Abstract: Nanocomposite biocompatible hydrogels (NCHGs) may be synthesised as model systems for in situ cured local drug delivery devices for treatment of inter alia periodontal infections. The composite includes the following components: nanoparticles (NPs), a matrix gel, and chlorhexidine (CHX) or other antibacterial drug. The NPs were obtained by free radical initiated copolymerization of the monomers, 2-hydroxyethyl methacrylate (HEMA) and polyethyleneglycol dimethacrylate (PEGDMA), in aqueous solution. The same monomers were used to prepare crosslinked matrices by photopolymerization. NCHGs were obtained by mixing NPs, monomers, and drug in an aqueous solution then crosslinked by photopolymerization.

Abstract: The invention relates to a novel herbicide composition, which comprises the (S) enantiomer or racemate of a compound of the general formula (I), ##STR1## wherein R stands for a methyl or ethyl group, as active ingredient in an amount of 0.01 to 95% by weight together with one or more solid and/or liquid carrier(s), preferably grist(s) of native or synthetic material(s) and/or with inert solvents(s), preferably xylene(s) and/or cyclohexanone; and optionally with surface active agents(s), preferably anionic and/or nonionic emulsifying or dispersing agent(s).The invention further relates to the above compounds of the general formula (I) as well as to a process for the preparation thereof.The compounds according to the invention possess an outstanding herbicidal effect (over 90%) and advantageous selectivity threshold values against cultivated plants.

Abstract: The invention relates to novel fungicidally active compounds, a process for the preparation thereof, composition comprising the said composition as active ingredient and their use for agricultural purpose.The novel (trifluoromethyl)-phenoxy benzoic acid derivate can be described by formula (I), ##STR1## wherein X is hydrogen or halogen, preferably chlorine, nitro or trifluoromethyl,Y is hydrogen or halogen, preferably chlorine,Z is hydrogen, trifluoromethyl or nitro,V is hydrogen, halogen, preferably chlorine, or nitro,W is hydrogen, nitro or trifluoromethyl,R.sub.1 is alkyl having 1-4 carbon atoms, preferably ethyl, hydrogen, alkali metal, preferably sodium, potassium, or ammonium or ammonium-ion having a formula (II),NH.sub.3.sup.+ R.sub.2 (II)whereinR.sub.

Abstract: A herbicide composition, which comprises (S)-1'-methoxycarbonylethyl 2-bromo-5-(2-chloro-4-trifluoromethylphenoxy) benzoate or (S)-1'-ethoxycarbonylethyl 2-bromo-5-(2-chloro-4-trifluoromethylphenoxy)benzoate as active ingredient in an amount of 0.01 to 95.0% by weight together with one or more solid and/or liquid carriers, preferably grists of native or synthetic materials; and/or with inert solvents, preferably xylenes and/or cyclohexanone; and optionally with surface active agents, preferably anionic and/or nonionic emulsifying or dispersing agents.

Abstract: The invention relates to a new process for the preparation of aminodiaryl sulfoxide derivatives of the formula (I), ##STR1## wherein X is halogen, alkoxy having from 1 to 6 carbon atoms or a group --(N,R,R.sup.1), in which p1 R and R.sup.1 are hydrogen or alkyl having from 1 to 6 carbon atoms,R.sup.2 is hydrogen, halogen, alkyl having from 1 to 6 carbon atoms, alkoxy having from 1 to 6 carbon atoms or phenyl or phenylthio both optionally substituted by one or more identical or different halogen(s) and/or amino group(s),and acid addition salts thereof.The compounds of formula (I) are pharmaceutically active, in particular are potent anthelmintics, or can be used as active ingredients in pesticidal compositions. The invention therefore relates to pharmaceutical and pesticidal compositions containing compounds of formula (I) or salts thereof as active ingredient.Compounds of formula (I), in which the substituents are as defined above, but if X stands for a group --N(R,R.sup.1) in which R and R.sup.

Abstract: An electro-optical light modulator having a reduced piezo-optical effect by providing a plurality of optically series-connected modulator crystals having geometric dimension differing from one another such that for pulse control the overlapping of acoustical transients generated in the individual modulator crystals is excluded, along the beam path and where periodical control is used, the overlapping of the piezo-electrical resonant frequencies of the individual modulator crystal is excluded.

Abstract: The invention relates to a new process for the preparation of aminodiaryl sulfoxide derivatives of the formula (I), ##STR1## wherein X is halogen, alkoxy having from 1 to 6 carbon atoms or a group --(N,R,R.sup.1), in whichR and R.sup.1 are hydrogen or alkyl having from 1 to 6 carbon atoms,R.sup.2 is hydrogen, halogen, alkyl having from 1 to 6 carbon atoms, alkoxy having from 1 to 6 carbon atoms or phenyl or phenylthio both optionally substituted by one or more identical or different halogen(s) and/or amino group(s),and acid addition salts thereof.The compounds of formula (I) are pharmaceutically active, in particular are potent anthelmintics, or can be used as active ingredients in pesticidal compositions. The invention therefore relates to pharmaceutical and pesticidal compositions containing compounds of formula (I) or salts thereof as active ingredient.Compounds of formula (I), in which the substituents are as defined above, but if X stands for a group --N(R,R.sup.1) in which R and R.sup.