Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Fluorescence molecular weight effect

Qualitatively, the observed molecular weight dependence of the fluorescence ratio can only be explained by resorting to a photophysical model that includes energy migration. It has been previously postulated that the molecular weight effect in fluid solution derives from differences in the effectiveness of rotational sampling for bonds near the ends and in the center of a chain [75-77], but the explanation cannot be used for the PS/PVME blend because of its high viscosity. It has also been proposed [75] that the trap concentration... [Pg.575]

Liquid crystal polymers are also used in electrooptic displays. Side-chain polymers are quite suitable for this purpose, but usually involve much larger elastic and viscous constants, which slow the response of the device (33). The chiral smectic C phase is perhaps best suited for a polymer field effect device. The abiHty to attach dichroic or fluorescent dyes as a proportion of the side groups opens the door to appHcations not easily achieved with low molecular weight Hquid crystals. Polymers with smectic phases have also been used to create laser writable devices (30). The laser can address areas a few micrometers wide, changing a clear state to a strong scattering state or vice versa. Future uses of Hquid crystal polymers may include data storage devices. Polymers with nonlinear optical properties may also become important for device appHcations. [Pg.202]

Approximately a minimum of 1 to 5,000 is required before complexation is no longer dependent on molecular weight for small anions such as KI and l-ariiLinonaphthaLine-8-sulfonate (ANS) (86,87). The latter anion is a fluorescent probe that, when bound in hydrophobic environments, will display increased fluorescence and, as expected, shows this effect in the presence of aqueous PVP. PVP, when complexed with Hl, shrinks in si2e as it loses hydrodynamic volume, possibly because of interchain complexation. ANS, on the other hand, causes the polymer to swell by charge repulsion because it behaves like a typical polyelectrolyte (88). [Pg.531]

Despite the technical problems in the latter film study, we conclude that there is no intramolecular excimer formation in the compounds of Richards et al.143, and probably little intermolecular excimer formation in the pure films. The absence of an effect of solvent power 25) on the possible excimer fluorescence of the R = CH3 polymer may not be significant, since little change in the coil dimensions would be expected for the short ( 300 backbone atoms) polymers 143> which were studied. Additional work is needed on the fluorescence of such polymers having higher molecular weights, different aryl substituents (R = 2-naphthyl, for example), and fewer adventitious impurities. [Pg.59]

We conclude that the difference between the experimental value and the no-transfer value of the fluorescence ratio of P2VN and PS is less in solution than in dilute miscible blends, because energy migration must compete with rotational processes in the generation of excimers in solution. This difference is also present when the effect of molecular weight on aryl vinyl polymers in solution and in dilute miscible blends is considered in the next section. [Pg.70]

Gel permeation chromatography of protein linear random coils in guanidinium chloride allows simultaneous resolution and molecular weight analysis of polypeptide components. Column calibration results are expressed in terms of a log M vs. Kd plot or of effective hydrodynamic radius (Re/). For linear polypeptide random coils in 6M GuHCl, Re is proportional to M0 555, and M° 555 or Re may be used interchangeably. Similarly, calibration data may be interpreted in terms of N° 555 (N is the number of amino acid residues in the polypeptide chain), probably the most appropriate calibration term provided sequence data are available for standards. Re for randomly coiled peptide heteropolymers is insensitive to amino acid residue side-chain composition, permitting incorporation of chromophoric, radioactive, and fluorescent substituents to enhance detection sensitivity. [Pg.316]


See other pages where Fluorescence molecular weight effect is mentioned: [Pg.70]    [Pg.71]    [Pg.260]    [Pg.220]    [Pg.246]    [Pg.194]    [Pg.271]    [Pg.637]    [Pg.65]    [Pg.178]    [Pg.63]    [Pg.317]    [Pg.92]    [Pg.592]    [Pg.91]    [Pg.48]    [Pg.150]    [Pg.74]    [Pg.1343]    [Pg.305]    [Pg.611]    [Pg.95]    [Pg.135]    [Pg.454]    [Pg.472]    [Pg.472]    [Pg.32]    [Pg.15]    [Pg.114]    [Pg.119]    [Pg.1343]    [Pg.160]    [Pg.127]    [Pg.690]    [Pg.328]    [Pg.185]    [Pg.74]    [Pg.348]    [Pg.49]    [Pg.297]    [Pg.85]    [Pg.600]    [Pg.200]    [Pg.222]    [Pg.249]   
See also in sourсe #XX -- [ Pg.70 ]




SEARCH



Effective molecular weight

Fluorescence effect

Molecular weight effect

© 2024 chempedia.info