the search for novel organic ferromagnetic polymers we devised synthet
ic routes to poly-p-phenylenevinylenes with nitroxide functional group
s. Reaction of the Grignard reagent derived from the ROC6H4(CH2)(n)Br
precursor (R=CH3, n=4; R=n-C6H13, n=6) with CO2 gave an acid which was
chloromethylated and subsequently coupled to the paramagnetic TEMPOL
group. The paramagnetic monomers could be readily converted to the dia
magnetic hydroxylamine salts to permit full NMR characterization. The
paramagnetic monomers were polymerized via the (KOBu)-Bu-t route to th
e corresponding PPV.