Processes for the preparation of hydroxygallium phthalocyanine
AssigneeXerox Corporation
InventorsRichard A. Burt, Cheng-Kuo Hsiao, Dasarao Murti, Roger E. Gaynor, Barkev Keoshkerian, James D. Mayo, George Liebermann
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Abstract
A process for the preparation of Type V hydroxygallium phthalocyanine which comprises the in situ formation of an alkoxy-bridged gallium phthalocyanine dimer, hydrolyzing said alkoxy-bridged gallium phthalocyanine dimer to hydroxygallium phthalocyanine, and subsequently converting the hydroxygallium phthalocyanine product obtained to Type V hydroxygallium phthalocyanine.
Claims34
A process for the preparation of Type V hydroxygallium phthalocyanine consisting essentially of the in situ formation of an alkoxy-bridged gallium phthalocyanine dimer, hydrolyzing said alkoxy-bridged gallium phthalocyanine dimer to hydroxygallium phthalocyanine, and subsequently converting the hydroxygallium phthalocyanine product obtained to Type V hydroxygallium phthalocyanine.
A process for the preparation of Type V hydroxygallium phthalocyanine which comprises the formation of an alkoxy-bridged gallium phthalocyanine dimer by the reaction of a gallium alkoxide, which has been formed from reacting gallium trichloride in a solvent, with a sodium alkoxide, and selecting the resulting mixture of gallium alkoxide and sodium chloride byproduct for the reaction with ortho-phthalodinitrile or 1,3-diiminoisoindoline and a diol;
- hydrolyzing the resulting alkoxy-bridged gallium phthalocyanine dimer to hydroxygallium phthalocyanine;
- and subsequently converting the product obtained to Type V hydroxygallium phthalocyanine by a solvent treatment;
- and wherein said diol is selected from the group consisting of ethylene glycol, 1,3-propanediol,2-methyl-1,3-propanediol,2,2-dimethyl-1,3-propanediol 1,3butanediol,2,3-butanediol,1,4-butanediol,1,4-cyclohexanediol and 1,6-hexanediol.
A process for the preparation of an alkoxy-bridged gallium phthalocyanine dimer by the reaction of gallium trichloride with an alkali metal alkoxide in a solvent;
- thereafter removing the alkali metal halide byproduct formed;
- and reacting the obtained gallium alkoxide solution with ortho-phthalodinitrile or 1,3-diiminoisoindoline, and a diol.
Dependencies are inferred from the claim text.