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Nicolaas A M Besseling

Publications and source records attributed to Nicolaas A M Besseling.

3 recordsLinked to original sources

Monte Carlo study of supramolecular polymer fractionation: selective removal of chain stoppers by phase separation.

Supramolecular polymers consist of bifunctional monomers that join and break reversibly. Supramolecular polymer solutions are often polluted by monofunctional contaminants, which drastically reduce the chain-forming capabilities of the system. Unfortunately, the monofunctional contaminants are difficult to remove due to the physical and chemical resemblance with the bifunctional counterparts. In this paper, we present a method to specifically remove the monofunctional contaminants from a supramolecular polymer solution. The general idea is to induce phase separation by decreasing the solvent quality and to remove the most dilute phase. This concept is explored by means of a recently developed Monte Carlo scheme to calculate the compositions of the coexisting liquid phases. The simulations provide a proof of principle that the proposed purification method is suitable to remove the monofunctional contaminants efficiently. The calculations indicate that, at the right experimental conditions, the vast majority of the monofunctional contaminants can be removed in this way while retaining most of the bifunctional monomers. Because of the general nature of the arguments presented here, it is to be expected that the results are applicable to a large variety of supramolecular systems. Moreover, the method is very suitable for large-scale applications because only solvent is added and no tedious chromatographic steps are required.

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Linear rheology of water-soluble reversible neodymium(III) coordination polymers.

The rheology of reversible coordination polymer networks in aqueous solution is studied. The polymers are formed by neodymium(III) ions and bifunctional ligands, consisting of two pyridine-2,6-dicarboxylate groups connected at the 4-positions by an ethylene oxide spacer. Neodymium(III) ions can bind three of these terdendate ligand groups. At high concentrations, the polymer networks yield viscoelastic materials, which can be described with the Maxwell model. The scaling of the elastic modulus, relaxation time, and zero-shear viscosity with concentration are in good agreement with the predictions of Cates' model that describes the dynamics of linear equilibrium polymers. This indicates that the networks have only few cross-links and can be described as linear equilibrium polymers. The gels are also thermo-reversible. At high temperatures, fast relaxation was found, resulting in liquidlike behavior. Upon cooling, the viscoelastic properties returned immediately. From the temperature dependence of the relaxation time, an activation energy of 49 kJ/mol was determined for the breaking and reptation of the polymers.

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Surface forces, supramolecular polymers, and inversion symmetry.

The effects of supramolecular equilibrium polymers on surface forces are studied by both a phenomenological Landau type analysis and a molecular model based on a Bethe-Guggenheim approximation. We point out that surface forces brought about by equilibrium polymers may be completely different from what can be found with "ordinary" polymers. The new feature is the role of inversion (a)symmetry or "directionality" of the associating unit molecules ("monomers"). Symmetric B-B monomers (where B denotes a self-complementary binding group) give rise to nondirectional chains and lead to attractive forces between similar surfaces. Asymmetric A-D monomers (where A and D denote complementary acceptor and donor groups, respectively) produce directional chains and can cause strong repulsion. The range of the attractive force has a maximum at intermediate concentration, while the range of the repulsive force increases over the whole concentration range.

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