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 (7/7 displayed)

  • 2024From generation to collection – impact of deposition temperature on charge carrier dynamics of high-performance vacuum-processed organic solar cells4citations
  • 2023Synthesis and characterization of poly(1,2,3-triazole)s with inherent high sulfur content for optical applicationscitations
  • 2023Synthesis and characterization of poly(1,2,3‐triazole)s with inherent high sulfur content for optical applications6citations
  • 2019Amphiphilic Block Copolymer Micelles in Selective Solvents: The Effect of Solvent Selectivity on Micelle Formation25citations
  • 2019Amphiphilic block copolymer micelles in selective solvents: The effect of solvent selectivity on micelle formationcitations
  • 2018Bioinspired thermoresponsive nanoscaled coatings: Tailor-made polymer brushes with bioconjugated arginine-glycine-aspartic acid-peptides5citations
  • 2010Design of new responsive materials based on functional polymer brushescitations

Places of action

Chart of shared publication
Riede, Moritz
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Mukherjee, Subhrangsu
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Wu, Jiaying
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Heger, Julian Eliah
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Mackenzie, Roderick C. I.
1 / 6 shared
Pfeiffer, Martin
1 / 1 shared
Müller-Buschbaum, Peter
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Ramirez, Ivan
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Durrant, James Robert
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Kaienburg, Pascal
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Voit, Brigitte
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Komber, Hartmut
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Banerjee, Susanta
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Mazumder, Kajari
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Horechyy, Andriy
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Kumar, Labeesh
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Nandan, Bhanu
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Uhlmann, Petra
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Stamm, Manfred
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Welzel, Petra B.
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Müller, Martin
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Guskova, Olga
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Psarra, Evmorfia
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König, Ulla
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Chart of publication period
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2023
2019
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Co-Authors (by relevance)

  • Riede, Moritz
  • Mukherjee, Subhrangsu
  • Wu, Jiaying
  • Heger, Julian Eliah
  • Mackenzie, Roderick C. I.
  • Pfeiffer, Martin
  • Müller-Buschbaum, Peter
  • Ramirez, Ivan
  • Durrant, James Robert
  • Dong, Yifan
  • Ade, Harald
  • Kaienburg, Pascal
  • Hosseini, Seyed Mehrdad
  • Pacalaj, Richard Adam
  • Voit, Brigitte
  • Komber, Hartmut
  • Banerjee, Susanta
  • Mazumder, Kajari
  • Horechyy, Andriy
  • Kumar, Labeesh
  • Nandan, Bhanu
  • Uhlmann, Petra
  • Fery, Andreas
  • Eichhorn, Klaus-Jochen
  • Stamm, Manfred
  • Welzel, Petra B.
  • Müller, Martin
  • Guskova, Olga
  • Psarra, Evmorfia
  • König, Ulla
OrganizationsLocationPeople

article

Synthesis and characterization of poly(1,2,3‐triazole)s with inherent high sulfur content for optical applications

  • Bittrich, Eva
  • Komber, Hartmut
  • Mazumder, Kajari
Abstract

<jats:title>Abstract</jats:title><jats:p>The synthesis of solution‐processable sulfur‐containing polytriazoles for optoelectronic applications is a relatively less explored domain in polymer research. The synthesis of novel bifunctional (DA) and trifunctional (TA) azido‐monomers with inherent high sulfur content and of organo‐soluble high refractive index poly(1,2,3‐triazole)s using the azido‐monomers via Cu(I) assisted click polymerization reactions are reported in this work. The azido‐monomers were synthesized by the conversion of previously reported amine‐functionalized compounds to azides using azidotrimethylsilane in a polar aprotic solvent. Dialkyne monomers were also synthesized and reacted with the azides to prepare a series of five linear and two hyperbranched poly(1,2,3‐triazole)s. Fourier transform infrared spectroscopy, nuclear magnetic resonance spectroscopy, differential scanning calorimetry and thermogravimetric analysis were used to characterize the synthesized polymers. It was also demonstrated that the use of the trifunctional azide in optimized conditions resulted in increased solubility of an otherwise insoluble linear poly(1,2,3‐triazole). The optical characterization of the polymers was carried out on thin polymer films with thickness in the nanometer range, which were successfully prepared by spin‐coating on silicon wafers. It was found that the increase in the sulfur and aromatic content in the polymer backbone successfully increased the refractive index of the polymers up to 1.743 at 589 nm.</jats:p>

Topics
  • impedance spectroscopy
  • compound
  • polymer
  • laser emission spectroscopy
  • thermogravimetry
  • Silicon
  • differential scanning calorimetry
  • Nuclear Magnetic Resonance spectroscopy
  • amine
  • Fourier transform infrared spectroscopy