Related Experiment Video
Updated: Feb 8, 2026

08:43
Molten-Salt Synthesis of Complex Metal Oxide Nanoparticles
Published on: October 27, 2018
18.8K
Synthesis of first row transition metal selenomaltol complexes
Michael T Spiegel1, Amanda Hoogerbrugge, Shamus Truksa
1Department of Chemistry and Biochemistry, Baylor University, Waco, Texas 76798, USA. Patrick_Farmer@baylor.edu.
Dalton Transactions (Cambridge, England : 2003)
|June 22, 2018
Summary
Researchers synthesized selenomaltol, a novel chelator, and its metal complexes. These compounds offer new possibilities for unusual O,Se-donor chelates in various applications.
Area of Science:
- Inorganic Chemistry
- Coordination Chemistry
- Organoselenium Chemistry
Background:
- Chelating agents are crucial in coordination chemistry for stabilizing metal ions.
- Exploring novel donor atoms like selenium can lead to unique complex properties.
- Selenomaltol represents an under-explored O,Se-donor ligand.
Purpose of the Study:
- To report an efficient synthesis of 3-hydroxy-2-methyl-4-selenopyrone (selenomaltol).
- To prepare and characterize metal complexes of selenomaltol with Fe(III), Ni(II), Cu(II), and Zn(II).
- To investigate the electronic and structural properties of these novel O,Se-donor chelates.
Main Methods:
- One-step synthesis of selenomaltol.
- Preparation and characterization of metal complexes.
- Spectroscopic studies (NMR, EPR, electronic absorption).
- X-ray crystallography and cyclic voltammetry.
- Nuclear Independent Chemical Shift (NICS) analysis for aromaticity.
Main Results:
- Efficient synthesis of selenomaltol achieved.
- Characterization of Fe(III), Ni(II), Cu(II), and Zn(II) selenomaltol complexes.
- Ni(II) and Cu(II) complexes exhibit chemically reversible, ligand-based oxidations.
- NICS analysis provides insights into the aromaticity of the ligand and its chelates.
Conclusions:
- The study successfully synthesized and characterized novel selenomaltol metal complexes.
- These O,Se-donor chelates display interesting redox properties.
- The findings expand the scope and utility of unusual chelating agents in coordination chemistry.
Related Concept Videos
Properties of Transition Metals
30.0K
Transition metals are defined as those elements that have partially filled d orbitals. As shown in Figure 1, the d-block elements in groups 3–12 are transition elements. The f-block elements, also called inner transition metals (the lanthanides and actinides), also meet this criterion because the d orbital is partially occupied before the f orbitals.
30.0K
Phase Transitions
23.3K
Whether solid, liquid, or gas, a substance's state depends on the order and arrangement of its particles (atoms, molecules, or ions). Particles in the solid pack closely together, generally in a pattern. The particles vibrate about their fixed positions but do not move or squeeze past their neighbors. In liquids, although the particles are closely spaced, they are randomly arranged. The position of the particles are not fixed—that is, they are free to move past their neighbors to...
23.3K
Crystal Field Theory - Octahedral Complexes
30.9K
Crystal Field Theory
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
30.9K
Formation of Complex Ions
26.2K
A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
26.2K
Metal-Ligand Bonds
24.4K
The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
24.4K
Cooperative Allosteric Transitions
8.8K
Cooperative allosteric transitions can occur in multimeric proteins, where each subunit of the protein has its own ligand-binding site. When a ligand binds to any of these subunits, it triggers a conformational change that affects the binding sites in the other subunits; this can change the affinity of the other sites for their respective ligands. The ability of the protein to change the shape of its binding site is attributed to the presence of a mix of flexible and stable segments in the...
8.8K

