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)

  • 2021POSS-enhanced colorless organic/inorganic nanocomposite (CORIN®) for atomic oxygen resistance in low earth orbit20citations
  • 2017Method of aerogel synthesis citations
  • 2014Large-aperture fast multilevel Fresnel zone lenses in glass and ultrathin polymer films for visible and near-infrared imaging applications38citations
  • 2011Polymeric coating for the protection of objectscitations
  • 2011Polymeric coating for protecting objects citations
  • 2011Solar panel with polymeric cover citations
  • 2009Color-matched polymer materials and method for forming the samecitations
  • 2007Anionic synthesis of epoxy end-capped polymers11citations
  • 2004Novel resin modified glass-ionomer cements with improved flexural strength and ease of handling37citations
  • 200331P and 1H NMR studies of the transesterification polymerization of polyphosphonate oligomers28citations

Places of action

Chart of shared publication
Poe, Garrett D.
1 / 1 shared
Seltzer, Aaron
1 / 1 shared
Steadfast, Daniel
1 / 1 shared
Hackett, James
1 / 1 shared
Dixit, Shamusundar N.
1 / 1 shared
Debruyckere, Michael
1 / 1 shared
Britten, Jerald A.
1 / 1 shared
Domber, Jeanette L.
1 / 1 shared
Patrick, Brian
1 / 1 shared
Atcheson, Paul D.
1 / 1 shared
Ji, Haining
1 / 1 shared
Dadmun, Mark
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Nonidez, William K.
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Kilbey, S. Michael
1 / 1 shared
Smith, Grant D.
1 / 1 shared
Mays, Jimmy W.
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Advincula, Rigoberto C.
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Wu, Wei
1 / 4 shared
Puckett, Aaron D.
1 / 1 shared
Xie, Dong
1 / 1 shared
Myrex, R. Dustan
1 / 1 shared
Wright, Young-Jin
1 / 1 shared
Dees, Jennifer
1 / 1 shared
Bharara, P. C.
1 / 1 shared
Byrd, Houston
1 / 1 shared
Branham, Keith E.
1 / 1 shared
Gray, Gary
1 / 1 shared
Chart of publication period
2021
2017
2014
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Co-Authors (by relevance)

  • Poe, Garrett D.
  • Seltzer, Aaron
  • Steadfast, Daniel
  • Hackett, James
  • Dixit, Shamusundar N.
  • Debruyckere, Michael
  • Britten, Jerald A.
  • Domber, Jeanette L.
  • Patrick, Brian
  • Atcheson, Paul D.
  • Ji, Haining
  • Dadmun, Mark
  • Nonidez, William K.
  • Kilbey, S. Michael
  • Smith, Grant D.
  • Mays, Jimmy W.
  • Advincula, Rigoberto C.
  • Wu, Wei
  • Puckett, Aaron D.
  • Xie, Dong
  • Myrex, R. Dustan
  • Wright, Young-Jin
  • Dees, Jennifer
  • Bharara, P. C.
  • Byrd, Houston
  • Branham, Keith E.
  • Gray, Gary
OrganizationsLocationPeople

article

Anionic synthesis of epoxy end-capped polymers

  • Ji, Haining
  • Dadmun, Mark
  • Nonidez, William K.
  • Kilbey, S. Michael
  • Farmer, Brandon
  • Smith, Grant D.
  • Mays, Jimmy W.
  • Advincula, Rigoberto C.
Abstract

The reaction of living anions of polystyrene (PS) or poly(methyl methacrylate) (PMMA) with epibromohydrin for the synthesis of well-defined epoxy end-functionalized polymers is reported. Polyanions were reacted with an excess of epibromohydrin in tetrahydrofuran (THF) at -78°C. The functionalities of the resulting polymers were analyzed by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS), NMR, and size exclusion chromatography (SEC). The epoxy end groups were reacted with 1,1-diphenyl- hexyllithium, and MALDI-TOF MS and NMR before and after this chemical modification were used to determine the presence of the epoxy end groups. The presence of the epoxy end group was confirmed by anionically polymerizing ethylene oxide from these epoxy end group. The formation of a block copolymer due to the epoxy end groups was proved by SEC analysis. The combined MALDI-TOF MS, 1 H NMR, and SEC results indicate that epoxy end-capped PS was obtained in quantitative yield. The method was extended to the synthesis of epoxy end-capped PMMA. With this polymer the extent of end-functionalization was high but not quantitative, with non-dimeric byproducts detected by MALDI-TOF MS.

Topics
  • impedance spectroscopy
  • copolymer
  • size-exclusion chromatography
  • Nuclear Magnetic Resonance spectroscopy
  • block copolymer
  • functionalization
  • matrix-assisted laser desorption–ionisation
  • spectrometry
  • time-of-flight mass spectrometry