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Synthesis of a Thiol Building Block for the Crystallization of a Semiconducting Gyroidal Metal-sulfur Framework
Published on: April 9, 2018
Coordination chemistry of poly(thioether)borate ligands
1Department of Chemistry and Biochemistry, University of Delaware, Newark, DE 19716, United States.
Summary
Tris(thioether)borate ligands offer versatile coordination chemistry with transition metals. These tripodal ligands are key in modeling metalloenzymes and activating small molecules like dioxygen and sulfur.
Area of Science:
- Inorganic Chemistry
- Organometallic Chemistry
- Coordination Chemistry
Background:
- Tris(thioether)borate ligands are tripodal ligands featuring highly polarizable thioether donors.
- These ligands have shown significant utility in coordination chemistry, particularly with transition metals.
Purpose of the Study:
- To review the development and applications of tris(thioether)borate ligands.
- To highlight their role in transition metal coordination, metalloenzyme active site modeling, and small molecule activation.
Main Methods:
- Review of existing literature on tris(thioether)borate ligand synthesis and coordination chemistry.
- Focus on complexes involving mid-to-late first-row transition metals (Fe, Ni, Co, Cu).
Main Results:
- Detailed coordination chemistry of iron, nickel, cobalt, and copper with tris(thioether)borate ligands.
- Demonstrated role of thioether substituents in directing complex formation.
- Successful modeling of zinc thiolate protein active sites and exploration of high-spin organometallic chemistry.
Conclusions:
- Tris(thioether)borate ligands are effective in stabilizing various oxidation states, including monovalent Fe, Co, and Ni.
- These complexes exhibit reactivity towards small molecules, such as dioxygen and sulfur activation by monovalent nickel.
- The unique electronic and steric properties of these ligands enable diverse applications in catalysis and bioinorganic chemistry.
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