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Photoluminescence coordination chemistry

This review deals with the applications of photolurainescence techniques to the study of solid surfaces in relation to their properties in adsorption, catalysis, and photocatalysis, After a short introduction, the review presents the basic principles of photolumines-cence spectrosajpy in relation to the definitions of fluorescence and phosphorescence. Next, we discuss the practical aspects of static and dynamic photoluminescence with emphasis on the spectral parameters used to identify the photoluminescent sites. In Section IV, which is the core of the review, we discuss the identification of the surface sites and the following coordination chemistry of ions at the surface of alkaline-earth and zirconium oxides, energy and electron transfer processes, photoluminesccncc and local structure of grafted vanadium oxide, and photoluniinescence of various oxide-... [Pg.119]

This review covers adsorption, catalysis, and photocatalysis that can be investigated and understood by photoluminescence spectroscopy. Most of the results discussed in this review have been obtained by photoluminescence techniques, but other, complementary techniques, are also discussed to emphasize the originality and potential value of photoluminescence spectroscopy, particularly with regard to anion coordination chemistry, excited states, and reaction dynamics. The latter field is of utmost importance in chemistry (35). Additional applications of photoluminescence spectroscopy to the study of solid surfaces are reviewed in the books Photochemistry on Solid Surfaces"(. 6) and Surface Photochemistry (37). [Pg.122]

Fluorescence and phosphorescence are emission processes which originate directly or indirectly (see 5 section ll.B) from the electronically excited singlet state and triplet state, respectively, produced by charge-transfer processes (Eqs. 1 and 2). Many publications deal with such charge-transfer transitions by diffuse reflectance spectroscopy (DRS) (2-6) showing the link between the latter technique and photoluminescence. It is worthwhile to recall that the emergence of the coordination chemistry of solid-state anions, namely, of surface lattice oxide ions, has almost entirely been based on the results of both photoluminescence and DRS analyses (7, 66). For some catalytic systems, vibrational structures can be detected (see Section IV.B) with an associated vibrational constant, which may be determined directly and independently by IR or Raman spectroscopy, evidencing the relation between these spectroscopies and photoluminescence (33, 34). [Pg.245]

Photoluminescence techniques will be applied to a broader range of systems, particularly oxide-supported sulfides (because of their important role in hydrotreating catalysis) as well as unsupported or oxide-supported (oxi)carbides or (oxi)nitrides (because of their growing importance as substitutes for noble metals and because they have metallic and acidic functions). Moreover, improved procedures for preparing catalytic materials will enable the design of tailored oxides with better defined characteristics, such as size, composition, and structure. The accumulation of data concerning the behavior of surface anions will also lead to a more refined view of the coordination chemistry of anions of nontransition elements. [Pg.249]

Figure 2.30 Representation of the asymmetric unit of [Nd(L )4(H20)][(TTF—CH=CH—Py+)] 2-The radical cation donors are drawn as balls and sticks the paramagnetic anionic coordination complexes of Nd(III) are drawn as capped sticks [23d], (Reprinted with permission from F. Pointillart, O. Maury, Y. Fe Gal, S. Golhen, O. Cador and F. Ouahab, 4-(2-Tetrathiafulvalenyl-ethenyl)pyridine (TTF—CH=CH—py) radical cation salts containing poly(P-diketonate) rare earth complexes synthesis, crystal structure, photoluminescent and magnetic properties, Inorganic Chemistry, 48, 7421-7429, 2009. 2009 American Chemical Society.)... Figure 2.30 Representation of the asymmetric unit of [Nd(L )4(H20)][(TTF—CH=CH—Py+)] 2-The radical cation donors are drawn as balls and sticks the paramagnetic anionic coordination complexes of Nd(III) are drawn as capped sticks [23d], (Reprinted with permission from F. Pointillart, O. Maury, Y. Fe Gal, S. Golhen, O. Cador and F. Ouahab, 4-(2-Tetrathiafulvalenyl-ethenyl)pyridine (TTF—CH=CH—py) radical cation salts containing poly(P-diketonate) rare earth complexes synthesis, crystal structure, photoluminescent and magnetic properties, Inorganic Chemistry, 48, 7421-7429, 2009. 2009 American Chemical Society.)...
Fig. 2 Photoluminescence and photoluminescence excitation spectra of Eu complex-capped ZnSe hybrid QDs synthesised from (a) Eu acetate hydrate, (b) Eu acetylacetonate hydrate and (c) CIE colour coordinates and images of ZnSe QDs (1), Eu-complexes (2) and Eu complex-capped ZnSe QDs (3). Reproduced with permission from reference 9. Copyright The Royal Society of Chemistry 2011. Fig. 2 Photoluminescence and photoluminescence excitation spectra of Eu complex-capped ZnSe hybrid QDs synthesised from (a) Eu acetate hydrate, (b) Eu acetylacetonate hydrate and (c) CIE colour coordinates and images of ZnSe QDs (1), Eu-complexes (2) and Eu complex-capped ZnSe QDs (3). Reproduced with permission from reference 9. Copyright The Royal Society of Chemistry 2011.

See other pages where Photoluminescence coordination chemistry is mentioned: [Pg.64]    [Pg.1]    [Pg.138]    [Pg.248]    [Pg.75]    [Pg.35]    [Pg.64]    [Pg.160]    [Pg.86]    [Pg.520]    [Pg.87]    [Pg.226]    [Pg.204]   
See also in sourсe #XX -- [ Pg.139 , Pg.140 , Pg.141 , Pg.142 , Pg.143 , Pg.144 , Pg.145 , Pg.146 , Pg.147 , Pg.148 , Pg.149 , Pg.150 , Pg.151 , Pg.152 , Pg.153 ]




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