2007
DOI: 10.1021/jp074485q
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Hydrodynamic Behavior of High Molar Mass Linear Polyglycidol in Dilute Aqueous Solution

Abstract: Six high molar mass polyglycidol samples were obtained by fractionation of polyglycidol synthesized by means of cationic polymerization of ethoxyethyl glycidyl ether followed by cleavage of the protective groups. The fractions covering the molar mass range from 0.1 to 2.4 x 10(6) were studied by dynamic and static light scattering. The weight-average molar masses (Mw), second virial coefficients (A2), radii of gyration (Rg), diffusion coefficients (D0), hydrodynamic radii (Rh), and dynamic virial coefficients … Show more

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Cited by 29 publications
(17 citation statements)
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References 58 publications
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“…This nding can be rationalized recalling that at lower temperatures polyglycidol exhibits behavior that is closer to that for polymer coils in marginal solvents. 46 At such conditions DDP and polyglycidol chains are not fully segregated and we can speculate that the polyglycidol chain partially covers the lipid mimetic anchor thus effectively decreasing the portion of DDP that is exposed to water; the longer the chain, the smaller the portion (Scheme 2). At elevated temperatures the solubility of polyglycidol increases; it goes preferentially in the aqueous phase thus exposing the whole hydrophobic anchor to water (Scheme 2), which is expected to facilitate the self-assembly and to decrease the CMCs.…”
Section: Determination Of the Critical Micellization Concentrations (mentioning
confidence: 99%
“…This nding can be rationalized recalling that at lower temperatures polyglycidol exhibits behavior that is closer to that for polymer coils in marginal solvents. 46 At such conditions DDP and polyglycidol chains are not fully segregated and we can speculate that the polyglycidol chain partially covers the lipid mimetic anchor thus effectively decreasing the portion of DDP that is exposed to water; the longer the chain, the smaller the portion (Scheme 2). At elevated temperatures the solubility of polyglycidol increases; it goes preferentially in the aqueous phase thus exposing the whole hydrophobic anchor to water (Scheme 2), which is expected to facilitate the self-assembly and to decrease the CMCs.…”
Section: Determination Of the Critical Micellization Concentrations (mentioning
confidence: 99%
“…PEO chains (based on a hydrodynamic radius of each PEO chain (11000 g/mol) of ~ 2.2 nm (calculated according to the method described in [22])). The functionalised β-CD-RGD is estimated to be of a similar size to the PEO (β-CD alone is 1.66 nm), meaning that at maximum packing on the outer rim of one cylinder composed of 75% PS-PEO-Ada, we may obtain ~27 conjugated CD-RGD molecules.…”
Section: The Outer Perimeter Of Each Peo Cylinder Of Diameter 19 Nm Imentioning
confidence: 99%
“…It has been shown, that if the propagating chain end is not a “free” alkoxide, high molecular weight polyglycidol can be obtained. By the use of partially hydrolyzed diethylzinc as catalyst, the basicity of the propagating alkoxide is suppressed by coordination to the zinc 41–43. Proton abstraction is efficiently avoided.…”
Section: Introductionmentioning
confidence: 99%