules remain of fundamental interest to chemists and biochemists. Indeed, they continue to be intensely investigated by researchers world-wide. Inspired by the importance of the porphyrins, a new research direction has emerged in recent years that is devoted to the preparation and study of non-porphyrin polypyrrole macrocycles. Here, the principal objectives have been to generate completely synthetic systems that bear some structural resemblance to naturally-occurring porphyrin derivatives while being quite different in their specific chemical makeup. Within this context, three different research directions have evolved, namely those involving the syntheses of contracted, isomeric, and expanded porphyrins, respectively. It is the chemistry of these systems that is the subject of this book. Because of the newness of the field, the emphasis of this book will be on synthesis and characterization (all work on porphyrin isomers and much of that associated with expanded porphyrins has only appeared in the last 10 years). One chapter on applications has, however, been included. Also, in the context of the preparative portions of the text, some efforts have been made to explain why various porphyrin analogue targets are of interest.

Table of Contents

Preface xi
Introduction
1(10)
Background
1(10)
Reasons for Interest
2(1)
Scope
3(1)
Nomenclature
3(3)
Graphical Overview of the Field
6(1)
References
7(4)
Contracted Porphyrins
11(116)
Introduction
11(116)
Corrole
13(4)
Synthesis of the Corrole Macrocycle
17(14)
Metallocorroles
31(31)
Reduction and Oxidation of Metallocorroles
62(2)
N-Substituted Corroles
64(20)
``Corrologen''
84(1)
Corrole--Corrole and Corrole--Porphyrin Dimers
85(3)
Isocorrole
88(1)
Synthesis
88(5)
Metalation Chemistry
93(2)
Contracted Porphyrins Containing Fewer than Four Pyrrole-like Subunits
95(1)
Subphthalocyanines
95(12)
Subtriazaporphyrins
107(1)
Heteroatom-bridged [18]Annulenes
107(9)
Other Systems of Interest
116(4)
References
120(7)
Isomeric Porphyrins
127(58)
Introduction
127(58)
[18]Porphyrin-(2.0.2.0) (``Porphycene'')
128(1)
Synthesis and Structure
128(13)
Metalloporphycenes
141(7)
Porphycene Transformations
148(14)
[18]Porphyrin-(2.1.0.1) (``Corrphycene'' or ``Porphycerin'')
162(1)
Synthesis
162(2)
Metal Complexes of Corrphycene
164(3)
[18]Porphyrin-(2.1.1.0) (``Hemiporphycene'')
167(3)
[18]Porphyrin-(3.0.1.0) (``Isoporphycene'')
170(1)
``Mutant'' or ``N-Confused'' Porphyrins
170(7)
Future Directions in Porphyrin Isomer Chemistry
177(4)
References
181(4)
Expanded Porphyrins Containing Four Pyrroles
185(68)
Introduction
185(68)
Homoporphyrins
185(16)
Vinylogous Porphyrins (Odd-Odd Systems)
201(1)
Historical Overview
202(1)
Bisvinylogous Porphyrins
203(6)
Tetravinylogous Porphyrins
209(6)
Octavinylogous Porphyrins
215(1)
Stretched Porphycenes (Even-Even Systems)
216(14)
Heteroatom-containing Stretched Porphycenes
230(7)
Odd-Even Systems
237(3)
Miscellaneous Systems of Interest
240(9)
References
249(4)
Contracted Expanded Porphyrins: Sapphyrins and Smaragdyrins
253(50)
Introduction
253(50)
Sapphyrins
253(6)
meso-Aryl-substituted Sapphyrins
259(6)
Heterosapphyrins
265(2)
Optical Properties of Sapphyrins and Heterosapphyrins
267(1)
Sapphyrins and meso-Aryl-substituted Sapphyrins
267(3)
Heterosapphyrins
270(2)
Metal Complexes of Sapphyrins
272(1)
Complexes with First-row Transition Elements
272(1)
Sitting-a-top Complexes
273(4)
Uranyl Cation Coordination by Modified Sapphyrins
277(3)
Metal Complexes of Heterosapphyrins
280(3)
Three-dimensional Sapphyrins and Sapphyrin Conjugates
283(1)
Sapphyrin Conjugates
284(5)
``Capped'' Sapphyrins
289(1)
Sapphyrin Oligomers
290(4)
Smaragdyrins and Heterosmaragdyrins (Norsapphyrins)
294(1)
Contributions from Grigg and Johnson
294(3)
Contributions from Woodward and coworkers
297(1)
Contributions from Sessler
298(1)
References
299(4)
Other Carbon-bridged Pentapyrrolic Systems
303(26)
Introduction
303(26)
Orangarin: Two Bridging Carbons
303(2)
Isosmaragdyrin: Three Bridging Carbons
305(3)
Sapphyrin ``Isomers'': Four Bridging Carbons
308(1)
Ozaphyrins
308(3)
[22]Dehydropentaphyrin-(2.1.0.0.1) and [22]Pentaphyrin-(2.1.0.0.1)
311(1)
Pentaphyrins
312(1)
Pentaazapentaphyrins
313(5)
Heteropentaphyrins
318(5)
Other Systems
323(1)
Pentaoxa[30]pentaphyrin-(2.2.2.2.2)
323(1)
Pentathia[30]pentaphyrin-(2.2.2.2.2)
324(2)
Decavinylogous Pentaphyrinogen
326(1)
``Inverted'' (Non-conjugated) Pentaphyrin
326(2)
References
328(1)
Carbon-linked Hexapyrrolic Systems and Heteroatom Analogs
329(40)
Introduction
329(40)
Hexaphyrins
329(1)
Synthesis
329(2)
Metalation Chemistry
331(3)
Hexathiahexaphyrinogen
334(1)
Rubyrins and Heterorubyrins
335(1)
Rubyrins
335(3)
Heterorubyrins
338(1)
Rosarins
339(1)
Synthesis
339(2)
Metalation Chemistry
341(2)
Rosarinogens and Heterorosarinogens
343(1)
Bronzaphyrins
344(4)
Amethyrins
348(1)
Synthesis
348(4)
Metalation Chemistry
352(4)
Other Systems of Interest
356(1)
Hexaoxa- and Hexathia[36]hexaphyrin-(2.2.2.2.2.2)
356(6)
Cram's Cavitand
362(1)
Hexathia[30]hexaphyrin-(2.0.2.0.2.0)
363(1)
Pyrazole-containing Hexaphyrin-like Systems
364(2)
References
366(3)
Higher Order Systems
369(16)
Introduction
369(16)
Turcasarin: Decaphyrin-(1.0.1.0.0.1.0.1.0.0)
369(2)
Cyclooctapyrroles
371(1)
Tetrahydrooctaphyrin-(2.1.0.1.2.1.0.1) and Octaphyrin-(2.1.0.1.2.1.0.1)
371(5)
Octaphyrin-(1.1.1.0.1.1.1.0)
376(3)
Octaphyrin-(1.0.1.0.1.0.1.0)
379(1)
Pyrrole-Thiophene Decamers: Hexathiatetraaza[44]decaphyrins-(2.0.0.0.0.2.0.0.0.0)
380(3)
References
383(2)
Nitrogen-bridged Expanded Porphyrins
385(44)
Introduction
385(44)
Schiff base-derived Expanded Porphyrins
386(1)
The ``[2 + 2]'' Approach
386(6)
The ``[1 + 1]'' Approach
392(17)
Other Nitrogen-bridged Expanded Porphyrins
409(1)
Superphthalocyanines
409(6)
Porphocyanines
415(4)
14-Aza[26]porphyrin-(5.1.5.1)
419(2)
Cryptand-like Expanded Porphyrins
421(3)
References
424(5)
Applications
429(76)
Introduction
429(76)
Magnetic Resonance Imaging
429(1)
Background: Utility of Contrast Agents
429(3)
Gadolinium(III) Texaphyrins
432(1)
Photodynamic Therapy and Photodynamic Viral Inactivation
433(1)
Introduction: Need for Photosensitizers
433(3)
Cadmium(II) and Lutetium(III) Texaphyrins
436(4)
Porphycenes and Expanded Porphycenes
440(2)
Sapphyrins and Vinylogous Porphyrins
442(1)
X-Ray Radiation Therapy Enhancement
442(1)
General Overview: Potential Benefit of Sensitizers
442(1)
Gadolinium(III) Texaphyrins
442(2)
Antisense Applications: RNA Hydrolysis and DNA Photolysis
444(1)
Introduction
444(3)
Photolytic Strategies
447(2)
RNA Hydrolysis: Lanthanide(III) Texaphyrins
449(4)
Combined Strategies: Yttrium(III) Texaphyrins
453(1)
Expanded Porphyrins as Anion-binding Agents
453(1)
Introduction
453(1)
Anion Binding in the Solid State
454(24)
Anion Binding in Solution: Sapphyrins, Rubyrins, Anthraphyrins
478(7)
Sapphyrin-Oligonucleotide Interactions
485(5)
References
490(15)
Index 505

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