01196nam0 22003011i 450 UON0039244520231205104618.786978-22-514-2042-420110510d2010 |0itac50 bafreFR|||| 1||||Etudes de patristique et d'histoire des conceptsPierre HadotParisLes Belles lettres2010406 p.22 cmVOA VII BA 525 NUON00351721001UON003517212001 ˆL' ‰âne d'or210 ParisLes Belles Lettres. VOA VII BA 525 NPATRISTICAUONC002934FIFRParisUONL002984VOC VII BVICINO ORIENTE CLASSICO - FILOSOFIAAHADOTPierreUONV055480163608Les Belles LettresUONV245913650ITSOL20240220RICASIBA - SISTEMA BIBLIOTECARIO DI ATENEOUONSIUON00392445SIBA - SISTEMA BIBLIOTECARIO DI ATENEOSI VOC VII B 014 SI SA 129774 5 014 Etudes de patristique et d'histoire des concepts250288UNIOR03957nam 2200613 450 991082999490332120180613002829.01-118-85885-91-118-85872-71-118-85898-0(CKB)3710000000521832(EBL)4548025(SSID)ssj0001579552(PQKBManifestationID)16255417(PQKBTitleCode)TC0001579552(PQKBWorkID)13190666(PQKB)10709661(PQKBManifestationID)14558238(PQKBWorkID)13299972(PQKB)20965169(MiAaPQ)EBC4548025(DLC) 2015033594(PPN)201592851(OCoLC)919316488(EXLCZ)99371000000052183220150818h20162016 uy| 0engur|n|---|||||txtccrOrganic redox systems synthesis, properties, and applications /edited by Tohru NishinagaHoboken, New Jersey :Wiley,[2016]©20161 online resource (862 p.)Description based upon print version of record.1-118-85874-3 Includes bibliographical references and index.TITLE 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 σ-BOND FORMATION/CLEAVAGE; 2.1 DYNAMIC REDOX ("DYREX") SYSTEMS; 2.2 ADVANCED ELECTROCHROMIC RESPONSE OF "ENDO"-TYPE DYREX SYSTEMS EXHIBITING REDOX SWITCHING OF A σ-BOND; 2.3 ADVANCED ELECTROCHROMIC RESPONSE OF "EXO"-TYPE DYREX SYSTEMS EXHIBITING REDOX SWITCHING OF A σ-BOND2.4 PROSPECT: REDOX SYSTEMS WITH MULTIPLE DYREX UNITSREFERENCES; 3 REDOX-CONTROLLED INTRAMOLECULAR MOTIONS TRIGGERED BY π-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; REFERENCES4 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 STUDY5.3 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 Π-SYSTEM7.5 THE LENGTH OF THE BRIDGEOxidation-reduction reactionOxidation-reduction reaction.547/.23Nishinaga TohruMiAaPQMiAaPQMiAaPQBOOK9910829994903321Organic redox systems4078876UNINA