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Photochemical properties

Photochemical decomposition in surfactant-intercalated saponite was investigated under visible light irradiation. The rate constant of the decomposition in C3F-saponite was the smallest. Photochemical decomposition of Rose Bengal is caused by the singlet oxygen, which is quenched by water molecules. The high water content around ammonium group shown in Section 15.2.4 was responsible for the decomposition [79]. [Pg.483]

The other photoprocesses such as photoinduced electron/energy transfer and photocatalysis, which have been reported in layered clays [89], are also expected in layered [Pg.484]


The photochemistry of transition metal 1,3-diketone chelate complexes has been known for some time [30,31], and their photophysical and photochemical properties and photocatalytic activity in different chemical reactions were reviewed in 1990 by Marciniak and Buono—Core [32]. Further discussion on the photochemistry of meta] chelate will not take place here since this subject is out of the scope of this chapter. [Pg.247]

Photochemical properties of copper complexes. G. Ferraudi and S. Muralidharan, Coord. Chem. Rev., 1981,36,45-88(115). [Pg.49]

Finally, phosphorus porphyrins, such as some of those detailed in Sect. 2.3.1 have attracted attention in organic chemistry for their unique photochemical properties. Aida reported that basic aqueous solutions of benzonitrile in the presence of 59a undergo under irradiation (A>420 nm) a clean transformation... [Pg.29]

As just mentioned, phosphorus porphyrins have unique photochemical properties. Their photophysics is also interesting. Emitter-quencher assemblies based on porphyrin building blocks have attracted attention due to their potential to serve as models in photosynthetic research (see [90] for an example) or for the development of photoswitches that could be used for the fabrication of molecular electronic/optical devices. In this context, Maiya and coworkers constructed a P(VI) porphyrin system 59b with two switchable azobenzene groups positioned in the apical positions of the pseudo-octahedral phosphorus atom [92]. Photoswitch ability (luminescence on/off) was demonstrated as... [Pg.30]

Table 25 Photochemical properties of selected poly(organophosphazenes)... Table 25 Photochemical properties of selected poly(organophosphazenes)...
Electrochemical and Photochemical Properties of Metal-Containing Dendrimers... [Pg.236]

The results of the above cited applications [18-28,45] have clearly shown that CS INDO method is fairly successful in combining equally satisfactory predictions of electronic spectra and potential surfaces (especially along internal rotation pathways) of conjugated molecules, a goal never reached by other NDO-type procedures. CS INDO shares, at least partly, the interpretative advantages of the CIPSI-PCILO-CNDO procedure [32,33,36,37], coming from using the same hybrid AO basis sets, but improves its predictive capabilities as far as spectroscopic and photochemical properties are concerned. [Pg.383]

Chan, C.-W., Wong, W.-T. and Che, C.-M. (1994) Gold(lll) photooxidants. Photophysical, photochemical properties, and crystal structure of a luminescent cyclometallated gold(lll) complex of 2,9-diphenyl- 1,10-phenanthroline. Inorganic Chemistry, 33, 1266-1272. [Pg.281]

Redox participants are chosen to facilitate spectroscopic, biochemical and electrochemical probing of DNA CT. These include metallointercalators, organic intercalators, and modified bases that possess useful, well-described, and varied redox, photophysical and photochemical properties (Table 1). Our probes are readily incorporated into DNA assemblies where CT distances ranging from 3.4 to 200 A and driving forces spanning over two volts can be modulated with certainty. Most importantly, all redox probes which afford fast and/or efficient CT through DNA are well-coupled to the 7r-stack. [Pg.82]

However, examination of the spectral properties of the starting ketones and isolated photoproducts indicated that the product distribution was determined by the photochemical properties of the molecules rather than their relative thermodynamic stabilities. These workers proposed that these... [Pg.84]

In Chapter 2 we discussed a number of techniques used to study the various photophysical and photochemical processes occurring in anthracene and similar molecules. In that discussion we were primarily interested in the singlet state. In this chapter we will discuss some of the techniques available for studying the photophysical and photochemical properties of the triplet state. Most of our discussion will be directed to the photochemistry of simple ketones. [Pg.344]

Foote, C.S. Photophysical and Photochemical Properties of Fullerenes. 169,347-364 (1994). Fossey, J., Sorba, J., and Lefort, D. Peracide and Free Radicals A Theoretical and Experimental Approach. 164, 99-113 (1993). [Pg.294]

The 977-pyrido[3,4- ]pyrrolizin-9-one 145 has been prepared for its photochemical properties. The preparation involves an intramolecular Friedel-Crafts acylation of the acid chloride formed from 3-(l-pyrrolyl)pyridine-4-carboxy-late (Scheme 40). The product is a photosensitizer, which absorbs visible light its absorption spectra are pH, solvent, and concentration dependent <1994SAA57>. [Pg.797]

Fluorophores are relative small molecules that, with some exceptions, are not naturally occurring and have to be synthesized chemically. There has been a large development in the synthesis of fluorescent molecules and nowadays there is a vast range of alternatives including dyes with improved photochemical properties, solubility or modified reactivity that allow for conjugation to other molecules of interest and the synthesis and application of fluorescent sensors [10, 13], Although a lot is known about the physics of fluorescence and a lot of information is available about the properties of dyes, their prediction from the chemical structures cannot be accurately done. For this reason, there has been a... [Pg.241]

Fluorescein is excited at 494 nm, which fits to the argon-ion laser line at 488 nm, a very convenient feature for many microscopy experiments. It emits at 520 nm and the emission band is far from being sharp. The broad fluorescence emission spectrum varies with pH [18]. The advantageous photochemical properties of fluorescein are its high absorption (emax = 79,000M-1cm-1) and quantum... [Pg.242]

The scientific group from Turkey62 studied photophysical and photochemical properties and behaviour of an azlactone derivative, 4-(p-N,N - dimethylaminophenylmethylene)-2-phenyl-5-oxazolone in sol-gel... [Pg.367]

Many studies on the photochemical properties of carbazolyl chromophores... [Pg.269]


See other pages where Photochemical properties is mentioned: [Pg.2954]    [Pg.9]    [Pg.440]    [Pg.349]    [Pg.163]    [Pg.163]    [Pg.214]    [Pg.127]    [Pg.222]    [Pg.64]    [Pg.278]    [Pg.163]    [Pg.256]    [Pg.162]    [Pg.28]    [Pg.69]    [Pg.203]    [Pg.29]    [Pg.29]    [Pg.140]    [Pg.157]    [Pg.243]    [Pg.14]    [Pg.15]    [Pg.30]    [Pg.295]    [Pg.205]    [Pg.259]    [Pg.239]   
See also in sourсe #XX -- [ Pg.87 ]




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Metal photochemical properties

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Photochemical properties centers

Photochemical properties of macrobicyclic complexes

Photochemical properties of metal

Photochemical properties of the

Photochemical properties, copper

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