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 (6/6 displayed)

  • 2013Complexes between poly(amido amine) dendrimers and poly(methacrlyic acid): insight from molecular dynamics simulations3citations
  • 2013Structure and dynamics of hyperbranched polymer/layered silicate nanocomposites41citations
  • 2012Conformational effects in non-stoichiometric complexes of two hyperbranched molecules with a linear polyelectrolyte9citations
  • 2012Conformational effects in non-stoichiometric complexes of two hyperbranched molecules with a linear polyelectrolytecitations
  • 2007Effects of topology and size on statics and dynamics of complexes of hyperbranched polymers with linear polyelectrolytes24citations
  • 2006Local polymer dynamics under strong connectivity constraints: The dendrimer case13citations

Places of action

Chart of shared publication
Laurini, Erik
1 / 9 shared
Tanis, I.
2 / 3 shared
Posocco, Paola
1 / 16 shared
Pricl, Sabrina
1 / 26 shared
Karageorgaki, C.
1 / 1 shared
Frick, B.
1 / 8 shared
Anastasiadis, S. H.
1 / 1 shared
Tragoudaras, D.
1 / 1 shared
Fotiadou, S.
1 / 1 shared
Chrissopoulou, K.
1 / 1 shared
Darinskii, A. A.
1 / 7 shared
Lyulin, Alexey V.
3 / 49 shared
Larin, S. V.
1 / 17 shared
Dalakoglou, G. K.
2 / 2 shared
Lyulin, S. V.
2 / 24 shared
Darinskiǐ, Aa
1 / 3 shared
Larin, Sergey V.
1 / 6 shared
Lyulin, A. Alexey
1 / 3 shared
Dalakoglou, Gk
1 / 1 shared
Lyulin, Sergey V.
1 / 8 shared
Chart of publication period
2013
2012
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Co-Authors (by relevance)

  • Laurini, Erik
  • Tanis, I.
  • Posocco, Paola
  • Pricl, Sabrina
  • Karageorgaki, C.
  • Frick, B.
  • Anastasiadis, S. H.
  • Tragoudaras, D.
  • Fotiadou, S.
  • Chrissopoulou, K.
  • Darinskii, A. A.
  • Lyulin, Alexey V.
  • Larin, S. V.
  • Dalakoglou, G. K.
  • Lyulin, S. V.
  • Darinskiǐ, Aa
  • Larin, Sergey V.
  • Lyulin, A. Alexey
  • Dalakoglou, Gk
  • Lyulin, Sergey V.
OrganizationsLocationPeople

article

Conformational effects in non-stoichiometric complexes of two hyperbranched molecules with a linear polyelectrolyte

  • Darinskii, A. A.
  • Lyulin, Alexey V.
  • Karatasos, K.
  • Larin, S. V.
  • Dalakoglou, G. K.
  • Lyulin, S. V.
Abstract

We report results from Brownian dynamics computer simulations of systems comprised by two terminally charged hyperbranched molecules preferentially branched in the periphery, with an oppositely charged linear chain of varying length. Comparison of the findings from the present study to stoichiometric counterparts and to analogous dendrimer-based complexes, reveal that the presence of the second hyperbranched molecule incurs significant changes in the conformational characteristics of both components of the complex. Instead of step-like changes in the average size and shape of the hyperbranched component that were noted in the previously studied stoichiometric systems, a rather smooth change is observed upon increase of the length of the linear component. In addition, a markedly different behavior is also noticed in the conformational characteristics of the linear chain when compared to that in similar dendrimer-based systems. The above findings are consistent with the higher degree of deformability of the peripherally branched molecules which allow appropriate rearrangements in shape in order to accommodate the favorable Coulombic interactions between the two components of the complex. This behavior offers new insight towards the design of more efficient hyperbranched-based systems which can take advantage of the multifunctionality and the structural properties of the highly branched polymer components.

Topics
  • impedance spectroscopy
  • polymer
  • simulation
  • dendrimer