Fe L- and K-edge XAS of low-spin ferric corrole: bonding and reactivity relative to low-spin ferric porphyrin. (1/174)

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DNA recognition by the DNA primase of bacteriophage T7: a structure-function study of the zinc-binding domain. (2/174)

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Coherent multidimensional optical probes for electron correlations and exciton dynamics: from NMR to X-rays. (3/174)

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X-ray absorption spectroscopy. (4/174)

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Biogenic formation of As-S nanotubes by diverse Shewanella strains. (5/174)

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Biophysical characterization of the iron in mitochondria from Atm1p-depleted Saccharomyces cerevisiae. (6/174)

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Extended X-ray absorption fine structure study on reaction of anti-tumor platinum complexes with reduced glutathione. (7/174)

Reactions of cis-diamminedichloroplatinum(II) (cisplatin) and 1,1-cyclobutanedicarboxylatodiammineplatinum(II) (carboplatin) with reduced glutathione, a tripeptide that is abundant in cells, were studied by means of X-ray absorption spectroscopy. Back-scattering amplitudes F(i)(k) and phase shifts Phi(i)(k) were theoretically derived, and validated by applying them to calculate extended X-ray absorption fine structure (EXAFS) oscillations of cisplatin and K(2)[Pt(SCN)(4)] in the solid state. EXAFS oscillations of reaction mixtures of cisplatin or carboplatin with reduced glutathione were fitted to the standard EXAFS equation using the F(i)(k) and Phi(i)(k) functions to give the coordination numbers of N or O atoms (N(N/O)) and of Cl or S atoms (N(Cl/S)). For both cisplatin and carboplatin, the N(N/O) value decreased and the N(Cl/S) values increased monotonically as the reaction proceeded. However, the reaction rate for carboplatin was significantly slower than that for cisplatin.  (+info)

The chemical forms of mercury in aged and fresh dental amalgam surfaces. (8/174)

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