Related Experiment Video
Updated: Jul 16, 2026

Synthesis of Antiviral Tetrahydrocarbazole Derivatives by Photochemical and Acid-catalyzed C-H Functionalization via Intermediate Peroxides (CHIPS)
Published on: June 20, 2014
Mercury binding sites in thiol-functionalized mesostructured silica.
Simon J L Billinge1, Emily J McKimmy, Mouath Shatnawi
1Department of Physics and Astronomy, Michigan State University, East Lansing, MI 48824, USA.
Thiol-functionalized silica effectively removes mercury from water. Research reveals mercury binds to sulfur, forming clusters and changing coordination with increasing mercury levels.
Area of Science:
- Materials Science
- Environmental Chemistry
- Nanotechnology
Background:
- Thiol-functionalized mesoporous silica demonstrates potential for heavy metal remediation.
- Understanding the mercury-binding mechanism is crucial for optimizing removal efficiency.
Purpose of the Study:
- To elucidate the mercury-binding mechanism in thiol-functionalized mesostructured silica.
- To investigate the structural and chemical changes upon mercury adsorption.
Main Methods:
- Synchrotron X-ray powder diffraction with atomic pair distribution function (PDF) analysis.
- Raman spectroscopy.
- Synthesis of thiol-functionalized mesoporous silica with varying functionalization levels (x=0.30, 0.50).
Main Results:
- Evidence of bridging thiolate sulfur atoms to mercury ions, forming surface chains.
- No significant Hg-O bonds detected, ruling out oxygen coordination.
- Mercury centers cluster via thiolate bridging, independent of loading.
- Mercury complexation changes from neutral (tetrahedral coordination) at low loading to cationic (linear coordination) at high loading, with nitrate as a counter-anion.
Conclusions:
- Thiol-functionalized silica binds mercury primarily through sulfur coordination.
- The binding mechanism and mercury speciation are dependent on the mercury loading.
- These findings provide insights for designing advanced sorbents for mercury removal.
Related Concept Videos
Covalent Bonding and Lewis Structures
Lewis Structures of Molecular Compounds and Polyatomic Ions
Structural Isomerism
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can be...
Resonance and Hybrid Structures
Resonance Structures and Resonance Hybrids
The Lewis structure of a nitrite anion (NO2−) may actually be drawn in two different ways, distinguished by the locations of the N–O and N=O bonds.
The Supercomplexes in the Crista Membrane
Introduction to Chemical Bonds
The electrons of the outermost energy level determine the energetic stability of the atom and its tendency to form chemical bonds with other atoms. The innermost electron shell has a maximum capacity of two electrons, but the next two electron shells can each have a maximum of eight electrons. This is known as the octet rule, which states that, with the exception of the innermost shell, atoms are most stable energetically when they have eight electrons in their valence shell, the...

