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(Z)-Stilbene, the Glossary

Index (Z)-Stilbene

(Z)-Stilbene is a diarylethene, that is, a hydrocarbon consisting of a cis ethene double bond substituted with a phenyl group on both carbon atoms of the double bond.[1]

Table of Contents

  1. 21 relations: Active laser medium, Conjugated system, Diarylethene, Dye, Dye laser, Electrocyclic reaction, Ethylene, Greek language, Hydrocarbon, Intramolecular reaction, Mallory reaction, Optical brightener, Phenyl group, Phosphor, Photoisomerization, Pterostilbene, Resveratrol, Scintillator, Steric effects, Stilbenoid, (E)-Stilbene.

  2. Laser gain media
  3. Phosphors and scintillators
  4. Stilbenoids

Active laser medium

The active laser medium (also called a gain medium or lasing medium) is the source of optical gain within a laser. (Z)-Stilbene and active laser medium are laser gain media.

See (Z)-Stilbene and Active laser medium

Conjugated system

In theoretical chemistry, a conjugated system is a system of connected p-orbitals with delocalized electrons in a molecule, which in general lowers the overall energy of the molecule and increases stability.

See (Z)-Stilbene and Conjugated system

Diarylethene

Diarylethene is the general name of a class of chemical compounds that have aromatic functional groups bonded to each end of a carbon–carbon double bond.

See (Z)-Stilbene and Diarylethene

Dye

A dye is a colored substance that chemically bonds to the substrate to which it is being applied.

See (Z)-Stilbene and Dye

Dye laser

A dye laser is a laser that uses an organic dye as the lasing medium, usually as a liquid solution.

See (Z)-Stilbene and Dye laser

Electrocyclic reaction

In organic chemistry, an electrocyclic reaction is a type of pericyclic rearrangement where the net result is one pi bond being converted into one sigma bond or vice versa.

See (Z)-Stilbene and Electrocyclic reaction

Ethylene

Ethylene (IUPAC name: ethene) is a hydrocarbon which has the formula or.

See (Z)-Stilbene and Ethylene

Greek language

Greek (Elliniká,; Hellēnikḗ) is an independent branch of the Indo-European family of languages, native to Greece, Cyprus, Italy (in Calabria and Salento), southern Albania, and other regions of the Balkans, the Black Sea coast, Asia Minor, and the Eastern Mediterranean.

See (Z)-Stilbene and Greek language

Hydrocarbon

In organic chemistry, a hydrocarbon is an organic compound consisting entirely of hydrogen and carbon.

See (Z)-Stilbene and Hydrocarbon

Intramolecular reaction

In chemistry, intramolecular describes a process or characteristic limited within the structure of a single molecule, a property or phenomenon limited to the extent of a single molecule.

See (Z)-Stilbene and Intramolecular reaction

Mallory reaction

In organic chemistry, the Mallory reaction is a photochemical-cyclization–elimination reaction of diaryl-ethylene structures to form phenanthrenes and other polycyclic form polycyclic aromatic hydrocarbons and heteroaromatics.

See (Z)-Stilbene and Mallory reaction

Optical brightener

Optical brighteners, optical brightening agents (OBAs), fluorescent brightening agents (FBAs), or fluorescent whitening agents (FWAs), are chemical compounds that absorb light in the ultraviolet and violet region (usually 340-370 nm) of the electromagnetic spectrum, and re-emit light in the blue region (typically 420-470 nm) through the phenomenon of fluorescence. (Z)-Stilbene and optical brightener are fluorescent dyes and luminescence.

See (Z)-Stilbene and Optical brightener

Phenyl group

In organic chemistry, the phenyl group, or phenyl ring, is a cyclic group of atoms with the formula, and is often represented by the symbol Ph (archaically φ). (Z)-Stilbene and phenyl group are phenyl compounds.

See (Z)-Stilbene and Phenyl group

Phosphor

A phosphor is a substance that exhibits the phenomenon of luminescence; it emits light when exposed to some type of radiant energy. (Z)-Stilbene and phosphor are luminescence and phosphors and scintillators.

See (Z)-Stilbene and Phosphor

Photoisomerization

In chemistry, photoisomerization is a form of isomerization induced by photoexcitation.

See (Z)-Stilbene and Photoisomerization

Pterostilbene

Pterostilbene (trans-3,5-dimethoxy-4-hydroxystilbene) is a stilbenoid chemically related to resveratrol. (Z)-Stilbene and Pterostilbene are stilbenoids.

See (Z)-Stilbene and Pterostilbene

Resveratrol

Resveratrol (3,5,4′-trihydroxy-trans-stilbene) is a stilbenoid, a type of natural phenol or polyphenol and a phytoalexin produced by several plants in response to injury or when the plant is under attack by pathogens, such as bacteria or fungi. (Z)-Stilbene and Resveratrol are stilbenoids.

See (Z)-Stilbene and Resveratrol

Scintillator

A scintillator is a material that exhibits scintillation, the property of luminescence, when excited by ionizing radiation. (Z)-Stilbene and scintillator are phosphors and scintillators.

See (Z)-Stilbene and Scintillator

Steric effects

Steric effects arise from the spatial arrangement of atoms.

See (Z)-Stilbene and Steric effects

Stilbenoid

Stilbenoids are hydroxylated derivatives of stilbene. (Z)-Stilbene and Stilbenoid are stilbenoids.

See (Z)-Stilbene and Stilbenoid

(E)-Stilbene

(E)-Stilbene, commonly known as trans-stilbene, is an organic compound represented by the condensed structural formula CHCH. (Z)-Stilbene and (E)-Stilbene are fluorescent dyes, laser gain media, luminescence, phenyl compounds, phosphors and scintillators and stilbenoids.

See (Z)-Stilbene and (E)-Stilbene

See also

Laser gain media

Phosphors and scintillators

Stilbenoids

References

[1] https://en.wikipedia.org/wiki/(Z)-Stilbene

Also known as Cis-stilbene.