LEADER 05267nam 2200625 a 450 001 996203742303316 005 20170809175845.0 010 $a1-281-84341-5 010 $a9786611843410 010 $a3-527-61921-6 010 $a3-527-61922-4 035 $a(CKB)1000000000553773 035 $a(EBL)482064 035 $a(OCoLC)298072160 035 $a(SSID)ssj0000120606 035 $a(PQKBManifestationID)11142214 035 $a(PQKBTitleCode)TC0000120606 035 $a(PQKBWorkID)10081826 035 $a(PQKB)11383332 035 $a(MiAaPQ)EBC482064 035 $a(PPN)156596415 035 $a(EXLCZ)991000000000553773 100 $a19940616d1994 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 14$aThe chemistry of the fullerenes$b[electronic resource] /$fAndreas Hirsch 210 $aStuttgart ;$aNew York $cG. Thieme Verlag$d1994 215 $a1 online resource (218 p.) 225 1 $aThieme organic chemistry monograph series 300 $aDescription based upon print version of record. 311 $a3-527-30890-3 320 $aIncludes bibliographical references and index. 327 $aThe Chemistry of the Fullerenes; Contents; Chapter 1. The Parent Fullerenes; 1.1 The Fullerenes: Molecular Allotropes of Carbon; 1.2 The Discovery of the Fullerenes; 1.3 Fullerene Production; 1.3.1 Fullerene Generation by Vaporization of Graphite; 1.3.1.1 Resitive Heating of Graphite; 1.3.1.2 Arc heating of Graphite; 1.3.1.3 Solar Generators; 1.3.1.4 Inductive Heating of Graphite; 1.3.2 Fullerene Synthesis in Combustion; 1.3.3 Formation of Fullerenes by Pyrolysis of Naphthalene; 1.3.4 Endohedrals; 1.3.5 The Formation Process; 1.4 Separation and Purification; 1.5 Properties; 1.5.1 Structures 327 $a1.5.2 Physical and Spectroscopic PropertiesReferences; Chapter 2. Reduction; 2.1 Introduction; 2.2 Fulleride Anions; 2.3 Reductive Electrosynthesis; 2.3.1 Electrocrystallization; 2.3.2 Electrophilic Additions to Fulleride Anions; 2.4 Reduction with Metals; 2.4.1 Alkali Metal Fullerides; 2.4.1.1 Generation in Solution and Quenching Experiments; 2.4.1.2 Synthesis and Properties of Alkali Metal Fulleride Solids; 2.4.2 Alkaline Earth Metal Fullerides; 2.4.3 Reduction with Mercury; 2.5 Reduction with Organic Donor Molecules; References; Chapter 3. Nucleophilic Additions; 3.1 Introduction 327 $a3.2 Addition of Carbon Nucleophiles3.2.1 Hydroalkylation and Hydroarylation of C60 and C70; 3.2.2 Langmuir - Blodgett Films of C60Ht-Bu; 3.2.3 Addition of Macromolecular Carbanions - Fullerene Polymers; 3.2.4 Cyclopropanation of C60 and C70; 3.3 Addition of Amines; 3.4 Addition of Hydroxide; References; Chapter 4. Cycloadditions; 4.1 Introduction; 4.2 [4+2] Cycloadditions; 4.3 [3+2] Cycloadditions; 4.3.1 Addition of Diazomethanes. Diazoacetates and Diazoamides; 4.3.2 Addition of Azides; 4.3.3 Addition of Trimethylenemethanes; 4.3.4 Addition of Azomethine Ylides 327 $a4.3.5 Addition of Nitrile Oxides4.3.6 Addition of Sulfinimides; 4.3.7 Addition of Disiliranes; 4.4 [2+2] Cycloadditions; 4.4.1 Addition of Benzyne; 4.4.2 Addition of Enones; 4.4.3 Addition of Quadricyclane; 4.4.4 Addition of Electron Rich Alkynes; 4.4.5 Photopolymerization of C60; 4.5 [2+1] Cycloadditions; 4.5.1 Addition of Carbenes; 4.5.2 Addition of Silylenes; References; Chapter 5. Hydrogenation; 5.1 Introduction; 5.2 Oligohydrofullerenes C60Hzn and C70H2n (n = 1 - 6); 5.2.1 Hydrogenation via Hydroboration, Hydrozirconation and Zinc/Acid Reduction; 5.2.2 Theoretical Investigations 327 $a5.3 Polyhydrofullerenes C60H2n and C70H2n (n = 7 - 70)5.3.1 Birch - Huckel Reduction; 5.3.2 Transfer Hydrogenation of C60 and C70; 5.3.3 Catalytic Hydrogenation; 5.3.4 Theoretical Investigations; References; Chapter 6. Radical Additions; 6.1 Introduction; 6.2 ESR Investigations of Radical Additions; 6.2.1 Addition of Single Radicals; 6.2.2 Multiple Radical Additions; 6.3 Metalation of C60 with Pentacarbonylrhenium Radicals; 6.4 Hydrostannylation of C60; 6.5 Addition of Bis(trifluoromethyl)nitroxide; 6.6 Radical Copolymerization of C60 and Paracyclophane; References 327 $aChapter 7. Transition Metal Complex Formation 330 $aAlthough synthetic fullerenes have only been around for a few years, there are thousands of scientific articles dealing with them. This is the first monograph in the field and thus represents a vital source of information summarizing the most important and fundamental aspects of the organic and organometallic chemistry of the fullerenes. The book is logically arranged so that information is easy to retrieve, and the style lends itself to effortless reading and to learning more about the chemical properties of a family of molecules that constitute new building blocks for novel architectures 410 0$aThieme organic chemistry monograph series. 606 $aFullerenes 615 0$aFullerenes. 676 $a543.0894 676 $a546.681 700 $aHirsch$b Andreas$cDr. rer. nat.$0916471 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a996203742303316 996 $aThe chemistry of the fullerenes$92273853 997 $aUNISA LEADER 01618oam 2200457 450 001 9910713670803321 005 20220405110242.0 035 $a(CKB)5470000002502964 035 $a(OCoLC)1159227079$z(OCoLC)1164154050$z(OCoLC)1182541615$z(OCoLC)1182634219 035 $a(EXLCZ)995470000002502964 100 $a20200622d2020 ua 0 101 0 $aeng 135 $aurbn||||a|||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aAssessing the value of the NATO alliance $ehearing before the Committee on Foreign Relations, United States Senate, One Hundred Fifteenth Congress, second session, September 5, 2018 210 1$aWashington :$cU.S. Government Publishing Office,$d2020. 215 $a1 online resource (iii, 58 pages) 225 1 $aS. hrg. ;$v115-780 517 $aAssessing the value of the NATO alliance 606 $aBallistic missile defenses$zEurope 606 $aNational security$xInternational cooperation 606 $aSecurity, International 607 $aRussia (Federation)$xForeign relations$zEurope 607 $aEurope$xForeign relations$zRussia (Federation) 608 $aLegislative hearings.$2lcgft 615 0$aBallistic missile defenses 615 0$aNational security$xInternational cooperation. 615 0$aSecurity, International. 801 0$bGPO 801 1$bGPO 801 2$bGPO 801 2$bOCLCF 801 2$bOCLCA 801 2$bOCLCQ 801 2$bGPO 906 $aBOOK 912 $a9910713670803321 996 $aAssessing the value of the NATO alliance$93444424 997 $aUNINA LEADER 02126oam 2200625I 450 001 9910713675503321 005 20201019065457.0 035 $a(CKB)5470000002502916 035 $a(OCoLC)1127388932 035 $a(EXLCZ)995470000002502916 100 $a20191113d1927 ua 0 101 0 $aeng 135 $aurbn||||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$a"ALCLAD" $ea new corrosion resistant aluminum product /$fby E.H. Dix, Jr 210 1$aWashington, [D.C.] :$cNational Advisory Committee for Aeronautics,$d1927. 215 $a1 online resource (13 pages, 3 unnumbered pages) $cillustrations 225 1 $aTechnical notes / National Advisory Committee for Aeronautics ;$vNo. 259 300 $a"August 1927." 300 $a"Read before the Committee on Materials for Aircraft of the National Advisory Committee for Aeronautics, at the annual aircraft conference at Langley Field, Va., May 24, 1927"--Page 1. 300 $aNo Federal Depository Library Program (FDLP) item number. 517 $a"ALCLAD" 606 $aAluminum alloys 606 $aMetal cladding 606 $aCorrosion resistant alloys 606 $aCorrosion resistant materials 606 $aMetal cladding$2fast 606 $aAluminum alloys$2fast 606 $aCorrosion resistant alloys$2fast 606 $aCorrosion resistant materials$2fast 615 0$aAluminum alloys. 615 0$aMetal cladding. 615 0$aCorrosion resistant alloys. 615 0$aCorrosion resistant materials. 615 7$aMetal cladding. 615 7$aAluminum alloys. 615 7$aCorrosion resistant alloys. 615 7$aCorrosion resistant materials. 700 $aDix$b E. H.$01408843 712 02$aUnited States.$bNational Advisory Committee for Aeronautics, 801 0$bTRAAL 801 1$bTRAAL 801 2$bTRAAL 801 2$bOCLCO 801 2$bOCLCF 801 2$bGPO 801 2$bMUB 801 2$bOCL 801 2$bGPO 906 $aBOOK 912 $a9910713675503321 996 $a"ALCLAD"$93493754 997 $aUNINA