Abstract: Branched polycarbonates are prepared by melt equilibration of aromatic cyclic polycarbonate oligomers with a polyhydric phenol having more than two hydroxy groups per molecule, preferably 1,1,1-tris-(4-hydroxyphenyl)ethane, in the presence of a carbonate equilibration catalyst, preferably tetrabutylammonium tetraphenylborate. In an additional embodimetn of the invention, a linear aromatic polycarbonate is added to the reaction mixture. Branched polycarbonates prepared according to this inventin have high melt strength and high shear sensitivity characteristics and are useful in extrusion and injection molding processing applications and particularly useful in blow molding applications for preparing relatively large articles and panels.

Abstract: The present invention relates to a mercapto compound, a process for preparing the mercapto compound, a process for preparing a polythiourethane base resin containing the mercapto compound, and a process for preparing plastic lenses containing the resin.

Abstract: The invention relates to new polythiophenes containing structural units of the formula ##STR1## in which A denotes an optionally substituted C.sub.1 -C.sub.4 -alkylene radical, their preparation by oxidative polymerization of the corresponding thiophenes and the use of the polythiophenes for imparting antistatic properties on substrates which only conduct electrical current poorly or not at all, in particular on plastic mouldings, and as electrode material for rechargeable batteries.

Abstract: Polycyclic polycarbonate (or thiol analog) oligomers are prepared from a mixture of at least one bishaloformate with at least one tetraphenol, or thio analogs thereof. Such mixture may also contain at least one dihydroxy or dimercapto compound. The oligomers are formed by the reaction of such mixtures with alkali metal hydroxides and various amines. The polycyclic oligomer mixtures may be converted to crosslinked polycarbonates or their thiol analogs.

Abstract: The invention relates to new polythiophenes containing structural units of the formula ##STR1## in which A denotes an optionally substituted C.sub.1 -C.sub.4 -alkylene radical,their preparation by oxidative polymerization of the corresponding thiophenes and the use of the polythiophenes for imparting antistatic properties on substrates which only conduct electrical current poorly or not at all, in particular on plastic mouldings, and as electrode material for rechargeable batteries.

Abstract: A process for preparing a copoly(arylene sulfide) corresponding to the structure[(--A--S--).sub.1-x (--A--S--S--).sub.x ].sub.nwherein x is in the range of 0.5 to 0.001 by reacting a mixture of a diiodoaromatic compound and elemental sulfur in the absence of a basic material and in the presence of a catalytic amount of an organic amine-containing compound.

Abstract: A process for preparing a copoly(arylene sulfide) corresponding to the structure[(--A--S--).sub.1-x (--A--S--S--).sub.x ].sub.nwherein x is in the range of 0.5 to 0.001 by reacting a mixture of a diiodoaromatic compound and elemental sulfur in the absence of a basic material and in the presence of a catalytic amount of iron.

Abstract: A process for preparing a copoly(arylene sulfide) corresponding to the structure[(--A--S--).sub.1-x (--A--S--S--).sub.x ].sub.nwherein x is in the range of 0.5 to 0.001 by reacting a mixture of a diiodoaromatic compound and elemental sulfur in the absence of a basic material.

Abstract: A phenol or bisphenol has been found effective as a chain transfer agent in the polymerization of cyclic carbonates to make hydroxyl-terminated polycarbonate oligomer of varying molecular weight.

Abstract: This invention relates to novel conductive thienylene- and furanylene-vinylene polymers and to a process for their preparation. The polymer can be formed into coherent films in which no voids are visible up to magnifications of up to 5000 times. These polymers have band gaps below 2 eV which makes them more suitable than conventional polyphenylene and poly(phenylene vinylene) polymers for use e.g. in batteries.

Abstract: Cyclic polycarbonate (or thiol analog) oligomer mixtures are prepared by the reaction of bishaloformates or their thio analogs, or mixtures thereof with dihydroxy or dimercapto compounds, with alkali metal hydroxides and various amines. The oligomer mixtures may be converted to polycarbonates or their thiol analogs by a method which is particularly adaptable to integration with polycarbonate processing operations. Polymerization may be conducted simultaneously with molding, extrusion and the like. The oligomer mixtures are adaptable to the preparation of filled prepregs.

Abstract: A polymer having an isothianaphthene structure represented by the formula (Ia) and/or Ib): ##STR1## wherein R.sup.1 and R.sup.2 each represents a hydrogen atom or a hydrocarbon residue having 1 to 5 carbon atoms such as methyl, methoxy and thiomethyl, with the proviso that R.sup.1 and R.sup.2 may link together to form, along with the benzene ring, a fused ring which is naphthalene; X is sulfur, selenium or tellurium; Y.sup.- represents an anion of an electrolyte; z represents a number from 0.01 to 1 showing a ratio of the anion per mol of a monomer; and n represents a number of from 5 to 500 showing a degree of polymerization.

Abstract: Cyclic polycarbonate oligomers are converted to linear polycarbonate resins by heating with a polycarbonate formation catalyst which generates aryl carbanions at temperatures up to about 300.degree. C. The preferred catalysts are tetraarylborates such as tetramethylammonium tetraphenylborate.

Abstract: A process for producing a novel cross-linked resin which comprises: reacting a bis(2-oxazoline) compound with a reactive compound which has at least one active hydrogen in the molecule, the reactive compound being at least one selected from the group consisting of a sulfonamide, an acid imide, an aromatic hydroxy-carboxylic acid and a bisphenol sulfone compound, in a molar ratio of the reactive compound to the bis(2-oxazoline) compound of not more than about 2, at an elevated temperature. About 5 to about 95 mole % of the reactive compound is replaceable by a dicarboxylic acid.The cross-linked resin may be usable for the production of machinery parts such as rolls and gears and embedded moldings of electrical machinery and apparatus parts as well as for electric insulating materials and dental uses. The cross-linked resin may further find applications in, for example, adhesives and various coating compositions.

Abstract: A linear poly(3-alkyl-2,5-thienylene) polymer having the formula: ##STR1## wherein R represents a lower alkyl group and n is 20 to 100. The polymer can be used to provide a semiconductor. A method for making the polymer comprises reacting 3-alkyl-2,5-dihalogenated thiophene with magnesium in an inert solvent in the substantial absence of water, in the presence of a nickel compound as a catalyst in an inert atmosphere.

Abstract: The polymer material is made from a first monomer and from a second monomer. The first monomer Ar includes at least one aromatic nucleus and the second monomer is a five links conjugated heterocyclic ring. The polymer material has the following general chemical formula: ##STR1## in which: X represents the group constituted by sulphur and selenium; R.sub.1 and R.sub.2 are chosen from the group constituted by hydrogen, and by the alkyl, alkoxyl, and hydroxyl groups; and n is the degree of polymerization. Such materials can be made conductive by adding a doping agent, and they can then be used for manufacturing electrodes, junctions, Schottky barriers, etc.

Abstract: Substances (I) capable of being converted into higher-molecular weight materials under the influence of a cationic catalyst, such as 1,2-epoxides, aminoplasts, vinyl monomers and prepolymers, or phenoplasts, are so converted by exposure to actinic radiation in the presence of an aryl- or aroyl- carbamoylsulfoxonium salt (II) of formula ##STR1## where p is zero or 1,q is 1 to 4,Ar denotes an aromatic group,R.sup.6 denotes --H or group --COR.sup.9 or --CONH(CO).sub.r R.sup.10,R.sup.7 denotes an alkyl, alkenyl, cycloalkyl, cycloalkylalkyl, aryl, or aralkyl group,R.sup.8 has the same meaning as R.sup.7 but may alternatively represent a dialkylamino group or, if R.sup.7 denotes alkyl, it may alternatively represent an arylamino group,R.sup.9 and R.sup.10 each denote a saturated or ethylenically unsaturated radical,r is zero or 1,t is 1, 2, or 3, andZ.sup.t- denotes a t-valent anion of a protic acid.

Abstract: A polymer having aromatic or heterocyclic rings as the only structural elements said aromatic or heterocyclic rings containing at least two nitro groups is disclosed as well as a method of preparing the same. The polymers are useful as binding agents for thermo stable propellants and can be easily formed into films. They remain thermally stable up to temperatures of at least 200.degree. C.

Abstract: Poly(organophosphazenes) containing repeating units of the structure: ##STR1## wherein X and X' represent organic substituents which may be the same or different and n is from 20 to 50,000, are prepared by a process which involves reacting a poly(dichlorophosphazene) having the formula --(NPCl.sub.2).sub.n --, in which n is from 20 to 50,000, with an active hydrogen-containing compound in the presence of a bicyclic amidine represented by the structure: ##STR2## in which m is an integer of from 1 to 10. A unique aspect of the process of the invention is that it can be utilized to prepare such poly(organophosphazenes) utilizing either soluble or gelled (insoluble) poly(dichlorophosphazenes) as starting materials.

Abstract: Polyphosphazene polymers are prepared which contain units represented by the formulas: ##STR1## wherein X is ##STR2## in which R is alkylene radical containing from 0 to 10 carbon atoms, R' is hydrogen or alkyl containing from 1 to 10 carbon atoms and n is an integer of from 0 to 10; wherein X' is X or is selected from the group consisting of substituted or unsubstituted alkoxy, aryloxy, amino and mercapto groups and wherein 20.ltoreq. (a+b+c).ltoreq.50,000 per polymer.The polymers of the invention can be utilized to form films and may also be utilized in applications such as moldings, coatings, foams and the like.

Abstract: Polyphosphazene copolymers are prepared which contain units represented by the formulas: ##STR1## wherein X is a sulfone radical selected from the group consisting of --CR.sub.1 R.sub.2 --SO.sub.2 --R and ##STR2## in which R is alkyl containing from 1 to 12 carbon atoms, cycloalkyl containing from 3 to 12 carbon atoms or aryl and R.sub.1 and R.sub.2 are individually selected from the group consisting of hydrogen, alkyl radicals containing from 1 to 11 carbon atoms, cycloalkyl radicals containing from 3 to 11 carbon atoms and aryl radicals; wherein X' is an organic radical selected from the group consisting of substituted or unsubstituted alkoxy, aryloxy, amino and mercapto groups and wherein 20.ltoreq.(a+b+c).ltoreq.50,000 per polymer.The copolymers of the invention can be utilized to form films and may also be utilized in applications for moldings, coatings and the like.

Abstract: Episulfides are reacted with mono, di or trithiols in the presence of tertiary aliphatic amines or tertiary aliphatic phosphines, to form corresponding thioether thiols by a highly selective anionic mechanism. Increasing episulfide-thiol ratios result in polythioether thiols of increasing molecular weights. Using two or more episulfides, block copolymers can be prepared. The reactive terminal thiol functionality and the segmented crystalline and amorphous block structure of the new polymers makes them particularly useful for castable rubber applications.