Abstract: Provided is a novel and effective process for the synthesis of aryl sulfides substituted with an alkanoylamino or (N-alkyl)alkanoylamino substituent. The process comprises reacting an appropriately substituted aromatic compound with a sulfur dihalide, preferably sulfur dichloride, in the presence of an alkali metal tetrafluoroborate catalyst and an ether comprising solvent.

Abstract: Novel poly-aromatic ethynyl-terminated enyne compounds of the formula: ##STR1## are provided together with a method of production thereof, wherein R.sub.1 is a strong electron withdrawing moiety and n is equal to or greater than 1.

Abstract: Accelerated curing rates of certain acetylene-terminated aromatic sulfones and polyimide oligomers are obtained by thermally curing the resins with an effective amount of a diethynylbiphenyl.

Abstract: Provided is a novel process for the synthesis of aryl sulfides substituted with an alkoxy or phenoxy substituent. The process comprises reacting an alkoxy or phenoxy substituted aromatic compound with a sulfur dihalide, preferably sulfur dichloride, in the presence of an alkali metal tetrafluoroborate catalyst, with the amount of said aromatic reactant compound preferably being sufficient to solvate the sulfur dichloride and catalyst sufficiently to allow the reaction to occur.

Abstract: In one aspect, thermosetting liquid resinous polyepoxides are upgraded or advanced in molecular weight by a process including (A) providing a catalyst-free mixture of a dihydric phenol, preferably bisphenol-A and a liquid resinous polyepoxide containing 1,2-epoxy groups, preferably a low molecular weight epoxy resin consisting essentially of the diglycidyl ether of bisphenol-A, at a temperature above about a minimum reaction temperature for a catalytic liquid upgrade reaction between the dihydric phenol and the polyepoxide; and (B) subsequently introducing the catlyst, preferably an organic phosphine and most preferably triphenylphosphine, into the mixture of the dihydric phenol and polyepoxide at reaction temperature and maintaining the mixture containing the catalyst at reaction temperature for a time sufficient to produce the upgraded version of the thermosetting resinous polyepoxide.

Abstract: An improved overall process is provided wherein poly(bisbenzimidazobenzophenanthroline) is formed on an expeditious basis and is recovered from the reaction mass in substantially pure form. Appropriate quantities of 1,4,5,8-tetracarboxy naphthalene dianhydride and 3,3',4,4' -tetraaminobiphenyl are condensed as defined) in a reaction zone while dissolved in molten antimony trichloride, and the resulting reaction mass containing the dissolved product is discharged into a precipitation zone containing hydrochloric acid (as defined). The resulting solid product is separated and dried. The liquid portion which is separated from the solid product contains antimony trichloride dissolved in hydrochloric acid and is subjected to distillation which substantially separates these components. The antimony trichloride is recycled to the reaction zone, and the hydrochloric acid is recycled to the precipitation zone.