Abstract: Copolymers are produced when a 4-vinyl-1,3 dioxolane monomer is copolymerized with an imidized maleic anhydride (for example, maleimide) monomer in the presence of a free radical initiator. Alternatively, a maleamic acid or maleimide functionally may be introduced into a copolymer containing a 4-vinyl-1,3 dioxolane and maleic anhydride by introducing a primary amine into the reaction mixture. Also, the dioxolane reactant may be introduced into the polymer by reacting 3,4-epoxy-1-butene in a ketone reaction solvent. The structure and composition of the product copolymer are controlled by both the sequence and conditions of the reaction. Products of the present invention can be cast as clear films and can also be used as reactive polymers.

Abstract: Copolymers are produced when a 3,4-epoxy-1-butene monomer is copolymerized with a maleimide monomer in the presence of a free radical initiator. The copolymerization involves both 1,2-propagation and 1,4-propagation of 3,4-epoxy-1-butene. Products of this invention can be cast as clear films and can also be used as reactive polymers.

Abstract: There is disclosed a composite of 1) a polymer containing repeating units derived from a vinyl carboxylic ester having at least one organo terminated poly(alkylene oxide) side chain with the proviso that the poly(alkylene oxide) is present in an amount greater than 35 mole percent of the total of all backbone monomer units and alkylene oxide units in the polymer and 2) a metal oxide wherein the metal oxide comprises between about 1 and about 60 percent by weight of the composite. The composites can be made by a process comprising the steps of:combining the described polymer and a metal oxide precursor in a solvent solution;casting or coating the resulting solution onto a substrate;curing the resulting sample to form acomposite of the polymer and the metal oxide. Optionally, the composite can be removed from the substrate to form a transparent free standing film. These composites have a variety of desirable properties.

Abstract: A method for preparing a polymer including the step of reacting carbon monoxide and a reactant pair having respective general formulas ##STR1## a reactant having the general formula ##STR2## in the presence of catalyst and free iodo or bromo ions. X is --Br or --I. n is an integer from 0 to 4. R.sup.1 is selected from the group consisting of alkyl, arylalkyl, aryl, heteroaryl, and cycloalkyl. R.sup.2 is selected from the group consisting of ##STR3## wherein each R.sup.5 is independently selected from the group consisting of alkyl and aryl, m is an integer from 1-12, and j is an integer between 0 and 300.

Abstract: A method for preparing a polymer including the step of reacting carbon monoxide and a reactant pair having respective general formulas ##STR1## and or a reactant having the general formula ##STR2## in the presence of catalyst and free iodo or bromo ions. X is a nonortho halide selected from --Br and --I. n is an integer from 0 to 4. R.sup.1 is selected from the group consisting of alkyl, arylalkyl, aryl, heteroaryl, and cycloalkyl. R.sup.2 is selected from the group consisting of ##STR3## and Each R.sup.5 is independently selected from the group consisting of alkyl and aryl, m is an integer from 1-12, and j is an integer between 0 and 300. R.sup.3 is selected from the group consisting of substituted aryl, unsubstituted aryl, substituted heteroaryl, and unsubstituted heteroaryl.

Abstract: A process for the preparation of aromatic imide sulfide polymers and polymers produced. In the process, elemental sulfur is reacted with a compound having the general formula ##STR1## wherein Z.sup.1 is a direct link and Z.sup.2 is H, or Z.sup.1 has the general structure ##STR2## or Z.sup.1 and Z.sup.2 together complete a moiety having the general structure ##STR3## n= 0-4 . R.sup.1 is substituted or unsubstituted: aryl or heteroaryl. ##STR4## which R.sup.3 is an independently selected aryl group, m is an integer from 1 to 12, and j is an integer from 0 to 300.

Abstract: A multiply-branched aliphatic-aromatic polyester and a method for producing that polymer. The method comprises condensing a branching reactant represented by the general formula ##STR1## Each j is 1 or 2, each Ar is independently selected from the group consisting of aromatic and heteroaromatic moieties having a total of ring carbons and heteroatoms of from 5 to about 20, each R.sup.1 is a linking group independently selected from alkyl having from 1 to about 6 carbons, fluoroalkyl having from 1 to about 6 carbons, --O--, --S--, --C.tbd.C--, and ##STR2## Z.sup.1 is selected from the group consisting of hydroxyl and --OSi(CH.sub.3).sub.3, and each Z.sup.2 is independently selected from groups having the structural formula ##STR3## wherein each R.sup.2 is independently selected from the group consisting of hydroxy, chloro, bromo, monovalent alkoxide having from 1 to about 6 carbons, and --O--(CH.sub.2).sub.g --OH, wherein g is an integer from 1 to 3, or Z.sup.

Abstract: A multiply-branched aliphatic-aromatic polyester and a method for producing that polymer. The method comprises condensing Z.sup.1 and Z.sup.2 groups of a branching reactant having the general formula Z.sup.1 --Ar--(Z.sup.2)j. In this formula, j is 2 or 3 and Ar is an aryl or heteroaryl group having from 1 to 3, solitary or linked or fused, substituted or unsubstituted, five or six membered rings. One of Z.sup.1 and Z.sup.2 is a group having the ##STR1## general formula in which R.sup.1 is selected from the group consisting of hydroxy, chloro, bromo, monovalent alkoxide having from 1 to about 6 carbons, and --O--(CH.sub.2).sub.d --OH, wherein d is an integer from 1 to 3; and the other is a group having the general formula ##STR2## in which R.sup.2 is a divalent alkyl group having from 1 to about 6 carbon atoms, and g is an integer from 0 to about 100.

Abstract: A method for preparing polyimides comprising reacting carbon monoxide, a primary diamine and a reactant selected from the group consisting of bis(o-iodoaromatic ester)s and bis(o-bromoaromatic ester)s, in the presence of solvent and catalyst, said catalyst being a compound of a metal seIected from the group consisting of platinum, palladium and nickel.

Abstract: A multiply-branched cycloalkyl polyester and a method for producing that polymer. The method comprises condensing Z.sup.1 and Z.sup.2 groups of a branching reactant having the general formula (Z.sup.1)j-CYCLO-(Z.sup.2)k, in which j is 1 or 2, k is 1 or 2, j+k is 3, 4, or 5. CYCLO is selected from the group consisting of non-aromatic ring systems having from 1 to 8, solitary or fused or linked alkyl or heteroalkyl rings. One of Z.sup.1 and Z.sup.2 is a group having the general formula ##STR1## and the other is --OH, --OSi(CH.sub.3).sub.3, or a group having the general formula ##STR2## R.sup.1 is selected from the group consisting of hydroxy, chloro, bromo, monovalent alkoxide having from 1 to about 6 carbons, and --O-- (CH.sub.2).sub.d --OH, wherein d is an integer from 1 to 3. R.sup.2 is a divalent alkyl group having from 1 to about 6 carbon atoms, and g is an integer from 0 to about 100. If CYCLO is a solitary ring then j+k is 3, 4, or 5. If Z.sup.1 is bonded to a linear aliphatic linking group then Z.sup.

Abstract: A process for the preparation of aromatic polyamides comprises reacting carbon monoxide and an aromatic iodoamine characterized by having at least one iodine atom covalently bonded to an aromatic ring and at least one amino group. The process is conducted in the presence of a solvent, a catalyst and a base at a pressure greater than about 1 kg/cm.sup.2.

Abstract: A method for preparing poly(imide-amide)s comprising reacting carbon monoxide, an aromatic or heteroaromatic diamine, and an aromatic or heteroaromatic di(trifluoromethane sulfonate), in the presence of solvent and a catalyst One of the aromatic reactants has a nucleus including a phthalimide ring system. The catalyst is a compound of a metal selected from the group consisting of platinum, palladium and nickel.

Abstract: An improved method for producing multiply-branched polyester comprising condensing a reactant having the general formula Z.sup.1 --Ar--(Z.sup.2).sub.j, wherein j is 2 or 3, Ar is an aryl or heteroaryl group having from 1 to 3, solitary or linked or fused, five or six membered rings, and one of Z.sup.1 and Z.sup.2 is a carboxyl group and the other is a group having the general formula ##STR1## wherein R is an alkyl group having from 1 to 3 carbon atoms, X is selected from the group consisting of fluoro and chloro and g is an integer from 0 to about 7.

Abstract: There is provided a method for the production of an arylamide bisnadimide. The arylamide bisnadimide is useful as a prepolymer. The method includes the step of: condensing a nadimide compound having the nitrogen of said nadimide substituted with a halogen substituted aromatic group, with a dinucleophile in the presence of carbon monoxide, a base and a palladium catalyst.

Abstract: A process for the preparation of aromatic polyamides comprises reacting carbon monoxide, a diamine and an aromatic polyiodide having at least two iodine atoms covalently bonded to an aromatic ring in non-ortho positions. The process is conducted in the presence of a solvent, a catalyst and a base at a pressure greater than about 15 psia (1.05 kg/cm.sup.2).

Abstract: Copolymers are made by reacting maleic anhydride or a related compound with a 4-vinyl-1,3-dioxolane in the presence of a free radical initiator. The dioxolane reactant can be made by reacting a ketone with 3,4-epoxy-1-butene, or a substituted derivative thereof.

Abstract: Copolymers are produced when 3,4-epoxy-1-butene (EpB) is copolymerized with maleic anhydride. The copolymerization is initiated by free radicals, and comprises both 1,2-propagation and 1,5-propagation of EpB. When an ether is used as the reaction solvent, the product is soluble, and essentially composed of (a) a monomer derived from maleic anhydride, and (b) two monomers derived from EpB. When the reaction solvent is a ketone, the polymer product is also soluble, and additionally contains (c) a moiety derived from a dioxolane formed in situ. When the reaction is conducted in the presence of a non polar (e.g., hydrocarbon or a halocarbon) solvent, or neat (i.e., in the absence of a solvent), the polymer product is insoluble in common organic solvents and contains (d) a symmetrical EpB dimer. This dimer apparently does not form, or is formed to only a very slight extent, when the polymerization is conducted in polar reaction solvents.

Abstract: Copolymers are produced when 3,4-epoxy-1-butene (EpB) is copolymerized with maleic anhydride. The copolymerization is initiated by free radicals, and comprises both 1,2-propagation and 1,5-propagation of EpB. When an ether is used as the reaction solvent, the product is soluble, and essentially composed of (a) a monomer derived from maleic anhydride, and (b) two monomers derived from EpB. When the reaction solvent is a ketone, the polymer product is also soluble, and additionally contains (c) a moiety derived from a dioxolane formed in situ. When the reaction is conducted in the presence of a non polar (e.g., hydrocarbon or a halocarbon) solvent, or neat (i.e., in the absence of a solvent), the polymer product is insoluble in common organic solvents and contains (d) a symmetrical EpB dimer. This dimer apparently does not form, or is formed to only a very slight extent, when the polymerization is conducted in polar reaction solvents.

Abstract: Copolymers are produced when 3,4-epoxy-1-butene (EpB) is copolymerized with maleic anhydride. The copolymerization is initiated by free radicals, and comprises both 1,2-propagation and 1,5-propagation of EpB. When an ether is used as the reaction solvent, the product is soluble, and essentially composed of (a) a monomer derived from maleic anhydride, and (b) two monomers derived from EpB. When the reaction solvent is a ketone, the polymer product is also soluble, and additionally contains (c) a moiety derived from a dioxolane formed in situ. When the reaction is conducted in the presence of a non polar (e.g., hydrocarbon or a halocarbon) solvent, or neat (i.e., in the absence of a solvent), the polymer product is insoluble in common organic solvents and contains (d) a symmetrical EpB dimer. This dimer apparently does not form, or is formed to only a very slight extent, when the polymerization is conducted in polar reaction solvents.

Abstract: Copolymers are made by reacting maleic anhydride or a related compound with a 4-vinyl-1,3-dioxolane in the presence of a free radical initiator. The dioxolane reactant can be made by reacting a ketone with 3,4-epoxy-1-butene, or a substituted derivative thereof.