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Interpnictogen cations: exploring new vistas in coordination chemistry
Alasdair P M Robertson1, Paul A Gray, Neil Burford
1Department of Chemistry, University of Victoria, Victoria, BC V8W 3V6 (Canada).
Pnictine derivatives act as Lewis acids or bases, forming complexes with p-block elements. This review explores new coordination chemistry extending from transition metals to p-block elements, focusing on enhanced Lewis acidity.
Area of Science:
- Inorganic Chemistry
- Coordination Chemistry
- P-block Element Chemistry
Background:
- Pnictine derivatives exhibit dual Lewis acid/base behavior.
- Amines and phosphines are common ligands for transition metals and p-block Lewis acids.
- Pnictogen-centered acceptors are key in coordination chemistry.
Purpose of the Study:
- To review recent advancements in pnictogen coordination chemistry.
- To explore the extension of coordination chemistry into the p-block.
- To highlight compounds with enhanced Lewis acidity and homoatomic bonding.
Main Methods:
- Review of literature on pnictine derivatives and p-block Lewis acids.
- Analysis of coordination compounds involving pnictogen centers.
- Discussion of factors influencing Lewis acidity, such as cationic charge.
Main Results:
- Pnictine derivatives can function as both electron donors and acceptors.
- Coordination complexes with p-block Lewis acids, particularly pnictogen-centered ones, have been developed.
- Introduction of cationic charge enhances Lewis acidity of pnictogen centers.
- Compounds with homoatomic coordinate bonding (Pn-Pn and Pn-Pn') and lone pairs at acceptor centers have been synthesized.
Conclusions:
- Coordination chemistry is systematically expanding from transition metals to the p-block.
- Enhanced Lewis acidity in pnictogen centers opens new avenues for complex formation.
- Homoatomic bonding in pnictogen complexes offers unique electronic properties and reactivity.
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