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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Materials Map under construction

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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1.080 Topics available

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (12/12 displayed)

  • 2022Toughening Polylactide with Graft-Block Polymers16citations
  • 2020Spatial Control of the Self-assembled Block Copolymer Domain Orientation and Alignment on Photopatterned Surfaces8citations
  • 2020Unusual Thermal Properties of Certain Poly(3,5-disubstituted styrene)s3citations
  • 2020Grain Growth and Coarsening Dynamics in a Compositionally Asymmetric Block Copolymer Revealed by X-ray Photon Correlation Spectroscopy6citations
  • 2019Physical Aging of Polylactide-Based Graft Block Polymers46citations
  • 2018Dynamics of a Supercooled Disordered Sphere-Forming Diblock Copolymer as Determined by X-ray Photon Correlation and Dynamic Mechanical Spectroscopies7citations
  • 2017Directed Self-Assembly and Pattern Transfer of Five Nanometer Block Copolymer Lamellae112citations
  • 2016A Hybrid Chemo-/Grapho-Epitaxial Alignment Strategy for Defect Reduction in Sub-10 nm Directed Self-Assembly of Silicon-Containing Block Copolymers27citations
  • 2016Orthogonally Spin-Coated Bilayer Films for Photochemical Immobilization and Patterning of Sub-10-Nanometer Polymer Monolayers5citations
  • 2016Pattern Transfer of Sub-10 nm Features via Tin-Containing Block Copolymers22citations
  • 2016Synthesis and characterization of Si-containing block co-polymers with resolution beyond 10 nm4citations
  • 2015Modulating Solubility and Enhancing Reactivity of Photo-Cross-Linkable Poly(styrene sulfonyl azide-alt-maleic anhydride) Thin Films8citations

Places of action

Chart of shared publication
Lee, Bongjoon
2 / 5 shared
Schibur, Haley J.
2 / 2 shared
Bates, Frank S.
4 / 90 shared
Cheng, Joy Y.
1 / 1 shared
Blachut, Gregory
5 / 7 shared
Asano, Yusuke
5 / 5 shared
Kline, R. Joseph
1 / 3 shared
Lynd, Nathaniel A.
2 / 7 shared
Sanders, Daniel P.
1 / 1 shared
Bates, Christopher M.
3 / 5 shared
Sunday, Daniel F.
1 / 1 shared
Carlson, Matthew C.
2 / 2 shared
Willson, C. Grant
5 / 8 shared
Callan, Devon H.
1 / 1 shared
Rettner, Charles T.
1 / 2 shared
Liu, Philip
1 / 1 shared
Baiz, Carlos R.
1 / 1 shared
Kim, Ji Yeon
1 / 2 shared
Zhu, Qingjun
1 / 3 shared
Mapesa, Emmanuel U.
1 / 1 shared
Sangoro, Joshua R.
1 / 3 shared
Ha, Heonjoo
1 / 6 shared
Cater, Henry L.
1 / 1 shared
Koh, Jai Hyun
1 / 2 shared
Kim, Sung Soo
1 / 4 shared
Lewis, Ronald M.
2 / 5 shared
Jackson, Grayson L.
2 / 2 shared
Narayanan, Suresh
2 / 5 shared
Zografos, Aristotelis
1 / 4 shared
Haugan, Ingrid N.
1 / 1 shared
Jones, Seamus D.
1 / 1 shared
Beech, Haley K.
1 / 1 shared
Yang, Xiaomin
1 / 1 shared
Sirard, Stephen M.
3 / 3 shared
Mallavarapu, Akhila
1 / 1 shared
Someya, Yasunobu
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Lane, Austin P.
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Dinhobl, Andrew M.
2 / 2 shared
Gronheid, Roel
1 / 4 shared
Durand, William J.
2 / 3 shared
Hymes, Diane
1 / 1 shared
Janes, Dustin W.
2 / 10 shared
Kim, Chae Bin
1 / 9 shared
Gurer, Emir
1 / 1 shared
Strahan, Jeffrey R.
1 / 1 shared
Mori, Kazunori
1 / 1 shared
Grantwillson, C.
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Sirard, Stephen
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Carroll, Gregory T.
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Saylor, David M.
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Chart of publication period
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2020
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2016
2015

Co-Authors (by relevance)

  • Lee, Bongjoon
  • Schibur, Haley J.
  • Bates, Frank S.
  • Cheng, Joy Y.
  • Blachut, Gregory
  • Asano, Yusuke
  • Kline, R. Joseph
  • Lynd, Nathaniel A.
  • Sanders, Daniel P.
  • Bates, Christopher M.
  • Sunday, Daniel F.
  • Carlson, Matthew C.
  • Willson, C. Grant
  • Callan, Devon H.
  • Rettner, Charles T.
  • Liu, Philip
  • Baiz, Carlos R.
  • Kim, Ji Yeon
  • Zhu, Qingjun
  • Mapesa, Emmanuel U.
  • Sangoro, Joshua R.
  • Ha, Heonjoo
  • Cater, Henry L.
  • Koh, Jai Hyun
  • Kim, Sung Soo
  • Lewis, Ronald M.
  • Jackson, Grayson L.
  • Narayanan, Suresh
  • Zografos, Aristotelis
  • Haugan, Ingrid N.
  • Jones, Seamus D.
  • Beech, Haley K.
  • Yang, Xiaomin
  • Sirard, Stephen M.
  • Mallavarapu, Akhila
  • Someya, Yasunobu
  • Lane, Austin P.
  • Dinhobl, Andrew M.
  • Gronheid, Roel
  • Durand, William J.
  • Hymes, Diane
  • Janes, Dustin W.
  • Kim, Chae Bin
  • Gurer, Emir
  • Strahan, Jeffrey R.
  • Mori, Kazunori
  • Grantwillson, C.
  • Sirard, Stephen
  • Carroll, Gregory T.
  • Saylor, David M.
OrganizationsLocationPeople

article

Modulating Solubility and Enhancing Reactivity of Photo-Cross-Linkable Poly(styrene sulfonyl azide-alt-maleic anhydride) Thin Films

  • Janes, Dustin W.
  • Carroll, Gregory T.
  • Saylor, David M.
  • Maher, Michael J.
Abstract

<p>To formalize our understanding of indiscriminate grafting chemistries as they pertain to cross-linkable polymers and emerging patterning technologies, we designed a new polymer, poly(styrene sulfonyl azide-alt-maleic anhydride) (PSSMA). By modulating its solubility, it can be deposited into smooth, ultrathin films atop polar and nonpolar polymers. Upon heating above 120 °C or exposure to UV light, highly reactive nitrene intermediates are generated from the azide groups which form covalent adducts and cross-link the PSSMA. Azide photolysis and polymer gelation were studied in the context of a statistical model to gain insight into the network outcomes of nitrenes in a polymer film. For every azide group converted to a nitrene in ambient atmosphere, it has an 11% likelihood of grafting to another chain and a 5% chance of causing a scission. These values can be increased over 3-fold by reducing the O<sub>2</sub> content by 85%. Alternatively, the effects of quenching by ground-state O<sub>2</sub> can be mitigated by adding Michler's ketone (MK) to the film. PSSMA/MK blend films possess a 39% (±13) likelihood for grafting and 29% (±10) for scission. The higher ratio of scission to grafting is a consequence of the sensitized azides producing triplet-state nitrenes, which favor hydrogen abstraction. These broadly generalizable considerations will be useful to others who wish to maximize light sensitivity in related polymer systems.</p>

Topics
  • impedance spectroscopy
  • polymer
  • thin film
  • reactive
  • Hydrogen
  • ketone
  • quenching
  • gelation