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The thiourea hydrogen bonds to the nitro group and stabilizes the incoming negative charge, while the amine acts a specific base to activate the nucleophile. This is an example of bifunctional catalysis. Hydrogen-bond catalysis is a type of organocatalysis that relies on use of hydrogen bonding interactions to accelerate and control organic ...
One example is titanium dihydride, which forms when titanium sponge is heated to 400-700 °C under an atmosphere of hydrogen. These reactions typically require high surface area metals. The direct reaction of metals with H 2 is a step in catalytic hydrogenation. For solutions, classic example involves Vaska's complex: [7]
An ubiquitous example of a hydrogen bond is found between water molecules. In a discrete water molecule, there are two hydrogen atoms and one oxygen atom. The simplest case is a pair of water molecules with one hydrogen bond between them, which is called the water dimer and is often used as a model system. When more molecules are present, as is ...
Researchers have since conducted increasingly detailed investigations of the triad's exact catalytic mechanism. Of particular contention in the 1990s and 2000s was whether low-barrier hydrogen bonding contributed to catalysis, [18] [19] [20] or whether ordinary hydrogen bonding is sufficient to explain the mechanism.
Thioureas are often found to be stronger hydrogen-bond donors (i.e., more acidic) than ureas [7] because their amino groups are more positively charged. Quantum chemical analyses revealed that this counterintuitive phenomenon, which is not explainable by the relative electronegativities of O and S, results from the effective steric size of the ...
a = the contribution from hydrogen-bond basicity (because a basic sorbent will interact with an acidic solute); and; b = the contribution from hydrogen-bond acidity to the transfer of the solute from air to the aerosol phase. Similarly, the correlation of solvent–solvent partition coefficients as log SP, is given by
Asymmetric hydrogenation is a chemical reaction that adds two atoms of hydrogen to a target (substrate) molecule with three-dimensional spatial selectivity.Critically, this selectivity does not come from the target molecule itself, but from other reagents or catalysts present in the reaction.
The term agostic is reserved to describe two-electron, three-center bonding interactions between carbon, hydrogen, and a metal. Two-electron three-center bonding is clearly implicated in the complexation of H 2 , e.g., in W(CO) 3 (PCy 3 ) 2 H 2 , which is closely related to the agostic complex shown in the figure. [ 8 ]