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Luminescence devices

A similarly wide choice of lumophores can be found within photophysics and photochemistry.191 The excitation (or absorption) and emission bands of luminescence come in a variety of wavelength positions, intensities and shapes. Another parameter, which is gaining in popularity among designers, is the luminescence lifetime. Time-resolved observation is a neat way of dissecting out the response of the luminescent device from the emissive noise of real-life matrices. Photostability of lumophores is a parameter which perhaps deserves more attention as more and more demanding applications are being tackled. [Pg.308]

U.S. 6,486,601 Organic luminescence device with reduced leakage current... [Pg.652]

Lanthanide Complexes of Encapsulating Ligands at Luminescent Devices... [Pg.179]

A large fraction of the research in ionically switchable luminescent devices is in this category. Several reviews of the early work are available.Figure 1... [Pg.4]

Lumophores other than hydrocarbons have been incorporated into the aminoalkyl aromatic family of ionically switchable luminescent devices. For instance, metal-loporphyrin systems such as have been used to good advantage. These cases absorb and emit at wavelengths as long as 596 and 650 nm, respectively. Such red-shifted systems are particularly attractive for monitoring ion movements in... [Pg.6]

Lumophore-spacer-receptor systems are not by any means limited to the ami-noalkyl aromatic family even if we focus on the receptor unit. Still, the latter family is likely to remain a major provider of ionically switchable luminescent devices. Aminoalkyl aromatics also serve as the platform for the development of luminescent PET sensors for a whole class of nonionic saccharides. While aliphatic amines, either singly or in arrays, can serve as receptors for a variety of cationic... [Pg.9]

As Figure 3 illustrates, redox active guests introduce PET processes almost by definition and luminescent on-off switching is the norm. However, the inhibitions outlined in Section 5 have not prevented the designers of switchable luminescent devices from exploring systems which bind redox active guests. The combined forces of inorganic coordination chemistry and supramolecular science have proved to be too attractive in many of these instances. It is to be hoped that some of this effort will filter across to the examination of more on-off systems like 17 and 18. [Pg.19]

While many metal centers can be reversibly cycled between two (or more) oxidation states, few organic moieties can match such reversibility especially in protic media. Nevertheless, the first supramolecular example of an electroswitch-able luminescent device involved the benzoquinone-hydroquinone couple. The luminescence of 55 " is switched off due to PET in the benzoquinone state of the redox couple. Electrochemical or chemical reduction of the benzoquinone under protic conditions to hydroquinone recovers the luminescence of the tris(2,2 -bipyridyl) Ru(II) unit. It is noted that the luminescence of tris(2,2 -bipyridyl) Ru(Il) itself is electroswitchable. Indeed tris(2,2 -bipyridyl) Ru(II) came to fame as a solar energy material from more humble beginnings as a luminescent redox indicator. However 55 achieves the same switching at a lower magnitude of reduction potential. Here lies the advantage of the supramolecular design. Like tris(2,2 -bipyridyl) Ru(II), many lumophores show electroswitchable luminescence. An... [Pg.23]

Observations Organic light-emitting diodes are self-luminescent devices that emit tight... [Pg.376]

Sabbatini, N. Guardigli, M. Lehn, J.-M. Luminescent lanthanide complexes as photochemical supramolecular devices. Coord. Chem. Rev. 1993,123, 201-228. Sabbatini, N. Guardigli, M. Manet, I. Lanthanide complexes of encapsulating ligands as luminescent devices. Adv. Photochem. 1997, 23, 213—278. [Pg.419]

The opposite of the AND gate is the NAND operation. In the context of a luminescent device this logic corresponds to an emission only if neither one of two different chemical imputs are present. A good... [Pg.791]

Most of the time-resolved emission spectroscopy setups are home made in the sense that they are built from individual devices (laser, detection system,. ..) hence they are not of a plug and press type, so that their exact characteristics may vary from one installation to the other. Some of these differences have no impact on the overall capabilities of the system but some have a drastic influence on the way the collected data are processed and analysed. This aspect will be detailed in the next section, while this section deals with a general description of the apparatus. The most basic type of apparatus will be described, with no reference to sophisticated techniques such as Time Correlated Single Photon Counting or Circularly Polarized Luminescence devices. [Pg.469]

In an earlier investigation by the author [2] poly(phenylene-co-vinylene) containing 2,5-thienylene vinylene, (I), was prepared and used as semiconductors in luminescent devices. [Pg.404]

Title Polymeric Compound and Organic Luminescence Device... [Pg.427]


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See also in sourсe #XX -- [ Pg.24 , Pg.26 ]




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