Claims
- 1. Distyryl-dibenzofuranes of the formula ##STR40## wherein R.sub.x is selected from the group consisting of sulphonic acid, benzyl ester of sulphonic acid, phenylester or alkylester of sulphonic acid with 1 to 18 carbon atoms in the alkyl part, alkylsulphone of 1 to 4 carbon atoms, phenylsulphone, a sulphonamide, a carboxylic acid, a carboalkoxy of 2 to 9 carbon atoms or a nitrile, R.sub.x '] is selected from the group consisting of sulphonic acid, benzylester of sulphonic acid, phenylester or alkylester or sulphonic acid with 1 to 18 carbon atoms in the alkyl part, alkylsulphone of 1 to 4 carbon atoms, phenylsulphone, a carboxylic acid, a carboalkoxy of 2 to 9 carbon atoms, nitrile, alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms, chlorine or hydrogen, and R.sub.y and R.sub.y ' independently of one another are hydrogen, sulphonic acid or a salt thereof, chlorine, alkyl of 1 to 4 carbon atoms or alkoxy of 1 to 4 carbon atoms.
- 2. Distyryl-dibenzofuranes according to claim 1, corresponding to the formula ##STR41## wherein R.sub.1 is selected from the group consisting of sulphonic acid or its salts, a sulphonamide, benzylester of sulphonic acid, phenylester or alkylester of sulphonic acid with 1 to 4 carbon atoms in the alkyl part, carboxylic acid or its salts, carboalkoxy of 2 to 9 carbon atoms, nitrile, alkylsulphone of 1 to 4 carbon atoms or phenylsulphone, and R.sub.2 is selected from the group consisting of hydrogen, chlorine, alkyl with 1 to 4 carbon atoms, alkoxy with 1 to 4 carbon atoms or a sulphonic acid or its salts.
- 3. Distyryl-dibenzofuranes according to claim 1, corresponding to the formula ##STR42## wherein R.sub.3 is selected from the group consisting of sulphonic acid or its salts, aminosulphonyl, monoalkylaminosulphonyl or dialkylaminosulphonyl with 1 to 4 carbon atoms per alkyl part, phenoxysulphonyl, alkyloxysulphonyl with 1 to 4 carbon atoms, alkylsulphonyl with 1 to 4 carbon atoms, phenylsulphonyl, carboxylic acid or its salts, carboalkoxy with 2 to 9 carbon atoms, aminocarbonyl, monoalkylaminocarbonyl or dialkylaminocarbonyl with 1 to 4 carbon atoms per alkyl part or nitrile.
- 4. Distyryl-dibenzofuranes according to claim 1, corresponding to the formula ##STR43## wherein R.sub.4 is selected from the group consisting of hydrogen, sulphonic acid or its salts, chlorine or methyl, R.sub.5 is selected from the group consisting of hydrogen, sulphonic acid or its salts, aminosulphonyl, monoalkylaminosulphonyl or dialkylaminosulphonyl with 1 to 4 carbon atoms per alkyl part, phenoxysulphonyl, alkoxysulphonyl with 1 to 4 carbon atoms, alkylsulphonyl with 1 to 4 carbon atoms, phenylsulphonyl, carboxylic acid or its salts, carboalkoxy with 2 to 9 carbon atoms, aminocarbonyl, monoalkylaminocarbonyl or dialkylaminocarbonyl with 1 to 4 carbon atoms per alkyl part or nitrile, R.sub.6 is selected from the group consisting of hydrogen, sulphonic acid or its salts, chlorine, alkyl with 1 to 4 carbon atoms or alkoxy with 1 to 4 carbon atoms and M is a salt-forming cation.
- 5. Distyryl-dibenzofuranes according to claim 1, corresponding to the formula ##STR44## wherein R.sub.8 is hydrogen, chlorine, methyl or methoxy, R.sub.9 represents hydrogen, the sulphonic acid group or its salts, chlorine, methyl or methoxy, R.sub.10 is hydrogen, chlorine, methyl or methoxy and M is a salt-forming cation.
- 6. Organic materials of polyamides and cellulose, containing 0.0001 to 1 percent by weight, calculated relative to the total amount of organic material, of at least one of the distyryl-dibenzofurane compounds as defined in claim 1.
- 7. Washing agent for textile organic materials of polyamides and celluloses, which contains 0.01 to 2 percent by weight of at least one distyryl-dibenzofurane compound, as defined in claim 1.
- 8. A process for the optical brightening of organic materials selected from the group consisting of polyamides and celluloses, wherein the improvement comprises incorporating into said materials to be optically brightened or applying to the surface of said materials to be optically brightened effective amounts of distyryl-dibenzofurance compounds of claim 1.
Priority Claims (1)
Number |
Date |
Country |
Kind |
9854/72 |
Jun 1972 |
CH |
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Parent Case Info
This is a continuation of application Ser. No. 374,141, filed on June 27, 1973, now abandoned.
US Referenced Citations (2)
Number |
Name |
Date |
Kind |
3627758 |
Weber et al. |
Dec 1971 |
|
3697513 |
Siegrist |
Oct 1972 |
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Non-Patent Literature Citations (1)
Entry |
Siegrist et al. Helvetia Chimica Acta 52 (1969) pp. 1282-1284, 1307. |
Continuations (1)
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Number |
Date |
Country |
Parent |
374141 |
Jun 1973 |
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