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Triethylene glycol formal,

Fig. 3.5. Time-conversion curve for the consumption of monomer (Mt), formation of polymer (P) and formation of cyclic dimer (M2) during the polymerization of triethylene glycol formal (0.5 mol 1 1... Fig. 3.5. Time-conversion curve for the consumption of monomer (Mt), formation of polymer (P) and formation of cyclic dimer (M2) during the polymerization of triethylene glycol formal (0.5 mol 1 1...
Figure 9. Monomer concentration at equilibrium in the polymerization of triethylene glycol formal /3/... Figure 9. Monomer concentration at equilibrium in the polymerization of triethylene glycol formal /3/...
Figfire 10. HP-GPC curves of the reaction mixture during the polymerization of the dimer of triethylene glycol formal (M,)... [Pg.91]

In this way the unstable 1,3-dioxacycloalkanes and their oligomers would be converted into stable ethers. This has been proved experimentally, and the reaction offers some exciting synthetic possibilities [17, 18]. In particular, it provides a new route to a variety of new crown ethers, such as the l,4,7,10-tetraoxa-ll,ll-dimethylcyclotridecane (a 13-crown-[4]-ether) from isobutene and the formal of triethylene glycol but that is another story ... [Pg.752]

See other pages where Triethylene glycol formal, is mentioned: [Pg.491]    [Pg.44]    [Pg.186]    [Pg.278]    [Pg.85]    [Pg.87]    [Pg.187]    [Pg.491]    [Pg.44]    [Pg.186]    [Pg.278]    [Pg.85]    [Pg.87]    [Pg.187]    [Pg.426]   
See also in sourсe #XX -- [ Pg.491 ]



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