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  2. Hydrogen-bond catalysis - Wikipedia

    en.wikipedia.org/wiki/Hydrogen-bond_catalysis

    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 ...

  3. Thiourea organocatalysis - Wikipedia

    en.wikipedia.org/wiki/Thiourea_organocatalysis

    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 ...

  4. Hydrogenation - Wikipedia

    en.wikipedia.org/wiki/Hydrogenation

    For example, the addition of hydrogen to ethene has a Gibbs free energy change of -101 kJ·mol −1, which is highly exothermic. [11] In the hydrogenation of vegetable oils and fatty acids, for example, the heat released, about 25 kcal per mole (105 kJ/mol), is sufficient to raise the temperature of the oil by 1.6–1.7 °C per iodine number drop.

  5. Active site - Wikipedia

    en.wikipedia.org/wiki/Active_site

    Hydrogen bond: A hydrogen bond is a specific type of dipole-dipole interaction between a partially positive hydrogen atom and a partially negative electron donor that contain a pair of electrons such as oxygen, fluorine and nitrogen. The strength of hydrogen bond depends on the chemical nature and geometric arrangement of each group.

  6. Catalytic triad - Wikipedia

    en.wikipedia.org/wiki/Catalytic_triad

    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.

  7. Photosystem II - Wikipedia

    en.wikipedia.org/wiki/Photosystem_II

    Photosystem II (of cyanobacteria and green plants) is composed of around 20 subunits (depending on the organism) as well as other accessory, light-harvesting proteins. Each photosystem II contains at least 99 cofactors: 35 chlorophyll a, 12 beta-carotene , two pheophytin , two plastoquinone , two heme , one bicarbonate, 20 lipids, the Mn

  8. Heterogeneous catalysis - Wikipedia

    en.wikipedia.org/wiki/Heterogeneous_catalysis

    Note that no chemical bonds are formed between adsorbate and adsorbent, and their electronic states remain relatively unperturbed. Typical energies for physisorption are from 3 to 10 kcal/mol. [ 2 ] In heterogeneous catalysis, when a reactant molecule physisorbs to a catalyst, it is commonly said to be in a precursor state, an intermediate ...

  9. Photosystem I - Wikipedia

    en.wikipedia.org/wiki/Photosystem_I

    Photosystem I (PSI, or plastocyanin–ferredoxin oxidoreductase) is one of two photosystems in the photosynthetic light reactions of algae, plants, and cyanobacteria. Photosystem I [1] is an integral membrane protein complex that uses light energy to catalyze the transfer of electrons across the thylakoid membrane from plastocyanin to ferredoxin.