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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Publications (1/1 displayed)

  • 2000Occurrence of radical cation localization in chemically modified poly(methylphenylsilane): Poly(methylphenyl-co-4-dimethylaminophenylmethylsilane)s and poly (methylphenyl-co-4-bromophenylmethylsilane)s9citations

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Jenneskens, Lw
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Cleij, Thomas J.
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2000

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  • Jenneskens, Lw
  • Cleij, Thomas J.
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article

Occurrence of radical cation localization in chemically modified poly(methylphenylsilane): Poly(methylphenyl-co-4-dimethylaminophenylmethylsilane)s and poly (methylphenyl-co-4-bromophenylmethylsilane)s

  • Jenneskens, Lw
  • King, Jk
  • Cleij, Thomas J.
Abstract

Chemical modification of poly(methylphenylsilane) 1 using triflate chemistry gave two series of random copolymers with different composition ratios, viz., poly(methylphenyl-co-4-dimethylaminophenylmethylsilane)s 3-7 and poly(methylphenyl-co-4-bromophenylmethylsilane)s 8-9. The optical and electronic properties of the copolymers have been studied and are compared with those of the homopolymers 1 and poly(4-dimethylaminophenyl-methylsilane) 2. Electrochemical measurements in THF/LiClO4 give strong evidence that, in marked contrast to the results observed for 1 and 2, the onset of oxidation (V-i) of 3-7 and 8-9, respectively, does not represent the silicon backbone valence band. Instead, in these copolymers, a mixture of decoupled electronic domains exists of which those possessing the lowest V-i govern the electrochemical response. As a consequence, the radical cations become confined, i.e. localization occurs. This interpretation is further supported by fluorescence emission spectroscopy, the presence of a confined exciton is indicated by the appearance of an additional broad band for the copolymers. Remarkably, copolymers with optical and electronic properties comparable to those of 3-7 are also accessible by (reversible) protonation of the 4-dimethylamino substituents of 2.

Topics
  • impedance spectroscopy
  • Silicon
  • random
  • copolymer
  • homopolymer
  • random copolymer