Covalent grafting of m -phenylene-ethynylene oligomers to oxide surfaces

Justin M Notestein, Christian Canlas, John Siegfried, Jeffrey S. Moore

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Oligomeric phenylene ethynylene is potentially a useful molecule for organic photovoltaics, light emitting diodes, sensor materials, or as intrinsically porous polymers for gas storage and separation. In the former two applications, the organic molecules are supported on an inorganic material for structural support or for charge collection at an electrode. Here, a 12 repeat unit oligomer of m-phenylene ethylene is covalently attached to high surface area and planar oxide supports as an alternate route to materials development, which displays novel properties and applications due to the covalent connection to the surface. Oligomers and model dimers are attached to alkyl-azide decorated surfaces via Cu-catalyzed 1,3-dipolar Huisgen cycloaddition or covalently linked with silane-bearing surfaces via Rh-catalyzed hydrosilylation. Surface structures and densities are verified by FTIR, TGA, transmission UV-visible spectroscopy, N2 physisorption, and transmission electron microscopy. On high-surface-area materials, hydrosilylation routes yield loadings up to 0.09 molecules nm-2, whereas on planar surfaces, densities reach 0.22 molecules nm-2, comparable to the footprint of the extended Tg side groups. Grafted molecules retain the solvation-dependent "folding" behavior of soluble oligomers as determined by solvent- and temperature- dependent photoluminescence spectra of grafted oligomers suspensions. Grafted oligomers can be suspended in liquids in which the oligomers are not intrinsically soluble, demonstrating, for example, that dodecane and decalin have opposite association behavior, in spite of both their very low polarity parameters. Photoluminescence spectra are consistent with coexisting folded and unfolded oligomers when grafted, in contrast with highly cooperative changes in solution. Highly loaded surfaces show significant hysteresis upon heating, suggesting a kinetic as well as thermodynamic solvent effect. Pinene guest molecules enhance folding of the grafted oligomers, demonstrating a responsive adsorbent surface. Having demonstrated proof of concept, covalently grafted oligo(PE) materials are applicable as a new class of tunable adsorbent materials and optoelectronic materials.

Original languageEnglish
Pages (from-to)5319-5327
Number of pages9
JournalChemistry of Materials
Volume22
Issue number18
DOIs
Publication statusPublished - Sep 28 2010

Fingerprint

Oligomers
Oxides
Molecules
Hydrosilylation
Adsorbents
Photoluminescence
Bearings (structural)
Silanes
Physisorption
Azides
Cycloaddition
Solvation
Surface structure
Dimers
Optoelectronic devices
Light emitting diodes
Hysteresis
Suspensions
Polymers
Ethylene

ASJC Scopus subject areas

  • Materials Chemistry
  • Chemical Engineering(all)
  • Chemistry(all)

Cite this

Covalent grafting of m -phenylene-ethynylene oligomers to oxide surfaces. / Notestein, Justin M; Canlas, Christian; Siegfried, John; Moore, Jeffrey S.

In: Chemistry of Materials, Vol. 22, No. 18, 28.09.2010, p. 5319-5327.

Research output: Contribution to journalArticle

Notestein, Justin M ; Canlas, Christian ; Siegfried, John ; Moore, Jeffrey S. / Covalent grafting of m -phenylene-ethynylene oligomers to oxide surfaces. In: Chemistry of Materials. 2010 ; Vol. 22, No. 18. pp. 5319-5327.
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