LEADER 01002nam 2200313 450 001 996422950403316 005 20210617083842.0 010 $a978-88-921-3736-3 100 $a20210617d2021----km y0itay5003 ba 101 0 $aita 102 $aIT 105 $ay 00 y 200 1 $aEconomia politica del terzo settore$fFrancesco Amati, Salvatore D'Acunto, Marco Musella 210 1 $aTorino$cGiappichelli$d2021 215 $aXIV, 213 p.$d24 cm 225 2 $aWelfare, economia sociale e sviluppo$v14 410 0 $aWelfare, economia sociale e sviluppo$v14 606 0 $aEnti senza scopo di lucro$xEconomia$2BNCF 676 $a338.47361763 700 1$aAMATI,$bFrancesco$f<1977- >$0804839 701 1$aD'ACUNTO,$bSalvatore$0118106 701 1$aMUSELLA,$bMarco$0118105 801 0$aIT$bcba$gREICAT 912 $a996422950403316 951 $a338.473 AMA 1$b92068 G.$c338.473$d539792 959 $aBK 969 $aECO 996 $aEconomia politica del terzo settore$91806901 997 $aUNISA LEADER 04956nam 2200625Ia 450 001 9910830959503321 005 20170814175535.0 010 $a1-282-11847-1 010 $a9786612118470 010 $a3-527-62713-8 010 $a3-527-62714-6 035 $a(CKB)1000000000785746 035 $a(EBL)481649 035 $a(OCoLC)435820278 035 $a(SSID)ssj0000251887 035 $a(PQKBManifestationID)11237341 035 $a(PQKBTitleCode)TC0000251887 035 $a(PQKBWorkID)10170659 035 $a(PQKB)10888908 035 $a(MiAaPQ)EBC481649 035 $a(PPN)152559027 035 $a(EXLCZ)991000000000785746 100 $a20081125d2009 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aStrained hydrocarbons$b[electronic resource] $ebeyond the van't Hoff and Le Bel hypothesis /$fedited by Helena Dodziuk 210 $aWeinheim $cWiley-VCH$dc2009 215 $a1 online resource (495 p.) 300 $aDescription based upon print version of record. 311 $a3-527-31767-8 320 $aIncludes bibliographical references and index. 327 $aStrained Hydrocarbons; Foreword; Preface; Contents; List of Contributors; 1 Introduction; 1.1 Initial Remarks; 1.2 Hydrocarbons with Unusual Spatial Structure: the Need to Finance Basic Research; 1.3 Computations on Strained Hydrocarbons; 1.4 Gallery of Molecules That Could Have Been Included in This Book; 1.4.1 Introductory Remarks; 1.4.2 Saturated Hydrocarbons; 1.4.3 Distorted Double Bonds; 1.4.4 Benzene Rings with Nontypical Spatial Structures; 1.4.5 Cumulenes; 1.4.6 Acetylenes; References; 2 Distorted Saturated Hydrocarbons; 2.1 Molecules with Inverted Carbon Atoms; 2.1.1 Introduction 327 $a2.1.2 Small-ring Propellanes: Computational and Physicochemical Studies2.1.3 Small-ring Propellanes: Experimental Results; 2.1.3.1 Preparation and Reactivity of [1.1.1]Propellane; 2.1.3.2 Preparation and Reactivity of [2.1.1]Propellane and [2.2.1]Propellane; 2.1.3.3 [1.1.1]Propellane as the Precursor for the Synthesis of Other Unusual Molecules; 2.1.4 New Hypothetical Molecules with Inverted Carbon Atoms; 2.2 Molecules with Planar and Pyramidal Carbon Atoms; 2.3 A Theoretical Approach to the Study and Design of Prismane Systems; 2.3.1 Introduction; 2.3.2 Prismanes; 2.3.3 Expanded Prismanes 327 $a2.3.3.1 Asteranes2.3.3.2 Ethynyl-expanded Prismanes; 2.3.4 Dehydroprismanes; 2.3.5 Polyprismanes; 2.3.5.1 Cubane Oligomers; 2.3.5.2 Fused Prismanes; 2.3.6 Conclusions; 2.4 (CH)(2n) Cage Structures, 'in'-'out' Isomerism in Perhydrogenated Fullerenes and Planar Cyclohexane Rings; 2.4.1 (CH)(2n) Cage Structures; 2.4.1.1 Tetrahedrane; 2.4.1.2 Triprismane; 2.4.1.3 Cubane 61, Cuneane 100 and Octabisvalene 101 C(8)H(8); 2.4.1.4 C(10)H(10) Saturated Cages; 2.4.1.5 C(12)H(12) Saturated Cages; 2.4.1.6 Higher [n]Prismanes, Dodecahedrane 327 $a2.4.1.7 'In'-'out' Isomerism in Perhydrogenated Fullerenes C(60)H(60)2.4.1.8 Summary; 2.4.2 Planar Cyclohexane Rings; 2.5 Ultralong C-C Bonds; 2.5.1 Introduction; 2.5.2 Ultralong C-C Bonds Confined in a Stiff Molecular Frame; 2.5.3 Tetraphenylnaphthocyclobutene as a Scaffold to Produce Ultralong C-C Bonds; 2.5.4 'Clumped' Hexaphenylethane Derivatives with Elongated and Ultralong C-C Bonds; 2.5.5 HPE Derivatives with a Super-ultralong C-C Bond; 2.5.6 'Expandability' of the Ultralong C-C Bond: Conformational Isomorphs with Different Bond Lengths; 2.5.7 Future Outlook; 2.6 Ultrashort C-C Bonds 327 $a2.6.1 Introduction2.6.2 Tricyclo[2.1.0.0(2,5)]pentanes: Ultrashort Endocyclic Bridging C-C Bonds; 2.6.3 Coupled Cage Compounds: Ultrashort Exocyclic Intercage C-C Bonds; 2.6.4 Sterically Congested in-Methylcyclophanes: Ultrashort C-C(Me) Bonds; 2.6.5 Conclusions; References; 3 Distorted Alkenes; 3.1 Nonplanar Alkenes; 3.1.1 Introduction and Context; 3.1.2 Bridgehead Alkenes; 3.1.2.1 t-Butyl-substituted Ethylenes; 3.1.2.2 Investigations of t-Butylated Ethylenes and Other Acyclic Alkenes; 3.1.2.3 Cyclo and Bicycloalkenes ... and on to Polycyclic Analogs 327 $a3.1.2.4 Adamantylideneadamantane and its Derivatives 330 $aIn clearly structured chapters, this book covers the fascinating world of hydrocarbons, providing an insight into the fundamental principles of chemistry. The monograph covers modern aspects of the topic, such as carbon nanotubes, molecular flask inclusion, and fullerenes, with new synthetic procedures for the build up of the structural lattice included. 606 $aHydrocarbons 606 $aChemistry, Organic 615 0$aHydrocarbons. 615 0$aChemistry, Organic. 676 $a547.01 676 $a547/.01 701 $aDodziuk$b Helena$0563740 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830959503321 996 $aStrained hydrocarbons$93933297 997 $aUNINA