Surface plasmon resonance study of the interaction of a beta-cyclodextrin polymer and hydrophobically modified poly(N-isopropylacrylamide)

Surface plasmon resonance (SPR) technique is used to follow, both in real time and in situ, the association between a physically adsorbed polymer of beta-cyclodextrin (pbetaCD) and different hydrophobically modified poly(N-isopropylacrylamide) (PNIPAM) copolymers containing either adamantyl or dodecyl groups. This association is due to the complex formation between the hydrophobic groups and the betaCD cavities. Therefore, the adsorbed amount of PNIPAM onto the pbetaCD layer depends on the substituent and on its substitution level. The association and dissociation rate constants are evaluated from the kinetics of PNIPAM adsorption. An estimation of the association constants leads to values higher than 10(4) M(-1), reflecting the strong interaction between these polymers.     

Synthesis of unsaturated esters of pyridine- and quinolinedicarboxylic acids

The divinyl, diallyl, and dipropargyl esters of pyridine-2,4-, pyridine-2,6-, and quinoline-2,4-dicarboxylic acids and the divinyl and dipropargyl esters of pyridine-2,5-dicarboxylic acid have been synthesized.     

Cyclization of o-nitrosoacylbenzenes to anthranils

5-Bromo- and 5-methoxy-3-ethylanthranils, respectively, were obtained by cyclization of o-nitrosopropiophenone under the influence of hydrogen bromide in benzene and hydrogen chloride in methanol. In these reactions, the starting nitroso ketone undergoes redox transformations that also proceed readily in an inert solvent in the absence of any cyclizing reagents.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 886–890, July. 1976.     

Five-membered-ring-substituted 1-methyl-1H-indeno[1,2-b]pyridines

1-Methyl-1H-indeno[1,2-b]pyridine and 1-methyl-1H-5-(, -dicarbomethoxyvinyl)-(formyl, acetyl)indeno[3,2-b]pyridines were obtained by treatment of N-methyl-4-azafluorenium iodide, as well as mixtures of it with acetylenedicarboxylic ester, dimethylformamide (DMF), and phosphorus oxychloride or acetic anhydride, with bases. 4-Azafluoronenone was used to synthesize 9-(p-methoxyphenyl)-4-azafluoren-9-ol, which was reduced to 9-(p-methoxyphenyl)-4-azafluorene, and 1-methyl-1H-5-(p-methoxyphenyl)indeno[3,2-b]pyridine was obtained from the methiodide of the latter.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1382–1386, October, 1981.