LEADER 00955nam1 22002653i 450 001 VAN00218532 005 20240806101251.855 100 $a20210928f |0itac50 ba 101 $aeng 102 $aCH 105 $a|||| ||||| 200 1 $aSemiconductor optics$fHeinz Kalt, Claus F. Klingshirn 210 $aCham$cSpringer 215 $avolumi$cill.$d24 cm 463 1$1001VAN00218534$12001 $aˆ1: ‰Linear Optical Properties of Semiconductors$fHeinz Kalt, Claus F. Klingshirn$1205 $a5. ed$1210 $aCham$cSpringer$d2019$1215 $axix, 559 p.$cill.$d24 cm$v1 500 1$3VAN00218539$aSemiconductor optics$92983258 620 $aCH$dCham$3VANL001889 700 1$aKalt$bHeinz$3VANV185968$0294630 701 1$aKlingshirn$bClaus F.$3VANV026656$0542529 712 $aSpringer $3VANV108073$4650 801 $aIT$bSOL$c20240906$gRICA 912 $fN 912 $aVAN00218532 996 $aSemiconductor optics$92983258 997 $aUNICAMPANIA LEADER 05417nam 22007094a 450 001 9910828098003321 005 20200520144314.0 010 $a9786612237539 010 $a9781282237537 010 $a1282237535 010 $a9780470516683 010 $a0470516682 010 $a9780470516676 010 $a0470516674 035 $a(CKB)1000000000376503 035 $a(EBL)454455 035 $a(OCoLC)609844468 035 $a(SSID)ssj0000353954 035 $a(PQKBManifestationID)11251614 035 $a(PQKBTitleCode)TC0000353954 035 $a(PQKBWorkID)10302226 035 $a(PQKB)10299653 035 $a(MiAaPQ)EBC454455 035 $a(Au-PeEL)EBL454455 035 $a(CaPaEBR)ebr10317837 035 $a(CaONFJC)MIL223753 035 $a(OCoLC)122701726 035 $a(FINmELB)ELB178412 035 $a(Perlego)2755417 035 $a(EXLCZ)991000000000376503 100 $a20070402d2007 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aChemistry and technology of carbodiimides /$fHenri Ulrich 205 $a1st ed. 210 $aChichester, England ;$aHoboken, NJ $cJohn Wiley & Sons$d2007 215 $a1 online resource (312 p.) 300 $aDescription based upon print version of record. 311 08$a9780470065105 311 08$a0470065109 320 $aIncludes bibliographical references and index. 327 $aChemistry and Technology of Carbodiimides; Contents; Preface; Acknowledgements; 1 General Introduction; 1.1 References; 2 Alkyl- and Arylcarbodiimides; 2.1 Introduction; 2.2 Synthesis of Alkyl- and Arylcarbodiimides; 2.2.1 From Thioureas, Isothioureas and Selenoureas; 2.2.2 By Dehydration of Ureas; 2.2.3 From Isocyanates or Isothiocyanates; 2.2.4 From Cyanamides; 2.2.5 By Nitrene Rearrangements; 2.2.6 From Haloformamidines or Carbonimidoyl Dihalides; 2.2.7 By Thermolysis Reactions; 2.2.8 By Miscellaneous Other Methods; 2.3 References I; 2.4 Reactions of Alkyl- and Arylcarbodiimides 327 $a2.4.1 Oligomerization and Polymerization2.4.2 Cycloaddition Reactions; 2.4.3 Reaction of Ylides with Carbodiimides; 2.4.4 Insertion Reactions; 2.4.5 Nucleophilic Reactions; 2.4.6 Heterocycles from Carbodiimides; 2.4.7 Use of Carbodiimides In Condensation Reactions; 2.4.8 Miscellaneous Reactions; 2.5 References II; 3 Unsaturated Carbodiimides; 3.1 Introduction; 3.2 Synthesis of Unsaturated Carbodiimides; 3.2.1 From Thioureas; 3.2.2 From Unsaturated Isocyanates; 3.2.3 From Unsaturated Iminophosphoranes and Isocyanates or Isothiocyanates; 3.2.4 By Other Methods 327 $a3.3 Reactions of Unsaturated Carbodiimides3.3.1 Polymerization Reactions; 3.3.2 Cycloaddition Reactions; 3.3.3 Other Reactions; 3.4 References; 4 Halogenated Carbodiimides; 4.1 Introduction; 4.2 Synthesis of Halogenated Carbodiimides; 4.2.1 From -Haloisocyanates; 4.2.2 By Halogenation of Carbodiimides; 4.2.3 From Carbonimidoyl Dichlorides or Imidoyl Chlorides; 4.2.4 By Other Methods; 4.3 Reactions of Halogenated Carbodiimides; 4.3.1 Cycloaddition Reactions; 4.3.2 Nucleophilic Reactions; 4.3.3 Other Reactions; 4.4 References; 5 Acyl-, Thioacyl- and Imidoylcarbodiimides; 5.1 Introduction 327 $a5.2 Synthesis of Acyl-, Thioacyl- and Imidoylcarbodiimides5.2.1 From Thioureas; 5.2.2 From Ureas; 5.2.3 From Isocyanates; 5.2.4 From Carbonimidoyl Dichlorides or Chloroformamidines; 5.2.5 From Cyanamides; 5.2.6 From Other Carbodiimides; 5.2.7 By Other Methods; 5.3 Reactions of Acyl-, Thioacyl- and Imidoylcarbodiimides; 5.3.1 Cycloaddition Reactions; 5.3.2 Other Reaction; 5.4 References; 6 Silicon Substituted Carbodiimides; 6.1 Introduction; 6.2 Synthesis of Silicon Substituted Carbodiimides; 6.2.1 From Cyanamides; 6.2.2 From Ureas; 6.2.3 From Isocyanates and Isothiocyanates 327 $a6.2.4 From Silylamines6.2.5 From Other Carbodiimides; 6.2.6 By Other Methods; 6.3 Reactions of Silicon Substituted Carbodiimides; 6.3.1 Oligomerization Reactions; 6.3.2 Cycloaddition Reactions; 6.3.3 Other Reactions; 6.4 References; 7 Nitrogen Substituted Carbodiimides; 7.1 Introduction; 7.2 Synthesis of Nitrogen Substituted Carbodiimides; 7.3 Reactions of Nitrogen Substituted Carbodiimides; 7.4 References; 8 Phosphorous Substituted Carbodiimides; 8.1 Introduction; 8.2 Synthesis of Phosphorous Substituted Carbodiimides; 8.2.1 From Thioureas; 8.2.2 From Iminophosphoranes 327 $a8.2.3 From Carbonimidoyl Dichlorides 330 $aCarbodiimides play an important role as condensation agents in the synthesis of polypeptides, polynucleotides, polysaccharides and numerous other chemical transformations. Chemistry and Technology of Carbodiimides is the first book to examine both the chemistry and technology of carbodiimides. This book provides a comprehensive and in-depth coverage of the synthesis and reactions of this industrially important class of chemicals while focusing on industrial applications, including the M-sectors of biochemical synthesis, pharmaceuticals, polymers, ceramics, and herbicides. Written by a w 606 $aCarbodiimides 615 0$aCarbodiimides. 676 $a661/.894 700 $aUlrich$b Henri$f1925-$01658044 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910828098003321 996 $aChemistry and technology of carbodiimides$94011827 997 $aUNINA