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Biblioteca

MARC Lista (tabellare)
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
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Chemistry and Technology of Natural and Synthetic Dyes and Pigments
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  
London : , : IntechOpen, , 2020
Materiale a stampa
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
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
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Colore : una biografia / Philip Ball
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  
Milano : BUR, 2005
Materiale a stampa
Lo trovi qui: Univ. del Salento
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Colour chemistry [[electronic resource] /] / R.M. Christie
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  
Cambridge, U.K., : Royal Society of Chemistry, c2001
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Colour chemistry [[electronic resource] /] / R.M. Christie
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  
Cambridge, U.K., : Royal Society of Chemistry, c2001
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Colour chemistry / / R.M. Christie
Colour chemistry / / R.M. Christie
Autore Christie R. M
Edizione [1st ed.]
Pubbl/distr/stampa Cambridge, U.K., : Royal Society of Chemistry, c2001
Descrizione fisica 1 online resource (218 p.)
Disciplina 667.2
Collana ISSN
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-9910961884303321
Christie R. M  
Cambridge, U.K., : Royal Society of Chemistry, c2001
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Colour chemistry / R.M. Christie
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.  
Cambridge : Royal Society of Chemistry, c2001
Materiale a stampa
Lo trovi qui: Univ. del Salento
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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