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Absorption oligomer

Decafluorobiphenyl [434-90-2] C F C F (mol wt, 334.1 mp, 68°C bp, 206°C), can be prepared by I Jllmann coupling of bromo- [344-04-7] chloro- [344-07-0] or iodopentafluorobenzene [827-15-6] with copper. This product shows good thermal stabiHty decafluorobiphenyl was recovered unchanged after 1 h below 575°C (270). Decafluorobiphenyl-based derivatives exhibit greater oxidative stabiHty than similar hydrocarbon compounds (271). Therm ally stable poly(fluorinated aryl ether) oligomers prepared from decafluorobiphenyl and bisphenols show low dielectric constant and moisture absorption which are attractive for electronic appHcations (272). [Pg.328]

A second type of uv curing chemistry is used, employing cationic curing as opposed to free-radical polymerization. This technology uses vinyl ethers and epoxy resins for the oligomers, reactive resins, and monomers. The initiators form Lewis acids upon absorption of the uv energy and the acid causes cationic polymerization. Although this chemistry has improved adhesion and flexibility and offers lower viscosity compared to the typical acrylate system, the cationic chemistry is very sensitive to humidity conditions and amine contamination. Both chemistries are used commercially. [Pg.248]

In order to summarize this section it must be noted that the possibility to evaporate conjugated oligomers in such a way that their chain axes point predominantly in one direction allows us to determine the anisotropic electronic properties of conjugated molecules. From these studies it becomes evident that in order to obtain polarized absorption or emission of light as required in polarization Filters or LCD-backlights, the application of conjugated molecules is one of the most attractive areas of application for these materials. [Pg.147]

The polaron is characterized by the reversal of bond alternation, which, in the case of polythiophene, extends over five monomer units [30-32], and the appearance of two localized stales in the band gap ). These states have been indeed observed by UV-V1S absorption of both oligomers and polymers, in solution [33— 40] and in the solid state [41-45]. [Pg.255]

Figure 4-2. INDO/SCI-siuiulaled linear absorption spectrum of the eleven-ring PPV oligomer. The vertical lines represent the oscillator strength of the transitions that are described the site labeling used tor the wavcluiiclion analyses is shown on lop. Figure 4-2. INDO/SCI-siuiulaled linear absorption spectrum of the eleven-ring PPV oligomer. The vertical lines represent the oscillator strength of the transitions that are described the site labeling used tor the wavcluiiclion analyses is shown on lop.
Figure 4-3. Absolute values of the INDO/SCI-calculalcd electron wavcfunctions v/(a, jt, = 34) calculated for the eleven-ring PPV oligomer as a function of carbon site (hole fixed on site 34) for the excited stales corresponding to (a) die first absorption peak (3.0 cV) (b) the second absorption peak (3.8 eV) (c) the third absorption peak (5.6 eV) (d) lire fourth absorption peak (6.3 eV) and (e) lire fifth absorption peak (7.0 cV). The energies given between parentheses refer to the theoretical values. Figure 4-3. Absolute values of the INDO/SCI-calculalcd electron wavcfunctions v/(a, jt, = 34) calculated for the eleven-ring PPV oligomer as a function of carbon site (hole fixed on site 34) for the excited stales corresponding to (a) die first absorption peak (3.0 cV) (b) the second absorption peak (3.8 eV) (c) the third absorption peak (5.6 eV) (d) lire fourth absorption peak (6.3 eV) and (e) lire fifth absorption peak (7.0 cV). The energies given between parentheses refer to the theoretical values.
Another way of obtaining information on the time-averaged mobility of charge carriers on their way across a sample of arbitrary thickness is, to simultaneously measure the current and the stationary charge earners density via transient absorption and to infer the mobility from j-rnpF. Such experiments have been performed on blends of conjugated oligomers derived from /m-siilbene amine and a... [Pg.527]

For the three oclyloxy-subslitulcd five-ring oligomers, the normalized photoluminescence spectra of the single crystals are depicted in Figure 16-26. Due to the large absorption coefficient (more than 105 cm"1 at the maximum) we were not able to measure the absorption spectra of the relatively thick (20-30 pm) single crystals (see Table 16-5 in Section 16.3.3.3.1). [Pg.617]

Liquid crystalline main chain polymers with siloxane spacer groups were obtained by the hydrosilation of (Si—H) terminated polydimethylsiloxane oligomers and mesogenic groups with terminal double bonds as shown in Reaction Scheme XVII-(a). Reactions were usually carried out in THF with the Wacker Oil catalyst 255). Completion of the reactions was followed by the disappearance of the strong (Si—H) absorption band at 2140 cm-1 using IR spectroscopy. [Pg.47]

Barium and strontium salts of polystyrene with two active end-groups per chain were prepared by Francois et al.82). Direct electron transfer from tiny metal particles deposited on a filter through which a THF solution of the monomer was percolated yields the required polymers 82). The A.max of the resulting solution depends on the DPn of the formed oligomers, being identical with that of the salt of polymers with one active end-group per chain for DPn > 10, but is red-shifted at lower DPn. Moreover, for low DPn, (<5), the absorption peak splits due to chromophor-chromophor interaction caused by the vicinity of the reactive benzyl type anions. [Pg.117]

Although the above profusion of in vivo studies evidence their health potentialities, the problem of the bioavailabihty of proanthocyanidins supplied by dietary supplementation has still not been completely resolved since unequivocal evidence for absorption is missing so far [11]. However, studies carried out using radio-labelled procyanidins revealed that dimers and trimers may be absorbed by intestinal cells, whereas a recent study demonstrated that procyanidin oligomers are readily adsorbed in rats [55], while it has been shown that colon microflora may be able to degrade proanthocyanidins to low-molecular-weight aromatic compounds [56]. [Pg.249]

Strong MLCT bands appear in the neutral form of azo-bridged ferrocene oligomers, as noted above. The absorption of the MLCT band at 534 nm diminishes, and a new band appears and increases at 672 nm with the oxidation to 25+. The new band can be assigned to a ligand-to-... [Pg.74]

Advances in size-exclusion chromatography, coupled with refractive index, absorption, viscosity, and lightscattering detectors, and MALDI-ToFMS, have made it possible to accurately determine molecular weight distribution (oligomer profiling), even at the relatively low values of polymeric additives (up to about 5000 Da). Advances in column design, e.g. high-resolution PS/DVB columns (> 105 plates m-1) mean that SEC can provide a valuable alternative to conventional HPLC techniques for the separation of small molecules. [Pg.733]


See other pages where Absorption oligomer is mentioned: [Pg.348]    [Pg.395]    [Pg.280]    [Pg.430]    [Pg.61]    [Pg.139]    [Pg.200]    [Pg.217]    [Pg.424]    [Pg.57]    [Pg.58]    [Pg.300]    [Pg.307]    [Pg.373]    [Pg.404]    [Pg.529]    [Pg.611]    [Pg.600]    [Pg.68]    [Pg.131]    [Pg.140]    [Pg.65]    [Pg.209]    [Pg.211]    [Pg.135]    [Pg.83]    [Pg.659]    [Pg.219]    [Pg.245]    [Pg.248]    [Pg.251]    [Pg.254]    [Pg.255]    [Pg.153]    [Pg.260]    [Pg.265]    [Pg.215]    [Pg.185]   
See also in sourсe #XX -- [ Pg.365 ]




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