A New Porous Reaction Layer for Developing Addressable Molecular Libraries

Libo Hu, Jennifer L. Bartels, Jeremy W. Bartels, Karl Maurer and Kevin D. Moeller*
Department of Chemistry, Washington University in St. Louis, St. Louis, Missouri 63130, and CombiMatrix Corporation, 6500 Harbor Heights Parkway, Suite 301, Mukilteo, Washington 98275
J. Am. Chem. Soc., 2009, 131 (46), pp 16638–16639
DOI: 10.1021/ja907000m
Publication Date (Web): October 29, 2009
Copyright © 2009 American Chemical Society
moeller@wustl.edu, †

Washington University in St. Louis.

, ‡

CombiMatrix Corporation.

Abstract

Abstract Image

A new diblock copolymer-derived porous reaction layer for microelectrode arrays has been tested for its stability and its compatibility with both site-selective synthesis and electrochemical signaling experiments. The diblock copolymer consisted of a cinnamoyl-substituted polymethacrylate block for attachment to the surface of the array and a bromo-substituted polystyrene block for selective functionalization of the surface proximal to microelectrodes in the array. Site-selective Suzuki, Heck, and Cu(I)-coupling reactions were all performed on the new reaction layer along with electrochemical impedance studies.

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This article has been cited by 7 ACS Journal articles (5 most recent appear below).

  • Cover Image

    Building Addressable Libraries: Amino Acid Derived Fluorescent Linkers

    Takamasa Tanabe, Bo Bi, Libo Hu, Karl Maurer, and Kevin D. Moeller
    Langmuir2012 28 (3), 1689-1693
    • Building Addressable Libraries: Amino Acid Derived Fluorescent Linkers

      Takamasa Tanabe, Bo Bi, Libo Hu, Karl Maurer, and Kevin D. Moeller
      Langmuir2012 28 (3), 1689-1693

      A new amino acid derived fluorescent linker for attaching molecules to the surface of a microelectrode array has been developed. Molecules to be monitored on an array are attached to the C-terminus of the linker, the N-terminus is then used to attach the ...

  • Cover Image

    Site-Selective, Cleavable Linkers: Quality Control and the Characterization of Small Molecules on Microelectrode Arrays

    Bo Bi, Richard Y.-C. Huang, Karl Maurer, Ceng Chen, and Kevin D. Moeller
    The Journal of Organic Chemistry2011 76 (21), 9053-9059
    • Site-Selective, Cleavable Linkers: Quality Control and the Characterization of Small Molecules on Microelectrode Arrays

      Bo Bi, Richard Y.-C. Huang, Karl Maurer, Ceng Chen, and Kevin D. Moeller
      The Journal of Organic Chemistry2011 76 (21), 9053-9059

      A “safety-catch” linker strategy has been used to release a portion of the products of a Diels–Alder reaction conducted on a microelectrode array for characterization of stereochemistry. The attachment and cleavage of organic compounds from the surface of ...

  • Cover Image

    Site-Selectively Functionalizing Microelectrode Arrays: The Use of Cu(I)-Catalysts

    Jennifer Bartels, Peng Lu, Karl Maurer, Amy V. Walker, and Kevin D. Moeller
    Langmuir2011 Article ASAP
    • Site-Selectively Functionalizing Microelectrode Arrays: The Use of Cu(I)-Catalysts

      Jennifer Bartels, Peng Lu, Karl Maurer, Amy V. Walker, and Kevin D. Moeller
      Langmuir2011 Article ASAP

      Site-selective Cu(I)-catalyzed reactions have been developed on microelectrode arrays. The reactions are confined to preselected electrodes on the arrays using oxygen as the confining agent. Conditions initially developed for the Cu(I)-catalyzed click ...

  • Cover Image

    Building Addressable Libraries: The Use of “Safety-Catch” Linkers on Microelectrode Arrays

    Bo Bi, Karl Maurer, and Kevin D. Moeller
    Journal of the American Chemical Society2010 132 (49), 17405-17407
    • Building Addressable Libraries: The Use of “Safety-Catch” Linkers on Microelectrode Arrays

      Bo Bi, Karl Maurer, and Kevin D. Moeller
      Journal of the American Chemical Society2010 132 (49), 17405-17407

      A “safety-catch” linker strategy has been used to site-selectively cleave and characterize molecules from a microelectrode array. The linkers are attached to the array by means of an ester and contain either a protected amine or protected alcohol ...

  • Cover Image

    Building Addressable Libraries: Site-Selective Use of Pd(0) Catalysts on Microelectrode Arrays

    Libo Hu, Melissae Stuart, Jun Tian, Karl Maurer, and Kevin D. Moeller
    Journal of the American Chemical Society2010 132 (46), 16610-16616
    • Building Addressable Libraries: Site-Selective Use of Pd(0) Catalysts on Microelectrode Arrays

      Libo Hu, Melissae Stuart, Jun Tian, Karl Maurer, and Kevin D. Moeller
      Journal of the American Chemical Society2010 132 (46), 16610-16616

      Site-selective Pd(0)-catalyzed reactions have been developed to functionalize a microelectrode array. Heck, Suzuki, and allylation reactions have all been accomplished. The reactions are compatible with both 1K and 12K arrays and work best when a nonsugar ...

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History

  • Published In Issue November 25, 2009
  • Article ASAPOctober 29, 2009
  • Received: August 18, 2009

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