LEADER 00919nam0-2200289 --450 001 9910678701203321 005 20230403102844.0 010 $a9783775748155 100 $a20230403d2021----kmuy0itay5050 ba 101 0 $aeng 102 $aDE 105 $aa 001yy 200 1 $aErik Dhont$elandscape architects$ework 1999-2020$f[authors: Erik Dhont, Michael Jakob, Suzanne Kr?i?z?enecky?] 210 $aBerlino$cHatje Cantz$d2021 215 $a237 p.$cill.$d30 cm 610 0 $aArchitettura del paesaggio$aDisegni e progetti 610 0 $aArchitetti del paesaggio$aBelgio$aBruxelles 700 1$aDhont,$bErik$01346950 701 1$aJacob,$bMichael$0291535 701 1$aKr?i?z?enecky?,$bSuzanne$01346951 801 0$aIT$bUNINA$gREICAT$2UNIMARC 901 $aBK 912 $a9910678701203321 952 $aMON C 900$b109/2023$fFARBC 959 $aFARBC 996 $aErik Dhont$93081899 997 $aUNINA LEADER 05179nam 2200649Ia 450 001 9910831025203321 005 20230213211443.0 010 $a1-282-30674-X 010 $a9786612306747 010 $a0-470-18679-8 010 $a0-470-18829-4 035 $a(CKB)1000000000376537 035 $a(EBL)469485 035 $a(OCoLC)814414716 035 $a(SSID)ssj0000336453 035 $a(PQKBManifestationID)11929272 035 $a(PQKBTitleCode)TC0000336453 035 $a(PQKBWorkID)10279735 035 $a(PQKB)10547141 035 $a(MiAaPQ)EBC469485 035 $a(EXLCZ)991000000000376537 100 $a19840208d1964 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 14$aThe cyanine dyes and related compounds$b[electronic resource] /$fFrances M. Hamer 205 $a99th ed. 210 $aNew York $cInterscience$d1964 215 $a1 online resource (830 p.) 225 1 $aThe chemistry of heterocyclic compounds, a series of monographs ;$vv. 18 300 $aDescription based upon print version of record. 311 $a0-470-38181-7 320 $aIncludes bibliographies. 327 $aTHE CYANINE DYES AND RELATED COMPOUNDS; Contents; I. Mainly Introductory; 1. The Connection of the Cyanines with Photography; 2. The Chemistry of the First Sixty-Three Years (up to 1919); 3. Establishment of the Constitution of the Typical Cyanines Known in 1920; A. The Constitution of Isocyanine; B. The Constitution of Cyanine; C. The Constitution of Pinacyanol; D. The Constitution of Cyanines of the Benzothiazole Series; E. Preparation of Unsymmetrical Methincyanines; F. The Constitution of Kryptocyanine; G. The Constitution of Dicyanine; H. The Constitution of the Apocyanines 327 $aI. Summary, and Some Developments4. Definition and Nomenclature; 5. Cyanines in which the Nuclei are Directly Linked (Apocyanines); A. General; B. Preparation and Properties; C. Nomenclature; II Methincyanines; 1. 4'-Cyanine Condensation (Involving Elimination of HX + Ha); A. General; B. 4,4'-Cyanines; C. 2,4'-Cyanines; D. Thia-4'-, Oxa-4'-, and Selena-4'-cyanines; E. Thizolo-4'- and Thiazolino-4'-cyanines; F. Thiacyanines; 2. ?-Cyanine Condensation (Involving Reactive I, CI, CN, or SO3R, and Elimination of 2HX); A. General; B. 2,2'-Cyanines; C. 2,4'-Cyanines 327 $aD. Thia-4'- and Selena-4'-cyaninesE. Indo-2'-cyanines; F. Thia-2'-, Oxa-2'-, and Selena-2'-cyanines; G. Thiazolo-a'-. Thiazolino-Z'-. Ox&olo-2'-. and Selenazolo-2'- cyanines; H. 2-Pyrido-2'-, 2-Pyrido4'-, 4-Pyrido.2'-, and 4-Pyrido-4'- cyanines; I. 2-Pyridothia- and Oxa-2'-pyrido-cyanines; J. 2.2'-, 2.4'-, and 4.4'- Pyridocyanines; K. Thiazolo-2'-, Thiazolino-2'-, Oxazolo-2'-, and Selenazolo-2'- pyridocyanines; L. Thiacyanines; 3. Nitrite Method; A. General; B. Indocyanines and Intermediate Compounds; C. Thiacyanines; D. Oxa- and Selena-cyanines; 4. Alkyl- or Aryl-thio Method; A. General 327 $aB. 2,2'- and 2,4'-CyaninesC. Thia-4'- and Oxa-4'-cyanines; D. Indo-2'-cyanines; E. Thia-2'- Oxa-2'-, and Selena-2'-cyanines; F. Thiazolo-2'-, Thiazolino-2'- and Oxazolo-2'-cyanines; G. 2-Pyrido-2'- and 4-Pyrido-4'-cyanines; H. Oxa-2'-pyrido- and 2-Pyridothia-cyanines; I. 4,4 '-Pyridocyanines; J. Thiazolo-2'- and Thiazolino-2'-pyridocyanines; K. Thia-, Oxa-, Oxathia- and Selenathia-cyanines; L. Indoxa- and Indothia-cyanines; M. Oxaoxazolo-, Oxathiamlo-, Oxazolothia-, and Thiathiazolo- cyanines; N. Oxazolo-, Thiazolo-, and Oxazolothiazolocyanines; 5. Condensations Depending on Reactive : N . R 327 $aA. GeneralB. Thia-2'cyanines; C. Thiacyanines; 6. Other Methods; A. Use of Grignard Reagent for Thiacyanines; B. Use of Ethyl Malonate for Synthesising Thiacyanines; C. Disulphide Method for Thia-, Thia-2'-, Thia-4'-, 2-Pyridothia-, and Thiathiazolo-cyanines; D. Malonic Acid Method for 2,2'-, Thia-, Oxa-, and Thiazolo- cyanines; E. 4,4'-Cyanine by Cleavage of 4,4'-Carbocyanine with Lepidine Ethiodide; F. Thia-, Oxa-, and Selena-cyanines by Reaction of a Quaternary Salt, Having a Methylthio-Group, with Acetic Anhydride; III . Methincyanines with Substituents on the Chain; A. General 327 $aB. 2,2'-Cyanines 330 $aChemistry of Heterocyclic Compounds publishes articles, letters to the Editor, reviews, and minireviews on the synthesis, structure, reactivity, and biological activity of heterocyclic compounds including natural products. The journal covers investigations in heterocyclic chemistry taking place in scientific centers of all over the world, including extensively the scientific institutions in Russia, Ukraine, Latvia, Lithuania and Belarus. 410 0$aChemistry of heterocyclic compounds ;$vv. 18. 606 $aCyanines 606 $aDyes and dyeing$xChemistry 615 0$aCyanines. 615 0$aDyes and dyeing$xChemistry. 676 $a547/.59/05 676 $a667.25 700 $aHamer$b Frances M$01275227 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910831025203321 996 $aThe cyanine dyes and related compounds$93004706 997 $aUNINA