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ChemInform Abstract: Synthesis and Separation of Structural Isomers of 2(3),9(10),16(17),23(24)-Tetrasubstituted Phthalocyanines.

✍ Scribed by Bernd Goerlach; Markus Dachtler; Tobias Glaser; Klaus Albert; Michael Hanack

Publisher: John Wiley and Sons
Year: 2010
Weight: 29 KB
Volume: 33
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200207175

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ChemInform Abstract: The Solid Phase, Room-Temperature Synthesis of Metal-Free and Metallophthalocyanines, Particularly of 2,3,9,10,16,17,23,24-Octacyanophthalocyanines.

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Synthesis and Aggregation Properties in Solution of a New Octasubstituted Copper Phthalocyanine: {2,3,9,10,16,17,23,24-Octakis-[(dioctylaminocarbonyl)methoxy]phthalocyaninato}copper(II)

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Unit cell determination of 2,3,9,10,16,17,23,24-octapentoxyphthalocyanine and its nickel derivative using electron and X-ray powder diffraction

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2,3,9,10,16,17,23,24-Octapentoxyphthalocyanine and its nickel derivative have been studied by means of electron and X-ray powder diffraction. The results reveal that the metal-free compound forms monoclinic crystals (space group C2/c) with unit cell constants a = 4.202 nm , b = 0.4977 nm , c = 3.345

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Formation and spectroelectrochemical characterization of multilayer and submonolayer thin films of 2,3,9,10,16,17,23,24-octa(2-benzyloxy-ethoxy) phthalocyninato copper (CuPc(OC2OBz)8)

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We review here the self-assembly, electrochemical and spectroelectrochemical properties of 2,3,9,10,16,17,23,24-octa(2-benzyloxyethoxy) phthalocyaninato copper ( CuPc ( OC ~2~ OBz )~8~), where terminal benzyl groups on the eight ethylene oxide side chains assist in forming unusually ordered, mechani