Home Chemistry Organic Building Blocks Aryls Triphenylene
Electrophilic Substitution Reactions: Triphenylene, like other PAHs, can undergo electrophilic aromatic substitution reactions. In these reactions, an electrophile (an electron-deficient species) attacks the π-electron cloud of the aromatic ring.
Diels-Alder Reactions: Triphenylene can participate in Diels-Alder reactions. This is a cycloaddition reaction where a conjugated diene (like triphenylene) reacts with an alkene (dienophile) to form a cyclic compound.
Oxidation Reactions: Triphenylene can undergo various oxidation reactions. This might involve the addition of oxygen, removal of hydrogen, or other processes that increase the oxidation state of the molecule.
Reduction Reactions: Triphenylene can also be reduced, which typically involves the addition of electrons or the removal of oxygen.
Halogenation Reactions: Triphenylene can react with halogens (e.g., bromine or chlorine) to form halogenated derivatives.
Metalation Reactions: Triphenylene can interact with metals, forming complexes where the metal is coordinated to the aromatic rings.
Photochemical Reactions: Triphenylene, like many PAHs, can participate in photochemical reactions under the influence of light. This can lead to the formation of reactive intermediates.
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Triphenylene-2,3,6,7,10,11-hexaol hydrate
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Triphenylene-2,3,6,7,10,11-hexayl hexaacetate
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