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  2. Phenanthrene - Wikipedia

    en.wikipedia.org/wiki/Phenanthrene

    Phenanthrene is used to make dyes, plastics, pesticides, explosives, and drugs. It has also been used to make bile acids, cholesterol and steroids. [3] Phenanthrene occurs naturally and also is a man-made chemical. Commonly, humans are exposed to phenanthrene through inhalation of cigarette smoke, but there are many routes of exposure.

  3. List of polysubstance combinations - Wikipedia

    en.wikipedia.org/wiki/List_of_polysubstance...

    A drug combination chart designed for harm reduction by TripSit [1] Polysubstance use or multisubstance use is the use of combinations of psychoactive substances with both legal and illegal substances. This page lists polysubstance combinations that are entheogenic, recreational, or off-label indicated use of pharmaceuticals.

  4. Anthracene - Wikipedia

    en.wikipedia.org/wiki/Anthracene

    Anthracene is a solid polycyclic aromatic hydrocarbon (PAH) of formula C 14 H 10, consisting of three fused benzene rings. It is a component of coal tar. Anthracene is used in the production of the red dye alizarin and other dyes. Anthracene is colorless but exhibits a blue (400–500 nm peak) fluorescence under ultraviolet radiation. [13]

  5. Polycyclic aromatic hydrocarbon - Wikipedia

    en.wikipedia.org/wiki/Polycyclic_aromatic...

    A Polycyclic aromatic hydrocarbon (PAH) is a class of organic compounds that is composed of multiple aromatic rings.Most are produced by the incomplete combustion of organic matter— by engine exhaust fumes, tobacco, incinerators, in roasted meats and cereals, [1] or when biomass burns at lower temperatures as in forest fires.

  6. Diboraanthracene - Wikipedia

    en.wikipedia.org/wiki/Diboraanthracene

    Diboraanthracene is a class of boron heterocyclic compounds in which two boron atoms substitute two carbon atoms in anthracene (C₁₄H₁₀), one of the typical polycyclic aromatic hydrocarbons (PAHs). The most well-studied diboraanthracene is 9,10-disubstituted-9,10-diboraanthracene (DBA) and its doubly reduced dianion (DBA²⁻).

  7. Triplet-triplet annihilation - Wikipedia

    en.wikipedia.org/wiki/Triplet-Triplet_Annihilation

    A Jablonski diagram describing the mechanism of triplet-triplet annihilation. The energy of the first triplet excited state (T 1) is transferred to a second triplet excited state (T 1), resulting in (1) the first T 1 returning to the singlet ground state S0 and (2) the second T 1 promoting to the singlet excited state (S 1).

  8. Drug interaction - Wikipedia

    en.wikipedia.org/wiki/Drug_interaction

    When two drugs affect each other, it is a drugdrug interaction (DDI). The risk of a DDI increases with the number of drugs used. [1] A large share of elderly people regularly use five or more medications or supplements, with a significant risk of side-effects from drugdrug interactions. [2] Drug interactions can be of three kinds:

  9. Clar's rule - Wikipedia

    en.wikipedia.org/wiki/Clar's_rule

    As a result, while anthracene reacts with maleic acid, phenanthrene does not, and triphenylene is the most stable species of these three. [ 1 ] Three Clar structures with an increasing number of π-sextets: anthracene (on the left), phenanthrene (in the middle), and triphenylene (on the right).

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