Since their initial accidental synthesis and characterization in Scotland in the late 1920s, there has been a strong research focus on the use of phthalocyanines (Pcs) as dyes and pigments. In recent years, active research fields have included their use in electrophotography, photovoltaic and solar cells, molecular electronics, Langmuir-Blodgett films, photosensitizers, electrochromic display devices, gas sensors, liquid crystals, low-dimensional conductors, and optical disks. Phthalocyanines possess interesting biological, electronic, optical, catalytic, and structural properties. The main disadvantage is their insolubility in common solvents due to strong intermolecular - interactions. The solubility of phthalocyanines can be increased by various methods such as the formation of anionic and cationic species and both axial and peripheral substitution. Substitution at the nonperipheral and peripheral positions of the benzo moieties usually enhances their solubility in organic solvents. The most important advantage of phthalocyanines compared to porphyrins is that their Q bands lie at longer wavelengths and are considerably more intense. In this book, you will find synthesis and some applications of various phthalocyanine derivatives.
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Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. KlappentextrnrnSince their initial accidental synthesis and characterization in Scotland in the late 1920s, there has been a strong research focus on the use of phthalocyanines (Pcs) as dyes and pigments. In recent years, active research fields . N° de réf. du vendeur 449930644
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Buch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Since their initial accidental synthesis and characterization in Scotland in the late 1920s, there has been a strong research focus on the use of phthalocyanines (Pcs) as dyes and pigments. In recent years, active research fields have included their use in electrophotography, photovoltaic and solar cells, molecular electronics, Langmuir-Blodgett films, photosensitizers, electrochromic display devices, gas sensors, liquid crystals, low-dimensional conductors, and optical disks. Phthalocyanines possess interesting biological, electronic, optical, catalytic, and structural properties. The main disadvantage is their insolubility in common solvents due to strong intermolecular - interactions. The solubility of phthalocyanines can be increased by various methods such as the formation of anionic and cationic species and both axial and peripheral substitution. Substitution at the nonperipheral and peripheral positions of the benzo moieties usually enhances their solubility in organic solvents. The most important advantage of phthalocyanines compared to porphyrins is that their Q bands lie at longer wavelengths and are considerably more intense. In this book, you will find synthesis and some applications of various phthalocyanine derivatives. 254 pp. Englisch. N° de réf. du vendeur 9789535132554
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Buch. Etat : Neu. Phthalocyanines and Some Current Applications | Yusuf Yilmaz | Buch | 254 S. | Englisch | 2017 | IntechOpen | EAN 9789535132554 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu Print on Demand. N° de réf. du vendeur 116117123
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Buch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -Since their initial accidental synthesis and characterization in Scotland in the late 1920s, there has been a strong research focus on the use of phthalocyanines (Pcs) as dyes and pigments. In recent years, active research fields have included their use in electrophotography, photovoltaic and solar cells, molecular electronics, Langmuir-Blodgett films, photosensitizers, electrochromic display devices, gas sensors, liquid crystals, low-dimensional conductors, and optical disks. Phthalocyanines possess interesting biological, electronic, optical, catalytic, and structural properties. The main disadvantage is their insolubility in common solvents due to strong intermolecular - interactions. The solubility of phthalocyanines can be increased by various methods such as the formation of anionic and cationic species and both axial and peripheral substitution. Substitution at the nonperipheral and peripheral positions of the benzo moieties usually enhances their solubility in organic solvents. The most important advantage of phthalocyanines compared to porphyrins is that their Q bands lie at longer wavelengths and are considerably more intense. In this book, you will find synthesis and some applications of various phthalocyanine derivatives.Books on Demand GmbH, Überseering 33, 22297 Hamburg 254 pp. Englisch. N° de réf. du vendeur 9789535132554
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Buch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Since their initial accidental synthesis and characterization in Scotland in the late 1920s, there has been a strong research focus on the use of phthalocyanines (Pcs) as dyes and pigments. In recent years, active research fields have included their use in electrophotography, photovoltaic and solar cells, molecular electronics, Langmuir-Blodgett films, photosensitizers, electrochromic display devices, gas sensors, liquid crystals, low-dimensional conductors, and optical disks. Phthalocyanines possess interesting biological, electronic, optical, catalytic, and structural properties. The main disadvantage is their insolubility in common solvents due to strong intermolecular - interactions. The solubility of phthalocyanines can be increased by various methods such as the formation of anionic and cationic species and both axial and peripheral substitution. Substitution at the nonperipheral and peripheral positions of the benzo moieties usually enhances their solubility in organic solvents. The most important advantage of phthalocyanines compared to porphyrins is that their Q bands lie at longer wavelengths and are considerably more intense. In this book, you will find synthesis and some applications of various phthalocyanine derivatives. N° de réf. du vendeur 9789535132554
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