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Borepin
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thumb|rightBorepins are a class of boron-containing heterocycles used in main group chemistry. They consist of a seven-membered unsaturated ring with a tricoordinate boron in it. Simple borepins are analogues of cycloheptatriene, which is a seven-membered ring containing three carbon-carbon double bonds, each of which contributes 2π electrons for a total of 6π electrons. Unlike other seven-membered systems such as silepins and phosphepins, boron has a vacant p-orbital that can interact with the π and π* orbitals of the cycloheptatriene. This leads to an isoelectronic state akin to that of the
Chemical data
- Formula
- C6H7B
- Molecular weight
- 89.93 g/mol
- IUPAC name
- 1H-borepine
- SMILES
- B1C=CC=CC=C1
- InChIKey
- LYCCRAPWFYEFFC-UHFFFAOYSA-N
- Polar surface area
- 0 Ų
- H-bond donors
- 0
- H-bond acceptors
- 0
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- aromatic compound
- Mass
- 90.064080624
Show 2 more facts
- canonical SMILES
- B1C=CC=CC=C1
- chemical formula
- C₆H₇B
Sources (2)
via Wikidata · CC0
~12 min read
Encyclopedic overview
11 sectionsContents
- Synthesis
- First reported synthetic method
- Synthetic developments
- Isomerization
- Reactivity
- Lewis acid-base adducts
- Borepin cations, anions, and radicals
- Framework manipulation
- Photophysical properties
- Fluorescence/phosphorescence
- References
thumb|rightBorepins are a class of boron-containing heterocycles used in main group chemistry. They consist of a seven-membered unsaturated ring with a tricoordinate boron in it. Simple borepins are analogues of cycloheptatriene, which is a seven-membered ring containing three carbon-carbon double bonds, each of which contributes 2π electrons for a total of 6π electrons. Unlike other seven-membered systems such as silepins and phosphepins, boron has a vacant p-orbital that can interact with the π and π* orbitals of the cycloheptatriene. This leads to an isoelectronic state akin to that of the tropylium cation, aromatizing the borepin while also allowing it to act as a Lewis acid. The aromaticity of borepin is relatively weak compared to traditional aromatics such as benzene or even cycloheptatriene, which has led to the synthesis of many fused, π-conjugated borepin systems over the years. Simple and complex borepins have been extensively studied more recently due to their high fluorescence and potential applications in technologies like organic light-emitting diodes (OLEDs) and photovoltaic cells.
== Synthesis ==
Excerpted from Wikipedia’s “Borepin” article, available under the CC BY-SA 4.0 licence.