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Extended -conjugated systems

It may be said that the condition necessary for a molecule to be aromatic is a relatively high specific delocalization energy (DE divided by either the number of bonds over which the conjugated system extends or the number of electrons in conjugation) and that the sufficient condition is a relatively low reactivity (judged by the values of theoretical indices) under the conditions under which aromaticity is to be exhibited. Such a theoretical aromaticity (Ar) can be expressed formally as ... [Pg.55]

We have studied the electronic properties of the polythiophenes in relation to their structural and conformational characteristics. Their electronic properties come out of the TT-conjugated system extended along the polythiophene backbone. Since the electronic state is strongly coupled to the backbone conformation, a variety of electronic properties show themselves depending on the conformations of polymer chains. [Pg.80]

The treatment of conjugated systems in terms of electron systems that extend smoothly over all atoms allows the treatment of a variety of structural phenomena, as may be explained with a spedes that shows hindered rotation and with the nitro group. [Pg.65]

Huckel realized that his molecular orbital analysis of conjugated systems could be extended beyond neutral hydrocarbons He pointed out that cycloheptatrienyl cation also called tropyhum ion contained a completely conjugated closed shell six tt electron sys tern analogous to that of benzene... [Pg.456]

Carotenoids are natural pigments characterized by a tail to tail linkage between two C20 units and an extended conjugated system of double bonds They are the most widely dis tributed of the substances that give color to our world and occur m flowers fruits plants insects and animals It has been estimated that biosynthesis from acetate produces approximately a hundred million tons of carotenoids per year The most familiar carotenoids are lycopene and (3 carotene pigments found m numerous plants and easily isolable from npe tomatoes and carrots respectively... [Pg.1100]

The analogous structures 309, 310, and 311 have been suggested for the pyrophthalones. Early work favored structure 309 (see reference 385 and references therein). Later, ultraviolet spectral data showed the presence of an extended conjugated system, and comparison with the spectra of the A -methyl compounds suggested structure 310. ... [Pg.429]

It would be expected that the stabilization of the adsorbed species by an extended conjugated system should increase with the number of aromatic rings in the adsorbed azahydrocarbon. However, data suitable for comparison are available only for phenanthridine, benzo-[/]quinoline, and benzo[h] quinoline. The large difference in the yields of biaryl obtained from the last two bases could be caused by steric interaction of the 7,8-benz-ring with the catalyst, which would lower the concentration of the adsorbed species relative to that with benzo[/]quinoline. The failure of phenanthridine to yield any biaryl is also noteworthy since some 5,6-dihydrophenanthridine was formed. This suggests that adsorption on the catalyst via the nitrogen atom is possible, but that steric inhibition to the combination of the activated species is involved. The same effect could be responsible for the exclusive formation of 5,5 -disubstituted 2,2 -dipyridines from 3-substi-tuted pyridines, as well as for the low yields of 3,3, 5,5 -tetramethyl-2,2 -bipyridines obtained from 3,5-lutidine and of 3,3 -dimethyl-2,2 -... [Pg.196]

In view of the limited capacity of the sulfur atom in the sulfoxide and sulfone functional groups to transmit conjugative effects due to the insulating effect of the LUMO sulfur d-orbitals45,46,56, the application of the UV technique even in the case of the cyclic vinyl sulfones (e.g. thiete dioxides 6b) cannot be expected to find extensive use. UV spectra of substituted thiete dioxides in which an extended conjugated system (e.g. 194) exists in the molecule, did provide useful information for structure elucidation231. However, the extent... [Pg.442]

Notably, derivatives (19), (21) and (23) are all orange in colour, suggestive of the presence of an extended 71-conjugated system [19b, 27]. This is supported... [Pg.135]

Note Added in Proof This is nicely illustrated by the landmark publication of Protasiewicz et al. [94] who describe derivative (122), the first conjugated polymers featuring phosphorus-phosphorus multiple bonds (Scheme 33). The di-phosphene-PPV (122) exhibits an extended 71-conjugated system as shown by the optical HOMO-LUMO gap that is close to that of related PPV [94]. [Pg.159]

The line structures of three biologically important molecules that contain extended conjugated systems. The conjugated systems are highlighted with color screens. [Pg.720]

There have been many applications of the Wittig reaction in multistep syntheses. The reaction can be used to prepare extended conjugated systems, such as crocetin dimethyl ester, which has seven conjugated double bonds. In this case, two cycles of Wittig reactions using stabilized ylides provided the seven double bonds. Note the use of a conjugated stabilized ylide in the second step.250... [Pg.163]

The use of the term leuco dye is a common paradox. Leuco color formers are materials that undergo controlled chemical or physical changes resulting in a shift from a colorless state to an intense color. The preparation of leuco color formers takes advantage of the very nature of colored materials themselves. The existence of extended conjugated -system in dyes is responsible for the absorption in the visible region. The chemistry of such rc-system is noted for facile reactivity, particularly to reactions such as reduction, oxidation, and hydrolysis (not hydrolytic cleavage). When n-... [Pg.312]

Ajayaghosh A, George SJ, Schenning APHJ (2005) Hydrogen-Bonded Assemblies of Dyes and Extended jr-Conjugated Systems. 258 83-118 Akai S, Kita Y (2007) Recent Advances in Pummerer Reactions. 274-. 35-76 Albert M, Fensterbank L, l.acote E, Malacria M (2006) Tandem Radical Reactions. 264 1-62 Alberto R (2005) New Organometallic Technetium Complexes for Radiopharmaceutical Imaging. 252 1-44... [Pg.256]


See other pages where Extended -conjugated systems is mentioned: [Pg.41]    [Pg.32]    [Pg.579]    [Pg.266]    [Pg.47]    [Pg.678]    [Pg.350]    [Pg.41]    [Pg.32]    [Pg.579]    [Pg.266]    [Pg.47]    [Pg.678]    [Pg.350]    [Pg.349]    [Pg.251]    [Pg.303]    [Pg.401]    [Pg.423]    [Pg.162]    [Pg.22]    [Pg.149]    [Pg.134]    [Pg.401]    [Pg.423]    [Pg.229]    [Pg.194]    [Pg.96]    [Pg.7]    [Pg.133]    [Pg.136]    [Pg.142]    [Pg.335]    [Pg.27]    [Pg.327]    [Pg.2]    [Pg.245]    [Pg.27]    [Pg.175]    [Pg.356]   
See also in sourсe #XX -- [ Pg.71 ]




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Acetylene-extended cross-conjugated systems

Conjugate system

Conjugated system conjugation)

Conjugated systems

Cross-Conjugated Systems in Acetylene-Extended Radiaannulene Frameworks

Extended conjugation

Extended jr-conjugated systems

System extended

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