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BODIPY Dyes : A Privilege Molecular Scaffold with Tunable Properties / / edited by Jorge Bañuelos-Prieto and Rebeca Sola Llano
BODIPY Dyes : A Privilege Molecular Scaffold with Tunable Properties / / edited by Jorge Bañuelos-Prieto and Rebeca Sola Llano
Pubbl/distr/stampa London, United Kingdom : , : IntechOpen, , 2019
Descrizione fisica 1 online resource (100 pages) : illustrations some color
Disciplina 667.25
Soggetto topico Chemistry, Organic
Dyes and dyeing - Chemistry
ISBN 1-83881-816-2
1-78985-082-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti BODIPY dyes
Record Nr. UNINA-9910317765103321
London, United Kingdom : , : IntechOpen, , 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The cyanine dyes and related compounds [[electronic resource] /] / Frances M. Hamer
The cyanine dyes and related compounds [[electronic resource] /] / Frances M. Hamer
Autore Hamer Frances M
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Interscience, 1964
Descrizione fisica 1 online resource (830 p.)
Disciplina 547/.59/05
667.25
Collana The chemistry of heterocyclic compounds, a series of monographs
Soggetto topico Cyanines
Dyes and dyeing - Chemistry
Soggetto genere / forma Electronic books.
ISBN 1-282-30674-X
9786612306747
0-470-18679-8
0-470-18829-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto THE 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
I. 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. ψ-Cyanine Condensation (Involving Reactive I, CI, CN, or SO3R, and Elimination of 2HX); A. General; B. 2,2'-Cyanines; C. 2,4'-Cyanines
D. 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
B. 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
A. 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
B. 2,2'-Cyanines
Record Nr. UNINA-9910144284603321
Hamer Frances M  
New York, : Interscience, 1964
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The cyanine dyes and related compounds [[electronic resource] /] / Frances M. Hamer
The cyanine dyes and related compounds [[electronic resource] /] / Frances M. Hamer
Autore Hamer Frances M
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Interscience, 1964
Descrizione fisica 1 online resource (830 p.)
Disciplina 547/.59/05
667.25
Collana The chemistry of heterocyclic compounds, a series of monographs
Soggetto topico Cyanines
Dyes and dyeing - Chemistry
ISBN 1-282-30674-X
9786612306747
0-470-18679-8
0-470-18829-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto THE 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
I. 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. ψ-Cyanine Condensation (Involving Reactive I, CI, CN, or SO3R, and Elimination of 2HX); A. General; B. 2,2'-Cyanines; C. 2,4'-Cyanines
D. 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
B. 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
A. 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
B. 2,2'-Cyanines
Record Nr. UNINA-9910643446403321
Hamer Frances M  
New York, : Interscience, 1964
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The cyanine dyes and related compounds [[electronic resource] /] / Frances M. Hamer
The cyanine dyes and related compounds [[electronic resource] /] / Frances M. Hamer
Autore Hamer Frances M
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Interscience, 1964
Descrizione fisica 1 online resource (830 p.)
Disciplina 547/.59/05
667.25
Collana The chemistry of heterocyclic compounds, a series of monographs
Soggetto topico Cyanines
Dyes and dyeing - Chemistry
ISBN 1-282-30674-X
9786612306747
0-470-18679-8
0-470-18829-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto THE 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
I. 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. ψ-Cyanine Condensation (Involving Reactive I, CI, CN, or SO3R, and Elimination of 2HX); A. General; B. 2,2'-Cyanines; C. 2,4'-Cyanines
D. 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
B. 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
A. 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
B. 2,2'-Cyanines
Record Nr. UNISA-996202928903316
Hamer Frances M  
New York, : Interscience, 1964
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
The cyanine dyes and related compounds [[electronic resource] /] / Frances M. Hamer
The cyanine dyes and related compounds [[electronic resource] /] / Frances M. Hamer
Autore Hamer Frances M
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Interscience, 1964
Descrizione fisica 1 online resource (830 p.)
Disciplina 547/.59/05
667.25
Collana The chemistry of heterocyclic compounds, a series of monographs
Soggetto topico Cyanines
Dyes and dyeing - Chemistry
ISBN 1-282-30674-X
9786612306747
0-470-18679-8
0-470-18829-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto THE 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
I. 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. ψ-Cyanine Condensation (Involving Reactive I, CI, CN, or SO3R, and Elimination of 2HX); A. General; B. 2,2'-Cyanines; C. 2,4'-Cyanines
D. 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
B. 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
A. 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
B. 2,2'-Cyanines
Record Nr. UNINA-9910831025203321
Hamer Frances M  
New York, : Interscience, 1964
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The cyanine dyes and related compounds / / Frances M. Hamer
The cyanine dyes and related compounds / / Frances M. Hamer
Autore Hamer Frances M
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Interscience, 1964
Descrizione fisica 1 online resource (830 p.)
Disciplina 547/.59/05
667.25
Collana The chemistry of heterocyclic compounds, a series of monographs
Soggetto topico Cyanines
Dyes and dyeing - Chemistry
ISBN 1-282-30674-X
9786612306747
0-470-18679-8
0-470-18829-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto THE 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
I. 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. ψ-Cyanine Condensation (Involving Reactive I, CI, CN, or SO3R, and Elimination of 2HX); A. General; B. 2,2'-Cyanines; C. 2,4'-Cyanines
D. 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
B. 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
A. 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
B. 2,2'-Cyanines
Record Nr. UNINA-9910877876903321
Hamer Frances M  
New York, : Interscience, 1964
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
I coloranti di sintesi per la tintura dei tessili naturali, artificiali e sintetici / Paolo Luigi Tazzetti
I coloranti di sintesi per la tintura dei tessili naturali, artificiali e sintetici / Paolo Luigi Tazzetti
Autore TAZZETTI, Paolo Luigi
Edizione [Rist. della 2. ed. riv. e corr.]
Pubbl/distr/stampa Torino : Levrotto e Bella, 1984
Descrizione fisica VIII, 270 p. ; 24 cm
Disciplina 667.25
Soggetto topico Coloranti sintetici
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione ita
Record Nr. UNISA-990002740210203316
TAZZETTI, Paolo Luigi  
Torino : Levrotto e Bella, 1984
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Industrial dyes [[electronic resource] ] : chemistry, properties, applications / / Klaus Hunger (editor)
Industrial dyes [[electronic resource] ] : chemistry, properties, applications / / Klaus Hunger (editor)
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2003
Descrizione fisica 1 online resource (686 p.)
Disciplina 667.2
667.25
Altri autori (Persone) HungerKlaus
Soggetto topico Dyes and dyeing - Chemistry
Dyes and dyeing - Industrial applications
Soggetto genere / forma Electronic books.
ISBN 3-527-60606-8
9786612118388
1-282-11838-2
1-280-56073-8
9786610560738
3-527-60201-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Industrial 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
2.1.3 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
2.4.1 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
2.6.1 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
2.8.4 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
3.1.2 Chemical Constitution of Reactive Systems
Record Nr. UNINA-9910146244403321
Weinheim, : Wiley-VCH, c2003
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