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Published on: August 17, 2018
A well-defined hydrocarbon-soluble calcium hydroxide: synthesis, structure, and reactivity
Christian Ruspic1, Sharanappa Nembenna, Anja Hofmeister
1Anorganische Chemie, Universität Duisburg-Essen, Universitätsstrasse 5-7, 45117 Essen, Germany.
A stable calcium hydroxide complex, synthesized via controlled hydrolysis, offers a novel route for calcium carbonate coatings from organic solvents. This complex also forms unique benzophenone adducts.
Area of Science:
- Inorganic Chemistry
- Materials Science
- Organometallic Chemistry
Background:
- Calcium hydroxide (Ca(OH)2) is typically insoluble in organic solvents, limiting its applications.
- Developing soluble and stable calcium hydroxide precursors is crucial for advanced material synthesis.
Purpose of the Study:
- To synthesize a novel, stable, and hydrocarbon-soluble calcium hydroxide complex.
- To explore the reactivity of this complex for material applications, including calcium carbonate formation and organic reactions.
Main Methods:
- Controlled hydrolysis of a (beta-diketiminate)calcium-amide precursor.
- Structural characterization of the resulting dimeric calcium-hydroxide complex.
- Investigating reactions with carbon dioxide and benzophenone.
Main Results:
- A stable, heteroleptic (beta-diketiminate)calcium-hydroxide complex was successfully synthesized.
- The complex demonstrated solubility in hydrocarbons and stability against ligand exchange.
- Rapid reaction with CO2 yielded a gel, enabling sol-gel coating with amorphous CaCO3.
- Reaction with benzophenone formed a red adduct, indicating no nucleophilic attack by the hydroxide.
Conclusions:
- The synthesized complex serves as a viable precursor for hydrocarbon-soluble calcium hydroxide.
- The observed reactivity enables novel sol-gel coating techniques for calcium carbonate.
- The complex exhibits unique reactivity patterns with organic carbonyl compounds.
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Covalent Bonds
When two atoms share electrons to complete their valence shells, they create a covalent bond. An atom's electronegativity—the force with which shared electrons are pulled towards an atom—determines how the electrons are shared. Molecules formed with covalent bonds can be either polar or nonpolar. Atoms with similar electronegativities form nonpolar covalent bonds; the electrons are shared equally. Atoms with different electronegativities share electrons unequally, creating polar bonds.

