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Conjugated polyene

Reductive elimination from 2-en-l,4-diol derivatives has been used to generate 1,3-dienes. Low-valent titanium generated from TiCl3-LiAlH4 can be used directly with the diols. This reaction has been used successfully to create extended polyene conjugation.305... [Pg.461]

Since 1987 numerous metallocenes, in particular ferrocenes, have been found to possess NLO properties, many of which have substituents containing polyene conjugate groups,72 Scheme 14. [Pg.204]

The table below shows the approximate wavelengths of light absorbed by a polyene conjugated system containing various numbers n of double bonds. Note that the colour absorbed is complementary to the colour transmitted—a red compound must absorb blue and green light to appear red. [Pg.149]

Streptomyces rosecflavus. which has the polyene conjugated to the lactone... [Pg.325]

Ultraviolet and visible light spectroscopy makes use of the quantized nature of the electronic structure of molecules. One example that is commonly observed by eye is the yellow color of polymeric materials that have been slightly degraded by heat or oxidation. Frequently this is due to the appearance of conjugated double bonds (5). For example, the 10-polyene conjugated structure absorbs light at 473 nm in the blue region. [Pg.32]


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See also in sourсe #XX -- [ Pg.217 ]




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Alkenes conjugated polyenes

COSY spectroscopy of conjugated polyenes

Conjugated polyene sequences

Conjugated polyene structures

Conjugated polyene systems

Conjugated polyene systems molecular orbital theory

Conjugated polyene, electrocyclic

Conjugated polyene, electrocyclic molecular orbitals

Conjugated polyene, electrocyclic reactions

Conjugated polyenes

Conjugated polyenes

Conjugated polyenes NMR spectra

Conjugated polyenes Subject inde

Conjugated polyenes acyclic

Conjugated polyenes cis/trans interconversion

Conjugated polyenes cyclic

Conjugated polyenes cyclization

Conjugated polyenes dimerization

Conjugated polyenes electrocyclic ring closure

Conjugated polyenes electronic spectra

Conjugated polyenes excited triplet states

Conjugated polyenes linear, electronic structure

Conjugated polyenes monocyclic

Conjugated polyenes planar

Conjugated polyenes rearrangement

Conjugated polyenes structure

Conjugated polyenes synthesis

Conjugated polyenic systems

Cross-conjugated polyene

Double-bond migration to give conjugated polyenes

Excitation energies linear conjugated polyenes

Hiickel molecular orbital theory for conjugated polyenes

Hydrogenation conjugated polyenes

Irradiation conjugated polyenes

Linear Conjugated Molecules The Polyenes

Nuclear Overhauser enhancement spectroscopy of conjugated polyenes

Nuclear magnetic resonance spectroscopy of conjugated polyenes

Polyene conjugated double bonds

Polyenes conjugated type

Polyenes conjugation

Polyenes conjugation

Polyenes cross-conjugated—

Polyenes, conjugated, Amax values

Some Conjugated Cyclic Polyenes

Subject conjugated polyenes

Substituted 1,3-Butadienes and Non-conjugated Polyenes

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