Macrocyclic and supramolecular chemistry: how Izatt-Christensen Award winners shaped the field
Commemorates the 25th anniversary of the Izatt-Christensen Award, which has been presented since 1991 at the annual meeting of the International Symposium on Macrocyclic and Supramolecular Chemistry (ISMSC). ...
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| Format: | Book |
| Language: | English |
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Chichester, West Sussex
Wiley
2016
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| Online Access: | Inhaltsverzeichnis Klappentext |
| Summary: | Commemorates the 25th anniversary of the Izatt-Christensen Award, which has been presented since 1991 at the annual meeting of the International Symposium on Macrocyclic and Supramolecular Chemistry (ISMSC). ... |
| Physical Description: | xix, 481 Seiten Illustrationen, Diagramme (teilweise farbig) |
| ISBN: | 9781119053842 |
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| 245 | 1 | 0 | |a Macrocyclic and supramolecular chemistry |b how Izatt-Christensen Award winners shaped the field |c edited by Reed M. Izatt, IBC Advanced Technologies, Inc., American Fork; Department of Chemistry and biochemistry, Brigham Young Unviersity, Provo, UT, USA |
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| 600 | 1 | 4 | |a Izatt, Reed M. |d 1926- |
| 600 | 1 | 4 | |a Christensen, James J. |d 1931- |
| 650 | 4 | |a Chemie | |
| 650 | 4 | |a Izatt-Christensen Award in Macrocyclic and Supramolecular Chemistry | |
| 650 | 4 | |a Supramolecular chemistry |x Awards | |
| 650 | 4 | |a Chemistry |x Awards | |
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| adam_text | Contents
List of Contributors
Preface
Acknowledgements
XV
xviii
XX
1 The Izatt-Christensen Award in Macrocyclic and Supramolecular Chemistry:
A 25-Year History (1991-2016)
Reed M. Izait, Jerald S. Bradshaw, Steven R. Izatt, and Roger G. Harrison
1.1 Introduction
1.2 International Izatt-Christensen Award in Macrocyclic and Supramolecular Chemistry
1.3 International Symposium on Macrocyclic and Supramolecular Chemistry
1.4 Izatt-Christensen award sponsor: IBC Advanced Technologies, Inc.
1.5 Summary
References
1
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2 Supramolecular Chemistry with DNA
Pongphak Chidchob and Hanadi Sleiman
2.1 Introduction
2.2 Motifs in structural DNA nanotechnology
2.2.1 DNA structural properties
2.2.2 The beginning of DNA nanotechnology: DNA tile assembly
2.2.3 DNA origami and single-stranded tiles
2.2.4 Perspective
2.3 Dynamic assembly and molecular recognition with DNA
2.4 Supramolecular assembly with hybrid DNA materials: increasing the letters of the alphabet
2.4.1 Three-dimensional structures: DNA cages
2.4.1.1 Synthesis
2.4.1.2 Simplified and DNA-minimal design of DNA cages
2.4.1.3 Perspective
2.4.2 Three-dimensional structures: DNA nanotubes
2.4.2.1 Synthesis
2.4.2.2 Control of nanotube length and stability
2.4.2.3 Temporal growth of DNA assembly
2.4.2.4 Perspective
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vi Contents
2.4.3 Biological applications of DNA cages and nanotubes 21
2.4.3.1 Tools for conditional drug delivery 21
2.4.3.2 Biological stability and gene-silencing activity 21
2.4.3.3 Interaction with lipid bilayers 21
2.4.3.4 Perspective 21
2.4.4 Effect of small-molecule insertions on DNA structure and stability 23
2.4.5 Non-covalent small molecule-mediated DNA assembly 23
2.4.5.1 Perspective 25
2.4.6 DNA-polymer and DNA-lipid conjugates 25
2.4.6.1 Synthesis 25
2.4.6.2 Dynamic behavior 25
2.4.6.3 Sequence-defined DNA-polymer conjugates 27
2.4.6.4 Perspective 27
2.4.7 3D organization of polymers with DNA nanostructures 27
2.4.7.1 Perspective 29
2.4.8 Metal-DNA assemblies 29
2.4.8.1 Strategy for incorporation of metal into DNA 29
2.4.8.2 Metal-DNA nanostructures 30
2.4.83 Perspective 30
2.4.9 Gold nanoparticle-DNA structures 32
2.5 Conclusion 33
References 34
3 Anion, Cation and Ion-Pair Recognition by Macrocyclic
and Interlocked Host Systems 38
Paul D. Beer and Matthew J. Langton
3.1 Introduction 38
3.2 Electrochemical molecular recognition 38
3.2.1 Electrochemical cation recognition 39
3.2.2 Electrochemical anion recognition 42
3.3 Anion recognition and sensing by macrocyclic and interlocked hosts 44
3.3.1 Transition metal bipyridyl-based macrocyclic receptors for anion
recognition and sensing 44
3.3.2 Interlocked host structures for anion recognition and sensing 45
3.3.3 Rotaxane and catenane host structures for sensing anions 48
3.4 Halogen-bonding anion recognition 55
3.5 Ion-pair recognition 59
3.6 Metal-directed self-assembly 62
3.7 Conclusions 67
3.8 Acknowledgements 67
References 67
4 Perspectives in Molecular Tectonics 73
Mir Wais Hasseini
4.1 Preamble: dreams and pathway 73
4.2 introduction 75
Contents vii
4.3 From tectons to networks 75
4.3.1 Inclusion networks: an interplay between concave and convex tectons 79
4.3.2 H-bonded networks 79
4.3.3 Neutral ID helical H-bonded networks 81
4.3.4 Charge-assisted H-bonded networks 82
4.3.5 H-bonded networks based on recognition of hexacyanometallates 83
4.3.6 From hydrogen-bonded networks to core-shell crystals 84
4.3.7 Coordination networks: an interplay between organic and metallic tectons 84
4.3.8 Helical coordination networks 84
4.3.9 Directional 1D coordination networks 85
4.4 Summary and outlook 87
4.5 Acknowledgements 88
References 88
5 Three Tales of Supramolecular Analytical Chemistry 92
Margaret K. Meadows and Eric V. Anslyn
5.1 Introduction 92
5.2 Citrate sensing 93
5.2.1 Receptor design 93
5.2.2 Indicator-displacement assays 94
5.2.3 Soda analysis 95
5.2.4 Wine analysis 95
5.2.5 Scotch analysis 97
5.2.6 Calcium and citrate multianalyte sensing 98
5.2.7 Dialysis 98
5.2.8 Conclusion 101
5.3 Rapid analysis of enantiomeric excess 101
5.3.1 Enantioselective indicator-displacement assays 101
5.3.1.1 ee Analysis with boronic acids 101
5.3.1.2 ee Analysis of amino acids 104
5.3.2 ee Determination using circular dichroism 104
5.3.2.1 CD analysis using metal-to-ligand charge transfer 105
5.3.2.2 ECCD analysis of alcohols 106
5.3.2.3 ECCD analysis of amines 108
5.3.2.4 Adaptation to high-throughput methods 108
5.3.3 Conclusion 108
5.4 Differential sensing 109
5.4.1 Chemometric analysis 110
5.4.2 An electronic tongue HO
5.4.3 Phosphopeptide classification 111
5.4.4 Serum albumin receptors for terpenes 112
5.4.5 Serum albumin receptors for glycerides 114
5.4.6 Mitogen-activated protein kinases differentiation 115
5.4.7 Wine 118
5.5 Conclusion 123
References 123
viii Contents
6 Robust Host-Guest Chemistry of Cucurbit[«]uril: Fundamentals and Applications
of the Synthetic Receptor Family 127
Kimoon Kim, Dinesh Shetty, and Kyeng Min Park
6.1 Personal pathway to the discovery of cucurbit[w]uril and early
day developments 127
6.2 Structures and physical properties of CB[w] 129
6.3 General host-guest chemistry of CB[n] 129
6.4 High-affinity host-guest pairs 130
6.4.1 High-affinity CB[6]-guest complexes 131
6.4.2 High-affinity CB[7]-guest complexes 131
6.5 Functionalized CBs 133
6.6 Applications of high-affinity CB[6] complexes 134
6.6.1 Pseudorotaxane formation and biological applications 134
6.6.2 Modular multi-functionalities through non-covalent modification 136
6.6.3 Hydrogelation through non-covalent crosslinking 136
6.7 Applications of high-affinity CB[7] complexes 137
6.7.1 Immobilization of biomolecules on a solid surface 137
6.7.2 Plasma membrane protein fishing 138
6.7.3 Supramolecular velcro system 138
6.7.4 Other applications 139
6.8 Conclusions 140
6.9 Acknowledgements 141
References 141
7 Molecular Recognition in Biomimetic Receptors 146
Peter C. Knipe, Sam Thompson, and Andrew D. Hamilton
7.1 Molecular recognition in biological systems 146
7.2 Model systems to investigate fundamental forces 146
7.2.1 Hydrogen bonding 147
7.2.2 Aromatic stacking 147
7.2.3 A first foray into mimicry - minimalist vancomycin analogues 148
7.3 Recognition of more complex systems - into the realm of peptides 149
7.3.1 Carboxylic acid binding 149
7.3.2 Peptide mimicry as a strategy for the inhibition of a key protein-protein interaction:
preny ltransferases 151
7.4 A general approach to peptide mimicry - targeting secondary structure 152
7.4.1 Terphenyls: the first class of a-helix mimic 152
7.4.2 The development of next-generation a-helix mimetics 153
7.4.3 Approaches to P-strand mimicry 154
7.4.4 p-sheet templation 154
7.5 Super-secondary structures and beyond 156
7.5.1 The p-meander 156
7.5.2 Mimicking a-helix bundles 156
7.5.3 Binding multiple sites through multivalent receptors 157
7.5.4 Self-assembly of receptors - binding quaternary structures 158
7.6 Outlook 159
References 160
Contents ix
8 A Lifetime Walk in the Realm of Cyclam 165
Luigi Fcibbrizzi
8.1 Synthesis and development of cyclam and related macrocycles 165
8.2 Macrocyclic effects and the importance of being 14-membered 170
8.3 Cyclam promotes the redox activity of the encircled metal ion 176
8.4 Scorpionands: cyclam derivatives with an aggressive tail,
biting a chelated metal from the top 180
8.5 Azacyclams: cyclam-like macrocycles with built-in functionalization 187
8.6 Conclusion J 93
8.7 Acknowledgements 195
References 196
9 Porosity in Metal-Organic Compounds
Alexander Schoedel and Omar M. Yaghi
9.1 Introduction
9.2 Werner complexes
9.3 Hofmann clathrates
9.4 Coordination polymers
9.5 Porosity in metal-organic frameworks
9.6 The discovery of MOF-5: the golden age of metal-organic
frameworks
9.7 The Cambridge Structural Database - an essential tool for MOF
chemists
9.8 Concluding remarks
9.9 Acknowledgement
References
200
200
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209
214
215
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215
10 Cyclodextrin-based Supramolecular Systems 220
Akira Harada
10.1 Introduction 220
10.2 Cyclodextrin-containing polymers 220
10.2.1 Preparation 220
10.2.2 Cooperativity 222
10.2.3 Optical resolution by CD 222
10.3 CD-organometallic complexes 222
10.4 Complex formation of cyclodextrin with polymers 223
10.4.1 Macromolecular recognition 223
10.4.2 Polyrotaxanes 224
10.4.3 Tubular polymers 224
10.5 Polymerization by CDs 225
10.6 Supramolecular polymers 228
10.7 Side-chain recognition by CDs 230
10.8 CD-based molecular machines 230
10.9 Macroscopic self-assembly through molecular recognition 233
10.9.1 Macroscopic self-assembly 233
10.9.2 Selectivity 234
x Contents
10.10 Self-healing by molecular recognition 235
10.11 Stimuli-responsive polymers 236
10.11.1 Photoresponsive polymers 236
10.11.2 Redox responsive gel 236
10.11.3 Metal-ion responsive system 237
10.12 Conclusion 238
References 238
11 Making the Tiniest Machines 241
David A. Leigh
11.1 Introduction 241
11.1.1 From a macrocyclic receptor for CO, to a [2]catenane 241
11.1.2 From rotaxanes to molecular shuttles 243
11.1.3 From shuttles to switches: stimuli-responsive molecular shuttles 244
11.2 Property effects using molecular shuttles 245
11.2.1 Switching “on” and “off’ fluorescence with a molecular shuttle 246
11.2.2 Rotaxane-based photoresponsive surfaces and macroscopic transport
by molecular machines 248
11.3 Molecular motors and ratchet mechanisms 248
11.3.1 From molecular switches to molecular motors 249
11.3.2 A [3]catenane rotary molecular motor 250
11.3.3 Controlled rotation in either direction: a [2]catenane reversible rotary
molecular motor 250
11.3.4 Molecular information ratchets 250
11.4 Small molecules that can “walk” along molecular tracks 254
11.5 Making molecules that make molecules 257
11.6 Outlook 257
11.7 Acknowledgements 259
References 259
12 Clipping an Angel’s Wings 261
Roeland JM. Nolte, Alan E. Rowan, and Johannes A.A.W. Elemans
12.1 Introduction 261
12.2 Molecular clips 263
12.2.1 Synthesis 263
12.2.2 Binding properties 265
12.2.3 Self-assembly 266
12.2.4 Functional clips 268
12.2.5 Biomimetic systems 272
12.2.6 Porphyrin clips: processive catalysis 274
12.3 Molecular capsules 278
12.4 Outlook 282
12.5 Acknowledgements 282
References 283
Contents xi
13 From Lanthanide Shift Reagents to Molecular Knots: The Importance
of Molecular and Mental Flexibility 288
Jeremy K.M. Sanders
13.1 Introduction: 1969-76 288
13.2 Metalloporphyrins 289
13.2.1 Model photosynthetic systems 289
13.2.2 Flexible porphyrin dimers: n-n interactions and model enzymes 290
13.2.3 The Anderson butadiyne system 292
13.2.4 Chemistry inside cavities 295
13.3 Macrocycles based on cholic acid 296
13.4 Designed donor-acceptor catenanes 297
13.5 Dynamic combinatorial chemistry 298
13.5.1 Conception and principles 298
13.5.2 Hydrazones 299
13.5.3 Disulfides 299
13.6 Conclusions 304
References 305
14 Texaphyrins: Life, Death, and Attempts at Resurrection 309
Jonathan L. Sessler
14.1 Introduction 309
14.2 Early days 309
14.3 Starting Pharmacyclics, Inc. 311
14.4 Early biological studies of texaphyrins 314
14.5 Clinical studies of texaphyrins at Pharmacyclics, Inc. 316
14.6 Changes in direction at Pharmacyclics, Inc. 316
14.7 Current research efforts involving texaphyrin 317
14.8 Texaphyrin-platinum conjugates 318
14.9 Acknowledgements 321
References 321
15 Macrocyclic Coordination Chemistry of Resorcin[4]arenes and PyrogaIIoI[4]arenes 325
Harshita Kumari, Carol A. Deakyne, and Jerry L. Atwood
15.1 Introduction 325
15.2 History of hydrogen-bonded pyrogallol[4]arene- and resorcin[4]arene-based nanocapsules 326
15.3 Metal-seamed pyrogallol[4]arene- and resorcin[4]arene-based complexes 327
15.3.1 Copper-seamed pyrogallol[4]arene hexamers 327
15.3.2 Zinc-seamed pyrogallol[4]arene dimers 329
15.3.3 Zinc-seamed pyrogallol[4]arene tethering complexes 330
15.3.4 Copper-seamed C-methylpyrogallol[4]arene dimer coordination polymers 330
15.3.5 Gallium-seamed pyrogallol[4]arene complexes 330
15.3.6 Nickel-seamed pyrogallol[4]arene dimers and hexamers 333
15.3.7 Ferrocene-containing pyrogallol[4]arene complexes 334
15.3.8 Iron-seamed pyrogallol[4]arene nanotubes 335
15.3.9 Holmium-seamed pyrogallol[4]arene dodecamer 335
336
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Contents
15.3.10 Insulin-enclosing hydrogen-bonded resorcin(4]arene nanocapsules
15.3.11 Zinc-seamed pyrogallol[3Jresorcin[l]arene dimer
15.3.12 Ionic dimeric Cs-containing pyrogallol[4]arene nanocapsule
15.3.13 Zirconium, silver, and iron-seamed resorcin[4]arene complexes
15.3.14 Manganese and cobalt complexes enclosed within resorcin[4]arenes
15.4 Concluding remarks
References
Dynamic Control of Recognition Processes in Host-Guest Systems
and Polymer-Polymer Interactions
Seiji Shinkai
16.1 Introduction
16.2 Dynamic control of crown ether functions by chemical and physical signals
16.3 Stereochemical studies of calix[n]arene derivatives
16.4 Ion and molecule recognition by functionalized calix[n]arenes and their
application to super Na+-sensors and novel [60]fullerene isolation
methods
16.5 Molecular design of novel sugar-sensing systems using boronic acid-diol
macrocyclization
16.6 From molecular machines to allosteric effects
16.7 From allosteric effects to aggregation-induced emission (AIE)
16.8 Extension of cooperative actions to polymeric and biological systems
16.9 Summary
16.10 Acknowledgements
References
Cation Binders, Amphiphiles, and Membrane Active Transporters
George W. Gokel, Saeedeh Negin, Joseph W. Meisel, Mohit B. Patel,
Michael R. Gokel, and Ryan Cantwell
17.1 Introduction
17.2 Conceptual development of lariat ethers for transport
17.3 Recognition of the ability of lariat ethers to form membranes
17.4 Use of lariat ethers to demonstrate cation-jt interactions
17.5 Development of synthetic cation channels based on crown ethers
17.6 Development of synthetic anion channels based on amphiphilic peptides
17.7 Membrane active amphiphiles as biologically active and applicable compounds
17.8 Conclusion
References
Supramolecular Technology
David N. Reinhoudt
18.1 Introduction
18.2 Chemical sensing
18.3 Membrane transport
18.4 Nonlinear optical materials
18.5 Supramolecular technology for nanofabrication
References
Contents xiii
19 Synthesis of Maerocydic Complexes Using Metal Ion Templates 383
Daryle H. Busch
19.1 Introduction 383
19.2 Macrocycle synthesis 384
19.2.1 The first planned macrocycle 384
19.2.2 Theoretical considerations 385
19.2.3 Oxygen carriers and enzyme mimics 385
References 386
20 Serendipity 388
Paul R. McGonigal and J. Fraser Stoddart
20.1 Serendipity in scientific discovery 388
20.2 Donor-acceptor charge transfer interactions 390
20.2.1 Introduction 390
20.2.2 Mechanically interlocked molecules 392
20.2.2.1 Molecular switches 394
20.2.2.2 Molecular electronic devices 396
20.2.2.3 Drug delivery systems 396
20.2.3 Lock-arm supramoiecular ordering (LASO) 398
20.2.3.1 Emergent ferroelectric properties 398
20.3 Cyclodextrins (CDs) 400
20.3.1 Introduction 400
20.3.2 Cyclodextrin Metal-Organic Frameworks (CD-MOFs) 401
20.3.2.1 CO? Sequestration and sensing 403
20.3.2.2 Chromatographic separations 404
20.3.3 Selective interactions with gold salts 406
20.3.3.1 Second-sphere coordination 407
20.3.3.2 A greener solution in the isolation of gold 408
20.4 Conclusions and outlook 410
References 41 i
21 Evolution of Znn-Macrocyelic Polyamines to Biological Probes
and Supramoiecular Assembly 415
Eiichi Kitmtra, Tohru Koike, and Shin Aoki
21.1 Introduction 415
21.2 Zinc enzyme models from Zn11 macrocyclic polyamine complexes 415
21.2.1 The CA-mimicking anion affinity of model 11 417
21.2.2 The CA-mimicking sulfonamide inhibition of model 11 418
21.2.3 Development of new Zn11 fluorophores and apoptosis sensors 418
21.2.4 From the Zn“-aldolase model to aldol synthesis catalyst 419
21.2.5 Reaction of ZnH-macrocyclic polyamines with phosphomono-, di-,
and triesters 421
21.2.6 A dinuclear Zn11 phosphomonoesterase model 29 421
21.2.7 Development of “Phos-tag,? for protein phosphorylation analysis 422
21.2.8 Cooperative phosphate dianion recognition by multiple Znn-cyclens 422
21.2.9 Discovery that guanidine is a Znn-binding ligand at neutral pH 423
xiv Contents
21.2.10 MB NMR sensing of Zn11 ion in vitro and in vivo using phenylboronic
acid-pendant cyclen 425
21.2.11 From the (3-lactamase model to development of new magnetic
beads device for purification of thiol-containing biomolecules 426
21.3 Znn-cyclens for selective recognition of nucleobases (thymine and uracil)
and manipulation of genes 427
21.3.1 Recognition of thymine and uracil in single- and double-stranded synthetic
nucleic acids 428
21.3.2 Recognition of thymine in native DNA 429
21.3.3 Recognition of AT-rich TATA box DNA 430
21.3.4 Simple detection of single nucleotide polymorphisms (SNP) by Znü-cyclen
polyacrylamide gel electrophoresis (PAGE) 430
21.3.5 Recognition of TpT with Ws(Znu-cyclen) 59 and TpTpT with
/m(Zn,l-cyclen) 60 431
21.3.6 Inhibition of photo[2+2] cycloaddition and promotion of photosplitting of
the e/s-syn-cyclobutane thymine dimer 431
21.3.7 Potent inhibition of HIV-1 TAR RNA -TAT peptide binding 433
21.4 New supramolecular assemblies with Zn!I-cyclen 434
21.4.1 Supramolecular cuboctahedron cages 434
21.4.2 Supramolecular trigonal prisms 437
21.4.3 Supramolecular catalysts mimicking dimetallic phosphomonoesterases 437
21.5 Acknowledgements 438
References 438
22 Contractile and Extensile Molecular Systems: Towards Molecular Muscles 444
Jean-Pierre Sauvage, Vincent Duplan, and Frédéric Niess
22.1 Preamble: the Izatt-Christensen award and Jean-Pierre Sauvage 444
22.2 Introduction 446
22.3 Interlocking ring compounds 447
22.3.1 Transition metal-based system 447
22.3.2 Cyclodextrin-type molecular muscles 450
22.3.3 Donor-acceptor based systems coupled to protonation/deprotonation processes 453
22.3.4 Other muscle-like systems based on the mechanical bond 455
22.4 Non-interlocking compounds 456
22.4.1 A contractile and extensible molecular figure-of-eight 456
22.5 Conclusion 458
22.6 Acknowledgements 461
References 461
Index
465
This book commemorates the 25th anniversary of the International
Izatt-Christensen Award in Macrocyclic and Supramolecular Chemistry.
The award, one of the most prestigious of small awards in chemistry,
recognizes excellence in the developing field of macrocyclic and
supramolecular chemistry.
Macrocyclic and Supramolecular Chemistry: How Izatt-Christensen Award
Winners Shaped the Field features chapters written by the award recipients,
who provide unique perspectives on the spectacular growth in these
expanding and vibrant fields of chemistry over the past half century, and
on the role of these award winners in shaping this growth. During this
time there has been an upsurge of interest in the design, synthesis, and
characterization of increasingly complex macrocyclic ligands and in the
application of this knowledge to understanding molecular recognition
processes in host-guest chemistry in ways that were scarcely envisioned
only a decade or two earlier.
This book will be useful as a reference text for a wide range of practitioners
in the fields of macrocyclic and supramolecular chemistry, as well as for
younger researchers and students, who will see great opportunities for
further creative work on the molecular scale in the research presented
here by the Izatt-Christensen Award winners.
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| discipline | Chemie / Pharmazie |
| format | Book |
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| id | DE-604.BV043833779 |
| illustrated | Illustrated |
| indexdate | 2024-07-10T07:36:19Z |
| institution | BVB |
| isbn | 9781119053842 |
| language | English |
| lccn | 016016106 |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-029244518 |
| oclc_num | 965122636 |
| open_access_boolean | |
| owner | DE-355 DE-BY-UBR DE-11 DE-19 DE-BY-UBM |
| owner_facet | DE-355 DE-BY-UBR DE-11 DE-19 DE-BY-UBM |
| physical | xix, 481 Seiten Illustrationen, Diagramme (teilweise farbig) |
| publishDate | 2016 |
| publishDateSearch | 2016 |
| publishDateSort | 2016 |
| publisher | Wiley |
| record_format | marc |
| spelling | Macrocyclic and supramolecular chemistry how Izatt-Christensen Award winners shaped the field edited by Reed M. Izatt, IBC Advanced Technologies, Inc., American Fork; Department of Chemistry and biochemistry, Brigham Young Unviersity, Provo, UT, USA Chichester, West Sussex Wiley 2016 xix, 481 Seiten Illustrationen, Diagramme (teilweise farbig) txt rdacontent n rdamedia nc rdacarrier Commemorates the 25th anniversary of the Izatt-Christensen Award, which has been presented since 1991 at the annual meeting of the International Symposium on Macrocyclic and Supramolecular Chemistry (ISMSC). ... Izatt, Reed M. 1926- Christensen, James J. 1931- Chemie Izatt-Christensen Award in Macrocyclic and Supramolecular Chemistry Supramolecular chemistry Awards Chemistry Awards Macrocyclic compounds Makrocyclische Verbindungen (DE-588)4168678-0 gnd rswk-swf Supramolekulare Chemie (DE-588)4306141-2 gnd rswk-swf Makrocyclische Verbindungen (DE-588)4168678-0 s Supramolekulare Chemie (DE-588)4306141-2 s DE-604 Izatt, Reed M. 1926- (DE-588)1113688882 edt Erscheint auch als Online-Ausgabe, EPUB 978-1-119-05386-6 Erscheint auch als Online-Ausgabe, PDF 978-1-119-05387-3 Digitalisierung UB Regensburg - ADAM Catalogue Enrichment application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=029244518&sequence=000003&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis Digitalisierung UB Regensburg - ADAM Catalogue Enrichment application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=029244518&sequence=000004&line_number=0002&func_code=DB_RECORDS&service_type=MEDIA Klappentext |
| spellingShingle | Macrocyclic and supramolecular chemistry how Izatt-Christensen Award winners shaped the field Izatt, Reed M. 1926- Christensen, James J. 1931- Chemie Izatt-Christensen Award in Macrocyclic and Supramolecular Chemistry Supramolecular chemistry Awards Chemistry Awards Macrocyclic compounds Makrocyclische Verbindungen (DE-588)4168678-0 gnd Supramolekulare Chemie (DE-588)4306141-2 gnd |
| subject_GND | (DE-588)4168678-0 (DE-588)4306141-2 |
| title | Macrocyclic and supramolecular chemistry how Izatt-Christensen Award winners shaped the field |
| title_auth | Macrocyclic and supramolecular chemistry how Izatt-Christensen Award winners shaped the field |
| title_exact_search | Macrocyclic and supramolecular chemistry how Izatt-Christensen Award winners shaped the field |
| title_full | Macrocyclic and supramolecular chemistry how Izatt-Christensen Award winners shaped the field edited by Reed M. Izatt, IBC Advanced Technologies, Inc., American Fork; Department of Chemistry and biochemistry, Brigham Young Unviersity, Provo, UT, USA |
| title_fullStr | Macrocyclic and supramolecular chemistry how Izatt-Christensen Award winners shaped the field edited by Reed M. Izatt, IBC Advanced Technologies, Inc., American Fork; Department of Chemistry and biochemistry, Brigham Young Unviersity, Provo, UT, USA |
| title_full_unstemmed | Macrocyclic and supramolecular chemistry how Izatt-Christensen Award winners shaped the field edited by Reed M. Izatt, IBC Advanced Technologies, Inc., American Fork; Department of Chemistry and biochemistry, Brigham Young Unviersity, Provo, UT, USA |
| title_short | Macrocyclic and supramolecular chemistry |
| title_sort | macrocyclic and supramolecular chemistry how izatt christensen award winners shaped the field |
| title_sub | how Izatt-Christensen Award winners shaped the field |
| topic | Izatt, Reed M. 1926- Christensen, James J. 1931- Chemie Izatt-Christensen Award in Macrocyclic and Supramolecular Chemistry Supramolecular chemistry Awards Chemistry Awards Macrocyclic compounds Makrocyclische Verbindungen (DE-588)4168678-0 gnd Supramolekulare Chemie (DE-588)4306141-2 gnd |
| topic_facet | Izatt, Reed M. 1926- Christensen, James J. 1931- Chemie Izatt-Christensen Award in Macrocyclic and Supramolecular Chemistry Supramolecular chemistry Awards Chemistry Awards Macrocyclic compounds Makrocyclische Verbindungen Supramolekulare Chemie |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=029244518&sequence=000003&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=029244518&sequence=000004&line_number=0002&func_code=DB_RECORDS&service_type=MEDIA |
| work_keys_str_mv | AT izattreedm macrocyclicandsupramolecularchemistryhowizattchristensenawardwinnersshapedthefield |