LEADER 03924nam 2200601 450 001 9910137222703321 005 20180613002829.0 010 $a1-118-85885-9 010 $a1-118-85872-7 010 $a1-118-85898-0 035 $a(CKB)3710000000521832 035 $a(EBL)4548025 035 $a(SSID)ssj0001579552 035 $a(PQKBManifestationID)16255417 035 $a(PQKBTitleCode)TC0001579552 035 $a(PQKBWorkID)13190666 035 $a(PQKB)10709661 035 $a(PQKBManifestationID)14558238 035 $a(PQKBWorkID)13299972 035 $a(PQKB)20965169 035 $a(MiAaPQ)EBC4548025 035 $a(DLC) 2015033594 035 $a(PPN)201592851 035 $a(EXLCZ)993710000000521832 100 $a20150818h20162016 uy| 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aOrganic redox systems $esynthesis, properties, and applications /$fedited by Tohru Nishinaga 210 1$aHoboken, New Jersey :$cWiley,$d[2016] 210 4$dİ2016 215 $a1 online resource (862 p.) 300 $aDescription based upon print version of record. 311 $a1-118-85874-3 320 $aIncludes bibliographical references and index. 327 $aTITLE PAGE; TABLE OF CONTENTS; LIST OF CONTRIBUTORS; PREFACE; 1 INTRODUCTION: BASIC CONCEPTS AND A BRIEF HISTORY OF ORGANIC REDOX SYSTEMS; 1.1 REDOX REACTION OF ORGANIC MOLECULES; 1.2 REDOX POTENTIAL IN NONAQUEOUS SOLVENTS; 1.3 A BRIEF HISTORY OF ORGANIC REDOX COMPOUNDS; REFERENCES; 2 REDOX-MEDIATED REVERSIBLE ?-BOND FORMATION/CLEAVAGE; 2.1 DYNAMIC REDOX ("DYREX") SYSTEMS; 2.2 ADVANCED ELECTROCHROMIC RESPONSE OF "ENDO"-TYPE DYREX SYSTEMS EXHIBITING REDOX SWITCHING OF A ?-BOND; 2.3 ADVANCED ELECTROCHROMIC RESPONSE OF "EXO"-TYPE DYREX SYSTEMS EXHIBITING REDOX SWITCHING OF A ?-BOND 327 $a2.4 PROSPECT: REDOX SYSTEMS WITH MULTIPLE DYREX UNITSREFERENCES; 3 REDOX-CONTROLLED INTRAMOLECULAR MOTIONS TRIGGERED BY ?-DIMERIZATION AND PIMERIZATION PROCESSES; 3.1 INTRODUCTION; 3.2 OLIGOTHIOPHENES; 3.3 PHENOTHIAZINE; 3.4 NAPHTHALENE AND PERYLENE BISIMIDES; 3.5 para-PHENYLENEDIAMINE; 3.6 PYRIDINYL RADICALS; 3.7 VIOLOGEN DERIVATIVES; 3.8 VERDAZYL; 3.9 PHENALENYL; 3.10 PORPHYRINS; 3.11 BENZENOID; 3.12 CYCLOPHANE; 3.13 TETRATHIAFULVALENE; 3.14 CONCLUSION; ACKNOWLEDGMENTS; REFERENCES 327 $a4 TETRATHIAFULVALENE: A REDOX UNIT FOR FUNCTIONAL MATERIALS AND A BUILDING BLOCK FOR SUPRAMOLECULAR SELF-ASSEMBLY4.1 INTRODUCTION: PAST AND PRESENT OF TTF CHEMISTRY; 4.2 BASIC REDOX PROPERTIES OF TTF AND STACKED TTF; 4.3 TTF AS A FAITHFUL REDOX ACTIVE UNIT IN FUNCTIONAL MATERIALS; 4.4 ELECTROCONDUCTING PROPERTIES OF TTF DERIVATIVES BASED ON SUPRAMOLECULAR SELF-ASSEMBLY; 4.5 SUMMARY AND OUTLOOK; REFERENCES; 5 ROBUST AROMATIC CATION RADICALS AS REDOX TUNABLE OXIDANTS; 5.1 INTRODUCTION; 5.2 DESIGNING MOLECULES FOR THE FORMATION OF STABLE CATION RADICALS (CRs)-A CASE STUDY 327 $a5.3 METHODS OF PREPARATIVE ISOLATION OF AROMATIC CATION RADICALS5.4 QUANTITATIVE OXIDATION OF ELECTRON DONORS USING THE-ORANGE+· SbCl6- AS ONE-ELECTRON OXIDANT; 5.5 READILY AVAILABLE ELECTRON DONORS FOR THE REDOX-TUNABLE AROMATIC OXIDANTS; 5.6 CONCLUSION; REFERENCES; 6 AIR-STABLE REDOX-ACTIVE NEUTRAL RADICALS: TOPOLOGICAL SYMMETRY CONTROL OF ELECTRONIC-SPIN, MULTICENTERED CHEMICAL BONDING, AND ORGANIC BATTERY APPLICATION; 6.1 INTRODUCTION; 6.2 OPEN-SHELL GRAPHENE FRAGMENT: DESIGN AND SYNTHESIS OF AIR-STABLE CARBON-CENTERED NEUTRAL RADICALS BASED ON FUSED-POLYCYCLIC ?-SYSTEM 327 $a7.5 THE LENGTH OF THE BRIDGE 606 $aOxidation-reduction reaction 615 0$aOxidation-reduction reaction. 676 $a547/.23 702 $aNishinaga$b Tohru 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910137222703321 996 $aOrganic redox systems$92072115 997 $aUNINA