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EN
The model isomerization reaction of 1,4-diallyloxybutane catalyzed by [RuClH(CO)(PPh3)3] has been studied. This reaction practically solely leads to the formation of 1-propenyl derivatives in mild and solventless reaction conditions. A mixture of isomer products, i.e. (Z,Z)-, (Z,E)-, (E,E)-l,4-di(l-propenyloxy)butanes is formed. The effect of the reaction conditions on the yield of 1-propenyl ether and the isomers contents was examined. The temperature, the catalyst concentration, the atmosphere of the reaction gas (air or inert gas) and the reaction time were changed. From the viewpoint of a minimal concentration of ruthenium pre-catalyst, the optimal parameters for the quantitative synthesis of 1-propenyl ether have been determined. Additionally, the 100%-yield reaction time was evaluated depending on the temperature and ruthenium pre-catalyst concentration.
2
Content available remote The synthesis of 1-propenyl ethers and their photopolymerization
EN
The di(l-propenyl) ether has been observed to be a highly reactive monomer in photoinitiated cationic polymerization undergoing very high conversions to polymer at very short irradiation times. The polymerization process was investigated for various UV-systems containing: the model 1-propenyl ether 1,4-dipropenoxybutane, the epoxy resin Epidian 6 or the unsaturated polyester resin Estromal 103 and cationic or radical initiator. The amounts of ether and initiators were changed in compositions.
3
Content available remote Non-waste synthesis of 1-propenoxyl monomers
EN
Non-waste synthesis of 1-propenoxyl monomers of C4 diols ((Z)-butane-2-ene-l,4-diols) via isomerization of the corresponding allyl ethers of diols catalysed by the ruthenium(II) complexes has been investigated. [RuHCl(CO)(PPh3)3] is a very active and selective catalyst precursor of isomerization of allyl ethers of diols, containing neither a triple bond nor unprotected primary allylic hydroxyl group. The optimal parameters for the synthesis of 1-propenyl ethers and their physic-chemical properties ('H NMR, MS, boiling point) are given. Synthesized propenyl ether monomers were of high purity, therefore, they are suitable directly for use in photointiated cationic polymerization.
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