4.6 Article

New linker systems for superior immobilized catalysts

Journal

NEW JOURNAL OF CHEMISTRY
Volume 34, Issue 12, Pages 2729-2731

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c0nj00482k

Keywords

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Funding

  1. National Science Foundation [CHE-0911207]
  2. Welch Foundation, Texas AM University [A-1706]
  3. DFG [SFB 623]
  4. Division Of Chemistry [0911207] Funding Source: National Science Foundation

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The rigid linkers E(p-C6H4PPh2)(4) (E = Si, Sn) have been synthesized from the corresponding precursors E(p-C6H4Br)(4) and immobilized by forming one (E = Si) or three (E = Sn) phosphonium groups that are attached to the silica support by electrostatic interactions. The remaining unquaternized phosphines are coordinated to Wilkinson-type Rh complexes. The catalyst immobilized by the rigid scaffold with three surface-bound phosphonium groups (E = Sn) displays superior catalytic activity and lifetime with respect to the hydrogenation of dodecene. This catalyst can be recycled 30 times in a batchwise manner under standardized conditions.

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