GB496970A - Improvements in the manufacture and production of dyestuffs of the phthalocyanine series - Google Patents

Improvements in the manufacture and production of dyestuffs of the phthalocyanine series

Info

Publication number
GB496970A
GB496970A GB1706437A GB1706437A GB496970A GB 496970 A GB496970 A GB 496970A GB 1706437 A GB1706437 A GB 1706437A GB 1706437 A GB1706437 A GB 1706437A GB 496970 A GB496970 A GB 496970A
Authority
GB
United Kingdom
Prior art keywords
chloride
halides
aluminium
carboxylic acid
phthalocyanine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB1706437A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to DEI58248D priority Critical patent/DE686054C/en
Application filed by IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB1706437A priority patent/GB496970A/en
Publication of GB496970A publication Critical patent/GB496970A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B47/00—Porphines; Azaporphines
    • C09B47/04—Phthalocyanines abbreviation: Pc
    • C09B47/08—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Photoreceptors In Electrophotography (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Dyes of the phthalocyanine series are made by heating phthalocyanines with organic acid halides. As accelerators there may be used the halides of iron, aluminium, zinc, arsenic, antimony, phosphorus and copper and also sulphuric acid. When starting from metal-free phthalocyanines, metal may be introduced into the phthalocyanine nucleus at the same time. Acid halides specified are acetyl-, chloracetyl-, propionyl-, butyryl-, oxalyl-, benzoyl- and phthalyl chlorides, phthalic acid - 4 - sulphochloride, p-toluenesulphochloride; halides of acids of the naphthalene, anthracene or anthraquinone series, e.g. 1-naphthoyl chloride, naphthalene - 1 - sulphochloride, 1 - naphthol - 2 - carboxylic acid-4-sulphochloride, anthraquinone-1-sulphonic- or carboxylic acid chloride or 1-nitroanthraquinone - 2 - carboxylic acid chloride; halides of heterocyclic acids, e.g. pyridine carboxylic acid chlorides. Diluents may be used such as carbon tetrachloride, tetrachlorethane, di- and trichlorbenzenes, nitrobenzene, pyridine, quinoline or phthalic anhydride, common salt, sodium sulphate, kieselguhr, mixtures of aluminium halides and alkali metal salts or aluminium halide-sulphur dioxide addition compounds. Green-blue to green products are obtained. In examples: (1) and (6) metal-free phthalocyanine (cf. Specification 410,814) is heated with benzoyl chloride or p-toluenesulphochloride in nitrobenzene or trichlorbenzene in presence of antimony trichloride; (2), (3), (7), (10) copper phthalocyanine is heated with benzoyl chloride in presence of copper meal with or without nitrobenzene, with a mixture of aluminium and sodium chlorides and 2 : 5-dichlorobenzoyl chloride or phthalyl chloride or 1-anthraquinonesulphochloride or 1-nitroanthraquinone-2-carboxylic acid chloride; (4) and (5) copper phthalocyanine sulphonic acid sodium salt is heated with oxalyl or benzoyl chloride in presence of sodium sulphate. Cobalt, nickel, zinc and aluminium phthalocyanines are also specified as starting materials.
GB1706437A 1937-06-13 1937-06-18 Improvements in the manufacture and production of dyestuffs of the phthalocyanine series Expired GB496970A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
DEI58248D DE686054C (en) 1937-06-13 1937-06-13 Process for the preparation of dyes of the phthalocyanine series
GB1706437A GB496970A (en) 1937-06-18 1937-06-18 Improvements in the manufacture and production of dyestuffs of the phthalocyanine series

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1706437A GB496970A (en) 1937-06-18 1937-06-18 Improvements in the manufacture and production of dyestuffs of the phthalocyanine series

Publications (1)

Publication Number Publication Date
GB496970A true GB496970A (en) 1938-12-09

Family

ID=10088607

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1706437A Expired GB496970A (en) 1937-06-13 1937-06-18 Improvements in the manufacture and production of dyestuffs of the phthalocyanine series

Country Status (1)

Country Link
GB (1) GB496970A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2648674A (en) * 1949-11-24 1953-08-11 Muehlbauer Fritz Cobalt phthalocyanine-acetic acid and chlorinated derivatives thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2648674A (en) * 1949-11-24 1953-08-11 Muehlbauer Fritz Cobalt phthalocyanine-acetic acid and chlorinated derivatives thereof

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