Abstract: Disclosed is a composition which comprises a polymer containing at least some monomer repeat units with water-solubility- or water-dispersability-imparting substituents and at least some monomer repeat units with photosensitivity-imparting substituents which enable crosslinking or chain extension of the polymer upon exposure to actinic radiation, said polymer being of the formula ##STR1## wherein x is an integer of 0 or 1, A is one of several specified groups, such as ##STR2## B is one of several specified groups, such as ##STR3## or mixtures thereof, and n is an integer representing the number of repeating monomer units. In one embodiment, a single functional group imparts both photosensitivity and water solubility or dispersability to the polymer. In another embodiment, a first functional group imparts photosensitivity to the polymer and a second functional group imparts water solubility or dispersability to the polymer.

Abstract: A digital video disc substrate comprising a polycarbonate is herein disclosed in which a main chain has a structure represented by the general formula (I) ##STR1## and at least 25 mol % of this terminal group is represented by the formula (III) or (IV) ##STR2## and a viscosity-average molecular weight is in the range of 10,000 to 17,000, preferably 12,500 to 14,500.

Abstract: Novel functionalized peroxides which may be used as crosslinking, grafting and curing agents, initiators for polymerization reactions and as monomers for condensation polymerizations to form peroxy-containing polymers, which in turn can be used to prepare block and graft copolymers, have the following Formula I: ##STR1## R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, X, Y.sup.1, Y.sup.2, Y.sup.3, Z.sup.1, Z.sup.2, x, y and z are as defined in the Summary of the Invention. The compounds of Formula I may be prepared by reacting hydroxy-containing tertiary hydroperoxides with diacid halides, phosgene, dichloroformates, diisocyanates, anhydrides and lactones to form the functionalized peroxides. These reaction products may be further reacted, if desired, with dialcohols, diamines, aminoalcohols, epoxides, epoxy alcohols, epoxy amines, diacid halides, dichloroformates and diisocyanates to form additional functionalized peroxides.

Abstract: Perfluoroalkylene oxide copolymer having acid fluoride moieties are prepared by reaction of hexafluoropropylene oxide and 1,2-epoxypentafluoropropane 3-fluorosulfate in the presence of a cesium alkoxide initiator. The copolymers may be cured at room temperature and are useful in sealant and coating formulations. Derivatives of the copolymers containing ester, amide, nitrile, and ether moieties are also disclosed.

Abstract: Novel functionalized peroxides which may be used as crosslinking, grafting and curing agents, initiators for polymerization reactions and as monomers for condensation polymerizations to form peroxy-containing polymers, which in turn can be used to prepare block and graft copolymers, have the following Formula I: ##STR1## R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, X, Y.sup.1, Y.sup.2, Y.sup.3, Z.sup.1, Z.sup.2, x, y and z are as defined in the Summary of the Invention. The compounds of Formula I may be prepared by reacting hydroxy-containing tertiary hydroperoxides with diacid halides, phosgene, dichloroformates, diisocyanates, anhydrides and lactones to form the functionalized peroxides. These reaction products may be further reacted, if desired, with dialcohols, diamines, aminoalcohols, epoxides, epoxy alcohols, epoxy amines, diacid halides, dichloroformates and diisocyanates to form additional functionalized peroxides.

Abstract: This invention relates to polymers having non-linear optical properties which polymers include fluorene moieties having at least one electron accepting group and at least one electon donating group substituted to different phenyl rings of the fluorene moiety.

Abstract: A process is disclosed whereby a polymeric resin (containing ester and/or carbonate bonds) is readily converted into a resin having a modified molecular structure. Accordingly, a cyclic carbonate (a monomer or oligomer) is transesterified with the polymer resin in the melt, preferably upon extrusion, optionally in the presence of a catalyst. Significantly, the cyclic carbonate which may include any of a variety of functional groups may, by the inventive process, be inserted into the structure of the polymer, effecting a modification to the structure and the properties of the resin. Among the disclosed beneficial modifications thus imparted to the resin are improved thermal stability, altered rheology and optical properties.

Abstract: Novel functionalized peroxides which may be used as crosslinking, grafting and curing agents, initiators for polymerization reactions and as monomers for condensation polymerizations to form peroxy-containing polymers, which in turn can be used to prepare block and graft copolymers, have the following Formula I: ##STR1## R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, X, Y.sup.1, Y.sup.2, Y.sup.3, Z.sup.1, Z.sup.2, x, y and z are as defined in the Summary of the Invention. The compounds of Formula I may be prepared by reacting hydroxy-containing tertiary hydroperoxides with diacid halides, phosgene, dichloroformates, diisocyanates, anhydrides and lactones to form the functionalized peroxides. These reaction products may be further reacted, if desired, with dialcohols, diamines, aminoalcohols, epoxides, epoxy alcohols, epoxy amines, diacid halides, dichloroformates and diisocyanates to form additional functionalized peroxides.

Abstract: Disclosed is a coating composition comprising:(1) a polycarbonate polyol having an average molecular weight of 400-10,000 and a hydroxyl value of 50-350, and(2) a melamine resin curing agent, wherein polyhydric alcohols constituting said polycarbonate polyol comprises at least 10 mol % of branched diols, at least 10 mol % of tri- or higher-hydric alcohols and the balance of the other polyhydric alcohols, and a ratio of component (1) / component (2) is within the range of 90/10-50/50 based on solid weight.

Abstract: A process for preparing a polyestercarbonate copolymer which is nearly devoid of diaryl-carbonates and that exhibits a glass transition temperature lower than bisphenol-A carbonate homopolymer, and that shows improved processability is herein described. The desired lower Tg and improved flow can be achieved by the polycondensation of a dihydric phenol and aliphatic dicarboxylic acid. The condensate is polymerized with a carbonate forming reagent.

Abstract: A curable resin composition, which is not thickened nor gels during storage, can be high solids, cures even at low temperatures and is excellent in electrostatic coating properties, and which contains as main components, a polymer having in one molecule epoxy group(s), and functional group(s) in each of which a carbonate ester group (--O--CO--O--) is directly bound to an aromatic ring; or a mixture of a compound having in one molecule at least two epoxy groups and a compound having in one molecule at least two functional groups in each of which a carbonate ester group (--O--CO--O--) is directly bound to an aromatic ring, and a curing reaction catalyst.

Abstract: Macrocyclic polyester oligomer compositions comprising alkylene isophthalate or terephthalate units or the like are prepared by the reaction of a diol with a diacid chloride in the presence of at least one amine characterized by substantially no steric hindrance around the basic nitrogen atom. The reaction is conducted under substantially anhydrous conditions and at a temperature from about -25.degree. to about +25.degree. C. The resulting macrocyclic oligomers may be converted to linear polyesters by contact with catalysts including basic reagents, stannous alkoxides, organotin compounds, titanate esters and metal acetylacetonates.

Abstract: Bischloroformate oligomer compositions are prepared by passing phosgene into a heterogeneous aqueous-organic mixture containing at least one dihydroxyaromatic compound, with simultaneous introduction of a base at a rate to maintain a specific pH range and to produce a specific volume ratio of aqueous to organic phase. By this method, it is possible to employ a minimum amount of phosgene. The reaction may be conducted batchwise or continuously. The bischloroformate composition may be employed for the preparation of cyclic polycarbonate oligomers or linear polycarbonate, and linear polycarbonate formation may be integrated with bischloroformate composition formation in a batch or continuous process.

Abstract: A gamma radiation-resistant polycarbonate-disulfide resin is disclosed. The incorporation of disulfide linkages in the structure of polycarbonate was found to enhance the resistance of the resin to the discoloration caused by exposure to gamma radiation. Accordingly, processes for the incorporation of disulfide linkages in the molecular backbone, as end-groups or as side chains are disclosed. The polycarbonate-disulfide resin may be used as a molding resin in the context of thermoplastic molding compositions as well as a stabilizing additive in polycarbonate resin.

Abstract: The present invention provides a second-order nonlinear optical polymer including a polymer backbone and side groups bonded to the polymer backbone, wherein the side groups include one or more of a first nonlinear optical group represented by the following formula (C-1) and one or more of a second nonlinear optical group represented by the following formula (C-2) or (C-2)': ##STR1## wherein .pi..sub.1 to .pi..sub.n, .pi.'.sub.1, .pi.'.sub.2, and .pi.".sub.1 each represent independently a .pi.-conjugated cyclic compound group; X.sub.1 to X.sub.n-1, X'.sub.1, Y.sub.1 to Y.sub.n-1, and Y'.sub.1 each represent independently CH, N, or N.fwdarw.O; A.sub.1, A.sub.2, and A.sub.3 each represent independently an electron attracting group; D.sub.1, D.sub.2, and D.sub.3 each represent independently an electron donating group; and n represents an integer of 3 or greater.

Abstract: Substituted triphenyl compounds endowed with chain extension activity for formulations such as polyurethanes are disclosed, and which have the general formula: ##STR1## wherein n is 0-1000; R.sub.1 .dbd.R.sub.2, and R.sub.1 and R.sub.2 are from the group --CH.sub.2 --CH.sub.2, --CH.sub.2 --C(CH.sub.3)H--; and --C(CH.sub.3)H--CH.sub.2 --.

Abstract: A cyclic polycarbonate oligomer having a low melting point useful in the preparation of high molecular weight resins. The cyclic polycarbonate oligomers have structural units with long alkyl chains which may contain ester substituents.

Abstract: A coating composition useful for shatter-proofing glass, capable of forming a film which allows an elongation of at least 400%. The coating composition includes (A) a polyurethane compound obtained by reaction of (a) a polycarbonate diol and/or (b) an aliphatic polyester diol, (c) an organic diisocyanate and (d) a chain extender possessing an active hydrogen-containing group in amounts to give an isocyanate group/active hydrogen-containing group equivalent ratio not exceeding 1.0, (B) an organic polyisocyanate compound and (C) a reactive silicone oil.

Abstract: This invention provides synthetic routes for novel single isomers of monocarbamate diols and their polymerization to provide novel polyesters, polyurethanes, polycarbonates, and the like having pendant carbamate groups on the polymer chain. Devices using some of these novel polymers which demonstrate nonlinear optical activity are also disclosed.

Abstract: Provided are a cyclodextrin polymer containing cyclodextrin in the backbone chain of a high-molecular weight compound selected from a polyurethane, a polyurea, an unsaturated polyester, a polyester, a polycarbonate, a polyamide and a polysulfone, as well as a cyclodextrin membrane prepared using said polymer.In accordance with the present invention, an increased amount of cyclodextrin unit can be immobilized and the function thereof is significantly improved; further, by using a specific high-molecular weight compound, the polymer obtained is rendered insoluble in water, etc. and yet decomposable with enzymes and it can accordingly be used as a degradable polymer. Further, there can be provided a cyclodextrin membrane which contains a large extent of cyclodextrin and which can be used alone as a membrane.

Abstract: Poly (Reissert compounds) can be formed by reaction of a coupled bis(isoquinoline), e.g., a 4,4' -coupled bis(isoquinoline), a diacid chloride, e.g. adipoyl chloride, and a source of cyanide, e.g., trimethylsilyl cyanide.

Abstract: Disclosed are fluorinated macromonomers containing one or more hydroxy groups, which are useful as monomers in other polymerization. Also disclosed are processes and an intermediate for making such macromonomers, and condensation and free radically made polymers which contain the macromonomers. The macromonomers are useful for modifying the properties of the polymers into which they are incorporated.

Abstract: In thermoplastic elastomers selected from the group consisting of the thermoplastic polyurethanes, of the polyetheresters and of the polyetheramides which are derived from polyetherpolycarbonatediols as diol components, the polyetherpolycarbonatediols used are reaction products of phosgene, dialkyl carbonates having C.sub.1 -C.sub.4 -alkyl groups or cyclic carbonates having C.sub.2 -C.sub.4 -alkylene bridges or mixtures thereof with mixtures ofa.sub.1) from 10 to 100 mol % of polyoxytetramethylenediol having a number average molecular weight M.sub.n of from 150 to 500 anda.sub.2) from 0 to 90 mol % of polyoxyalkylenediols which differ from a.sub.1) and have C.sub.2 -C.sub.8 -alkylene groups, aliphatic alkanediols of 2 to 14 carbon atoms, alicyclic alkanediols of 3 to 14 carbon atoms or alkylene oxides of 2 or 3 carbon atoms, or mixtures thereof.

Abstract: Ester polyphenols such as the tris(bisphenol A) ester of trimellitic acid are prepared by the reaction of the corresponding aromatic poly(acyl halide) with a dihydroxyaromatic compound such as bisphenol A. They may be employed in the preparation of branched polycarbonates via chloroformate oligomer compositions.

Abstract: Polyetherpolycarbonatediols are composed essentially ofA) from 3 to 63.7 mol % of units derived from a polyoxytetramethylenediol,B) from 63.7 to 3 mol % of units derived from a polyoxy-C.sub.2 -C.sub.8 -alkylenediol other than A), an aliphatic alkanediol of from 2 to 14 carbon atoms, an alicyclic alkanediol of from 3 to 14 carbon atoms or an alkylene oxide of 2 to 3 carbon atoms, or a mixture thereof, andC) from 33.3 to 50 mol % of units derived from phosgene, a dialkyl carbonate having C.sub.1 -C.sub.4 -alkyl groups or a cyclic carbonate having C.sub.2 -C.sub.4 -alkylene bridges, or a mixture thereof.

Abstract: A method for the preparation of a variety of engineering polymers and copolymers, in particular aromatic polymers and copolymers which comprises reacting a stannylated reactant containing a first monomeric or polymeric moiety with an electrophilic reactant, usually a di(acid chloride) containing a second monomeric or polymeric moiety. The intermediate and second compound react by way of a condensation reaction to eliminate the tin and polymerise together the first and second moieties. Some novel polymers and copolymers can be prepared using this method.

Abstract: Copolyester-diol polycarbonates fluid at room temperature, having a number average molecular weight comprised within the range of from 1,500 to 6,000 with a glass transition temperature (T.sub.g) lower than -45.degree. C., useful in the sector of polyurethanes and in the sector of sealants, are obtained by means of a reaction of transesterification by starting from:(a) and organic carbonate,(b) an aliphatic diol,(c) an oligopolyester-diol.This latter is the product of reaction of an aliphatic bicarboxy acid with a mixture of two or more diols, comprising neopentyl glycol.

Abstract: This invention provides synthetic routes for novel single isomers of monocarbamate diols and their polymerization to provide novel polyesters, polyurethanes, polycarbonates, and the like having pendant carbamate groups on the polymer chain. Devices using some of these novel polymers which demonstrate nonlinear optical activity are also disclosed.

Abstract: A new class of transition metal bis(dithiolene) complex polymers having improved physical characteristics. These polymers are generally prepared by first preparing a bifunctionalized transition metal bis(dithiolene) complex, then reacting the bifunctionalized complex with one or more other bifunctional compounds. A wide variety of flexible linkage can be incorporated into the polymer chain via the bifunctional reactant to vary the physical properties of the resulting polymer. The polymers can be used as near infrared filters, both as supported and freestanding films.

Abstract: This invention relates to aliphatic polycarbonates including sequential copolymers based on cyclic aliphatic carbonates and esters and block copolymers of blocks of polymerised cyclic aliphatic carbonates and blocks of polymerised vinyl compounds stabilized against thermal degradation containing 0.01 to 3.0% by weight, based on polymer, of a compound of trivalent phosphorus.

Abstract: Aromatic polycarbonates are prepared by initially phosgenating a mixture of bisphenol and aqueous alkali metal hydroxide under interfacial reaction conditions to form an oligomeric bisphenol monochloroformate followed by the further introduction of phosgene and base and thereafter the elimination of reacted phosgene and the incorporation of endcapping phenol and tertiary organic amine and additional alkali metal hydroxide into the mixture. Reduced phosgene usage, the substantial elimination of emulsion formation, increased pH measurement accuracy and avoidance of production of diarylcarbonates are substantially provided.

Abstract: Macrocyclic polyester oligomer compositions comprising alkylene isophthalate or terephthalate units or the like are prepared by the reaction of a diol with a diacid chloride in the presence of at least one amine characterized by substantially no steric hindrance around the basic nitrogen atom. The reaction is conducted under substantially anhydrous conditions and at a temperature form about -25.degree. to about +25.degree. C. The resulting macrocyclic oligomers may be converted to linear polyesters by contact with catalysts including alkali metal salicylates, stannous alkoxides and organotin compounds.

Abstract: A polymeric peroxide comprising a dilvalent recurring unit having the formula: ##STR1## wherein the recurring unit of Formula I has a 10 hour half-life temperature of at least 80.degree. C. and optionally a divalent recurring unit having the formula: ##STR2## wherein R.sup.1, R.sup.2, R.sup.3, R.sup.5, X, X.sup.1, Y, Z, y and z are as defined in the Detailed Description of the Preferred Embodiments and the polymeric peroxide has a molecular weight of 1,000 to 200,000. The polymeric peroxides are derived from hydroxy-hydroperoxides of dihydroxy dialkyl peroxides. These polymeric peroxides can be used for preparing block copolymers and compatibilizing polymer blends and alloys.

Abstract: Bischloroformate oligomer compositions are prepared by passing phosgene into a heterogeneous aqueous-organic mixture containing at least one dihydroxyaromatic compound, with simultaneous introduction of a base at a rate to maintain a specific pH range and to produce a specific volume ratio of aqueous to organic phase. By this method, it is possible to employ a minimum amount of phosgene. The reaction may be conducted batchwise or continuously. The bischloroformate composition may be employed for the preparation of cyclic polycarbonate oligomers or linear polycarbonate, and linear polycarbonate formation may be integrated with bischloroformate composition formation in a batch or continuous process.

Abstract: Aromatic bischloroformates are prepared by the reaction of a dihydroxyaromatic compound such as bisphenol A with phosgene in the presence of water, base and an organic liquid such as methylene chloride. Initially, a mixture of the bisphenol, organic liquid and about 5-15% of the total base is prepared, and phosgene is passed into said mixture. The remainder of the base is added initially at a constant rate, and then only when the measured pH of the aqueous mixture is below a targeted value in the range of about 8-11 and in about 5-10% excess with respect to the phosgene then being introduced. This method minimizes hydrolysis of phosgene and formation of such by-products as monochloroformates and hydroxy-terminated polycarbonate oligomers.

Abstract: Oligomeric carbonate dihydroxyaromatic-based chainstoppers are disclosed. One example of this type of chainstopper is a bisphenol A bischloroformate oligomer monocapped with phenol. These chainstoppers may be prepared by phosgenating a dihydroxyaromatic compound to terminate one or both of the terminal oxygen atoms with chlorocarbonyl groups, followed by reaction of the chlorocarbonyl-terminated material with a phenolic-type compound in the presence of an amine catalyst. The chainstoppers of the present invention are very useful in accurately controlling the molecular weight of polycarbonates formed by various processes, while also preventing the formation of undesirable by-products, such as diarylcarbonates.

Abstract: Liquid crystalline bis-chlorocarbonic acid esters are 4-hydroxybenzoic acid-(4'-hydroxyphenyl) esters corresponding to the following formula ##STR1## wherein R.sub.1, R.sub.2, R.sub.3 and R.sub.4 denote, independently of one another, hydrogen, a halogen atom or a C.sub.1 to C.sub.6 alkyl group. Preparation of (I) and liquid crystalline N-alkyl polyurethanes and polycarbonates prepared form (I) are other invention embodiments.

Abstract: Bischloroformates of bisphenol compositions comprising hydroquinone or a hydroquinone-bisphenol A mixture are prepared by passing phosgene into a vigorously agitated mixture of water, an alkaline earth metal hydroxide, the bisphenols and a substantially inert, water-immiscible organic liquid such as methylene chloride. The molar ratio of water to alkaline earth metal hydroxide is in the range of about 3-8:1. The bisphenols and at least a portion of the organic liquid are preferably initially present in the reaction mixture, and the alkaline earth metal hydroxide is preferably added during phosgenation.

Abstract: Aromatic polycarbonates having a predetermined relatively low weight average molecular weight, as well as a low molecular weight distribution, are prepared by partially capping an aromatic bischloroformate composition, preferably a bisphenol A bischloroformate composition, with a monohydroxyaromatic compound and subsequently converting the partially capped composition to a polycarbonate, using a base which provides a buffered pH in the range of about 12-13. The preferred base is calcium hydroxide, which is soluble in water in precisely the amount required to provide the desired pH.

Abstract: A superabsorbent, thermoplastic polymeric composition comprising:(A) from about 86 to about 98 percent by weight, based on the total weight of the composition, of a poly(oxyethylene) diol soft segment having a weight average molecular weight in the range of from about 5,000 to about 50,000; and(B) from about 2 to about 14 percent by weight, based on the total weight of the composition, of a hard segment which has a melting point above ambient temperature and below the temperature at which decomposition of either the composition or the soft segment takes place, is essentially insoluble in water, and phase separates from the soft segment, said hard segment being selected from the group consisting of polyurethanes, polyamides, polyesters, polyureas, and combinations thereof;wherein the soft and hard segments are covalently bound together by means of urethane, amide, ester, or secondary urea linkages or combinations thereof.

Abstract: Cyclic copolycarbonate oligomer mixtures are prepared from mixtures of hydroquinone bischloroformate and bischloroformates of bisphenols, typically bisphenol A or a spirobiindane bisphenol, by condensation in the presence of an amine, an aqueous base and a non-polar organic liquid. They may be converted to solvent-resistant linear polycarbonates, many of which are crystalline.

Abstract: Cyclic polyphenylene ether-polycarbonate oligomer compositions are prepared from bishaloformates and bisphenols, at least one of which includes a spirobiindane moiety and the other of which is derived from a bisphenol-terminated polyphenylene ether oligomer. The cyclic compositions may be converted to linear copolycarbonates by treatment with a polycarbonate formation catalyst.

Abstract: High molecular weight polycarbonates are prepared by reacting a sterically hindered, substituted aromatic bischloroformate with an alkali metal hydroxide in the presence of a substituted pyridine.

Abstract: Novel polycarbonate latex compositions comprising 0.1 to 30 mole percent of recurring units containing a carboxyl or a tertiary amine acid addition salt component are disclosed.The latex compositions are made by:(a) preparing a polycarbonate comprising from about 0.1 to 30 mole percent of recurring units having a carboxyl or a tertiary amine acid additon component;(b) dissolving the polycarbonate in a water miscible solvent having a boiling point below about 100.degree. C.;(c) blending the solution of (b) with water; and(d) removing the water-miscible solvent.

Abstract: An organic condensation polymer made by reacting in solution of first compound having at least two anionic carbon sites bonded to each other either directly or through a chain of 1 to 30 carbon atoms, including a bisacetylide or a first compound having an anionic carbon site and a latent anionic carbon site bonded to each other either directly or through a chain of 1 to 30 carbon atoms, such as organometallic cyclopentadienides, with a second compound containing at least two electrophillic carbon sites bonded to each other either directly or through a chain of 1 to 30 carbon atoms, including diesters, dihalides, diamides or dianhydrides of polycarboxylic acids, and diisocyanates.

Abstract: A method for the preparation of a variety of engineering polymers and copolymers, in particular aromatic polymers and copolymers which comprises reacting a stannylated reactant containing a first monomeric or polymeric moiety with an electrophilic reactant, usually a di(acid chloride) containing a second monomeric or polymeric moiety. The intermediate and second compound react by way of a condensation reaction to eliminate the tin and polymerize together the first and second moieties. Some novel polymers and copolymers can be prepared using this method.

Abstract: Process for the preparation of polycarbonates by reacting at least one epoxy compound with carbon dioxide at 40.degree. to 200.degree. C. and 2 to 40 bar in the presence of a catalytic amount of a double metal cyanide complex and(a) one or more salts composed of at least bivalent metal ions and metal-free anions having a solubility in water of at least 1 g/100 ml at 25.degree. C., and/or(b) one or more no-metal containing acids of which a 0.1N solution in water at 25.degree. C. has a pH not exceeding 3.

Abstract: Process for the preparation of polycarbonates by reacting at least one epoxy compound with carbon dioxide at 40.degree. to 200.degree. C. and 2 to 40 bar in the presence of a catalytic amount of a double metal cyanide complex and (a) one or more salts composed of at least bivalent metal ions and metal-free anions having a solubility in water of at least 1 g/100 ml at 25.degree. C., and/or (b) one or more no-metal containing acids of which a 0.1 N solution in water at 25.degree. C. has a pH not exceeding 3.

Abstract: Polyether polycarbonate diols based on 1,6-hexanediol and having a molecular weight of from 500 to 12,000 are made by etherifying 50-100 mole % 1,6-hexane-diol in the presence of 0-50 mole % of specified diols and reacting the resultant polyether with a compound selected from diarylcarbonates, dialkyl carbonates, dioxolanones, hexanediol bischlorocarbonic acid esters, phosgene and urea. These diols are particularly useful in the production of polyurethanes having improved physical properties.

Abstract: A process, and product produced therefrom, for preparing a high molecular weight poly(arylene sulfide ketone) from the reaction product of an alkali metal bisulfide with an alkali metal hydroxide, employing molar excess of alkali metal bisulfide with respect to the alkali metal hydroxide. A process, and product produced therefrom, for preparing a high molecular weight poly(arylene sulfide ketone) employing an alkali metal sulfide and an alkali metal hydrosulfide, wherein the alkali metal .[.sulfide.]. .Iadd.hydrosulfide .Iaddend.is added in a molar excess with respect to the alkali metal .[.hydrosulfide.]. .Iadd.sulfide.Iaddend..