Abstract: Thermotropic liquid-crystalline aromatic polyesters processable in the molten state, comprising units derived from at least one dicarboxylic aromatic acid and from mono- and di-substituted (1-phenyl-ethyl)-hydroquinones in admixture with hydroquinone, and/or hydroquinones substituted with halogen or alky, aryl or cycloalkyl groups.

Abstract: Thermotropic liquid crystalline aromatic polyesters of 3,3'-diphenyl-4,4'-dihydroxydyphenyl containing units derived from mono-substituted hydroquinones in amounts over 10% by moles with respect to the total of the aromatic diols.

Abstract: Liquid-crystalline, thermotropic, aromatic polyesters processable in the molten state, comprising units derived from hydroquinones substituted with aryl, aralkyl and aroyl groups, and from phenoxy-hydroquinone.

Abstract: Thermotropic liquid crystalline polyesters which can be processed in the molten state containing moieties derived from a dicarboxylic aromatic acid and 2,5-dihydroxybenzophenone eventually in a mixture with a substituted hydroquinones.

Abstract: Thermotropic liquid-crystalline aromatic polyesters of 4,4'-dihydroxy-diphenyl substituted with a halogen or with an alkyl, cycloalkyl, aryl, aralkyl, keto or ether radical.

Abstract: Thermotropic liquid crystalline aromatic polyesters of 4,4'-dihydroxydiphenyl substituted in 3,3' positions by a halogen or by an alkyl, cycloalkyl or aralkyl radical.

Abstract: Thermotropic semiflexible polyesters are taught which are obtained by polycondensation of 4,4'-dihydroxybicyclohexyl with at least one .alpha.,.omega.- alkandioic acid of general formula:HOOC-(CH.sub.2).sub.n -COOH (I)wherein n is an integer comprised between 4 and 12.

Abstract: Process for the hydrogenation of bis-phenols by reacting bis-phenols with hydrogen in the presence of a catalytic system consisting of palladium supported on activated carbon.

Abstract: A process for the manufacture of o-nitrobenzaldehyde by oxidation of o-nitrotoluene, characterized in that o-nitrotoluene is made to react with an aqueous solution containing Cerium.sup.iv perchlorate and from 5 to 9 moles/liter of perchloric acid; according to a preferred embodiment, the dispersion of o-nitrotoluene in an aqueous solution containing from 5 to 9 moles per liter of perchloric acid is first prepared and then an aqueous solution is gradually added, containing Cerium.sup.iv perchlorate and 5-9 moles/liter of perchloric acid.

Abstract: Polyphenylenethers are prepared by oxidative polymerization of phenols in the presence of oxygen and of organic bases (amines), by using copper-based catalysts having general formula:(B).sub.n (Cu).sub.a X.sub.b Y.sub.zwhereinB=optionally substituted naphthiridie group,X=halogen, or nitro group or perchlorate group,Y=bridge compound between the copper atoms, of the pyrazole or imidazole type,z=0 or 1, wherefore: when z=0,a and n, either like or unlike each other, are 1 or 2,b=an integer from 1 to 3, extremes included, while, when z=1:n=a=2b=3.

Abstract: This invention relates to the preparation of esters or salts of aromatic or etheroaromatic acids having formula Y--Ar--CO--OR (I), where:Ar represents an aromatic group constituted by one or more benzene rings, optionally condensed, or an etheroaromatic nucleus optionally condensed with one or more benzene rings;Y represents from zero to more substituents, equal or different, chosen among a halogen; an alkyl group having up to 6 carbon atoms; an alkoxy group having up to 5 carbon atoms; an ester group --COOR', where R' contains up to 5 carbon atoms; a hydroxyl group; a phenyloxy group, optionally substituted with groups inert under reaction conditions; a trifluoromethyl group; a nitrile group; an amidic group (--CONH.sub.2); an acetamidic group (--NH--CO--CH.sub.3); or an acyl group --CO--R", where R" represents a hydrocarbon group having up to 8 carbon atoms;R represents an alkyl group R.sub.1 having up to 5 carbon atoms or an alkali metal or alkaline earth metal M.

Abstract: Alpha-arylpropionic acids and alkaline salts thereof are prepared by catalytic reaction with carbon monoxide of the corresponding secondary halids in an anhydrous low alcohol solvent in the presence of a salt of cobalt hydrocarbonyl and in further presence of alkaline hydroxides under substantially ambient temperature and pressure conditions.The products obtained find useful applications in the field of pharmaceutics (analgesics, antipyretics, etc.) and as intermediates for chemical syntheses of fine chemicals, phytodrugs, etc.

Abstract: A process is herein described for preparing carboxylated organic compounds (acids, esters, alkaline salts) of formula ##STR1## wherein R is a hydrocarbyl group having up to 11 carbon atoms (an aliphatic, alicyclic, aryl- or heteroarylalkyl group), also substituted, in its turn, by groups inert under the reaction conditions (alkyl, aryl, etheric, thioetheric, halogen, nitrile, ester, amide, ketonic groups), and R' is a hydrogen atom or an alkyl C.sub.1 -C.sub.8 group, by reaction of carbon monoxide with the corresponding hydrocarbyl halides, having the halogen bound to a non-tertiary carbon atom, in the presence of catalysts which are salts of cobalt hydrocarbonyl, or precursors thereof, in a hydro-alcoholic or alcoholic solvent and in the presence of bases.The process is characterized in that the catalytic system composed by the salt of cobalt hydrocarbonyl is supported on an anion exchange resin.

Abstract: Phenyl pyruvic acid and substituted derivatives thereof are synthesized by catalytic carbonylation of a benzyl halide in the presence of a catalytic system based on carbonyl complexes of cobalt or precursors thereof.

Abstract: A process is disclosed for preparing alpha-thienylacetic acid, alkyl esters and salts thereof by carbonylation of 2-chloromethylthiophene, characterized in that 2-chloromethylthiophene and carbon monoxide are reacted under atmospheric pressure and at a temperature ranging from 0.degree. to 60.degree. C., in an aqueous-alcoholic solution in the presence of a catalyst selected from the class consisting of Co.sub.2 (CO).sub.8, MCo(CO).sub.4 where M is selected from the class consisting of Na and K, and a system comprising a cobalt salt (such as cobaltous chloride), a ferro-manganese alloy and at least one sulphur-containing promoter (such as the alkaline sulphides and thiosulphates), and in the presence of an inorganic base, and the separating the alpha-thienylacetic acid from the resulting salt and/or ester obtained.

Abstract: This invention relates to a process for preparing phenylacetic acid. In particular, the present invention relates to a catalytic process for the synthesis of the alkaline salts of phenylacetic acid by carbonylation of benzyl halides in a diphase system in the presence of cobalt carbonyl complexes. More particularly, the present invention relates to a process for preparing alkaline salts of phenylacetic acid by reacting a benzyl halide selected from chloride and bromide with carbon monoxide in the presence of a catalyst consisting in a salt of cobalt hydrocarbonyl, characterized in that the reaction is conducted in an aqueous/organic diphase system consisting of (a) an aqueous solution of an inorganic alkaline base, and (b) the benzyl halide in an organic solvent, in the presence of a catalyst system composed by a quaternary alkylammonium salt and by a cobalt hydrocarbonyl salt, at atmospheric pressure and at a temperature ranging from 20.degree. to 70.degree. C about.

Abstract: A process for preparing carboxylic acids by reaction of carbon monoxide with aromatic and aliphatic organic halides, optionally further substituted by groups inert under the reaction conditions, and catalyzed by phosphinic palladium complexes and in the presence of quaternary alkyl-ammonium salts, characterized in that said process is conducted in a double liquid phase consisting essentially of (a) the organic halide and the catalytic palladium complex or their solutions in at least one hydrocarbon solvent immiscible with H.sub.2 O, and (b) an aqueous inorganic alkaline solution containing the quaternary alkyl-ammonium salt, at a temperature between about 50.degree. and 150.degree. C. More particularly, the reaction is conducted in the presence of at least one catalyst selected from among:A. at least one palladium complex of the formula:Pd[P(R).sub.3 ].sub.mwherein m is a whole number from 2 to 4, and (R).sub.