Abstract: Copolyetherimides are prepared by the reaction of an alkali metal salt of a dihydroxyaromatic compound with a bis(substituted phthalimide) and a third compound which may be a substituted aromatic ketone or sulfone or a macrocyclic polycarbonate or polyarylate oligomer. The reaction takes place the in presence of a solvent and a phase transfer catalyst having high thermal stability, such as a hexaalkylguanidinium halide. Random or block copolymers may be obtained, depending on the reaction conditions.

Abstract: Esterification reactions conducted in the presence of Lewis acids, including the reactions between aromatic carboxylic acids and alcohols and between epoxides and carboxylic acids, may be conducted with the use as the catalyst of a hexaalkylguanidinium or .alpha.,.omega.-bis(pentaalkylguanidinium)alkane salt such as hexaethyiguanidinium chloride or bromide.

Abstract: An improved process for preparing a nitrogen or oxygen containing organoalkoxysilane such as an isocyanurate or fumarate by reacting a haloalkylaikoxysilane such as a chloropropytrimethoxysilane and a reactant of either a cyanate or an ammonium salt of an organic acid of C1-C20 carbon atoms or a metal salt of an organic acid of C1-C20 carbon atoms or mixtures thereof to a reaction temperature of at least about 80.degree. C. to about 200.degree. C., the improvement is in carrying out the reaction in the presence of a guanidinium salt phase as a transfer catalyst such as hexaethylguanidinium chloride. The improved process also is reacted wherein the temperature increase from the exotherm reaction above the reaction temperature ranges from about 0.degree. C. to about 120.degree. C. A preferred metal cyanate is sodium cyanate.

Abstract: Hexasubstituted guanidinium chlorides are prepared by a method which affords them in high yield as aqueous solutions, optionally also containing alkali metal chlorides. The solutions may be employed as sources of hexasubstituted guanidinium salts useful as phase transfer catalysts and the reaction of alkali metal salts of dihydroxyaromatic compounds with substituted imides to form polyetherimides or their intermediates.

Abstract: Aromatic polyether polymers, illustrated by polyethersulfones, polyetherketones and polyetherimides, are prepared by a phase transfer catalyzed reaction between a salt of at least one dihydroxyaromatic compound and at least one substituted aromatic compound such as bis(4-chlorophenyl) sulfone, bis(4-chlorophenyl) ketone or 1,3-bis?N-(4-chlorophthalimido)!benzene, in a monoalkoxybenzene such as anisole as diluent and in the presence of a phase transfer catalyst, preferably a hexaalkylguanidinium salt.

Abstract: Diaminoalkyl quaternary ammonium salts are prepared by the reaction of alkyl halides with tertiary diamines having C.sub.2-20 primary alkyl radicals attached to nitrogen and an alkyl radical between the two nitrogen atoms in which at least three carbon atoms separate said nitrogen atoms. Said salts are preferably substantially free from corresponding diamines. They are useful as catalysts for interfacial polycarbonate preparation by the reaction of phosgene with at least one dihydroxyaromatic compound. Polycarbonate preparation using such catalysts is economical in phosgene consumption, is accompanied by a rapid conversion of chloroformate groups to desirable species and affords a product with a very low proportion of unreacted dihydroxyaromatic compound.

Abstract: Disclosed are copolycarbonate compositions comprising structural units of Formula I ##STR1## Formula II ##STR2## wherein R.sup.2 represents --CH.sub.3, --C.sub.2 H.sub.5, or propyl; A is a divalent organic moiety; and wherein the ratio of Formula I to Formula II in the copolycarbonate is from about 99.8:0.2 to about 90:10.

Abstract: Reaction mixtures prepared from tetraalkyl titanates and mixtures of glycols, said reaction mixtures comprising titanium bisglycoxide oligomers, may be used as depolymerization catalysts for conversion of linear polyesters to macrocyclic polyester oligomers.

Abstract: The invention relates to a novel process for depolymerizing polyesters by subjecting the polyesters to catalysts and organic solvents which are substantially free of oxygen and water in order to produce macrocyclic polyester oligomers substantially free of hydroxybutyl terminated linear impurities.

Abstract: Macrocyclic polyester oligomer compositions are polymerized to high molecular weight polyesters by heating with a titanate ester composition comprising moieties having oxygen or nitrogen chelated with a titanium atom or having two titanium atom connected by alkylene ester units. Depending on the chemical nature of the initiator, the polymerization reaction may be extremely rapid as desired for structural reaction injection molding, or may have an induction period as desired for resin transfer molding.

Abstract: A process for making high ductile and high melting point polyesters comprising the step of contacting macrocyclic copolyester oligomers having structural units with C.sub.4 alkylene bridging radicals and structural units with bridging radicals other than C.sub.4 alkylenes, and a polymerization catalysts.