Benzene, 1-ethynyl-4-(phenylethynyl)-

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CAS: 92866-00-7
MF: C16H10
MW: 202.2506
Synonyms: Benzene, 1-ethynyl-4-(phenylethynyl)-

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Jean-Luc Bredas

Georgia Institute of Technology
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Michael D. Hopkins

The University of Chicago
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Marcin Ptaszek

University of Maryland
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Jonathan S. Lindsey

North Carolina State University
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Kirk S. Schanze

University of Florida
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Co-reporter: Abigail H. Shelton, Randi S. Price, Luisa Brokmann, Barbara Dettlaff, and Kirk S. Schanze
pp: 7867
Publication Date(Web):July 29, 2013
DOI: 10.1021/am401834f
We report three platinum acetylide acrylate monomers containing known two-photon absorption (TPA) chromophores and their covalent incorporation into polymers via free radical polymerization with methyl methacrylate. The photophysical properties of the platinum acetylide monomers and resulting poly(methyl methacrylate) (PMMA) copolymers were investigated to determine if the one- and two-photon photophysical properties of the chromophores were maintained in the copolymers. The photophysical properties of the series of copolymers were studied in solution and solid state with minimum shifts exhibited in the ground state absorption, photoluminescence, and triplet–triplet transient absorption spectra. The polymer films displayed markedly stronger phosphorescence and longer triplet excited state lifetimes than the polymers in solution or the monomers. The incorporation of the platinum acetylide chromophores into the PMMA copolymers allows the materials to be cast as thin films or into free-standing monoliths. Films with ∼3.6 μm in thickness and monoliths with 1 mm path length were fabricated and examined. The nonlinear absorption responses of the polymers in solution were measured via the nanosecond z-scan method, and the solid state polymer monoliths were measured via nonlinear transmittance. Both measurements indicate that the polymers exhibited strong transmittance attenuation at input pulse energies exceeding 100 μJ.Keywords: nonlinear absorption; platinum acetylide; PMMA; polymer; z-scan;

David Lee Phillips

The University of Hong Kong
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