Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (10/10 displayed)

  • 2023Effect of polymer architecture on the adsorption behaviour of amphiphilic copolymers : A theoretical study4citations
  • 2021Theory of Microphase Segregation in ABA Triblock Comb-Shaped Copolymers : Lamellar Mesophase7citations
  • 2018Microphase segregation of diblock copolymers studied by the self-consistent field theory of Scheutjens and Fleer9citations
  • 2016Loss of bottlebrush stiffness due to free polymers9citations
  • 2016Loss of bottlebrush stiffness due to free polymers9citations
  • 2016Enhanced stiffness of silk-like fibers by loop formation in the corona leads to stronger gels1citations
  • 2015Liquid crystals of self-assembled DNA bottlebrushes23citations
  • 2015Liquid crystals of self-assembled DNA bottlebrushes23citations
  • 2009Interaction of particles with a polydisperse brush39citations
  • 2009Modeling the structure of a polydisperse polymer brush112citations

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Chart of shared publication
Mu, Mingduo
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Holmes, Melvin
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Chen, Jianshe
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Ettelaie, Rammile
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Zhulina, Ekaterina B.
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Borisov, Oleg V.
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Darinskii, Anatoly A.
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Mikhailov, Ivan V.
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Kamperman, Marleen
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Mocan, Merve
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Stuart, Martien A. Cohen
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Voets, Ilja K.
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Storm, Ingeborg M.
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Vries, Renko De
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Kornreich, Micha
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Beck, Roy
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De Vries, Renko
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Cohen Stuart, Martien A.
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De Vries, Renko J.
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Rombouts, Wolf H.
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Werten, Marc W. T.
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De Wolf, Frits A.
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Domeradzka, Natalia E.
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Hernandez-Garcia, Armando
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De Vos, Wiebe M.
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Kleijn, J. Mieke
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Keizer, Arie De
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Chart of publication period
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2021
2018
2016
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2009

Co-Authors (by relevance)

  • Mu, Mingduo
  • Holmes, Melvin
  • Chen, Jianshe
  • Ettelaie, Rammile
  • Zhulina, Ekaterina B.
  • Borisov, Oleg V.
  • Darinskii, Anatoly A.
  • Mikhailov, Ivan V.
  • Kamperman, Marleen
  • Mocan, Merve
  • Stuart, Martien A. Cohen
  • Voets, Ilja K.
  • Storm, Ingeborg M.
  • Vries, Renko De
  • Kornreich, Micha
  • Beck, Roy
  • De Vries, Renko
  • Cohen Stuart, Martien A.
  • De Vries, Renko J.
  • Rombouts, Wolf H.
  • Werten, Marc W. T.
  • De Wolf, Frits A.
  • Domeradzka, Natalia E.
  • Hernandez-Garcia, Armando
  • De Vos, Wiebe M.
  • Kleijn, J. Mieke
  • Keizer, Arie De
OrganizationsLocationPeople

article

Liquid crystals of self-assembled DNA bottlebrushes

  • Stuart, Martien A. Cohen
  • Voets, Ilja K.
  • Storm, Ingeborg M.
  • Vries, Renko De
  • Kornreich, Micha
  • Hernandez-Garcia, Armando
  • Leermakers, Frans A. M.
Abstract

<p>Early theories for bottlebrush polymers have suggested that the so-called main-chain stiffening effect caused by the presence of a dense corona of side chains along a central main chain should lead to an increased ratio of effective persistence length (l<sub>p,eff</sub>) over the effective thickness (D<sub>eff</sub>) and, hence, ultimately to lyotropic liquid crystalline behavior. More recent theories and simulations suggest that l<sub>p,eff</sub> ∼ D<sub>eff</sub>, such that no liquid crystalline behavior is induced by bottlebrushes. In this paper we investigate experimentally how lyotropic liquid crystalline behavior of a semiflexible polymer is affected by a dense coating of side chains. We use semiflexible DNA as the main chain. A genetically engineered diblock protein polymer C<sub>4</sub>K<sub>12</sub> is used to physically adsorb long side chains on the DNA. The C<sub>4</sub>K<sub>12</sub> protein polymer consists of a positively charged binding block (12 lysines, K<sub>12</sub>) and a hydrophilic random coil block of 400 amino acids (C<sub>4</sub>). From light scattering we find that, at low ionic strength (10 mM Tris-HCl), the thickness of the self-assembled DNA bottlebrushes is on the order of 30 nm and the effective grafting density is 1 side chain per 2.7 nm of DNA main chain. We find these self-assembled DNA bottlebrushes form birefringent lyotropic liquid crystalline phases at DNA concentrations as low as 8 mg/mL, roughly 1 order of magnitude lower than for bare DNA. Using small-angle X-ray scattering (SAXS) we show that, at DNA concentrations of 12 mg/mL, there is a transition to a hexagonal phase. We also show that, while the effective persistence length increases due to the bottlebrush coating, the effective thickness of the bottlebrush increases even more, such that in our case the bottlebrush coating reduces the effective aspect ratio of the DNA. This is in agreement with theoretical estimates that show that, in most cases of practical interest, a bottlebrush coating will lead to a decrease of the effective aspect ratio, whereas, only for bottlebrushes with extremely long side chains at very high grafting densities, a bottlebrush coating may be expected to lead to an increase of the effective aspect ratio.</p>

Topics
  • density
  • impedance spectroscopy
  • simulation
  • crystalline phase
  • strength
  • random
  • bottlebrush
  • small angle x-ray scattering
  • liquid crystal
  • light scattering