Abstract
The first example of a stable zincagermylene,:Ge(TBoN)(ZnL∗) (TBoN = N(SiMe3){B(DipNCH)2}, Dip = C6H3Pri2-2,6; L∗ = -N{C6H2[C(H)Ph2]2Me-2,6,4}(SiPri3)) is prepared and shown to have unprecedented reactivity for a germylene, with respect to the activation of dihydrogen. Computational analyses point towards this being partially derived from the electron releasing nature of the amido-zinc fragment, which leads to a narrowing of the HOMO-LUMO gap in the compound.
| Original language | English |
|---|---|
| Pages (from-to) | 12692-12695 |
| Number of pages | 4 |
| Journal | Chemical Communications |
| Volume | 53 |
| Issue number | 94 |
| DOIs | |
| Publication status | Published - 2017 |
| Externally published | Yes |
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