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Photoactive components

The incorporation of photoactive components into the molecular structure, which allows reversible switching of the output physical properties, such as light or redox potential, by an... [Pg.566]

Felekis and Tagmatarchis (2005) used this cycloaddition process to prepare SWNT derivatives possessing photoactive components, such as the addition of ferrocene groups. They used a short PEG-type spacer on the glycine to impart water solubility at the same time. [Pg.647]

The chemical linkage,, between A and B shown above can be of any sort, provided modification of the physical and chemical processes of excited states occurs when photoactive components form part of a supramolecular structure. [Pg.214]

Several different methods of sidewall functionalisation, such as fluorination, radical addition, nucleophilic addition, electrophilic addition and cycloaddition, have been developed (Tasis et al., 2006). The sidewalls of vertically aligned CNTs have been functionalised with DNA using azide units as photoactive components. The azi-dothymidine reacted photochemically with sidewalls of CNTs utilising [2+1] cycloaddition. The oligonucleotides were grown in situ on the sidewalls of CNTs and the DNA-modified CNTs were obtained after the deprotection of the nucleic acid (Moghaddam et al., 2004). [Pg.29]

The employment of a mesoporous semiconductor electrode dramatically increases the contact area between the semiconductor and the absorbed photoactive components and electrolyte, and eventually improves the conversion efficiency of the PECs. How-... [Pg.462]

The photoactive component in these cells is a dye adsorbed chemically onto the surface of the semi-conductor. When light hits this surface, the dye (S) absorbs a photon and becomes excited (S ) in this state it transfers an electron into the TiOj semi-conductor (injection). The positively charged dye (S+) then passes its positive charge to a redox mediator in the bulk electrolyte. The oxidised mediator is attracted to the counter electrode where it is reduced back by electron transfer, thus completing the circuit. [Pg.293]

PE, RIE and IM resistances for an extensive list of commercial photoresists are included as well for comparison with the vinyl systems and amongst themselves. Although the exact com-osition of these systems is not public information, the generic type of base resin or polymer binder is generally known. In addition, the photoactive components are all known to be aromatic azides or azo-compounds. [Pg.63]

In general, the photoresists exhibit greater dry-process resistance than the vinyl polymers of Table II. The greater dry-etch resistances of photoresists is attributed to the aromatic nature of the crosslinking agents, photoactive components, and novolac resins (positive photoresists only). In addition, the... [Pg.70]

The formation of supramolecular entities from photoactive components may be expected to pertub the ground-state and excited-state properties of the individual species, giving rise to novel properties that define a supramolecular photochemistry [8.2, A. 10, A.20J. [Pg.91]

Photoresists contain photoactive components, which absorb light of a specific wavelength and upon absorption undergo chemical transformation. As a result of such transformations, the extinction coefficient of the active ingredient changes. In addition, photoresists typically contain other components which may or may not absorb light, but do not undergo chemical reactions as result of exposure and whose extinction coefficients are therefore constant. [Pg.679]

Like proton transfer, photoisomerization is a fundamentally important photochemical process. The two most important forms of photoisomerization are valence isomerization and stereoisomerization. The latter is probably the most common photoinduced isomerization in supramolecular chemistry. It may occur in systems in which the photoactive component has unsaturated bonds which can be excited, and this effect may be exploited for optical switching applications. A number of interfacial supramolecular complexes capable of undergoing cis-trans photoisomerization have been studied from this perspective - some examples are outlined in Chapter 5. [Pg.49]

However, the photochemistry itself does not make a relief image. Rather it is used to modify the solubility of the polymeric binder. The diazoquinone compounds used in resists are referred to as dissolution inhibitors or photoactive components (PAC s). The addition of a diazoquinone molecule dramatically inhibits the dissolution rate of a thin film of a novolac resin. Upon exposure, the dissolution rate of the novolac based resist is considerably faster than the rate for the novolac alone. The accelerated dissolution rate may be caused by formation of acid eind its subsequent ionization during development or by enhauiced diffusion of the developer into the coating because of changes caused by the formation and fate of the nitrogen (2). [Pg.238]

The present examples are intended to demonstrate the potential of the copper catenates as mobile, electro- and photoactive components in the design of molecular devices which may be of use in the development of electron transfer-driven molecular machines. [Pg.2301]

CEPs have also been used as the photoactive component in photoelectrochemi-cal (Gratzel) cells40,41 as well as catalytic counter electrodes in place of platinum.42... [Pg.15]

The absorption behavior of the photoactive component does not say anything about the behavior of the excited state. Does it deactivate rapidly in the singlet channel with fluorescence or radiationless Does it undergo fast intersystem crossing into the triplet manifold What is the chemistry of all these excited states If we have the opportunity to measure them, fluorescence and phosphorescence spectra will supply us with lifetime and quantum yield data. A comprehensive up-to-date collection of photophysical data can be found in Murov s Handbook of Photochemistry (see Table 2). [Pg.6]

In one of India s sacred books Atharava-veda (1400 BC) it is described how seeds of the plant Psoralea corylifolia can be used for the treatment of vitiligo. Psoralens are the photoactive components of these seeds, just as in the extracts of the plant, Ammi majus, which grows on the banks of the Nile, was used by the Egyptians to treat vitiligo. For centuries photochemotherapy made no further progress until 1974 when PUVA (i.e. treatment with psoralens and UVA radiation) was reported to be an efficient treatment of psoriasis [13]. Photochemotherapy can also be tailored to act on the immune system such as in extracorporeal photophoresis of mucoses fungoides, cutaneous T-cell lymphoma [14]. [Pg.5]

It should be emphasized that one-component resists consisting of pure radiation-sensitive materials, which in modern times are comprised primarily of polymers that combine all of the necessary attributes of a resist, have now fallen out of favor. In contrast, modern advanced lithography relies almost exclusively on the multicomponent design concept in which resist functions are provided by separate components, comprising the resin/bmder on the one hand, and the photoactive compounds on the other. In these multicomponent systems, the resins/ binders are polymers and are typically inert to radiation, but can undergo radiation-induced reactions initiated by the photoactive components of the resists. ... [Pg.182]

The most commonly used form of the photoactive component in DNQ resists are DNQs substituted in the 5-position (I) or in the 4-position (II) with sulfonic acid derivatives. [Pg.292]

DNQs have some physical attributes that make them ideal candidates as photoactive components for near-UV hthography. These attributes, according to Reiser, include ... [Pg.294]

Zaynoun, S.T., B.E. Johnson, and W. Frain-Bell. 1977a. A study of oil of bergamot and its importance as a phototoxic agent. I. Characterization and quantification of the photoactive component. Br. J. Dermatol. 96(5) 475-482. [Pg.236]

Introduction. A representation of "photon-reads" devices is shown in Scheme III. Such devices are made of a photoactive component P bound to another component, M, which can undergo interaction with some external species X. The interaction with X perturbs the properties of M. This modifies the excited-state behavior of P. Thus, the photochemical and photophysical behavior of P can be used to reveal ("read") the interaction taking place between M and X. The "photon-reads" devices can be classified according to the type of interaction which modulates the photochemical and photophysical properties of the supramolecular system. [Pg.21]

Unlike the systems in the PV-electrolysis category, the photoactive components in the photoelectrode based systems configuration are immersed in solution, and typically include one or more PEC solid/liquid rectifying junctions. [Pg.214]


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Photoactive

Photoactivity

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