Synthetic methods for conjugated polymers and carbon materials:
Gespeichert in:
Format: | Buch |
---|---|
Sprache: | English |
Veröffentlicht: |
Weinheim
Wiley-VCH Verlag GmbH & Co. KGaA
[2017]
|
Schlagworte: | |
Online-Zugang: | Inhaltsverzeichnis |
Beschreibung: | x, 300 Seiten Illustrationen, Diagramme (teilweise farbig) |
ISBN: | 9783527339983 |
Internformat
MARC
LEADER | 00000nam a2200000 c 4500 | ||
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264 | 1 | |a Weinheim |b Wiley-VCH Verlag GmbH & Co. KGaA |c [2017] | |
264 | 4 | |c © 2017 | |
300 | |a x, 300 Seiten |b Illustrationen, Diagramme (teilweise farbig) | ||
336 | |b txt |2 rdacontent | ||
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653 | |a Carbon Materials | ||
653 | |a Chemie | ||
653 | |a Chemistry | ||
653 | |a Kohlenstoffmaterial | ||
653 | |a Kohlenstoffmaterialien | ||
653 | |a Materials Science | ||
653 | |a Materialwissenschaften | ||
653 | |a Organic Chemistry | ||
653 | |a Organische Chemie | ||
653 | |a Polymer Science & Technology | ||
653 | |a Polymer Synthesis | ||
653 | |a Polymersynthese | ||
653 | |a Polymerwissenschaft u. -technologie | ||
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Datensatz im Suchindex
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adam_text | CONTENTS
LIST OF CONTRIBUTORS
IX
1 STILLE POLYCONDENSATION: A VERSATILE SYNTHETIC APPROACH TO FUNCTIONAL
POLYMERS
1
TIANYUE ZHENG, ALEXANDER M. SCHNEIDER, AND LUPING YU
1.1 INTRODUCTION 1
1.1.1 HISTORY OF THE STILLE REACTION (AND POLYCONDENSATION) 2
1.2 REACTION MECHANISM 3
1.2.1 SIMPLIFIED MECHANISM 3
1.3 REACTION CONDITIONS 6
1.3.1 CATALYST AND LIGAND 7
1.3.2 SOLVENT 9
1.3.3 ADDITIVE 10
1.3.4 TEMPERATURE 11
1.4 EXAMPLES OF FUNCTIONAL MATERIALS SYNTHESIZED BY STILLE
POLYCONDENSATION 12
1.4.1 NONLINEAR OPTICAL (NLO) POLYMERS 13
1.4.1.1 BACKGROUND 13
1.4.1.2 EXAMPLES OF NLO POLYMERS SYNTHESIZED BY STILLE POLYCONDENSATION
13
1.4.2 ORGANIC PHOTOVOLTAIC POLYMERS 16
1.4.2.1 BACKGROUND 16
1.4.2.2 EXAMPLES OF DONOR POLYMERS 17
1.4.2.3 EXAMPLES OF ACCEPTOR MATERIALS 23
1.4.3 ORGANIC FIELD EFFECT TRANSISTOR (OFET) POLYMERS 28
1.4.3.1 BACKGROUND 28
1.4.3.2 EXAMPLES OF FET POLYMERS SYNTHESIZED BY STILLE POLYCONDENSATION
32
1.4.4 ORGANIC LIGHT-EMITTING DIODE (OLED) POLYMERS 35
1.4.4.1 BACKGROUND 35
1.4.4.2 EXAMPLES OF OLED POLYMERS SYNTHESIZED BY STILLE POLYCONDENSATION
36
1.4.5 OTHER FUNCTIONAL MATERIALS 38
1.5 CHALLENGE AND OUTLOOK 42
1.5.1 ADVANTAGES OF THE STILLE REACTION 42
1.5.2 DISADVANTAGES OF STILLE REACTION 44
1.6 SUMMARY 47
REFERENCES 48
2
SUZUKI POLYCONDENSATION
59
ANURAG KRISHNA, ANDREY V. LUNCHEV, AND ANDREW C GRIMSDALE
2.1 INTRODUCTION 59
2.2 MECHANISM OF SUZUKI COUPLING AND SUZUKI POLYCONDENSATION 60
2.3 CATALYSTS 62
2.4 REACTION CONDITIONS FOR SUZUKI COUPLING 65
2.4.1 BASES, WATER, SOLVENTS 66
2.4.2 MICROWAVE-ASSISTED REACTIONS 67
2.5 SIDE REACTIONS 67
2.6 AB VERSUS AA/BB SUZUKI POLYCONDENSATION 71
2.7 MONOMER PURITY, STOICHIOMETRY, AND SOLVENTS 73
2.8 MONOMERS FOR SPC 75
2.8.1 BORON MONOMERS 75
2.8.2 HALIDE AND OTHER MONOMERS
80
2.9 CHAIN GROWTH SPC 81
2.10 SCOPE AND APPLICATIONS OF SPC 82
2.11 CONCLUSION 85
REFERENCES 86
3 CONTROLLED SYNTHESIS OF CONJUGATED POLYMERS AND BLOCK
COPOLYMERS
97
TINE HARDEMAN, MARIE-PAULE VAN DEN EEDE, LIZE VERHEYEN, AND GUY
KOECKELBERGHS
3.1 INTRODUCTION 97
3.2 APPROACHES TO CONTROLLED POLYMERIZATIONS 97
3.2.1 CATALYST TRANSFER POLYMERIZATIONS 97
3.2.1.1 MECHANISM 97
3.2.1.2 KUMADA CATALYST TRANSFER POLYCONDENSATION 99
3.2.1.3 NEGISHI CATALYST TRANSFER POLYCONDENSATION 102
3.2.1.4 CTP BASED ON SUZUKI - MIYAURA COUPLINGS 102
3.2.1.5 CTP BASED ON OTHER COUPLING REACTIONS 103
3.2.2 CONTROLLED POLYMERIZATIONS BASED ON DEACTIVATION OF THE MONOMER
103
3.2.2.1 MECHANISM 103
3.2.2.2 . PD(RUPHOS) PROTOCOL 104
3.2.2.3 MISCELLANEOUS 104
3.3 END-FUNCTIONALIZED POLYMERS 106
3.3.1 INTRODUCTION 106
3.3.2 EXTERNAL FUNCTIONALIZED INITIATORS 106
3.3.2.1 PRINCIPLE 106
3.3.2.2 EXTERNAL INITIATORS WITH NI AS CATALYST 106
3.3.2.3 EXTERNAL INITIATORS WITH PD AS CATALYST 109
3.3.2.4 GRAFTING-FROM 110
3.3.3 END-CAPPING 111
3.3.3.1 PRINCIPLE 111
3.3.3.2 END-CAPPING WITH NI AS CATALYST 111
3.3.3.3 END-CAPPING WITH PD AS CATALYST 112
3.3.4 HETEROBIFUNCTIONAL CONJUGATED POLYMERS 112
3.4 BLOCK COPOLYMERS 112
3.4.1 GRAFTING-TO METHOD 112
3.4.2 END-FUNCTIONAL POLYMER COPOLYMERIZATION METHOD 113
3.4.3 GRAFTING-FROM METHOD 114
3.4.4 SEQUENTIAL MONOMER ADDITION 114
3.5 OTHER COPOLYMERS 117
REFERENCES 117
4 DIRECT (HETERO)ARYLATION POLYMERIZATION
131
MARIO LEDERE AND SERGE BEAUPRE
4.1 INTRODUCTION 131
4.2 FIRST EXAMPLES OF DIRECT (HETERO)ARYLATION POLYMERIZATION 134
4.3 SELECTIVITY AND REACTIVITY PROBLEMS 138
4.4 EN ROUTE TO DEFECT-FREE CONJUGATED POLYMERS 142
4.5 OUTLOOK 150
REFERENCES 150
5 CONTINUOUS FLOW SYNTHESIS OF CONJUGATED POLYMERS AND CARBON
MATERIALS
159
VALERIE D. MITCHELL AND WALLACE W.H. WONG
5.1 INTRODUCTION TO FLOW CHEMISTRY 159
5.2 CONJUGATED POLYMERS 161
5.3 CARBON MATERIALS 173
5.4 MATERIAL PROCESSING 177
5.5 SUMMARY 178
REFERENCES 178
6 SYNTHESIS OF STRUCTURALLY DEFINED NANOGRAPHENE MATERIALS THROUGH
OXIDATIVE CYCLODEHYDROGENATION
183
AKIMITSU NARITA
6.1 INTRODUCTION 183
6.2 SYNTHESIS OF NANOGRAPHENE MOLECULES THROUGH OXIDATIVE
CYCLODEHYDROGENATION 186
6.2.1 SOLUTION SYNTHESIS OF EXTENDED NANOGRAPHENE MOLECULES WITH FECL3
AND A1C13 186
6.2.2 COMPLEMENTARY CYCLODEHYDROGENATION METHODS FOR THE SOLUTION
SYNTHESIS
OF NANOGRAPHENE MOLECULES 188
6.2.3 SYNTHESIS OF NANOGRAPHENE MOLECULES WITH SEVEN- AND EIGHT-MEMBERED
RINGS 195
6.2.4 SYNTHESIS OF HETEROATOM-DOPED NANOGRAPHENE MOLECULES 198
6.2.5 NANOGRAPHENE MOLECULES THROUGH SURFACE-ASSISTED
CYCLODEHYDROGENATION 202
6.3 BOTTOM-UP SYNTHESIS OF GRAPHENE NANORIBBONS 204
6.3.1 GRAPHENE NANORIBBONS FROM SOLUTION-MEDIATED
CYCLODEHYDROGENATION 205
6.3.2 GRAPHENE NANORIBBONS FROM SURFACE-ASSISTED CYCLODEHYDROGENATION
208
6.4 CONCLUSIONS 217
REFERENCES 218
1
PHOTOCHEMICAL AND DIRECT C-H ARYLATION ROUTES TOWARD CARBON
NANOMATERIALS
229
JEAN-FRANCOIS MORIN, MAXIME DAIGLE, AND MAUDE DESROCHES
7.1 INTRODUCTION 229
12 PHOTOCHEMICAL ROUTES TOWARD PAHS AND CARBON NANOMATERIALS 231
7.2.1 PHOTOCHEMICAL DEHYDROGENATION 231
7.2.2 PHOTOCHEMICAL DEHYDROHALOGENATION (CDU) 237
7 2 3 MISCELLANEOUS PHOTOCYCLIZATION REACTION 242
7.3 INTRAMOLECULAR DIRECT ARYLATION C -H 243
7.3.1 CONCLUSION AND PERSPECTIVE 249
REFERENCES 250
8 CARBON-RICH MATERIALS FROM SP-CARBON PRECURSORS
255
DOMINIK PRENZEL AND RIK R. TYKWINSKI
8.1 INTRODUCTION 255
8.2 CARBYNE 256
8.3 SOLID-STATE REACTIONS OF POLYYNES: TOPOCHEMICAL POLYMERIZATIONS 261
8.4 DIYNE POLYMERIZATION 261
8.5 TUBULAR STRUCTURES 264
8.6 BEYOND DIYNES - TOPOCHEMICAL POLYMERIZATION OF POLYYNES 268
8.7 TOWARD NANOGRAPHENE* 272
8.8 PENTALENES 274
8.9 MODIFICATION OF SP-PRECURSORS WITH TETRACYANOETHYLENE (TCNE) 275
8.10 THERMAL DIMERIZATION OF CUMULENES 278
8.11 OUTLOOK: FROM SOLUTION TO SURFACE? 278
8.12 SUMMARIZING COMMENTS 282
ACKNOWLEDGMENTS 286
REFERENCES 286
INDEX
293
|
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dewey-ones | 540 - Chemistry and allied sciences |
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dewey-sort | 3540 |
dewey-tens | 540 - Chemistry and allied sciences |
discipline | Chemie / Pharmazie |
format | Book |
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indexdate | 2024-07-10T07:41:40Z |
institution | BVB |
institution_GND | (DE-588)16179388-5 |
isbn | 9783527339983 |
language | English |
oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-029439074 |
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physical | x, 300 Seiten Illustrationen, Diagramme (teilweise farbig) |
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spelling | Synthetic methods for conjugated polymers and carbon materials edited by Mario Leclerc and Jean-François Morin Weinheim Wiley-VCH Verlag GmbH & Co. KGaA [2017] © 2017 x, 300 Seiten Illustrationen, Diagramme (teilweise farbig) txt rdacontent n rdamedia nc rdacarrier Kohlenstoffwerkstoff (DE-588)4031677-4 gnd rswk-swf Konjugierte Polymere (DE-588)4236284-2 gnd rswk-swf Carbon Materials Chemie Chemistry Kohlenstoffmaterial Kohlenstoffmaterialien Materials Science Materialwissenschaften Organic Chemistry Organische Chemie Polymer Science & Technology Polymer Synthesis Polymersynthese Polymerwissenschaft u. -technologie (DE-588)4143413-4 Aufsatzsammlung gnd-content Konjugierte Polymere (DE-588)4236284-2 s Kohlenstoffwerkstoff (DE-588)4031677-4 s DE-604 Leclerc, Mario 1961- Sonstige (DE-588)1081309075 oth Morin, Jean-François 1978- Sonstige (DE-588)1125471239 oth Wiley-VCH (DE-588)16179388-5 pbl Erscheint auch als Online-Ausgabe, ePDF 978-3-527-69598-0 Erscheint auch als Online-Ausgabe, ePub 978-3-527-69596-6 Erscheint auch als Online-Ausgabe, Mobi 978-3-527-69597-3 Erscheint auch als Online-Ausgabe, oBook 978-3-527-69595-9 DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=029439074&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
spellingShingle | Synthetic methods for conjugated polymers and carbon materials Kohlenstoffwerkstoff (DE-588)4031677-4 gnd Konjugierte Polymere (DE-588)4236284-2 gnd |
subject_GND | (DE-588)4031677-4 (DE-588)4236284-2 (DE-588)4143413-4 |
title | Synthetic methods for conjugated polymers and carbon materials |
title_auth | Synthetic methods for conjugated polymers and carbon materials |
title_exact_search | Synthetic methods for conjugated polymers and carbon materials |
title_full | Synthetic methods for conjugated polymers and carbon materials edited by Mario Leclerc and Jean-François Morin |
title_fullStr | Synthetic methods for conjugated polymers and carbon materials edited by Mario Leclerc and Jean-François Morin |
title_full_unstemmed | Synthetic methods for conjugated polymers and carbon materials edited by Mario Leclerc and Jean-François Morin |
title_short | Synthetic methods for conjugated polymers and carbon materials |
title_sort | synthetic methods for conjugated polymers and carbon materials |
topic | Kohlenstoffwerkstoff (DE-588)4031677-4 gnd Konjugierte Polymere (DE-588)4236284-2 gnd |
topic_facet | Kohlenstoffwerkstoff Konjugierte Polymere Aufsatzsammlung |
url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=029439074&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
work_keys_str_mv | AT leclercmario syntheticmethodsforconjugatedpolymersandcarbonmaterials AT morinjeanfrancois syntheticmethodsforconjugatedpolymersandcarbonmaterials AT wileyvch syntheticmethodsforconjugatedpolymersandcarbonmaterials |