4.8 Article

Reversible Isomerizations between 1,4-Digermabenzenes and 1,4-Digerma-Dewar-benzenes: Air-Stable Activators for Small Molecules

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 141, Issue 6, Pages 2263-2267

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.9b00129

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Funding

  1. JSPS KAKENHI from MEXT (Japan) [JP15H03777, JP15K13640]
  2. Collaborative Research Program of the Institute for Chemical Research, Kyoto University
  3. DAIKO FOUNDATION
  4. JURC
  5. IRCCS
  6. KURCA (Kyoto University)
  7. [JP16J05501]

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The first examples of stable, crystalline, and air-sensitive 1,4-digermabenzenes were isolated. These species photochemically isomerize into the corresponding air-stable digerma-Dewar-benzenes. More importantly, alkyl-substituted Dewar-type-1,4-digermabenzenes can be considered as reversible air-stable activators for small molecules such as dihydrogen, carbon dioxide, and acetylene at room temperature. The regeneration of these activators can be accomplished via a thermal retro-isomerization that affords the corresponding 1,4-digermabenzenes.

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