DE1618197C - Use of asymmetric oxalic acid diarylamides as ultraviolet protective agents for organic materials - Google Patents

Description

The present invention relates to the protection of organic materials by Ultraviolet radiation can be damaged in various ways against exposure to it this radiation with the help of asymmetric oxalic acid diarylamides, which are free of hydroxyl groups in the o-position for bonding the aryl radicals to the amide nitrogen atoms are.

It has already been described that oxalic acid-bis-oxyarylamide as a protective agent against Ultraviolet radiation is suitable, but it was previously believed that the light stability of such compounds bound to the presence of two free hydroxyl groups o to the amide nitrogen may be. Compounds of this type are e.g. B. in the German Auslegeschrift 1 188 080 described. However, these compounds give different substrates discoloration when exposed to light, which Rendering substrates unusable in many cases.

In contrast to the above view, it has now been found that an extensive Class of oxalic acid diarylamides without the feature mentioned not only as technically extremely useful Ultraviolet absorbers show, but surprisingly show a higher light stability. There is no discoloration of the substrates.

The present invention then relates to the use of asymmetric oxalic acid diarylamides the general formula

NH - CO - CO - NH - B

wherein A is an unsubstituted naphthyl radical or an optionally in the p-position with a halogen atom, a lower alkyl group, a lower alkoxy group, the nitrile, nitro or benzoyloxy group or optionally Phenyl radical substituted by methyl groups in the p- and m-positions and B optionally with 1 to 3 identical or different substituents from the group consisting of halogen atoms and alkyl groups 1 to 12 carbon atoms, the oxy-lower alkyl, carboxy-lower alkyl ester, trifluoromethyl, nitro, Lower alkanoyl, amino, hydroxy, carboxyl, carboxyhalido, carbamido, N-alkyl-carbamido, Carboxy alkali, lower alkyl carboxy, carboxy-p-halophenyl ester groups substituted phenyl radical and A and B are different from one another and free from o-position hydroxyl groups, as ultraviolet protective agents for organic materials.

The oxalic acid diarylamides to be used according to the invention can each represent one or the other different amide grouping to meet the demand for asymmetrical structure - from the derive the amines listed below as an example:,

a) anilines

Aniline; 2-chloroaniline, 4-chloroaniline,

3-chloroaniline,

2,4-dichloroaniline, 3,4-dichloroaniline,
2,4,6-trichloroaniliri and the corresponding

Bromaniline,

2, -fluoroaniline, 3-fluoroaniline, 4-fluoroaniline,
2, -iodaniline, 4-iodaniline,

3,5-diiodaniline, '.

2-methyl-, 3-methyl- or 4-methylaniline,
2,4-dimethylaniline, 2,5-dimethylaniline,

2,6-diethylaniline,

2-methyl-5-isopropylaniline,

3-trifluoromethylaniline,

3,5-bis-trifluoromethylaniline,
4-nitro-, 2-nitro- and 3-nitroaniline,

3-hydroxy- or 4-hydroxyaniline,

2-aminodiphenyl,

m-aminoacetanilide, p-aminoacetanilide,

and their amides,

ίο Anthranilic acid and its methyl and
Ethyl ester,

p-amino-N.N-dimethylaniline,

4-aminomethyl benzoate and ethyl benzoate,

4-hydroxy-3,5-di-tert-butylaniline,
4-hydroxy-3,5-dichloroaniline,

4-methyl-3-chloroaniline,

2-chloro-4-trifluoromethylaniline,

2,4-dimethyl-6-nitroaniline.

b) naphthylamines

α-naphthylamine or / 3-naphthylamine.

The oxalic acid bis-arylamide of the general formula (1) to be used according to the invention can be obtained in a manner known per se. They can be obtained by amidating oxalic acid or its esters on one side in the first stage by reacting oxalic acid or oxalic acid esters, in particular alkyl esters, with approximately equimolar amounts of corresponding primary amines A - NH ₂ or B - NH ₂ ( where A and B have the abovementioned meaning). A preferred method is, for example, that oxalic acid, oxalic acid half esters or oxalic acid diesters with similar or different ester radicals with approximately equimolar amounts of one of the aforementioned amines in the melt or in organic solvents inert towards the reactants in the presence of anhydrous boric acid at a temperature between about 50 and 200 ° C are condensed.

After isolation of the amide ester or amic acid obtained in this way, the remaining carboxyl group or carboxylate group of the oxalic acid half-amide is condensed in the second stage with a second amine A - NH ₂ or B - NH ₂ under analogous conditions , where in general expediently a temperature which is 50 to 100 ° C. higher, ie

between about 100 and 250 ⁰ C, is selected.

Here too, roughly equimolecular amounts are normally used.

Suitable inert organic solvents as mentioned above are in particular those with a ^{boiling point above about 160 °} C., that is to say

z. B. higher benzene hydrocarbons or halogenated Benzenes such as di- or trichlorobenzenes.

On the other hand, the introduction of the second amide group can also be achieved by saponification of one side of the in first stage produced amide ester to the amic acid, conversion into the amide acid halide and subsequent Amidation of the acid halide group take place.

With the help of the oxalic acid diamides described above In principle, all such organic materials can be stabilized and protected, which by the influence of ultraviolet rays in any

a form can be damaged or destroyed. Such damage caused by the same cause, namely ultraviolet radiation, can have very different effects, for example color change, Change in mechanical properties (brittleness, cracks, tear strength, flexural strength, Abrasion resistance, elasticity, aging), initiation of undesired chemical reactions (decomposition of sensitive chemical substances, photochemically induced rearrangements, oxidation, etc; for example from oils containing unsaturated fatty acids) or triggering of symptoms of burns and irritation (e.g. in human Skin). The use of the asymmetric oxalic acid diarylamides defined above is of preferred importance to protect polycondensation products and polyaddition products against the effects of ultraviolet.

The organic materials to be protected can be in a wide variety of processing states and physical states exist, while their common feature in a sensitivity to There is ultraviolet radiation.

As low molecular weight or higher molecular weight substances for which the inventive method for Protection or stabilization comes into consideration, for example: organic natural substances such as they are used for pharmaceutical purposes, UV sensitive dyes or compounds that decomposed as food or in food by exposure to light (unsaturated fatty acids in oils).

Examples of high molecular weight organic substances are:

I. Synthetic organic high molecular or higher molecular materials such as:

a) Polymerization products based on at least one polymerizable carbon-carbon double bond containing organic compounds, d. H. their homo- or copolymers and their aftertreatment products such as for example crosslinking, grafting or degradation products, polymer blends, modification products by modifying reactive groups in the polymer molecule, such as. B. Polymers based on α, / 3-unsaturated Carboxylic acids (e.g. acrylates, acrylamides, acrylonitrile), olefin hydrocarbons such as. B. δ-olefins, ethylene, propylene or dienes, d. H. so also rubbers and rubber-like ones Polymers (also so-called ABS polymers), polymers based on vinyl and Vinylidene compounds (e.g. styrene, vinyl ester, vinyl chloride, vinyl alcohol), of halogenated Hydrocarbons, from unsaturated aldehydes and ketones or allyl compounds;

b) other polymerization products, such as. B. obtainable by ring opening, e.g. B. polyamides from Polycaprolactam type, also formaldehyde polymers or polymers that are available both via polyaddition and polycondensation are, such as polyethers, polythioethers, polyacetals, thioplasts.

c) Polycondensation products or precondensates based on bifunctional or polyfunctional compounds with condensable groups, their homo- and mixed condensation products and products post-treatment, for which examples include: polyester [saturated (e.g. Polyethylene terephthalate) or unsaturated (e.g. maleic acid - dialcohol - polycondensates as well their crosslinking products with polymerizable vinyl monomers), unbranched and branched (also based on higher alcohols such as alkyd resins)], polyamides (e.g. hexamethylenediamine adipate), Maleinate resins, melamine resins, phenolic resins (e.g. novolaks), aniline resins, furan resins, carbamide resins, and also their precondensates and similarly built products, polycarbonates and silicone resins.

d) Polyaddition products such as polyurethanes (crosslinked and uncrosslinked), epoxy resins.

II. Semi-synthetic organic materials, such as. B. cellulose esters or mixed esters (acetate, propionate), Nitrocellulose, cellulose ether, regenerated cellulose (viscose, copper ammonia cellulose) or their aftertreatment products, casein plastics.

III. Natural organic materials of animal or vegetable origin, for example based on cellulose or proteins such as wool, cotton, silk, raffia, jute, hemp, fur and hair, leather, wood masses in fine distribution, natural resins (such as rosin, especially paint resins), gelatine, Glues, also rubber, gutta-percha, balata and their aftertreatment and modification products, degradation products, products obtainable by modifying reactive groups.
The organic materials, especially plastics, such as polymers of vinyl chloride, saturated and unsaturated polyesters, celluloses and polyamides, can be used in the various

• The most varied processing states (raw materials, semi-finished products or finished products) and aggregate states are present. They can even be in the form of the most varied of shaped structures, i. H. so z. B. predominantly three-dimensionally extended bodies such as profiles, containers or a wide variety of Workpieces, chips or granulates, foams; predominantly two-dimensional bodies, such as films, foils, lacquers, impregnations and coatings, or predominantly one-dimensional Bodies, such as threads, fibers, bristles, wires. On the other hand, the said materials can also in unshaped states in the most varied of homogeneous and inhomogeneous distribution forms and Physical states exist, e.g. As powders, solutions, normal and reverse emulsions (Creams), dispersions, latices, sols, gels, putties, waxes, adhesives and fillers.

Fiber materials can be in a wide variety of predominantly non-textile processing forms, z. B. as threads, yarns, nonwovens, felts, wadding, flocking structures or as textile fabrics or textile composites, knitted fabrics, paper, cardboard, etc.

The new stabilizers can also be used, for example, as follows:

a) in cosmetic preparations such as perfumes, colored and uncolored soaps and bath additives, Skin and face creams, powders, repellants and in particular sun protection oils and creams;

b) as a mixture with dyes or pigments or as an additive to dye baths, printing, etching or Reserve pastes. Also for the aftertreatment of dyeings, prints or etching prints;

c) in mixtures with so-called "carriers", antioxidants, other light stabilizers, heat stabilizers or chemical bleaches;

d) in a mixture with crosslinkers, finishing agents such as starch or synthetically accessible finishes;

e) in combination with detergents. The detergents and stabilizers can be the ones to be used Wash baths can also be added separately;

f) in gelatin layers for photographic purposes;

g) in combination with polymeric carrier materials (polymerization, polycondensation or polyaddition products), in which the stabilizers are incorporated in dissolved or dispersed form, possibly alongside other substances, z. B. for coating, impregnating or binding agents (solutions, dispersions, emulsions) for Textiles, fleece, paper, leather;

h) as additives to a wide variety of industrial products to reduce their aging rate reduce, e.g. B. as an additive to glues, adhesives or paints, etc.

If the protective agents to be used according to the invention for the treatment of textile organic materials of natural or synthetic origin, z. B. textile fabrics are to be used, the same can be used in each phase of the finishing, such as finishing, anti-crease finishing, dyeing processes, other finishing by means of fixing processes Similar to dyeing processes can be applied to the substrate to be protected.

The new stabilizing agents to be used according to the invention are preferably added to the materials added or incorporated before or during their deformation. For example, you can use it at the production of films, foils, tapes or moldings of the molding compound or injection molding compound add or dissolve, disperse or otherwise finely distribute in the spinning mass before spinning. The protective agents can also be the starting substances, reaction mixtures or intermediates for the production of fully or semi-synthetic organic materials are added, so also before or during the chemical reaction, for example in the case of a polycondensation (including precondensates), in a polymerization (including prepolymers) or a polyaddition.

An important application variant for the stabilizers to be used according to the invention consists in the fact that these substances are incorporated into a protective layer, which is the one behind them Protect material. This can be done in such a way that the ultraviolet absorber is applied to the surface layer (a film, a fiber of a multi-dimensional molded body). This can be achieved, for example, by a kind of dyeing process or the active ingredient in one Embed polymer (polycondensate polyadduct) film according to known surface coating methods with polymeric substances, or one the active substance can diffuse or swell into the surface layer in dissolved form by means of a suitable solvent. One Another important variant is that the ultraviolet absorber is essentially self-supporting two-dimensional carrier material is embedded, e.g. B. a film or a vessel wall to thereby to keep ultraviolet radiation from the underlying substance (examples: shop windows, films, Transparent packs, bottles).

It goes without saying from the above that in addition to protecting the substrate or the carrier substance, which contains the ultraviolet absorber, at the same time also the protection from other accompanying substances of the substrate is reached, for example dyes, antioxidants, disinfectant additives, Antistatics and other finishes, plasticizers and fillers.

Depending on the type of substance to be protected or stabilized, on its sensitivity or the application form of protection and stabilization can determine the required amount of stabilizer vary within wide limits, for example between about 0.01 and 10 percent by weight, based on the amount of substrate to be protected. For most practical purposes, however, suffice Amounts from about 0.05 to 2%.

The resultant method of protecting organic materials from the action above from ultraviolet radiation and heat thus consists in using the oxalic acid diamides described homogeneously distributed in the organic materials to be protected, superficially on these materials applies or covers the materials to be protected with a filter layer, which the designated Contains connections.

In particular, it is expedient to proceed in such a way that the oxalic acid diarylamides described are used in substance, in dissolved or dispersed form in the organic to be protected Materials in amounts of 0.1 to 10, preferably 0.2 to 2.0 percent by weight based on the amount of the materials to be protected are incorporated in a homogeneous distribution before the final deformation.

If the substance to be used according to the invention is to be applied superficially to the substrate to be protected, e.g. If, for example, a fiber material (fabric) is applied, this can advantageously be done by introducing the substrate to be protected into a liquor which contains the UV absorber in dissolved or dispersed form. Suitable solvents can e.g. B. methanol, ethanol, acetone, ethyl acetate, methyl ethyl ketone, cyclohexanol or especially water. As in dyeing processes, the substrate to be treated is left in the liquor for a certain time - usually 10 minutes to 24 hours - at 10 to 120 ^° C., it being possible for the liquor to be moved if necessary. The material is then rinsed, optionally washed and dried.

It is often expedient to use the light stabilizers described above in combination with sterically hindered phenols, esters of thiodipropionic acid or organic phosphorus compounds.
The parts and percentages mentioned in the following manufacturing instructions and the examples always represent parts by weight and percentages by weight, unless stated otherwise.

1

Preparation method 9.1 parts of the compound of the formula O O

[^ V-NH-CC-OC ₂ H ₅ Cl

(13)

are with 6.5 parts of 3,4-dichloroaniline and 0.5 parts Boric acid stirred for 2 hours at 175 to 180 ° C, the. resulting alcohol continually is distilled off. The melt is then dissolved in dimethylformamide and the solution is added at 20.degree with water.

The product of the formula

O O

NH-C-C-NH

Cl

(14)

Cl Cl

It separates out in the form of almost colorless crystals. Yield: about 12 parts.

197

An analysis product recrystallized three times from benzene-methanol melts at 234 to 235 ° C. and shows following data:

C ₁₄ H ₉ O ₂ N ₂ CH ₃ :

Calculated ... C 48.94, H 2.64, N 8.15; found .... C 49.09, H 2.48, N 8.17.

The compounds listed in the tables below were produced in the same way or in a different manner manufactured. In these tables:

Column I formula no.

Columns II + III definition of the connection

Column IV melting point ⁰ C

(uncorrected) Column V analysis data C, H, N

(1st line calculated 2nd line found)

Regarding compound no. () In Table D ₂ , it should be noted that the C ₁₂ H ₂₅ radical is a mixture of differently branched isomers (from tetramerization of 4 propylene molecules).

D ₁ NH-CO-CO.-NH

(15)

I. II (V ₁ =) III (W, =) -NO ₂ IV 58.94
59.20 V 14.73
14.60 16 - H -NH ₂ 252 to 253 65.87
65.86 3.89
4.00 16.46
16.32 17th - H -NH-CO-CH ₃ 211 to 212 64.63
64.48 5.13
5.05 14.14
14.16 18th - H - COOH 295 to 297 63.38
63.66 5.09
4.94 9.86
10.01 19th - H - COCl > 330 59.51
59.85 4.26
4.39 9.25
9.22 20th - H - CONH ₂ 229 to 231 63.59
63.22 3.66
3.70 14.83
14.65 21 TT -CO-Nh-CH ₂ CH-CH ₂ CH ₃
(CH ₂ ) ₃ - CH ₃ > 33O 69.85
69.87 4.63
4.63 10.63
10.72 22nd TT - COONa 267 to 269 58.83
58.59 7.39
7.28 9.15
9.28 23 - H - COOC ₂ H ₅ > 330 65.37
65.59 3.62
3.70 8.97
8.98 24 - H C ₁₂ H ₂₅ 202 to 203 76.43
76.56 5.16
5.28 6.86
6.91 25th - H - Η 75 to 90 63.89
63.65 8.88
8.61 7.10
7.19 26th - COO- χζ ^ Cl 222 to 223 3.90
3.99

209 633/200

continuation

10

I. H (V ₁ =) HI (W ₁ =) IV 67.59
67.48 ν 9.85
9.89 27 - Η - CH ₂ CH ₂ - OH 217 to 218 64.42
64.47 5.67
5.58 9.39
9.32 28 TJ - CH ₂ COOH 254 to 256 72.95
72.93 4.73
4.75 9.45
9.58 29 - Η CH ₂ CH ₂ CH ₂ CH ₃ 178 to 180 6.80
6.61

V, - NH - CO - CO - NH - W ₇ (30)

π (V ₂ =)

III (W ₂ =) IV

■ V

CH,

CH,

CH,

Cl

Cl

CF ₃

Cl to 272

to 190

up to 250

to 290

to 204

to 210

to 228

to 192

62.40 4.54 9.70 62.30 4.51 9.59

46.79 2.21 6.82 47.00 2.45 6.81

43.33 2.34 7.22 43.24 2.24 7.25

54.00 3.91 8.42 54.13 3.92 8.45

42.73 2.15 6.64 42.53 2.40 6.61

42.22 1.99 6.15 42.12 1.82 6.36

55.75 3.74 8.67 56.04 3.49 8.86

53.87 3.39 7.85 54.09 3.65 7.92

11th

Continued 12

I. H (V ₂ =) III (W ₂ =) IV ν 39 CF ₃ 165 to 166 52.32 3.10 7.18
52.03 3.10 7.23

D,

V, - NH - CO - CO - NH - W ₂ (40)

H (V ₂ =)

IH (W ₂ =) IV

CH ₁

CH,

CH,

CH ₁

CH ₁

CH,

Cl

CF,

Cl

to 226

to 206

to 184

to 179

to 208

to 183

to 227

to 231

56.99 4.18 8.31 57.71 4.25 8.43

72.32 6.43 9.92 72.61 6.52 10.00

55.07 3.81 7.56 55.17 3.97 7.56

53.47 3.49 6.93 53.77 3.60 6.92

75.45 5.70 8.80 75.16 5.65 8.83

74.98 5.30 9.21 74.71 5.24 9.24

66.57 4.03 8.63 66.53 3.75 8.59

58.55 3.55 7.59 58.47 3.30 7.65

continuation

14th

I. II (V ₂ =) III (W ₂ =) IV 51.00
51.18 V 2.85
2.79 11.90
1100 ■ CF ₃ 49 O ₂ N - ^ y- 200 to 201

V ₂ - NH CO - CO - NH - W ₂

H (V ₂ =)

IH (W ₂ =)

IV

51

52

53

54

55

N = C

to 189

OH

OH

to 242

> 330

to 279

to 304

47.77 2.41 7.34 47.93 2.56 7.57

72.32 6.43 9.92 72.02 6.46 9.76

60.11 3.36 14.02

60.19 3.39 14.16

63.99 5.37 9.33

63.95 5.34 9.06

67.01 4.29 7.44 66.98 4.24 7.49

Examples

In the following examples, unless otherwise noted, parts are parts by weight and percentages are percentages by weight.

In each of these examples, typical representatives used for respective subgroups of compounds suitable according to the invention. In principle are all of the compounds mentioned in the preceding description and their equivalents equally suitable, with only the solubility of the compound in question to be taken into account in the substrate to be used or to be determined in a manual test. Possibly Finally, the fact that the absorption maximum of the to be incorporated must also be taken into account Compound is influenced by the substituents in the aromatic radical.

example 1

. It becomes an acetyl cellulose film about 50 μ thick by pouring out a 10% acetyl cellulose solution containing 1% (calculated on acetyl cellulose) dsr compound of formula (51) contains prepared. After drying, the following are obtained Values for the percentage of light transmission:

Light transmission in% exposed 45 wavelength in ηΐμ (100 hours unexposed Fadeometer) 0 260 to 310 0 5 ₅ o 320 5 20- 330 20th 50 340 50 75 . 350 75

55

6o

Similarly behave z. B. the compounds of the formulas (17), (27), (45), (47) and (53).

Example 2

A paste of 100 parts of polyvinyl chloride, parts by volume of dioctyl phthalate and 0.2 parts of the compound of the formula (45) is ^{rolled out on the calender at 145 to 150 °} C. to form a film of about 0.5 mm. The polyvinyl chloride film obtained in this way absorbs in the ultraviolet range from 280 to 350 πΐμ.

Instead of the compound of the formula (45), it is also possible, for example, to use one of the compounds of the formulas (24), (29), (33), (37). Or (41) can be used.

Example 3

A mixture of 100 parts of polyethylene and 0.2 parts of the compound of formula (42) is rolled on the calender at 130 to 14O ⁰ C into a sheet and pressed at 150 ⁰ C.

The polyethylene film thus obtained is practically impermeable to ultraviolet light in the area from 280 to 350 πΐμ.

Instead of the compound of the formula (42), it is also possible, for example, to use one of the compounds of the formulas (34), (46) or (47) can be used.

Example 4

A mixture of 100 parts of polypropylene and 0.2 parts of one of the compounds of the formulas (29), (32), (35), (45) or (51) is processed on the calender at 170 ^° C. to form a skin. This is pressed mm at 230 to 24O ⁰ C and a maximum pressure of 40 kg / cm ² into a plate of Figure 1.

The plates thus obtained are useful for ultraviolet light in the range of 280 to 350 πΐμ impermeable. Other compounds listed in the table behave similarly.

Example 5

0.2 parts of the compound of formula (14) are dissolved in 1.8 parts of monostyrene and 0.5 parts a cobalt naphthenate monostyrene solution (containing 1% cobalt). There are 40 parts on it an unsaturated polyester resin based on phthalic acid-maleic acid-ethylene glycol in monostyrene was added and the whole was stirred for 10 minutes. After the dropwise addition of 1.7 parts of a catalyst solution (Methyl ethyl ketone peroxide in dimethyl phthalate) is the well mixed, air-free mass poured out between two glass plates. After about 20 minutes the 1 mm thick polyester plate is ready solidified that it can be removed from the mold, it is in the range of 280 to UV light 350 πΐμ impermeable.

Instead of the compound of the formula (14), it is also possible, for example, to use one of the compounds of the formulas (31) or (32) can be used.

Example 6

25 g of distilled styrene monomer can be prepolymerized in a closed bottle in an oven at 90 ⁰ C for 2 days. In the viscous. Then 0.25 g of a compound of the formulas (45), (46), (48) or (51) and 0.025 g of benzoyl peroxide are slowly stirred in. The mixture is then poured into a cuboid form made of aluminum foil and ^{kept at 70 °} C. for 1 day. After the mass has completely solidified and cooled, the shape is broken apart. The block thus obtained is then pressed in a hydraulic press at a temperature of 138 ° C. and a pressure of 150 kg / cm ² to give a plate 1 mm thick.

The polystyrene plates produced in this way are impermeable to UV light in the range from 280 to 350 ηΐμ. They are completely colorless. When exposing in the fadeometer you can see a significant improvement Observe the light stability by placing polystyrene sheets containing compounds of the above formulas contain no yellowing when exposed to 200 hours, while plates are already yellowed without these additives. Others listed in the tables behave similarly Links.

B e i s ρ i e 1 7

8 g toluene - 2,4 - diisocyanate - toluene - 2,6 - diisocyanate mixture (65:35) and 20 g of a slightly branched polyester made from adipic acid, diethylene glycol and triol (hydroxyl number: 60) are stirred together for about 15 seconds. Then you give 2 ml of a catalyst mixture (consisting of 6 ml of a tertiary amine, 3 ml dispersant, 3 ml a stabilizer and 2 ml of water) and 0.28 g of a compound of the formulas (32), (35), (45) or (51) and stir briefly. A foam fleece is formed, which is placed in a water bath after 30 minutes will. After a further 30 minutes, it is washed thoroughly with water and dried at room temperature.

The addition of one of the above-mentioned UV absorbers increases the resistance during exposure in the xenotest apparatus. The above absorbers are also found in numerous other polyurethanes based on the isocyanate polyaddition process are based, easy to incorporate.

Other connections listed in the table behave similarly.

Example 8

0.2 g of the compound of the formula (14) are dissolved in 10 g of pure olive oil. The solution takes place quickly and without heating. A 50μ thick layer of this solution absorbs the UV light up to 340μ.

Likewise, other fatty oils and creams or emulsions that can be used as cosmetic Find purposes use to solve the above or other compounds such. B. (32), (39) or Use (51).

Example 9

12 g of polyacrylonitrile are sprinkled into 88 g of dimethylformamide with stirring until they are completely dissolved. Then 0.1 g of the instantly dissolving compound of the formula (46) is added. The viscous mass is then applied to a cleaned glass plate and spread with a film drawing rod. It is then dried in a vacuum drying cabinet at 120 ^° C. and a vacuum of 150 mm Hg for 20 minutes. The result is a film about 0.05 mm thick, which can easily be removed from the glass substrate. The film obtained in this way is completely colorless and absorbs UV light up to a wavelength of 350 πΐμ practically completely, while a film without the above compound of the formula (46) allows at least 80% of the UV light to pass through. In addition, the compounds mentioned for polystyrene are also suitable for incorporation into polyacrylonitrile.

Claims (1)

Claim: Use of asymmetrical oxalic acid diarylamides of the general formula A - NH - CO - CO - NH - B wherein A is an unsubstituted naphthyl radical or an optionally in the p-position with a halogen atom, a lower alkyl group, a lower 209 633/200 alkoxy group, the nitrile, nitro or benzoyloxy group or optionally in the p- and m-positions phenyl radical substituted by methyl groups and B is optionally 1 to 3 identical or various substituents from the group of halogen atoms, alkyl groups with 1 to 12 carbon atoms, the oxy lower alkyl, carboxy lower alkyl ester, trifluoromethyl, nitro, lower alkanoyl, amino, hydroxy, carboxyl, carboxyhalido, carbamidep, N-alkyl-carbamido, Carboxy alkali, lower alkyl carboxy, carboxy halophenyl ester groups is substituted phenyl and A and B are different from one another and free from o-hydroxy groups, as an ultraviolet protectant for organic materials.