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EntityQ5272284· pop 6· linked from 6 articles

Diborynes are low-valent main-group compounds that contain a formal boron–boron triple bond (B≡B). In most isolable examples, the B≡B unit is stabilized by strong σ-donor ligands and is often described as L→B≡B←L; N-heterocyclic carbenes (NHCs) are among the most common supporting ligands. Structurally, many diborynes exhibit an approximately linear B–B ligand arrangement, which makes them a useful point of comparison to other main-group multiple-bond systems where π-bonding can be harder to sustain.

~18 min read

Encyclopedic overview

12 sections
Contents
  • Synthesis
  • First reported synthetic method
  • Synthetic developments
  • Reactivity
  • [[Lewis acids and bases|Lewis acid-base]] adducts
  • Bond strength and bonding analysis
  • Chalcogen insertion reactions
  • [[Hydroboration]] and formation of boron clusters
  • Carbon monoxide binding and coupling
  • Photophysical properties
  • Conclusion
  • References

Diborynes are low-valent main-group compounds that contain a formal boron–boron triple bond (B≡B). In most isolable examples, the B≡B unit is stabilized by strong σ-donor ligands and is often described as L→B≡B←L; N-heterocyclic carbenes (NHCs) are among the most common supporting ligands. Structurally, many diborynes exhibit an approximately linear B–B ligand arrangement, which makes them a useful point of comparison to other main-group multiple-bond systems where π-bonding can be harder to sustain.

Their bonding description has been examined extensively. While the B≡B linkage is commonly discussed in terms of a σ bond and two π interactions, experimental and theoretical work has emphasized that ligand donation plays an important role in stabilizing this framework, and that the B–B multiple bond is generally weaker than the C≡C bond in alkynes. At the same time, diborynes can retain low-lying acceptor character at boron, which helps explain their tendency to engage in donor–acceptor interactions and their broader reactivity patterns.

Excerpted from Wikipedia’s “diboryne” article, available under the CC BY-SA 4.0 licence.

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