4.6 Article

Prediction of Boron-Boron Triple-Bond Polymers Stabilized by Janus-Type Bis(N-heterocyclic) Carbenes

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 21, Issue 21, Pages 7814-7819

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201500241

Keywords

boron; carbenes; density-functional calculations; main-group elements; polymers

Funding

  1. CNPq
  2. CAPES
  3. FAPERJ
  4. INOMAT

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A class of polymeric compounds containing boron-boron triple bonds stabilized by N-heterocyclic biscarbenes is proposed. Since a triply bonded B-2 is related to its third excited state, the predicted macromolecule would be composed by several units of an electronically excited first-row homonuclear dimer. Moreover, it is shown that the replacement of biscarbene with N-2 or CO as spacers could change the bonding profile of the boron-boron units to a cumulene-like structure. Based on these results, different types of diboryne polymers are proposed, which could lead to an unprecedented set of boron materials with distinct physical properties. The novel diboryne macromolecules could be synthesized by the reaction of Janus-type biscarbenes with tetrabromodiborane, B2Br4, and sodium naphthalenide, [Na(C10H8)], similarly to Braunschweig's work on the room temperature stable boron-boron triple bond compounds (Science, 2012, 336, 1420).

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