4.6 Article

Synthesis of Structurally Varied 1,3-Disiloxanediols and Their Activity as Anion-Binding Catalysts

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 22, Issue 51, Pages 18349-18353

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201604103

Keywords

anion-binding; hydrogen bonds; organocatalysis; self-assembly; silanol

Funding

  1. National Science Foundation [CHE-0847358, CHE-1363375]
  2. UC Davis Borge Fellowship
  3. Direct For Mathematical & Physical Scien
  4. Division Of Chemistry [1363375] Funding Source: National Science Foundation

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A series of new 1,3-disiloxanediols has been synthesized, including naphthyl-substituted and unsymmetrical siloxanes, and demonstrated as a new class of anion-binding catalysts. In the absence of anions, diffusion-ordered spectroscopy (DOSY) displays self-association of 1,3-disiloxanediols through hydrogen-bonding interactions. Binding constants determined for 1,3-disiloxanediol catalysts indicate strong hydrogen-bonding and anion-binding abilities with unsymmetrical siloxanes displaying different hydrogen-bonding abilities for each silanol group.

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