LEADER 01187nam0-22004211i-450- 001 990006021240403321 005 20160223124144.0 035 $a000602124 035 $aFED01000602124 035 $a(Aleph)000602124FED01 035 $a000602124 100 $a20130723d1987----km-u0itay50------ba 101 0 $aita 102 $aIT 105 $ay---y---001yy 200 1 $a<>invenzioni e i modelli industriali nella giurisprudenza$fGiovanni Lecce 210 $aMilano$cGiuffrè$d1987 215 $aVIII, 607 p.$d24 cm 225 1 $aRaccolta sistematica di giurisprudenza commentata$iNuova serie$v6 676 $a346.07 676 $a346.03 676 $a343 700 1$aLecce,$bGiovanni$0229442 801 0$aIT$bUNINA$gRICA$2UNIMARC 901 $aBK 912 $a990006021240403321 952 $aDPR 20-460$b3744$fDEC 952 $aVI F 642$b269$fDDA 952 $aCOLLEZ. 257BIS (6)$b3298*$fFGBC 952 $a2-C-IV-6$fDDCP 952 $aCOLLEZ. 1156 (6)$b7843$fFSPBC 959 $aDEC 959 $aFGBC 959 $aDDA 959 $aDDCP 959 $aFSPBC 996 $aInvenzioni e i modelli industriali nella giurisprudenza$9578933 997 $aUNINA LEADER 00836nam0-2200301---450 001 990002767400203316 005 20220601120951.0 035 $a000276740 035 $aUSA01000276740 035 $a(ALEPH)000276740USA01 035 $a000276740 100 $a20060627d1978----km-y0itaa50------ba 101 0 $afre 102 $aBE 105 $a||||z|||001fy 200 1 $a<> vieux médicin raconte...$fArmand Colard$gpréface de George Sion 210 $aBruxelles$cJ. Goemaere$d1978 215 $a155 p.$d22 cm 676 $a843.914 700 1$aCOLARD,$bArmand$0593726 801 0$aIT$bsalbc$gISBD 912 $a990002767400203316 951 $aXV.4.A. 1109$b185699 L.M.$cXV.4.A. 959 $aBK 969 $aFF 979 $aMARIASEN$b90$c20060627$lUSA01$h1041 996 $aVieux médicin raconte..$9997614 997 $aUNISA LEADER 04671nam 2200613 450 001 9910830515703321 005 20230421044619.0 010 $a1-281-84295-8 010 $a9786611842956 010 $a3-527-61613-6 010 $a3-527-61612-8 035 $a(CKB)1000000000376628 035 $a(EBL)482212 035 $a(OCoLC)723943581 035 $a(SSID)ssj0000354716 035 $a(PQKBManifestationID)11925310 035 $a(PQKBTitleCode)TC0000354716 035 $a(PQKBWorkID)10314535 035 $a(PQKB)10780593 035 $a(MiAaPQ)EBC482212 035 $a(EXLCZ)991000000000376628 100 $a20160820h19931993 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aReactivity in molecular crystals /$fedited by Yuji Ohashi 210 1$aTokyo, Japan ;$aWeinheim, [Germany] :$cKodansha :$cVCH,$d1993. 210 4$d©1993 215 $a1 online resource (362 p.) 300 $aDescription based upon print version of record. 311 $a3-527-29098-2 320 $aIncludes bibliographical references at the end of each chapters and index. 327 $aReactivity in Molecular Crystals; List of Contributors; Contents; Preface; 1. THEORETICAL APPROACH; 1.1 Potential Energy Calculations of Crystals; 1.2 A Novel Molecular-Dynamics Method to Predict Molecular Crystal Structures; 2. PHYSICO-CHEMICAL APPROACH; 2.1 Development of a New X-Ray Diffractometer (IPD-WAS) for Rapid Measurement; 2.2 Reaction Process in Solid State Studied by High Resolution Electron Spectromicroscopy; 2.3 Analysis of Charge Transfer Complex Formation in the Solid State by Penning lonilation Electron Spectroscopy 327 $a2.4 Analysis of Reactive Species by Time Resolved Infrared Reflection Absorption Spectroscopy2.5 Molecular Motion in Clathrate Crystals Analyred by Solid-state NMR Method; 2.6 Asymmetric Structure Analysis for Reaction Centers of a Molecular Crystal and on a Crystal Surface by EXAFS Spectroscopy; 2.7 Excitation Energy Transfer Between Metal Complexes in Solids; 3. CRYSTALLINE-STATE REACTION; 3.1 Dynamic Structure Analysis of Crystalline-State Reaction; 3.2 Reversible Intercalation of Guest Molecules in Crystals of Cholic Acid 327 $a3.3 How can Crystalline Environment Provide Outstanding Chemistry for Diarylcarbenes or Arylnitrenes4. Solid-to- Solid Organic Reactions; 4.1 Introduction; 4.2 Pinacol and Benzylic Acid Rearrangement; 4.3 Baeyer-Villiger Oxidation; 4.4 Reduction with NaBH4; 4.5 Grignard, Reformatsky and Luche Reactions; 4.6 Coupling Reactions; 4.7 Witting-Horner Reaction; 4.8 Aldol Condensation; 4.9 Dehydration, Rearrangement, Chlorination and Etherification of Secondary Alcohols; 4.10 Host-Guest Inclusion Complexation in the Solid State; 5. Streoselective Solid-State Photoreaction 327 $a5.1 Determining Factors of Molecular Arrangement and Reaction Course in the Crystalline-State Photoreaction of Unsymmetrically Substituted Diolefins5.2 Stereoselectivity in Reactions of Clathrate Crystals; 5.3 Solid-state Photochromism of Tetraphenyldihydro-1,3,5-Triazine and Related Heterocycles; 5.4 Solid-state Photoracemization and Photoisomerization of Alkyl Cobalt Complexes; 6. REACTIVITY AND CRYSTAL STRUCTURE; 6.1 Packing Effect in Solid-State Polymerization of Diethynylbenzene Derivatives by Radiation 327 $a6.2 High Selective Reaction Deduced by Tunneling Effect in the Crystalline Environment6.3 Formation of Bimolecular Films and Crystal Structure; 6.4 Reactivity and Reaction Pathway of the Sulfur Compounds; 6.5 Stereoselectivity and Molecular Recognition in Double Macrocyclic Inclusion Crystals; Index 330 $aDo you need to design syntheses that are* highly selective* fast* enantioselective with quantitative enantiomeric yield? This book describes in detail how best to exploit the enormous synthetic potential of solid state reactions. Written by leading experts, it provides in-depth information on* the theoretical and physico-chemical approach to solid state reactions* solid-to-solid organic reactions* stereoselective solid state photoreactions* reactivity and crystal structureAn ideal companion to Dunitz and Bu?rgi's 'Structure Correlation', this 606 $aMolecular crystals 606 $aChemical reactions 615 0$aMolecular crystals. 615 0$aChemical reactions. 676 $a548 676 $a548.85 702 $aO?hashi$b Yu?ji$f1941- 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830515703321 996 $aReactivity in molecular crystals$92016854 997 $aUNINA