Abstract: Modified cyclopentadiene resins comprising essentiallya) 20 to 80% by weight of cyclopentadiene compounds,b) 1 to 40% by weight of natural resin acids andc) 31 to 70% by weight of phenol resins.These compounds are suitable as binder resins for printing inks. They are distinguished by excellent compatibility with aromatics-free mineral oils and with vegetable oils.

Abstract: A continuous process for the preparation of perfluorinated carbonyl fluorides from hexafluoropropene oxide (HFPO), in which HFPO is continuously oligomerized in a catalyst solution in devices which allow separation of the heavy product phase from the catalyst phase during the reaction, is described. Different oligomer distributions can be achieved by choice of the catalyst and different operating temperatures. The reaction itself takes place always in the substantial absence of the product which is formed, and achieves a considerable saving in time.

Abstract: A process for the preparation of the dimer of hexafluoropropene oxide (HFPO), in which the HFPO is dimerized in an aprotic polar solvent in the presence of a catalyst mixture, is described. The catalyst mixture is composed of a metal salt of the elements of the 1st transition metal series of the periodic table and of a tertiary diamine. By bringing in a molar ratio of metal salt to tertiary diamine in the range from 2:1 to 1:2, in particular 1:1, the selectivity for the dimeric compound is greatest, with high yields of the dimer being obtained.

Abstract: A curing agent (A) for resins (B) which can be cured by means of isocyanates, which has an amine number of 20 to 150 mg of KOH/g and an OH number of not more than 20 mg of KOH/g and which contains per molecule at least two masked isocyanate groups which are reactive under the conditions of curing, obtained by reacting(a) an amine which contains at least one .beta.-hydroxylalkyl group per molecule and has an OH number of 100 to 1,200 mg of KOH/g and an amine number of 100 to 1,200 mg of KOH/g and which, if appropriate, also contains NHCO groups, if appropriate as a mixture with another OH-functional and/or NH-functional compound, with(b) a partly masked isocyanate, if appropriate as a mixture with an at least difunctional, OH-reactive and/or NH-reactive compound.These curing agents are readily dispersible in aqueous systems, if appropriate after neutralization, and frequently increase stability in aqueous paint formulations.

Abstract: Curing component (A) based on polyisocyanates for binders (B) which contain groups containing active hydrogen, wherein the curing component (A) is a product of the reaction of (a1) polyisocyanates with (a2) .alpha.-hydroxyalkylpyridines.Mixtures of (A) and (B), and also, if appropriate, diluents (C) and additives (D), are stable on storage and give, even at temperatures of 120.degree.-140.degree. C., curing products which are sufficiently solvent-stable. They are suitable, in particular, for surface-coating preparations.

Abstract: The invention relates to aminourethanes essentially composed of structural units derived from (.alpha.) polyamines of the general formula (I) ##STR1## and of structural units derived from (.beta.) oligomeric or polymeric compounds which contain at least one terminal 2-oxo-1,3-dioxolane group.The invention further relates to a process for preparing these aminourethanes and to their use in particular in paint formulations.The aminourethanes according to the invention are suitable in particular for use as curable water-dispersible binders in particular for cationic electrocoating.

Abstract: 2-(Meth)acrylamido-2-methylpropanephosphonic acid is prepared by reaction of 2-methylprop-1-ene-1-phosphonic acid or 2-methylpro-2-ene-1-phosphonic acid with (meth)acrylonitrile in the presence of an equimolar amount of a strong acid. The compounds are suitable as such or in the form of their salts as comonomer for the manufacture of copolymers, which are used inter alia as dyeing auxiliaries and as scale inhibitors.

Abstract: Cyanohydrine derivatives of the formula ##STR1## wherein R.sub.1 and R.sub.2 are alkyl, haloalkyl, cycloalkyl, aralkyl or aryl, R.sub.3 and R.sub.4 are hydrogen, alkyl, phenyl or benzyl, R.sub.5 is hydrogen, acyl, trialkylsilyl or alkoxycarbonyl, X is oxygen or sulfur and n is zero or 1, are intermediates for the manufacture of flame retardants, bactericides, fungicides and herbicides.

Abstract: Cyanohydrin acylates of aldehydes are manufactured by reacting aldehydes with aqueous solutions of cyanides and organic acid chlorides or anhydrides in the molar ratio of aldehyde:cyanide:acid chloride or anhydride of 1:1:1 with deviations of at most only about 10%, optionally in the presence of an inert organic solvent immiscible with water in a one-stage process. The process products are intermediates mainly in the fields of pharmaceuticals and plant protection.

Abstract: Herbicidal agents, containing as active ingredient a compound of the formula ##STR1## or their salts with acids, are useful for combatting a great variety of mono- and dicotyledonous weeds. In the formula R.sub.1 is methyl or halomethyl, R.sub.2 is OH, SH, OM or SM (M=equivalent of a base), R.sub.3 is the same as R.sub.2 or an ester, amide or hydrazide group, R.sub.4 and R.sub.5 are preferably hydrogen and X is oxygen or sulfur.

Abstract: Compounds of the formula ##STR1## WHEREIN Z is alkyl with 2 to 6 carbom atoms, x is oxygen, NH or sulfur, n and m are integers from 2 to 6, r is zero or 1, R.sup.4, R.sup.5 R.sup.6 and R.sup.7 are hydrogen or methyl and R.sup.3 is methyl, ethyl or phenyl. They are obtained by reacting 1 mole of a compound of formulaZ--(X--H).sub.nwith n.multidot.m moles of an alkylencoxide or alkylenecarbonate of the formulas ##STR2## and n(m+r) moles of a phospholane of formula ##STR3## These compounds are used as flameproofing agents especially for pile carpets.

Abstract: Preparation of 2,5-dioxo-1,2-oxa-phospholanes having general formula (I) ##STR1## wherein R.sup.1 represents an alkyl group being optionally substituted and having up to 18 carbon atoms, a cycloalkyl group having up to 8 carbon atoms, an alkenyl group having up to 8 carbon atoms, an aryl group having up to 14 carbon atoms being possibly substituted by lower alkyl groups, by alkoxy groups, by halogen or by lower alkyl radicals, by alkylated or dialkylated amino groups, or which represents an aralkyl group having up to 15 carbon atoms and being possibly substituted in the same way as the aryl group,Wherein R.sup.2 stands for a lower alkyl group or hydrogen and R.sup.3 stands for a lower alkyl radical, a phenyl radical being possibly substituted by halogen or lower alkyl groups, for a benzyl radical or for hydrogen.

Abstract: 2,5-Dioxo-1,2-oxa-phospholanes of the formula (I) ##STR1## wherein R.sup.1 is an organic radical and R.sup.2 and R.sup.3 each also represents an organic radical or hydrogen, are prepared by reacting 2-haloformylethyl-phosphinic acid halides of the formula (II) ##STR2## wherein R.sup.1, R.sup.2 and R.sup.3 are defined as in formula (I) and X means Cl or Br, preferably Cl, with an approximatey equimolar quantity of acrylic acid. The compounds (II) may also be produced in the reaction batch and in situ by reacting about equimolar quantities of a dihalophosphine of the formula (III) ##STR3## with an .alpha.,.beta.-unsaturated acid (IV)R.sup.4 -- OH (IV)In the formulae (III) and (IV) R.sup.1, R.sup.2, R.sup.3 and X are defined as indicated above.In the reaction there is formed, in addition to the compounds (I), practically exclusively .beta.-halopropionic acid and no free hydrogen halide.

Abstract: Compounds of the formula ##STR1## WHEREIN Z is alkyl with 2 to 6 carbon atoms, x is oxygen, NH or sulfur, n and m are integers from 2 to 6, r is zero or 1, R.sup.4, R.sup.5 R.sup.6 and R.sup.7 are hydrogen or methyl and R.sup.3 is methyl, ethyl or phenyl. They are obtained by reacting 1 mole of a compound of formulaZ--(X--H).sub.nwith n.m moles of an alkyleneoxide or alkylenecarbonate of the formulas ##STR2## and n(m+r) moles of a phospholane of formula ##STR3## These compounds are used as flameproofing agents especially for pile carpets.

Abstract: Process for preparing cyclic phosphinic acid esters of the formula (I) ##STR1## wherein R.sub.1 is an alkyl radical having up to 18 carbon atoms or a phenyl radical being optionally substituted by alkyl, halogen or alkylated amino groups, R.sub.2 stands for a hydrogen atom or has the same meaning as R.sub.1 and n is 1 or 2, which comprises reacting phosphinic acid monoesters of the formula (II) ##STR2## wherein R.sub.3 is an alkyl radical having up to 8 carbon atoms optionally substituted by chlorine atoms and R.sub.1 has the meaning given above, with an alkenol of the formula (III) ##STR3## wherein R.sub.2 and n have the aforesaid meaning, in the presence of catalytic quantities of free radical forming agents, splitting off the alcohol of formula (IV)r.sub.3 oh (iv)simultaneously or subsequently and separating the reaction products, preferably by distillation.

Abstract: Preparation of 2,5-dioxo-1,2-oxa-phospholanes of the formula (I) ##STR1## wherein R.sup.1 represents an optionally substituted alkyl having up to 18 carbon atoms, a cycloalkyl radical having up to 8 carbon atoms, an alkylene radical having up to 8 carbon atoms, an aryl radical having up to 14 carbon atoms which may be substituted by lower alkyl groups, lower alkoxy groups, halogen or by amino groups alkylated or dialkylated by lower alkyl groups, or an aralkyl radical having up to 15 carbon atoms which may be substituted in an analogous manner as the aryl radical, R.sup.2 represents a lower alkyl radical or hydrogen and R.sup.3 represents an alkyl radical having up to 6 carbon atoms, a phenyl radical which may be substituted by halogen or by lower alkyl groups, a benzyl radical or hydrogen, by reacting 2-halogenoformylethylphosphonic acid halides of the formula (II) ##STR2## wherein R.sup.1, R.sup.2 and R.sup.

Abstract: 2-Halo-ethane-phosphonic acid dihalides and vinyl-phosphonic acid dihalides are prepared by reacting hydroxyethane-phosphonic acid, its salts or functional derivatives, or the mono-thio-analogs thereof with acid halides of the formula (CO).sub.1 or 2 X.sub.2 wherein X represents halogen using as catalyst a compound containing at least one three- to penta-valent nitrogen or phosphorus atom bound by at least 3 valences to organic radical having up to 20 carbon atoms, two of the valences possibly forming a double bond; a one- to three-basic organic or inorganic fully amidated acid of three or penta-valent phosphorus the nitrogen atoms of which are alkylated by aliphatic radicals having up to 20 carbon atoms and the organic radical of which contains up to 20 carbon atoms, or a mixture of the aforesaid compounds. If desired the reaction is carried out in an inert solvent, preferably the reaction product and in the presence of a polymerization inhibitor.

Abstract: Process for preparing phosphonic acid dihalides of the formula ##EQU1## wherein R is alkyl of 1 to 18 carbon atoms, cycloalkyl of 4 to 8 carbon atoms, alkenyl of 2 to 18 carbon atoms, phenyl, phenalkyl or alkyl-phenyl of 7 to 8 carbon atoms, phenyl, phenalkyl or alkyl-phenyl of 7 to 8 carbon atoms, all radicals R optionally being substituted by chlorine, bromine, cyano or lower acyloxy, and wherein X is halogen such as 2-chloroethane phosphonic acid dichloride, by reacting phosphonic or thio-phosphonic acids of the formula ##EQU2## wherein Y is oxygen or sulfur, their salts or functional derivatives, with acid halides of the formula(CO).sub.n X.sub.2 (III)wherein X is chlorine or bromine and n is 1 or 2, in the presence of 0.2 - 5% or in the presence of 0.01 to 0.2% by weight of1.

Abstract: 2-Hydroxyethane-phosphonic acid diesters, 2-hydroxyethylphoshinic acid esters and the corresponding thiophoshonic acid-O,O-diesters or thiophosphinic acid-O-esters of the formula ##EQU1## wherein R.sub.1 is alkyl having from 1 to 18 carbon atoms, R.sub.2 has the meaning of R.sub.1 or represents cycloalkyl having up to 10 carbon atoms, alkenyl having up to 18 carbon atoms, aryl having up to 14 carbon atoms or aralkyl having up to 15 carbon atoms,R.sub.3 means hydrogen, alkyl having up to 18 carbon atoms, alkenyl having up to 18 carbon atoms, cycloalkyl having up to 10 carbon atoms, aryl having up to 14 carbon atoms or aralkyl having up to 15 carbon atoms, the substituents R.sub.1 -R.sub.

Abstract: Flame-repellant linear polyesters are obtained by incorporating by condensation phosphorus-compounds having the formula ##STR1## wherein R and R.sub.1 are organic radicals which may also contain hereto atoms into the linear polyesters, preferably those from terephthalic acid and ethylene glycol. These polyesters are materials of which flame-repellent filaments, fibers, sheets, press-moulded and injection-moulded articles may be made. Products of the invention can be used whereever especially acute risks of ignition and fire exist.