Darstellung und eigenschaften von N-3,5-dinitrobenzoyl- und N-2,4,6-trinitrophenyl-nylon 66

1978

Enantioselektive Trifluoracetylierung mit Hilfe chiraler Polyamide

1980

(S)-Poly(2-aminobutyric acid) (1) [(S)-poly(imino-1-methyl-3-oxotrimethylene)] was transformed into its N-trifluoroacetyl derivative 4. The IR spectra and the circular dichroism of both substances were compared. In addition, (S)-poly[N-(1-phenylethyl)acrylamide] (2) ((S)-poly-[1-(1-phenylethylaminocarbonyl)ethylene]) was trifluoroacetylated leading to polymer 5. 4 was found to react as trifluoroacetylating agent with L-1-phenylethylamine (L-3) twice as fast as it reacts with D-3. Accordingly, the reaction of 4 with D,L-3 leads preferentially to the L-form of N-(1-phenylethyl)trifluoroacetamide with optical yields up to 6%. The reaction of 5 with D,L-3 affords the D-form of N-(1-phenylethyl)…

Reaktionen bei der Bestrahlung von poly(N-chloramid)en

1980

On irradiating poly(N-chloroamide)s in films or in solution in the range of 325–375 nm carboxamide groups are formed. The irradiated polymer contains chlorine which is linked to C-atoms. This reaction can certainly not be explained with an intramolecular photorearrangement but with a sequence of photoreactions and dark reactions satisfactorily accounting for all observations.

Darstellung und eigenschaften von N-trichloracetyl-nylon 66

1978

N-trifluoracetyl-nylon 66 als polymeres reagenz

1979

N-Trifluoroacetyl-Nylon 66 (2) obtained by the reaction of Nylon 66 (1) with trifluoroacetic anhydride is very suitable as a polymeric reagent for the trifluoroacetylation of amines and alcohols. The advantages of 2 compared with low molecular trifluoroacetylating reagents are discussed. The selectivity against different substituted anilines and against structurally isomeric secondary amines was studied intensively by kinetic measurements.

Polarographische Untersuchungen an monomeren und polymeren N-Chlorcarbonamiden

1979

The polarographic reduction of low molecular and high molecular N-chlorocarboxamides at the dropping mercury electrode proceeds in two one-electron-transfer steps, which are highly irreversible. In the case of the low molecular models 1 and 2 the reaction is diffusion-controlled, whereas in the case of the poly(N-chloroamide) 3 the reaction is adsorption-controlled. Reduction of several poly(N-chloroamide)s shows always two reduction waves with a distance of 0,5 V. There is, however, no relation between the polyamide-type and the position of the half-wave potentials. The polarographic reduction can be used as an analytical method for quantitative determination of N-chlorocarboxamide groups …