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Biblioteca

MARC Lista (tabellare)
Covex Polytopes / Branko Grunbaum
Covex Polytopes / Branko Grunbaum
Autore Grünbaum, Branko <1929- >
Pubbl/distr/stampa London : Interscience, 1967
Descrizione fisica xiv, 456 p. ; 24 cm
Disciplina 516
Collana Pure and applied mathematics
Soggetto non controllato Geometria
Geometria - teoria generale
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-990002558140403321
Grünbaum, Branko <1929- >  
London : Interscience, 1967
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Cryophysics / K. Mendelssohn
Cryophysics / K. Mendelssohn
Autore Mendelssohn, K.
Pubbl/distr/stampa New York : Interscience, 1960
Disciplina 536.71
Collana Interscience Tracts on Physics and Astronomy
Soggetto non controllato Calore
Termodinamica
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-990001033720403321
Mendelssohn, K.  
New York : Interscience, 1960
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Crystal Structures / R.A.G. Wyckoff
Crystal Structures / R.A.G. Wyckoff
Autore Wyckoff, R.A.G.
Pubbl/distr/stampa New York : Interscience, 1966
Disciplina 538
Soggetto non controllato Cristallografia
Raggi x
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-990001079150403321
Wyckoff, R.A.G.  
New York : Interscience, 1966
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Crystal Structures / R.A.G. Wyckoff
Crystal Structures / R.A.G. Wyckoff
Autore Wyckoff, R.A.G.
Pubbl/distr/stampa New York : Interscience, 1964
Disciplina 548
Soggetto non controllato Cristallografia
Raggi x
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-990001079140403321
Wyckoff, R.A.G.  
New York : Interscience, 1964
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Crystal Structures / R.A.G. Wyckoff
Crystal Structures / R.A.G. Wyckoff
Autore Wyckoff, R.A.G.
Pubbl/distr/stampa New York : Interscience, 1963
Disciplina 538
Soggetto non controllato Cristallografia
Raggi x
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-990001079160403321
Wyckoff, R.A.G.  
New York : Interscience, 1963
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Crystalline olefin polymers / Editors: R.A.V. Raff, K.W. Doak
Crystalline olefin polymers / Editors: R.A.V. Raff, K.W. Doak
Autore Raff, Rudolf August Victor
Pubbl/distr/stampa New York [etc.] : Interscience, 1964
Disciplina 547
Collana High Polymers
Soggetto non controllato Chimica organica
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-990001050540403321
Raff, Rudolf August Victor  
New York [etc.] : Interscience, 1964
Materiale a stampa
Lo trovi qui: Univ. Federico II
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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
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