Abstract: A process for the preparation of a reaction product (A) comprises the following stage (i):

Abstract: The present invention provides a process for the free radical polymerization of one or more ethylenically unsaturated monomers, said process comprising polymerizing one or more ethylenically unsaturated monomers in the presence of one or more N-oxyl radicals of formula II, wherein X is S, NR5, O, SO or SO2, R5 is C1-C20-alkyl or C5-C8-cycloalkyl and R3 and R4 independently of one another, are C1-C4-alkyl, phenyl, naphthyl or an aromatic five-membered ring, or R3 and R4 together are —(CH2)o— and p and o, independently of one another, are an integer from 2 to 7.

Abstract: Cosmetic or dermatological preparations for avoiding or reducing skin damage by peroxides or hydroperoxides formed as a result of endogenous or exogenous factors, with a content of

Abstract: A reaction product (A) which can be prepared by reaction, under free radical conditions, of at least one monomer (a) capable of free radical reaction, in the presence of at least one free radical initiator and of a radical of the formula (III) 1

Abstract: The present invention relates to chiral 1,3-dioxane compounds and diastereomers thereof of the general formula I where R1, R2 and R3 are as defined in the description, and the use of these compounds as chiral dopants for liquid-crystalline systems. The invention further relates to non-polymerizable or polymerizable liquid-crystalline compositions comprising at least one chiral 1,3-dioxane compound of the formula (I) of the invention, the use of these non-polymerizable or polymerizable liquid-crystalline compositions for producing optical components, the use of the polymerizable liquid-crystalline compositions for printing or coating substrates, for preparing dispersions and emulsions, films or pigments and optical components, printed or coated substrates, dispersions and emulsions, films and pigments of this type.

Abstract: Disclosed are a detersive composition comprising a water-soluble or water-dispersible block copolymer preparable by controlled free-radical polymerization, a process for preparing such a detersive composition and the use of water-soluble or water-dispersible block copolymers preparable by controlled free-radical polymerization for preparing detersive compositions.

Abstract: The use of compounds of the general formula I in which the substituents are as defined in the description, as chiral dopants for nematic or cholesteric liquid crystals for the generation of layers which reflect in color in the UV or IR region or for the preparation of pigments having a liquid-crystalline cholesteric order.

Abstract: The present invention relates to 4-formylamino-N-methylpiperidine derivatives of the formula (I) 1

Abstract: A process for the preparation of polymers is described, wherein at least one first ethylenically unsaturated monomer is subjected to a free radical polymerization in the presence of stable free radicals or sources of stable free radicals and of a compound having at least one free thiol group to give a polymer, and wherein the molar ratio of compound having a free thiol group to stable free radicals is from 0.05 to 1.1.

Abstract: Improved liquid crystalline materials may be prepared by doping liquid crystalline materials with chiral, uncharged metal compounds of formula [(P1—Y1—A1—Y2—M1—Y3—)nL]2Me or [(P1—Y1—A1—Y2—M1—Y3—)nL]Me(L′(—Y6—M2—Y5—A2—Y4—P2)n′)m. Groups P1 and P2 may be, independently, hydrogen, C1-C12-alkyl groups, polymerizable groups, or radicals containing a polymerizable group. Y1 to Y6 may be, independently, single chemical bonds, ether groups, thio groups, carbonyl groups, acid groups, etc. Groups A1 and A2 are spacers having from 1 to 30 carbon atoms, and M1 and M2 are mesogenic groups. Me may be a transition metal from the fourth, fifth or sixth period of the periodic table, except for technetium, silver, cadmium, gold, mercury, or any of the lanthanoids, or Me may be a main group element from group 14 (IUPAC system), except for carbon and lead.

Abstract: 4,4-Diarylbutadienes of the formula I, where the diene system has the Z,Z; Z,E; E,Z or E,E configuration or a mixture thereof, and where the variables independently of one another have the following meanings: R1 and R2 are hydrogen, C1-C20-alkyl, C2-C10-alkenyl, C3-C10-cycloalkyl, C3-C10-cycloalkenyl, C1-C12-alkoxy, C1-C20-alkoxycarbonyl, C1-C12-alkylamino, C1-C12-dialkylamino, aryl, hetaryl, unsubstituted or substituted, substituents which confer solubility in water and are selected from the group consisting of carboxylate, sulfonate, or ammonium residues; R3 is COOR5, CONR5R6; R4 is COOR6, CONR5R6; R5 and R6 are hydrogen, C1-C20-alkyl, C2-C10-alkenyl, C3-C10-cycloalkyl, C7-C10-bicycloalkyl, C3-C10-cycloalkenyl, C7-C10-bicycloalkenyl, aryl, hetaryl, unsubstituted or substituted; n is 1 to 3; and R3 and R4 are not COOCH3 when R1 and R2 are hydrogen, are used as photostable UV filters in cosmetic and pharmaceutical preparations to protect the human skin or human hair from the sun's rays,

Abstract: A description is given of a stabilizer composition comprising

Abstract: A process for the preparation of a reaction product (A), which comprises the following stage (i):

Abstract: Use of amino-substituted hydroxybenzophenones of the formula I in which the variables have the meanings explained in the description, as photostable UV filters in cosmetic and pharmaceutical preparations for protecting human skin or human hair from the sun's rays, alone or together with compounds which absorb in the UV region and are known per se for cosmetic and pharmaceutical preparations.

Abstract: Disclosed are polymerizable liquid-crystalline compounds of the general formula (I) 1

Abstract: The present invention relates to liquid-crystalline compositions of matter comprising, as components,

Abstract: Flavonoids of the formula 1

Abstract: 4,4-Diarylbutadienes of the formula I, 1

Abstract: The present invention relates to chiral 1,3-dioxane compounds and diastereomers thereof of the general formula I 1

Abstract: 4,4-Diarylbutadienes of the formula I, where the variables have the meanings explained in the description, are used as photostable UV filters in cosmetic and pharmaceutical preparations to protect the human skin or human hair from the sun's rays, alone or together with compounds which absorb in the UV region and are known per se for cosmetic and pharmaceutical preparations.