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Abstract
The reaction of N-heterocyclic carbenes with polyaminoboranes [MeNH-BH2](n) or [NH2-BH2](n) at 20 degrees C led to depolymerisation and the formation of labile, monomeric aminoborane-NHC adducts, RNH-BH2-NHC (R = Me or H); a similar NHC adduct of Ph2N=BCl2 was characterized by single crystal X-ray diffraction.
| Original language | English |
|---|---|
| Pages (from-to) | 9098-9100 |
| Number of pages | 3 |
| Journal | Chemical Communications |
| Volume | 49 |
| Issue number | 80 |
| DOIs | |
| Publication status | Published - 2013 |
Keywords
- MOLECULAR-WEIGHT POLYAMINOBORANES
- AMINE-BORANE ADDUCTS
- AMMONIA-BORANE
- HYDROGEN-TRANSFER
- PHOSPHINE-BORANE
- DEHYDROGENATION
- CHEMISTRY
- MECHANISM
- PRECURSOR
- STORAGE
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Dive into the research topics of 'Polyaminoborane main chain scission using N-heterocyclic carbenes; formation of donor-stabilised monomeric aminoboranes'. Together they form a unique fingerprint.Projects
- 1 Finished
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Catalytic Dehydrocoupling of Amine-Borane Adducts: A Route to Polyaminoboranes, Boron-Nitrogen Analogues of Polyolefins
Manners, I. (Principal Investigator)
1/08/10 → 1/02/14
Project: Research
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