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 | ||
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Lo trovi qui: Univ. Federico II | ||
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Chemistry and Technology of Natural and Synthetic Dyes and Pigments |
Autore | Samanta Ashis Kumar |
Edizione | [1st ed.] |
Pubbl/distr/stampa | London : , : IntechOpen, , 2020 |
Descrizione fisica | 1 online resource (308 pages) |
Disciplina | 667.3 |
Altri autori (Persone) |
AwwadNasser S
AlgarniHamed Majdooa |
Soggetto topico |
Dyes and dyeing - Textile fibers
Dyes and dyeing - Chemistry |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910688600503321 |
Samanta Ashis Kumar
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London : , : IntechOpen, , 2020 | ||
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Lo trovi qui: Univ. Federico II | ||
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Chemistry and Technology of Natural and Synthetic Dyes and Pigments / / edited by Ashis Kumar Samanta, Nasser Awwad, Hamed Majdooa Algarni |
Pubbl/distr/stampa | London : , : IntechOpen, , 2020 |
Descrizione fisica | 1 online resource (304 pages) : illustrations |
Disciplina | 667.2 |
Soggetto topico |
Dyes and dyeing - Textile fibers
Dyes and dyeing - Chemistry |
ISBN | 1-78985-998-0 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910424649503321 |
London : , : IntechOpen, , 2020 | ||
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Lo trovi qui: Univ. Federico II | ||
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Colore : una biografia / Philip Ball |
Autore | Ball, Philip |
Pubbl/distr/stampa | Milano : BUR, 2005 |
Descrizione fisica | 367 p., [24] p. of plates : ill. (col.) ; 20 cm |
Disciplina | 701.85 |
Collana | BUR. Saggi |
Soggetto topico |
Coloring matter - History
Color in art Dyes and dyeing - Chemistry Art and industry |
ISBN | 8817000728 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | ita |
Record Nr. | UNISALENTO-991001220669707536 |
Ball, Philip
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Milano : BUR, 2005 | ||
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Lo trovi qui: Univ. del Salento | ||
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Colour chemistry [[electronic resource] /] / R.M. Christie |
Autore | Christie R. M |
Pubbl/distr/stampa | Cambridge, U.K., : Royal Society of Chemistry, c2001 |
Descrizione fisica | 1 online resource (218 p.) |
Disciplina | 667.2 |
Collana | RSC paperbacks |
Soggetto topico | Dyes and dyeing - Chemistry |
Soggetto genere / forma | Electronic books. |
ISBN |
1-62870-123-4
1-84755-059-2 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | CONTENTS; Chapter 1; Colour: A Brief Historical Perspective; Chapter 2; The Physical and Chemical Basis of Colour; Chapter 3; Azo Dyes and Pigments; Chapter 4; Carbonyl Dyes and Pigments; Chapter 5; Phthalocyanines; Chapter 6; Miscellaneous Chemical Classes of Organic Dyes and Pigments; Chapter 7; Textile Dyes (Excluding Reactive Dyes); Chapter 8; Reactive Dyes for Textile Fibres; Chapter 9; Pigments; Chapter 10; Functional or 'High Technology' Dyes and Pigments; Chapter 11; Colour and the Environment; Bibliography; Subject Index |
Record Nr. | UNINA-9910454066403321 |
Christie R. M
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Cambridge, U.K., : Royal Society of Chemistry, c2001 | ||
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Lo trovi qui: Univ. Federico II | ||
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Colour chemistry [[electronic resource] /] / R.M. Christie |
Autore | Christie R. M |
Pubbl/distr/stampa | Cambridge, U.K., : Royal Society of Chemistry, c2001 |
Descrizione fisica | 1 online resource (218 p.) |
Disciplina | 667.2 |
Collana | RSC paperbacks |
Soggetto topico | Dyes and dyeing - Chemistry |
ISBN |
1-62870-123-4
1-84755-059-2 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | CONTENTS; Chapter 1; Colour: A Brief Historical Perspective; Chapter 2; The Physical and Chemical Basis of Colour; Chapter 3; Azo Dyes and Pigments; Chapter 4; Carbonyl Dyes and Pigments; Chapter 5; Phthalocyanines; Chapter 6; Miscellaneous Chemical Classes of Organic Dyes and Pigments; Chapter 7; Textile Dyes (Excluding Reactive Dyes); Chapter 8; Reactive Dyes for Textile Fibres; Chapter 9; Pigments; Chapter 10; Functional or 'High Technology' Dyes and Pigments; Chapter 11; Colour and the Environment; Bibliography; Subject Index |
Record Nr. | UNINA-9910782761203321 |
Christie R. M
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Cambridge, U.K., : Royal Society of Chemistry, c2001 | ||
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Lo trovi qui: Univ. Federico II | ||
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Colour chemistry / R.M. Christie |
Autore | Christie, R. M. |
Pubbl/distr/stampa | Cambridge : Royal Society of Chemistry, c2001 |
Descrizione fisica | xi, 205 p. : ill. ; 25 cm |
Disciplina | 667.2 |
Collana | RSC Paperbacks |
Soggetto topico | Dyes and dyeing - Chemistry |
ISBN |
0854045732
9780854045730 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNISALENTO-991003324889707536 |
Christie, R. M.
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Cambridge : Royal Society of Chemistry, c2001 | ||
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Lo trovi qui: Univ. del Salento | ||
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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
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New York, : Interscience, 1964 | ||
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Lo trovi qui: Univ. Federico II | ||
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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
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New York, : Interscience, 1964 | ||
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Lo trovi qui: Univ. Federico II | ||
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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
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New York, : Interscience, 1964 | ||
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Lo trovi qui: Univ. di Salerno | ||
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