LEADER 05502nam 2200697 a 450 001 9910146244403321 005 20210209221235.0 010 $a3-527-60606-8 010 $a9786612118388 010 $a1-282-11838-2 010 $a1-280-56073-8 010 $a9786610560738 010 $a3-527-60201-1 035 $a(CKB)1000000000019306 035 $a(EBL)482076 035 $a(OCoLC)180264254 035 $a(SSID)ssj0000178558 035 $a(PQKBManifestationID)11183070 035 $a(PQKBTitleCode)TC0000178558 035 $a(PQKBWorkID)10229392 035 $a(PQKB)11623698 035 $a(MiAaPQ)EBC482076 035 $a(MiAaPQ)EBC5247780 035 $a(Au-PeEL)EBL5247780 035 $a(CaONFJC)MIL56073 035 $a(OCoLC)1027173788 035 $a(EXLCZ)991000000000019306 100 $a20030331d2003 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aIndustrial dyes$b[electronic resource] $echemistry, properties, applications /$fKlaus Hunger (editor) 210 $aWeinheim $cWiley-VCH$dc2003 215 $a1 online resource (686 p.) 300 $aDescription based upon print version of record. 311 $a3-527-30426-6 320 $aIncludes bibliographical references and index. 327 $aIndustrial Dyes Chemistry, Properties, Applications; Contents; Preface; List of Contributors; 1 Dyes, General Survey; 1.1 Introduction; 1.2 Classification Systems for Dyes; 1.3 Classification of Dyes by Use or Application Method; 1.4 Nomenclature of Dyes; 1.5 Equipment and Manufacture; 1.6 Economic Aspects; 1.7 References; 2 Important Chemical Chromophores of Dye Classes; Introduction; 2.1 Azo Chromophore; 2.1.1 Introduction; 2.1.2 General Synthesis; 2.1.2.1 Diazo Components; 2.1.2.2 Diazotization Methods; 2.1.2.3 Coupling Components; 2.1.2.4 Azo Coupling in Practice 327 $a2.1.3 Principal Properties2.1.3.1 Tautomerism; 2.1.3.2 Metallized Azo Dyes; 2.1.3.3 Carbocyclic Azo Dyes; 2.1.3.4 Heterocyclic Azo Dyes; 2.1.4 References; 2.2 Anthraquinone Chromophore; 2.2.1 Introduction; 2.2.2 General Synthesis; 2.2.3 Principal Properties; 2.2.3.1 Benzodifuranone Dyes; 2.2.3.2 Polycyclic Aromatic Carbonyl Dyes; 2.2.4 References; 2.3 Indigoid Chromophore; 2.3.1 Introduction; 2.3.2 General Synthesis; 2.3.3 Principal Properties; 2.3.3.1 Color; 2.3.3.2 Basic Chromophore; 2.3.3.3 Solvatochromism; 2.3.3.4 Redox System; 2.3.4 References; 2.4 Cationic Dyes as Chromophores 327 $a2.4.1 Introduction2.4.2 General Synthesis; 2.4.3 Chemical Structure and Classification; 2.4.3.1 Dyes with Delocalized Charge; 2.4.3.2 Dyes with Localized Charge; 2.4.4 Principal Properties; 2.4.4.1 Cationic Dyes for Synthetic Fibers; 2.4.4.2 Cationic Dyes for Paper, Leather, and Other Substrates; 2.4.5 References; 2.5 Polymethine and Related Chromophores; 2.5.1 Introduction; 2.5.2 General Synthesis; 2.5.3 Principal Properties and Classification; 2.5.3.1 Azacarbocyanines; 2.5.3.2 Hemicyanines; 2.5.3.3 Diazahemicyanines; 2.5.3.4 Styryl Dyes; 2.6 Di- and Triarylcarbenium and Related Chromophores 327 $a2.6.1 Introduction2.6.2 Chromophores; 2.6.3 General Synthesis; 2.6.4 Principal Properties; 2.6.5 References; 2.7 Phthalocyanine Chromophore; 2.7.1 Introduction; 2.7.2 General Synthesis; 2.7.3 Principal Properties; 2.7.4 Industrial Production; 2.7.4.1 Copper Phthalocyanine; 2.7.4.2 Phthalocyanine Derivatives; 2.7.4.3 Pthalocyanine Sulfonic Acids and Sulfonyl Chlorides; 2.7.5 References; 2.8 Sulfur Compounds as Chromophores; 2.8.1 Introduction; 2.8.2 Chromophores; 2.8.3 General Synthesis; 2.8.3.1 Sulfur Bake and Polysulfide Bake Dyes; 2.8.3.2 Polysulfide Melt Dyes; 2.8.3.3 Pseudo Sulfur Dyes 327 $a2.8.4 Principal Properties2.8.5 References; 2.9 Metal Complexes as Chromophores; 2.9.1 Introduction; 2.9.2 Azo/Azomethine Complex Dyes; 2.9.2.1 General Synthesis; 2.9.2.2 Principal Properties; 2.9.3 Formazan Dyes; 2.9.3.1 Introduction; 2.9.3.2 General Synthesis; 2.9.3.3 Principal Properties; 2.9.4 References; 2.10 Fluorescent Dyes; 2.11 Other Chromophores; 2.11.1 Quinophthalone Dyes; 2.11.2 Nitro and Nitroso Dyes; 2.11.3 Stilbene Dyes; 2.11.4 Formazan Dyes; 2.11.5 Triphenodioxazine Dyes; 2.11.6 References; 3 Dye Classes For Principal Applications; 3.1 Reactive Dyes; 3.1.1 Introduction 327 $a3.1.2 Chemical Constitution of Reactive Systems 330 $aWhat would life be like without color? Ever since one can think back, color has always accompanied mankind. Dyes - originally obtained exclusively from natural sources - are today also produced synthetically on a large scale and represent one of the very mature and traditional sectors of the chemical industry.The present reference work on Industrial Dyes provides a comprehensive review of the chemistry, properties and applications of the most important groups of industrial dyes, including optical brighteners. It also outlines the latest developments in the area of functional dyes.< 606 $aDyes and dyeing$xChemistry 606 $aDyes and dyeing$xIndustrial applications 608 $aElectronic books. 615 0$aDyes and dyeing$xChemistry. 615 0$aDyes and dyeing$xIndustrial applications. 676 $a667.2 676 $a667.25 701 $aHunger$b Klaus$0555711 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910146244403321 996 $aIndustrial dyes$92201394 997 $aUNINA LEADER 03363nam 2200661 a 450 001 9910782475803321 005 20200520144314.0 010 $a1-281-93672-3 010 $a9786611936723 010 $a90-474-3124-3 024 7 $a10.1163/ej.9789004162143.i-196 035 $a(CKB)1000000000556552 035 $a(EBL)467950 035 $a(OCoLC)646789890 035 $a(SSID)ssj0000269040 035 $a(PQKBManifestationID)11214513 035 $a(PQKBTitleCode)TC0000269040 035 $a(PQKBWorkID)10243243 035 $a(PQKB)10705392 035 $a(MiAaPQ)EBC467950 035 $a(OCoLC)154309346$z(OCoLC)153579286 035 $a(nllekb)BRILL9789047431244 035 $a(Au-PeEL)EBL467950 035 $a(CaPaEBR)ebr10271056 035 $a(PPN)174390203 035 $a(EXLCZ)991000000000556552 100 $a20070706d2007 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aWar, domination, and the monarchy of France$b[electronic resource] $eClaude de Seyssel and the language of politics in the Renaissance /$fby Rebecca Ard Boone 210 $aLeiden ;$aBoston $cBrill$d2007 215 $a1 online resource (212 p.) 225 1 $aBrill's studies in intellectual history ;$vv. 156 300 $aDescription based upon print version of record. 311 $a90-04-16214-3 320 $aIncludes bibliographical references and index. 327 $aIn medias res : the life of Claude de Seyssel -- The scholar-diplomat -- The translator of histories -- Seyssel in Italy : a scholar looks at war -- The scholar and the state -- Seyssel, the church, and the ideal prelate. 330 $aClaude de Seyssel's important political treatise, The Monarchy of France (1515) illuminates the link between warfare, the state, and the social order in the Renaissance. Raised and educated in Turin, Seyssel entered the service of the French king to facilitate the French invasion of Italy. His wide experience as a jurist, royal counselor, diplomat, propagandist, translator, historian, and prelate informed his unique political perspective. As a witness to the failures of the French in the Italian Wars, he maintained that successful conquest and occupation resulted from superior discipline and order as well as from the elimination of social conflict. In his view, a state with a well-ordered system of law and a wide base of popular support was best-suited to conquer and maintain an empire. His application of Italian political language to French society and government produced a vision of war, politics, and society with radical implications for French history. 410 0$aBrill's studies in intellectual history ;$vv. 156. 606 $aPolitical science$xHistory$y16th century 606 $aPolitics and war$xHistory$y16th century 606 $aMonarchy$zFrance$xHistory$y16th century 607 $aFrance$xPolitics and government$y1328-1589 615 0$aPolitical science$xHistory 615 0$aPolitics and war$xHistory 615 0$aMonarchy$xHistory 676 $a320.44409/024 700 $aBoone$b Rebecca Ard$01494352 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910782475803321 996 $aWar, domination, and the monarchy of France$93717783 997 $aUNINA