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• W1986907100 abstract "Using self-consistent field theory (SCFT), we study the conformational properties of polyelectrolyte dendrimers. We compare results for three different models of charge distributions on the polyelectrolytes: (1) a smeared, quenched charge distribution characteristic of strong polyelectrolytes; (2) a smeared, annealed charge distribution characteristic of weak polyelectrolytes; and (3) an implicit counterion model with Debye-Huckel interactions between the charged groups. Our results indicate that an explicit treatment of counterions is crucial for the accurate characterization of the conformations of polyelectrolyte dendrimers. In comparing the quenched and annealed models of charge distributions, annealed dendrimers were observed to modulate their charges in response to the density of polymer monomers, counterions, and salt ions. Such phenomena is not accommodated within the quenched model of dendrimers and is shown to lead to significant differences between the predictions of quenched and annealed model of dendrimers. In this regard, our results indicate that the average dissociated charge documentclass[12pt]{minimal}begin{document}$bar{alpha }$end{document}α¯ inside the dendrimer serves as a useful parameter to map the effects of different parametric conditions and models onto each other. We also present comparisons to the scaling results proposed to explain the behavior of polyelectrolyte dendrimers. Inspired by the trends indicated by our results, we develop a strong segregation theory model whose predictions are shown to be in very good agreement with the numerical SCFT calculations." @default.
• W1986907100 created "2016-06-24" @default.
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• W1986907100 date "2011-11-28" @default.
• W1986907100 modified "2023-10-18" @default.
• W1986907100 title "Mean field theory of charged dendrimer molecules" @default.
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• W1986907100 doi "https://doi.org/10.1063/1.3663382" @default.
• W1986907100 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22128954" @default.
• W1986907100 hasPublicationYear "2011" @default.
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