Condensation of α-ethoxyacrolein with secondary amines

Conclusions Morpholine, piperidine, and dibutylamine undergo both 1,2 and 1,4 addition to -ethoxyacrolein to form a mixture of 3,3- and 1,3-diamino-2-ethoxy-1-propenes. The N-formyl derivative of the starting amine is a side product. The reaction of -ethoxyacrolein with diethylamine gives only splitting of the C-C bond and formation of N-formyldiethylamine.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2610–2612, November, 1985.     

Reaction of α-alkoxyacroleins with acetone cyanohydrin

Conclusions -Alkoxyacroleins add acetone cyanohydrin in the presence of piperidine to give 1-N-piperidino-1-cyano-2-alkoxy-2-propenes, which in the presence of piperidine or on long storage are isomerized to 1-N-piperidino-1-cyano-2-alkoxy-1-propenes.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2122–2124, September, 1973.     

Far-IR spectra of charge-transfer complexes between IX (X = Cl,Br or I) and trans-1,2-bis(4-pyridyl)ethylene, 1,2-bis(4-pyridyl)ethane and 4,4′-

Far-IR spectra of charge-transfer complexes of trans-1,2-bis(4-pyridyl)ethylene (Bpe), 1,2-bis(4-pyridyl)ethane (Bpa) and 4,4′-bipyridyl (4,4′-     

The functional layered organosilica materials prepared with anion surfactant templates

A novel strategy for the synthesis of layered organosilica is demonstrated. The ionic interaction between the anionic group of a surfactant (sodium dodecyl sulfate) and the cationic organic group of an organosilane (3-aminopropyltrimethoxysilane, ATMS) under acidic conditions was utilized to create a layered organosilica at room temperature. The inorganic part of the organosilica layer was an Si-O hexagonal sheet, and organofunctional groups were alternately arranged on both sides of the sheet. The layered structure of the ATMS organosilica was retained after the removal of the surfactant with chloride anion. The properties of the layered ATMS organosilica were investigated. The layered ATMS-Cl organosilica is stable and possesses a definite layer structure in water or ethanol. Various kinds of anions can be intercalated in the interlayer space of the layered ATMS organosilicas and the layer was expanded dependent on the intercalated anions. The structure of the layered ATMS organosilica was well retained during the intercalation processes.     

Equilibrium anionic polymerization of 4,7-dioxaoctanal and n-octanal

Equilibrium anionic polymerization of 4,7-dioxaoctanal (DOA) and n-octanal (OA) was carried out in tetrahydrofuran in the temperature range of ?90 to ?68°C, and thermodynamic parameters were evaluated as follows: ΔH_ss = ?4.0 ± 0.1 kcal/mole, ΔS_ss = ?18.4 ± 0.5 cal/mole-deg, and T_c,ss = ?56°C for the DOA system; ΔH_sc = ?3.4 ± 0.1 kcal/mole, ΔS_sc = ?15.7 ± 0.4 cal/mole-deg, and T_c,sc = ?59°C for the OA system. Comparison of these values with those in the cases of β-methoxypropionaldehyde and n-valeraldehyde made it clear that the aliphatic aldehyde having a longer alkyl group polymerizes with smaller changes of enthalpy and entropy and that the polar-substituted aldehydes have higher polymerizability than the corresponding unsubstituted aliphatic aldehydes in the temperature range studied. These effects of substituents are interpreted from the viewpoint of the intermolecular interactions of polar groups in monomers and their polymers.