Heterocyclic compounds

Details Heterocyclic compounds Heterocyclic compounds

2000-06-08

2003-04-01

Klemanski, Helene (Department: 1755)

Compositions: coating or plastic

Coating or plastic compositions

Marking

C106S031770, C106S498000, C544S001000

Reexamination Certificate

active

06540820

ABSTRACT:

The present invention relates to colorants for the mass coloring of polymers. In the mass coloring of polar polymers in particular, examples being polyamides, polyesters, polycarbonates and ABS, stringent requirements in terms of their heat stability and light fastness are expected from the dyes used.
The object of the present invention is, therefore, to provide heat-stable, light-fast and readily polymer-soluble colorants.
It has been found that the compounds of the formula (I) defined below achieve the stated object.
The invention, therefore, relates to the use as a polymer-soluble colorant of a compound of the formula (I)
in which R
1
, R
2
, R
3
, R
4
, R
5
, R
6
, R
7
, R
8
, R′
5
, R′
6
, R′
7
, R′
8
are hydrogen, halogen, hydroxy, —NO
2
, —CN, —CF
3
, —CONH
2
, C
1-12
alkyl, phenyl, naphthyl, phenanthryl, anthryl, R
9
R
10
N—, R
9
—O— or R
9
—S—, —CONHR
10
, —CONR
9
R
10
in which R
9
and R
10
are C
1
-C
6
-alkyl, C
6
-C
10
-aryl, (C
6
-C
10
)-aryl-(C
1
-C
6
)-alkyl or (C
1
-C
6
)-alkyl-(C
6
-C
10
)-aryl, in which the alkyl and/or aryl radicals can be substituted by hydroxyl, C
1
-C
6
-alkoxy, C
6
-C
10
-aryloxy or halogen; and optionally two adjacent groups can form an isocyclic or heterocyclic group.
Preferred compounds of the formula (I) are those in which each R
1
, R
2
, R
3
, R
4
is hydrogen, halogen, methyl or nitro.
Compounds of the formula (I) which are also preferred are those in which R
5
, R
6
, R
7
, R
8
, R′
5
, R′
6
, R′
7
, R′
8
are hydrogen, methyl, chlorine, —CF
3
or CONH
2
.
Preference is also given to compounds of the formula (I) in which two adjacent groups of the series R
5-8
and R′
5-8
form heterocyclic rings of the following type:
in which R
11
, R
12
are independently hydrogen, C
1-12
alkyl, phenyl, naphthyl, phenanthryl.
Particular preference is given to compounds of the formula (I) in which R
11
, and R
12
are methyl, ethyl, phenyl.
Novel compounds according to the invention have the structure of formula (I) in which at least one of the substitutents R
1
, R
2
, R
3
, R
4
, R
5
, R
6
, R
7
, R
8
, R′
5
, R′
6
, R′
7
or R′
8
has the meaning —CN, —CF
3
, —CONH
2
, phenyl, naphthyl, phenanthryl, anthryl, R
9
R
10
N—, —CONHR
10
or —CONR
9
R
10
as defined above, as well as the compounds where two adjacent groups form an isocyclic or heterocyclic group.
The present invention also provides a process for preparing the novel compounds of the formula (I) as defined above, characterized in that a naphtoquinone of the formula (II)
in which Hal is halogen, preferably Cl or Br, is condensed with compounds of the formula (IIIa) and (IIIb)
in which Met is hydrogen, Na
+
, K
+
or Zn
2+
.
Condensation takes place in a molar ratio of (II):(IIIa):(IIIb) of approx. 1:1:1.
Condensation can be conducted without solvent in the melt at temperatures, for instance, of between 150° C. and 300° C., preferably up to 250° C., or in an inert solvent at temperatures between 25° C. and 300° C., preferably between 100° and 250° C., in the presence or absence of a catalyst, at atmospheric pressure or under pressure.
Examples of suitable solvents are relatively high-boiling aliphatic or aromatic, substituted or unsubstituted hydrocarbons, examples being xylene (mixture), biphenyl, nitrobenzene, chlorobenzenes, chloronaphthalene, glycol ethers, organic acids and acid amides, especially dimethylformamide, dimethylacetamide or N-methyl-pyrrolidone.
Examples of possible catalysts are inorganic or organic acids, such as hydrochloric or sulphuric acid, benzenesulphonic, toluenesulphonic acid, or acetic acid. The salts of organic acids, such as sodium or potassium acetate, are in many cases also suitable as catalysts.
Whereas the compound of formula (IV)
is not heat stable in polyester or polyamides, it is surprising that the compound of formula (V) for example is heat stable in polyamide (up to 300° C.) and also in polyester up to 320° C. The compound of formula (V) has also a very good light fastness in polyester.
The compounds of the invention are eminently suitable for the coloring of melts of synthetic polar polymers such as, for example, ABS, polyester, polycarbonate or polyamides. Polyamides are, for example, polycondensation products or addition polymerization products of dicarboxylic acids and diamines, e.g. of adipic acid and hexamethylenediamine, of lactams, e.g. &egr;-caprolactam, or of aminocarboxylic acids, e.g. &ohgr;-aminoundecanoic acid. The polyamide melt mixed with the pigment is brought into its final form by conventional methods—for example, in melt spinning, injection molding, extrusion or film blowing machines.
Some of the dyes of formula (I) give a fluorescent coloration in synthetic polar polymers such as, for example, ABS, polyester, polycarbonate or polyamides.
The dyes of the formula (I) are extremely stable to the heat stress which is necessarily part of the coloring of synthetic polyamides, and the substrates mass-colored with them also display excellent fastness properties, especially light fastness. Their high polymer-solubility is particularly noteworthy.
The compounds of the formula (I) are also suitable as colorants in electrophotographic toners and developers, such as one- or two-component powder toners (also called one- or two-component developers), magnetic toners, liquid toners, polymerization toners and specialty toners (literature: L. B. Schein, “Electrophotography and Development Physics”; Springer Series in Electrophysics 14, Springer Verlag, 2
nd
Edition, 1992).
Typical toner binders are addition polymerization, polyaddition and polycondensation resins, such as styrene, styrene-acrylate, styrene-butadiene, acrylate, polyester and phenol-epoxy resins, polysulphones, polyurethanes, individually or in combination, and also polyethylene and polypropylene, which may comprise further constituents, such as charge control agents, waxes or flow assistants, or may be modified subsequently with these additives.
The compounds of the formula (I) are suitable, furthermore, as colorants in powders and powder coating materials, especially in triboelectrically or electrokinetically sprayable powder coating materials which are used for the surface coating of articles made, for example, from metal, wood, plastic, glass, ceramic, concrete, textile material, paper or rubber (J. F. Hughes, “Electrostatics Powder Coating” Research Studies, John Wiley & Sons, 1984).
Powder coating resins that are typically employed are epoxy resins, carboxyl- and hydroxyl-containing polyester resins, polyurethane resins and acrylic resins, together with customary hardeners. Combinations of resins are also used. For example, epoxy resins are frequently employed in combination with carboxyl- and hydroxyl-containing polyester resins. Typical hardener components (as a function of the resin system) are, for example, acid anhydrides, imidazoles and also dicyanodiamide and its derivatives, blocked isocyanates, bisacylurethanes, phenolic and melamine resins, triglycidyl isocyanurates, oxazolines and dicarboxylic acids.
In addition, the compounds of the formula (I) are suitable as colorants in ink-jet inks, both aqueous and non-aqueous, and in those inks which operate in accordance with the hot-melt process.
In the examples below, parts are by weight.


REFERENCES:
patent: 3376298 (1968-04-01), Braun et al.
patent: 3408349 (1968-10-01), Matsunaga
patent: 3716534 (1973-02-01), Sieja
patent: 4992101 (1991-02-01), Jaffe et al.
patent: 5021573 (1991-06-01), Bitterli et al.
patent: 6046335 (2000-04-01), Boeglin et al.
patent: 6200378 (2001-03-01), Piastra et al.
patent: 6277536 (2001-09-01), Piastra et al.
patent: 6375732 (2002-04-01), Kaul et al.
British Search Report, 9/99.
K. Takagi, M. Kawabe, M. Matsuoka, & T, Kitao, Dyes & Pigments, 1985, vol. 6(3), p. 177-188, No month available.
N.L. Agarwal & R.L. Mital, Egypt, J. Chem., 1977, vol. 20, No. 2, p. 205-208, No month available.
Journal of Chemical and Engineering Data, 1975, vol. 20, No., 2, p. 199-201, No month available.
Journ

Affiliated with

Also associated with

Rating

Heterocyclic compounds does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Heterocyclic compounds, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Heterocyclic compounds will most certainly appreciate the feedback.

Rate now

Comments { 0 }

Profile ID: LFUS-PAI-O-3078174