[go: up one dir, main page]

GB1049766A - New dyes of the tetrazaporphin series - Google Patents

New dyes of the tetrazaporphin series

Info

Publication number
GB1049766A
GB1049766A GB3545363A GB3545363A GB1049766A GB 1049766 A GB1049766 A GB 1049766A GB 3545363 A GB3545363 A GB 3545363A GB 3545363 A GB3545363 A GB 3545363A GB 1049766 A GB1049766 A GB 1049766A
Authority
GB
United Kingdom
Prior art keywords
tetrazaporphin
sulphonic acid
arylene
aromatic
ring
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
GB3545363A
Inventor
Johannes Dehnert
Arnold Tartter
Walter Grosch
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.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik 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
Application filed by BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB1049766A publication Critical patent/GB1049766A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B62/00Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/44Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
    • C09B62/465Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring the reactive group being an acryloyl group, a quaternised or non-quaternised aminoalkyl carbonyl group or a (—N)n—CO—A—O—X or (—N)n—CO—A—Hal group, wherein A is an alkylene or alkylidene group, X is hydrogen or an acyl radical of an organic or inorganic acid, Hal is a halogen atom, and n is 0 or 1
    • C09B62/483Porphines; Azaporphines
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B47/00Porphines; Azaporphines
    • C09B47/04Phthalocyanines abbreviation: Pc
    • C09B47/08Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
    • C09B47/24Obtaining compounds having —COOH or —SO3H radicals, or derivatives thereof, directly bound to the phthalocyanine radical
    • C09B47/26Amide radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

The invention comprises tetrazaporphin dyes having the general formula <FORM:1049766/C4-C5/1> in which Pc is a tetrazaporphin nucleus, R is hydrogen or substituted or unsubstituted alkyl radical, X is an aromatic heterocyclic ring containing in the ring an unsubstituted imino group, the heterocyclic ring may be attached by a substituted or unsubstituted aryleneamino, arylene-sulphonylamino,arylene-carbonylamino, arylene-azo, alkylene or arylene radical which may be fused with the heterocycle, m is 0-5, n is 1-4, p is 0-2, the total of m, n and p amounting to between 2 and 8 inclusive The tetrazaporphin is preferably a phthalocyanine which may be metallized, e.g. copper, nickel or cobalt and iron, aluminium, zinc or chromium. The dyes are obtained by reacting a tetrazaporphin sulphonic acid halide, preferably chloride or bromide, which may contain free sulphonic acid radicals, with an aromatic-heterocyclic amine having an unsubstituted imino group in the ring, and hydrolysing unreacted sulphonic acid halide groups, or by reacting a tetrazaporphin sulphonic acid halide which may contain free sulphonic acid groups, in any sequence with an aromatic-heterocyclic amine containing an unsubstituted imino group in its ring, and with ammonia or any primary amine, and hydrolysing unreacted sulphonic acid halide groups. Aromatic-heterocyclic amines of the above type include, pyrrole, pyrazole, imidazole, triazole and tetrazole derivatives, indole and indazole derivatives are also specified.
GB3545363A 1962-09-11 1963-09-09 New dyes of the tetrazaporphin series Expired GB1049766A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB68801A DE1210109B (en) 1962-09-11 1962-09-11 Process for the preparation of dyes of the tetrazaporphin series

Publications (1)

Publication Number Publication Date
GB1049766A true GB1049766A (en) 1966-11-30

Family

ID=6976040

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3545363A Expired GB1049766A (en) 1962-09-11 1963-09-09 New dyes of the tetrazaporphin series

Country Status (3)

Country Link
CH (1) CH451372A (en)
DE (1) DE1210109B (en)
GB (1) GB1049766A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2621231C3 (en) * 1976-05-13 1978-10-26 Hoechst Ag, 6000 Frankfurt Phthalocyanine compounds, process for their preparation and their use as dyes

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1066305B (en) * 1959-10-01 Farbenfabriken Bayer Aktiengesellschaft, Leverkusen-Bayerwerk Process for the preparation of dyes of the phthalocyanine series
GB850159A (en) * 1958-04-16 1960-09-28 Bayer Ag Water-soluble sulphonium dyestuffs

Also Published As

Publication number Publication date
CH451372A (en) 1968-05-15
DE1210109B (en) 1966-02-03

Similar Documents

Publication Publication Date Title
GB1069952A (en) New class of n,n,n&#39;,n&#39;-tetrakis (p-substituted-phenyl)-p-phenylenediamines and benzidines
GB1207249A (en) New azo compounds and processes for their manufacture and use
GB1320921A (en) Fibre-reactive dyestuffs
US2808413A (en) Imidazoline derivatives of 2-aryl indolines
ES354601A1 (en) Anthraquinone reactive dyestuffs
GB1049766A (en) New dyes of the tetrazaporphin series
GB1391244A (en) 3-amino-1h-pyrazolo-3,4-b-pyridines and a process for their preparation
GB1114427A (en) Azophthalocyanine dyestuffs and processes for their manufacture
DE3374934D1 (en) 8-substituted pyrrolizidine derivatives and use thereof
GB1147546A (en) New basic azo dyestuffs and processes for their manufacture and use
GB1122249A (en) Novel diazo compounds and diazotype copying material
GB1035915A (en) N-(acylamino)-ephedrines and a method for their preparation
GB1227538A (en)
GB1134329A (en) Substituted pyrazolone compounds
ES411858A1 (en) Reactive dyestuffs
GB950698A (en) New dyes containing dihalopyridazone groups
ES259131A1 (en) Filter layer for photographic elements
GB956623A (en) Phenylpiperazinone derivatives
US2553989A (en) Hemicyanine dyestuffs
GB1086994A (en) Monazo heterocyclic dyes, cationic derivatives thereof, and their use
GB1448281A (en) 1,3-diphenylpyrazolines
ES394346A1 (en) Procedure for the preparation of new 2-alquiltio-4,6 -diamino - s - triacinas of activity herbicida. (Machine-translation by Google Translate, not legally binding)
ES328778A1 (en) Procedure for the preparation of cationic monoazoic colorants. (Machine-translation by Google Translate, not legally binding)
GB1099186A (en) New sultone condensation products and their use as levelling agents for electro-deposited coatings
GB1139361A (en) Cationic azo dyestuffs