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Metal ions Characterization

Table II reports the contact coupling constant for different aqua ion systems at room temperature. The contact coupling constant is a measure of the unpaired spin density delocalized at the coordinated protons. The values were calculated from the analysis of the contact contribution to the paramagnetic enhancements of relaxation rates in all cases where the correlation time for dipolar relaxation is dominated by x and Tig > x. In fact, in such cases the dispersion due to contact relaxation occurs earlier in frequency than the dispersion due to dipolar relaxation. In metalloproteins the contact contribution is usually negligible, even for metal ions characterized by a large contact contribution in aqua ion systems. This is due to the fact that the dipolar contribution is much larger because the correlation time increases by orders of magnitude, and x becomes longer than Tig. Under... Table II reports the contact coupling constant for different aqua ion systems at room temperature. The contact coupling constant is a measure of the unpaired spin density delocalized at the coordinated protons. The values were calculated from the analysis of the contact contribution to the paramagnetic enhancements of relaxation rates in all cases where the correlation time for dipolar relaxation is dominated by x and Tig > x. In fact, in such cases the dispersion due to contact relaxation occurs earlier in frequency than the dispersion due to dipolar relaxation. In metalloproteins the contact contribution is usually negligible, even for metal ions characterized by a large contact contribution in aqua ion systems. This is due to the fact that the dipolar contribution is much larger because the correlation time increases by orders of magnitude, and x becomes longer than Tig. Under...
Di Paola, A., Marci, G., Palmisano, L., Schiavello, M., Uosaki, K., Ikeda, S. and Ohtani, B. (2002). Preparation of polycrystalline Ti02 photocatalysts impregnated with various transition metal ions Characterization and photocatalytic activity for the degradation of 4-nitrophenol. J. Phys. Chem. B 106(3), 637-645. [Pg.504]

A few reports on metal ion characterization in metalloenzymes by hyphenated techniques with ICP-MS detection should also be mentioned. Inhibition, reactivation, and determination of metal ions in membrane metalloproteases of bacterial origin was studied by Leopold et al The results obtained by SEC-ICP-MS and the results of enzymological methods indicated that two different membrane proteases from Bacillus cereus and Pseudomonas aeruginosa were zinc metalloproteases. In another study, ICP-MS measurements helped in the characterization of a fibrinolytic metalloprotease from the ftniting bodies of an edible mushroom. " Using HPLC-ICP-MS, Suzuki et al. detected a zinc-binding protein present specifically in the livers of male adult rats. ... [Pg.6098]

Active carbon materials can be used for preconcentration (by adsorption) of diluted electroactive species (e.g.. metal ions). Characterizing the electrochemical behavior of these. systems is therefore important both for electroanalytical [248] and catalytic purposes [242-247,249]. On the other hand, how the adsorbed electroactive species interacts with the electrode material depends on its surface... [Pg.189]

Dunbar RC, Steill JD, Polfer NC, Berden G, Oomens J (2012) Peptide bond tautraneiizatimi induced by divalent metal ions characterization of the iminol configuration. Angew Chem Int... [Pg.221]

A. Di Paola, G. Marci, L. Palmisano, M. Schiavello, K. Uosaki, S. Ikeda, B. Ohtani, Preparation of Polycrystalline Ti02 Photocatalysts Impregnated with Various Transition Metal Ions Characterization and Photocatalytic Activity for the Degradation of 4-Nitrophenol. J. Phys. [Pg.500]

Inorganic flocculants are analyzed by the usual methods for compounds of this type. Residual metal ions in the effluent are measured by spectroscopic techniques such as atomic absorption. Polymeric aluminum species formed in solution have been characterized by Al-nmr (64). [Pg.36]

On the basis of data obtained the possibility of substrates distribution and their D-values prediction using the regressions which consider the hydrophobicity and stmcture of amines was investigated. The hydrophobicity of amines was estimated by the distribution coefficient value in the water-octanole system (Ig P). The molecular structure of aromatic amines was characterized by the first-order molecular connectivity indexes ( x)- H was shown the independent and cooperative influence of the Ig P and parameters of amines on their distribution. Evidently, this fact demonstrates the host-guest phenomenon which is inherent to the organized media. The obtained in the research data were used for optimization of the conditions of micellar-extraction preconcentrating of metal ions with amines into the NS-rich phase with the following determination by atomic-absorption method. [Pg.276]

The most common ions observed as a result of electron-stimulated desorption are atomic (e. g., H, 0, E ), but molecular ions such as OH", CO", H20, and 02" can also be found in significant quantities after adsorption of H2O, CO, CO2, etc. Substrate metallic ions have never been observed, which means that ESD is not applicable to surface compositional analysis of solid materials. The most important application of ESD in the angularly resolved form ESDIAD is in determining the structure and mode of adsorption of adsorbed species. This is because the ejection of positive ions in ESD is not isotropic. Instead the ions are desorbed along specific directions only, characterized by the orientation of the molecular bonds that are broken by electron excitation. [Pg.177]

Two classes of aldolase enzymes are found in nature. Animal tissues produce a Class I aldolase, characterized by the formation of a covalent Schiff base intermediate between an active-site lysine and the carbonyl group of the substrate. Class I aldolases do not require a divalent metal ion (and thus are not inhibited by EDTA) but are inhibited by sodium borohydride, NaBH4, in the presence of substrate (see A Deeper Look, page 622). Class II aldolases are produced mainly in bacteria and fungi and are not inhibited by borohydride, but do contain an active-site metal (normally zinc, Zn ) and are inhibited by EDTA. Cyanobacteria and some other simple organisms possess both classes of aldolase. [Pg.620]

Alkyl derivatives such as 1,4-S6(NR)2 and S4(NR)4 can be synthesized by reacting S2CI2 with primary amines RNH2 in an inert solvent. Compounds such as 1,4-S2(NR)4 (R = —C02Et) are now also well characterized.The bis-adduct [Ag(S4N4H4)2]" " has been isolated as its perchlorate this has a sandwich-like structure and is unique in being S-bonded rather than N-bonded to the metal ion. ... [Pg.736]

When the polymer was prepared by the suspension polymerization technique, the product was crosslinked beads of unusually uniform size (see Fig. 16 for SEM picture of the beads) with hydrophobic surface characteristics. This shows that cardanyl acrylate/methacry-late can be used as comonomers-cum-cross-linking agents in vinyl polymerizations. This further gives rise to more opportunities to prepare polymer supports for synthesis particularly for experiments in solid-state peptide synthesis. Polymer supports based on activated acrylates have recently been reported to be useful in supported organic reactions, metal ion separation, etc. [198,199]. Copolymers are expected to give better performance and, hence, coplymers of CA and CM A with methyl methacrylate (MMA), styrene (St), and acrylonitrile (AN) were prepared and characterized [196,197]. [Pg.431]

This is only the beginning of a process which ultimately results in the formation of solid state hydroxides or oxides. Actually, the solution species present in neutral or alkaline solutions of transition-metal ions are relatively poorly characterized. The formation of numerous hydroxy- and oxy-bridged polynuclear species makes their investigation very difficult. However, it is clear that there is a near-continuous transition from mononuclear solution species, through polynuclear solution species to colloidal and solid state materials. By the way, the first example of a purely inorganic compound to exhibit chirality was the olated species 9.11. [Pg.183]

The potential of reversed micelles needs to be evaluated by theoretical analysis of the metal ion distribution within micelles, by evaluation of the free energy of the solvated ions in the reversed micelle organic solution and the bulk aqueous water, and by the experimental characterization of reversed micelles by small-angle neutron and x-ray scattering. [Pg.137]

SIMS Cluster Ion Characterization During Oxygen Adsorption and Oxidation. For heavy oxidation, that is essentially bulk oxide films, the oxidation state of the metal can be determined from the positive and negative SIMS intensity distributions (1 ). Though similar attempts have been made to characterize the nature of the surface during the early stages of oxygen interactions (14,15), we now know from the extensive information available from other techniques that such interpretations are incorrect. We use the by now well-characterized W(100)/O and Ni(100)/0 systems as examples. [Pg.319]

The pectin/sucrose gels were characterized as follows (amounts per lOOg gel) 0.3 g AUA, 65% soluble solid substance, 0.01 mol sodium acetate / lactic acid buffer, pH 3.0 (20°C). The metal ions were added as combinations of chlorides according to a mixture design with constant amount of chloride ions (2.5 mmol / lOOg gel). Thus the total amount of metal ions... [Pg.584]

IR spectroscopy of adsorbed carbon monoxide has been used extensively to characterize the diluted, reduced Cr/silica system [48-54,60,76,77]. CO is an excellent probe molecule for Cr(ll) sites because its interaction is normally rather strong. The interaction of CO with a transition metal ion can be separated into electrostatic, covalent a-dative, and 7r-back donation contributions. The first two cause a blue shift of the vco (with respect to that of the molecule in the gas phase, 2143 cm ), while the last causes a red shift [83-89]. From a measurement of the vco of a given Cr(II) carbonyl complex, information is thus obtained on the nature of the Cr(II)- CO bond. [Pg.15]


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See also in sourсe #XX -- [ Pg.200 , Pg.408 ]




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