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Complexes of a Frustrated Lewis Pair-Supported P(-1) Ligand
Brandon L Frenette1, Michael J Ferguson1, Eric Rivard1
1Department of Chemistry, University of Alberta, 11227 Saskatchewan Dr. NW, Edmonton, Alberta, T6G 2G2, Canada.
Researchers developed novel metal phosphide complexes using an intramolecular frustrated Lewis pair (FLP) ligand. This work introduces new P(-1) ligand chemistry and unique metal-phosphorus bonding insights.
Area of Science:
- Organometallic Chemistry
- Main Group Chemistry
- Inorganic Synthesis
Background:
- Frustrated Lewis pairs (FLPs) enable unique reactivity.
- Low-valent phosphorus (P(-1)) ligands are synthetically challenging.
- Metal phosphides are important materials and catalysts.
Purpose of the Study:
- To synthesize and characterize novel metal complexes supported by an intramolecular FLP.
- To explore the reactivity of a P(-1) ligand with zinc and other metals.
- To investigate new routes to metal phosphide species and phosphorus-containing compounds.
Main Methods:
- Synthesis of a monomeric zinc bis(phosphido) complex.
- Transmetallation reactions to form tellurium and phosphorus complexes.
- In situ reduction of PCl3 with FLP ligand.
- Density Functional Theory (DFT) calculations.
Main Results:
- First monomeric zinc bis(phosphido) complex synthesized.
- New tellurium bis(phosphido) complex and PPCl2 adduct formed via transmetallation.
- Direct synthesis of PPCl2 adduct from PCl3 reduction.
- Characterization of a cobalt(-1) phosphaborene complex isoelectronic to olefins.
Conclusions:
- The intramolecular FLP ligand provides access to diverse low-valent phosphorus metal complexes.
- These complexes offer new avenues for studying metal-phosphorus bonding.
- The developed chemistry expands the scope of FLP-supported P(-1) ligand applications.
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