Characterization absorption spectroscopy

Wliat does one actually observe in the experunental spectrum, when the levels are characterized by the set of quantum numbers n. Mj ) for the nonnal modes The most obvious spectral observation is simply the set of energies of the levels another important observable quantity is the intensities. The latter depend very sensitively on the type of probe of the molecule used to obtain the spectmm for example, the intensities in absorption spectroscopy are in general far different from those in Raman spectroscopy. From now on we will focus on the energy levels of the spectmm, although the intensities most certainly carry much additional infonnation about the molecule, and are extremely interesting from the point of view of theoretical dynamics. 

The prepared catalysts were characterized by x-ray diffraction (XRD), N2 adsorption and CO chemisorption. Also, X-ray absorption spectroscopy (XAS) at the Ni K edge (8.333 keV) of reference and catalyst samples was carried out in the energy range 8.233 to 9.283 keV at beamline X18B of the... 

X-ray absorption spectroscopy was used for situ characterization of active, supported Pt catalysts. 

X-ray absorption spectroscopy combining x-ray absorption near edge fine structure (XANES) and extended x-ray absorption fine structure (EXAFS) was used to extensively characterize Pt on Cabosll catalysts. XANES Is the result of electron transitions to bound states of the absorbing atom and thereby maps the symmetry - selected empty manifold of electron states. It Is sensitive to the electronic configuration of the absorbing atom. When the photoelectron has sufficient kinetic energy to be ejected from the atom It can be backscattered by neighboring atoms. The quantum Interference of the Initial... 

Transition metal oxides, rare earth oxides and various metal complexes deposited on their surface are typical phases of DeNO catalysts that lead to redox properties. For each of these phases, complementary tools exist for a proper characterization of the metal coordination number, oxidation state or nuclearity. Among all the techniques such as EPR [80], UV-vis [81] and IR, Raman, transmission electron microscopy (TEM), X-ray absorption spectroscopy (XAS) and NMR, recently reviewed [82] for their application in the study of supported molecular metal complexes, Raman and IR spectroscopies are the only ones we will focus on. The major advantages offered by these spectroscopic techniques are that (1) they can detect XRD inactive amorphous surface metal oxide phases as well as crystalline nanophases and (2) they are able to collect information under various environmental conditions [83], We will describe their contributions to the study of both the support (oxide) and the deposited phase (metal complex). 

Dendrimer encapsulated Pt nanoparticles (DENs) were prepared via literature methods (1, 11). PtCl42 and dendrimer solutions (20 1 Pt2+ dendrimer molar ratio) were mixed and stirred under N2 at room temperature for 3 days. After reduction with 30 equivalents of BH4 overnight, dialysis of the resulted light brown solution (2 days) yielded Pt2o nanoparticle stock solution. The stock solution was filtered through a fine frit and Pt concentration was determined with Atomic Absorption Spectroscopy (11). Details on catalyst characterization and activity measurements have been published previously (11). 

Since mild activation conditions appear to be important, a number of solution activation conditions were tested. PAMAM dendrimers are comprised of amide bonds, so the favorable conditions for refro-Michael addition reactions, (low pH, high temperature and the presence of water) may be able to cleave these bonds. Table 1 shows a series of reaction tests using various acid/solvent combinations to activate the dendrimer amide bonds. Characterization of the solution-activated catalysts with Atomic Absorption spectroscopy, FTIR spectroscopy and FTIR spectroscopy of adsorbed CO indicated that the solution activation generally resulted in Pt loss. Appropriate choice of solvent and acid, particularly EtOH/HOAc, minimized the leaching. FTIR spectra of these samples indicate that a substantial portion of the dendrimer amide bonds was removed by solution activation (note the small y-axis value in Figure 4 relative... 

Vol. 21 Reilctance Spectroscopy. By Wesley Wm.Wendlandt and Harry G. Hecht Vol. 22 The Analytical Toxicology of Industrial Inorganic Poisons. By the late Morris B. Jacobs Vol. 23 The Formation and Properties of Precipitates. By Alan G.Walton Vol. 24 Kinetics in Analytical Chemistry. By Harry B. Mark, Jr. and Garry A. Rechnitz Vol. 25 Atomic Absorption Spectroscopy. Second Edition. By Morris Slavin Vol. 26 Characterization of Organometallic Compounds (in two parts). Edited by Minoru Tsutsui Vol. 27 Rock and Mineral Analysis. Second Edition. By Wesley M. Johnson and John A. Maxwell Vol. 28 The Analytical Chemistry of Nitrogen and Its Compounds (in two parts). Edited by C. A. Streuli and Philip R.Averell... 

Conclusions. Time-resolved CO laser absorption spectroscopy can provide information useful in characterizing the primary photochemical channels in gas-phase transition metal carbonyls. We have found that product vibrational energy distributions indicate that W(CO)g and Cr(CO>6 dissociate via different... 

S-C sMes)Ir1"(L)C1]1 complexes (L = bpy and phen derivatives) form stable hydrides upon oxidative addition of a proton to the doubly reduced [(775-C5Me5)Ir1(L)]° intermediate (Equations (14) and (15)),23 24 26 28 which have been characterized by absorption spectroscopy and H-NMR spectrometry. Additional electrochemical activation is thus required for efficient H2 evolution, by either spontaneous decomposition (Equation (17)) or protonation (Equation (18)) of the reduced hydride complex (ECE mechanism) 24,26,28... 

XPS has typically been regarded primarily as a surface characterization technique. Indeed, angle-resolved XPS studies can be very informative in revealing the surface structure of solids, as demonstrated for the oxidation of Hf(Sio.sAso.5)As. However, with proper sample preparation, the electronic structure of the bulk solid can be obtained. A useful adjunct to XPS is X-ray absorption spectroscopy, which probes the bulk of the solid. If trends in the XPS BEs parallel those in absorption energies, then we can be reasonably confident that they represent the intrinsic properties of the solid. Features in XANES spectra such as pre-edge and absorption edge intensities can also provide qualitative information about the occupation of electronic states. 

Paktunc, D. Dutrizac, J. 2003. Characterization of arsenate-for-sulfate substitution in synthetic jarosite using X-ray diffraction and X-ray absorption spectroscopy. Canadian Mineralogist, 41, 905-919. 

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