Details

<p>Preface ix</p> <p>Abbreviations xi</p> <p>Acknowledgments xv</p> <p>Author Biographies xvii</p> <p><b>1 Description of Diamondoids 1</b></p> <p>1.1 Nomenclature 2</p> <p>1.2 Strain 5</p> <p>1.3 Preparation of Diamondoids 8</p> <p>1.4 Physical Properties of Diamondoids 14</p> <p>1.5 Spectroscopy of Diamondoids 18</p> <p>1.6 Ionization Potentials 23</p> <p>1.7 Electron Affinities 24</p> <p>1.8 Vibrational Spectroscopy 25</p> <p><b>2 Naturally Occurring Diamondoids 35</b></p> <p>2.1 Diamondoid Occurrence in the Earth’s Crust 38</p> <p>2.2 Diamondoids in Geochemical Studies 40</p> <p>2.3 Diamondoid Formation in the Earth’s Crust 42</p> <p>2.4 Large-scale Isolation of Natural Diamondoids 44</p> <p>2.5 Alternative Natural Sources of Diamondoids 48</p> <p>2.6 Other Diamondoid Derivatives in Nature 50</p> <p><b>3 Diamondoids as Alkane CH Activation Models 63</b></p> <p><b>4 Preparative Diamondoid Functionalizations 75</b></p> <p>4.1 Halogenations 75</p> <p>4.2 Diamondoid Alcohols and Ketones 83</p> <p>4.3 Carboxylic Acids and Their Derivatives 98</p> <p>4.4 Nitrogen-Containing Compounds 103</p> <p>4.5 Phosphorous- and Sulfur-Containing Compounds 108</p> <p>4.6 Single Electron Oxidations of Diamondoids 113</p> <p>4.7 Other Diamondoid Derivatives 118</p> <p><b>5 Diamondoid Self-Assembly 137</b></p> <p>5.1 Adamantane-Containing SAMs on Surfaces 137</p> <p>5.2 Higher Diamondoids for SAM Formation 146</p> <p>5.3 Pristine Diamondoids on Surfaces 157</p> <p>5.4 Other Applications of Diamondoid SAM Materials 157</p> <p>5.5 Adamantane-stabilized Metal Nanoparticles 160</p> <p><b>6 Growing Diamond Structures from Diamondoids Via Seeding 171</b></p> <p>6.1 Diamondoid-Promoted Growth of Diamond Under HT-HP or CVD Conditions 171</p> <p>6.2 Higher Diamondoids for Diamond Nucleation 177</p> <p>6.3 Diamond Growth Inside Nanotubes 180</p> <p><b>7 Diamondoid Polymers 193</b></p> <p>7.1 Polymers Based on 1-Adamantyl-1-adamantane (1ADAD) 194</p> <p>7.2 Polymers Based on Monofunctionalized Diamantanes 197</p> <p>7.3 Polymers Based on Difunctionalized Diamantanes 199</p> <p><b>8 Diamondoids in Catalysis 213</b></p> <p><b>9 Medicinal Compounds 239</b></p> <p><b>10 Supramolecular Architectures 251</b></p> <p><b>11 Diamondoid Oligomers 279</b></p> <p>11.1 Saturated Diamondoid Oligomers 279</p> <p>11.2 Unsaturated Oligomers 287</p> <p><b>12 Doped Diamondoids 305</b></p> <p>12.1 @-Doping 306</p> <p>12.2 Internal Doping 308</p> <p>12.3 External Doping 318</p> <p><b>13 Perspective 339</b></p> <p>References 340</p> <p>Index 343</p>

<p><b>Prof. Andrey A. Fokin</b> is Full Professor and Head of the Department of Organic Chemistry and Technology at National Technical University "Igor Sikorsky Kiyv Polytechnic Institute" (Ukraine). He has been a visiting professor at the Universities of Minnesota and Georgia (USA) as well as in Giessen (Germany). His research mostly concentrates on the combination of computational and experimental studies with applications in organic, physical-organic, medical, agricultural chemistry and nanotechnology.</p> <p><b>Dr. Marina Sekutor</b> is senior research associate in the Division of Organic Chemistry and Biochemistry at the Ruder Boskovic Institute (Zagreb, Croatia). She was a postdoctoral Alexander-von-Humboldt fellow in the group of Prof. Schreiner at the Justus Liebig University Giessen (Germany) and a visiting scientist at the University of Maryland (USA). Her research interests include supramolecular host-guest chemistry of polycyclic compounds and the use of diamondoid derivatives in materials science.</p> <p><b>Prof. Peter R. Schreiner</b> is Professor of Organic Chemistry and Liebig-Chair at the Institute of Organic Chemistry at Justus Liebig University Giessen (Germany). His research interests include organic reaction dynamics and reactive intermediates, quantum mechanical tunneling as well as London dispersion interactions as probed in the realm of nanodiamonds and organocatalysis. He is an Editor for the <i>Journal of Computational Chemistry, WIRES - Computational Molecular Sciences,</i> and the <i>Beilstein Journal of Organic Chemistry</i>.</p>

<p> <b>Comprehensive resource on an important and fascinating compound class, covering synthesis, properties, functionalization, and applications in organic synthesis, materials science, and more</b> <p><i>The Chemistry of Diamondoids </i>gives a state-of-the-art overview of all aspects of diamondoid chemistry, covering nomenclature, natural occurrence, chemical and physical properties, along with synthesis and functionalization of diamondoids as well as their applications as molecular building blocks in organic synthesis, polymer and materials science, nanotechnology, and medicinal chemistry. The book concludes with a perspective towards future developments in the field, thereby drawing attention to areas open for discovery. <p>Written by experts in the field, <i>The Chemistry of Diamondoids </i>includes information on: <ul><li>Naturally occurring diamondoids, their formation, and the role they play in the petroleum industry and in geosciences, plus man-made approaches to prepare them on large scale</li><li>Growing diamond from diamondoids via seeding, preparation and properties of diamondoid oligomers and doped diamondoids</li><li>C–H-bond functionalization, a precondition for their use in many applications, and fine-tuning of diamondoid properties by precise cage substitution reactions</li></ul> <p>With its all-encompassing approach, <i>The Chemistry of Diamondoids </i>is a valuable guide for newcomers and researchers in organic chemistry and materials science interested in modern synthetic methods and organic functional materials.

DE