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  2. Allylic strain - Wikipedia

    en.wikipedia.org/wiki/Allylic_strain

    Allylic strain in an olefin. Allylic strain (also known as A 1,3 strain, 1,3-allylic strain, or A-strain) in organic chemistry is a type of strain energy resulting from the interaction between a substituent on one end of an olefin (a synonym for an alkene) with an allylic substituent on the other end. [1]

  3. Divergent synthesis - Wikipedia

    en.wikipedia.org/wiki/Divergent_synthesis

    In chemistry a divergent synthesis is a strategy with the aim to improve the efficiency of chemical synthesis. It is often an alternative to convergent synthesis or linear synthesis. In one strategy divergent synthesis aims to generate a library of chemical compounds by first reacting a molecule with a set of reactants. The next generation of ...

  4. Carrier generation and recombination - Wikipedia

    en.wikipedia.org/wiki/Carrier_generation_and...

    Likewise, when there is a deficit of carriers (i.e., <), the generation rate becomes greater than the recombination rate, again driving the system back towards equilibrium. [1] As the electron moves from one energy band to another, the energy and momentum that it has lost or gained must go to or come from the other particles involved in the ...

  5. Click chemistry - Wikipedia

    en.wikipedia.org/wiki/Click_chemistry

    Click chemistry is an approach to chemical ... Diels-alder reaction to release furan and give 1,2,3- or 1,4,5-triazoles. ... useful in a new generation of ...

  6. 1,3-Dipolar cycloaddition - Wikipedia

    en.wikipedia.org/wiki/1,3-Dipolar_cycloaddition

    [1] [2] Hence, the reaction is sometimes referred to as the Huisgen cycloaddition (this term is often used to specifically describe the 1,3-dipolar cycloaddition between an organic azide and an alkyne to generate 1,2,3-triazole). 1,3-dipolar cycloaddition is an important route to the regio-and stereoselective synthesis of five-membered ...

  7. Aryne - Wikipedia

    en.wikipedia.org/wiki/Aryne

    In organic chemistry, arynes [1] and benzynes [2] are a class of highly reactive chemical species derived from an aromatic ring by removal of two substituents. Arynes are examples of didehydroarenes (1,2-didehydroarenes in this case), although 1,3- and 1,4-didehydroarenes are also known. [3] [4] [5] Arynes are examples of alkynes under high strain.

  8. Molecular scale electronics - Wikipedia

    en.wikipedia.org/wiki/Molecular_scale_electronics

    In a few technology generations, the composition of the devices must be controlled to a precision of a few atoms [3] for the devices to work. With bulk methods growing increasingly demanding and costly as they near inherent limits, the idea was born that the components could instead be built up atom by atom in a chemistry lab (bottom up) versus ...

  9. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    The compound with the formula (C 5 H 5) 2 Fe 2 (CO) 4 exists as three isomers in solution. In one isomer the CO ligands are terminal. When a pair of CO are bridging, cis and trans isomers are possible depending on the location of the C 5 H 5 groups. [7] Another example in organometallic chemistry is the linkage isomerization of ...