Publisher's Synopsis
V rabote izucheny kineticheskie zakonomernosti reaktsii sinteza prostykh aromaticheskikh poliefirov na osnove fenolftaleina i 4,4-dikhlordifenilsul'fona, ob"yasnyayushchie osobennosti eye protekaniya, kinetika reaktsii vzaimodeystviya diana s "aktivirovannymi" aromaticheskimi 4,4-digalogenproizvodnymi, soderzhashchimi razlichnye mostikovye gruppy ili razlichnye galogeny. Ustanovlena vozmozhnost' obrazovaniya gomo- i geterokoordinatsionnykh sistem v srede DMSO-digalogenaren - difeno-ksidnyy anion, vliyayushchikh na reaktsionnuyu sposobnost' iskhodnykh monomerov i snizhayushchikh skorost' reaktsii. Predlozhen mekhanizm aromaticheskogo nukleofil'nogo zameshcheniya pri sinteze prostykh aromaticheskikh poliefirov na osnove 4,4-digalogendifenilketona s uchetom protekaniya pobochnykh reaktsiy obrazovaniya koordinatsionnykh sistem. Pokazana vozmozhnost' polucheniya digidroksilsoderzhashchego "dimera" pri vzaimodeystvii v DMSO 4,4-dikhlordifenilketona s difenolyatom diana v sootnoshenii 1:2. Na osnove sintezirovannogo "dimera" predlozhena skhema i osushchestvlen sintez novykh aromaticheskikh sopoliefirketonov: poliarilenefirketonsul'fonov (PAEKS), poliarilenefirketonformaley (PAEKF), poliarilenefiroketonsul'fonformaley (PAEKSF), poliarilenefirketonarilatov(PAEKA).
