Acyl derivatives of 2-aminopyridine, 2-aminopyrimidine, 4-amino-2,2,6,
6-tetramethyl-piperidine-1-oxyl, and 4-hydroxy-2,2,6,6-tetramethylpipe
ridine-1-oxyl were obtained from long-chain diacetylenic acyl chloride
s and the corresponding heterocyclic compounds. Spreading isotherms of
monolayers on a water surface show that lengthening of the hydrocarbo
n chain and replacement of the pyridyl groups in these compounds by th
e more hydrophilic pyrimidyl groups render the films more condensed. L
ong-chain acyl derivatives of nitroxyl radicals form monolayers posses
ing a low collapse pressure. ESR spectra of Langmuir-Blodgett films of
these radicals before and after photopolymerization were recorded.