Competitive complex forming reactions between monosubstituted and nonsubstituted poly(ethylene glycol)s with poly(methacrylic) acid
β Scribed by V. Yu. Baranovsky; S. Shenkov
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 364 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
Institute of Polymers, Bulgarian Academy of Sciences, BG-l 1 13 Sofia, Bulgaria
SYNOPSIS
A competitive complex forming reaction between a number of monosubstituted poly(ethy1ene glyco1)s (PEG*) containing a hydrophobic group of differing chemical nature and nonsubstituted PEG of various molecular weights with poly(methacry1ic acid) (PMAA) was studied. A UV spectroscopy method was used. During the transfer of the hydrophobic chromophoric group from the aqueous medium into the hydrophobic domains of the polycomplex (PMAA.PEG*), a bathochromic effect was observed. The introduction of a hydrophobic group into the PEG chain leads to stabilization of the polycomplex (PMAA.PEG) that is formally the same as growing the chain length of PEG. The polymerization degree of PEG having the same competitive power as PEG* can be used as the peculiar scale of the complex forming ability of PEG* in the complexation with PMAA.
π SIMILAR VOLUMES
Complex formation between polymethacrylic (PMAA) and polyacrylic acids, and star-shaped poly(ethy1ene glycol) prepared by ethoxylation of pyrogallol (Pyr-PEG) has been studied viscometrically and by potentiometric titration in water solution. The competitive ability of Pyr-PEG and of the derivatives
A~tract--Complex formation between poly(methacrylic acid) and monosubstituted poly(ethylene glycols) (PEG) in dilute aqueous solutions has been studied by potentiometric titration and viscometry. The presence of a hydrophobic group in the PEG chain results in a significant decrease of the critical c
Interpolymer reactions between poly(acrylic acid) and poly(vinyl ether) of ethylene glycol were studied by viscometric and spectroturbidimetric methods in aqueous and organic solutions of different nature. It is shown that the formation of interpolymer complexes strongly depends on the strength of t