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Anionic interactions platinum

The adsorption of anions on solid surfaces is of considerable interest, mainly because of its effect on the kinetics of electrochemical reactions. Several in-situ techniques have been applied toward this purpose. Infrared measurements were used to identify adsorbed species, estimate anion adsorption isotherms, and to gain information on anion interaction with electrode surfaces. " Sulfuric acid anions are possibly the conunonest anion adsorbates because of their specific adsorption on metal surfaces. Depending on the metal, its surface orientation, and the concentration of anion, either sulfate or bisulfate can be specifically adsorbed on the surface. Identifying the predominant adsorbate on platinum-group metals has engendered some controversy. While STM studies show that... [Pg.11]

Hydrogen bonding between an SiOH group and fluorine occurs in the platinum complex 44 [prepared by hydrolysis of a bis(alkylidene)-silacyclopropane] in which the SbF6 anion hydrogen bonds to the platinum-containing cation (O - F distance 2.77(2) A) (249). The platinum complex 45 is not reported (250) to form hydrogen bonds, and a more recent study (210) has confirmed that there do not appear to be any OH OH or OH tt interactions. [Pg.206]

In general, covalent coordination of platinum to phosphate groups has been neglected at the oligonucleotide level, although such interaction is feasible and has been observed with phosphate anions [109]. In N,N-di-methylformamide, ds-DDP seems to be able to coordinate to the phos-phodiester groups of d(TpT) and d(TpG)" [110]. In the case ofd(TpT)-,... [Pg.198]

The reaction of PtX and liquid ammonia gives mixtures of haloammine complexes [PtX (NH3)6 ]X4 n (X = Cl, Br, I n = 3, 2, 1, 0). The salts Pt(NH3)6]X, may be isolated as the main product only after several weeks of reaction. Interactions at room temperature of PtCl -and PtBr salts with liquid ammonia yield the dinuclear p-amido ammine complex [(NH3)4Pt(/i-NH2)2Pt(NH3)4]X6 quantitatively.1033 The structure shows a Pt-Pt separation of 3.16(1) A. 34 Interaction of PtXg with liquid or gaseous ammonia followed by addition of excess KNH2 yields the hexakis(amido) complex K2[Pt(NH2)6] (equation 333).1033 Complexes of the anionic ligand NC12 bonded to platinum(IV) have also been prepared. One method is by treatment of [PtCl(NH3)s]CI3 with chlorine (equation 334).1035... [Pg.429]

As far as we are aware, the number of luminescent extended systems with gold-platinum interactions is reduced to only one report. This is a puzzling situation since the situation of platinum in the periodic table suggests considerable relativistic effects for this atom and extended chains of squared-planar Pt(II) cation-anion complexes built by metal-metal interactions are not strange. In fact, salts such as [Pt(CNR)4][Pt(CN)4] ,67 which are luminescent and display vapochromic behavior, and the modified form of the Magnus salt [Pt(NH3)4][Pt(CN)4] ,68 which shows semiconducting properties, are examples of this type of supramolecular systems. Therefore, the stable combination of gold and platinum in cation/anion-acid/base systems should be anticipated. [Pg.359]

Ruiz J, Lorenzo J, Sanglas L, Cutillas N, Vicente C, Villa MD, Aviles FX, Lopez G, Moreno V, Perez J, Bautista D (2006) Palladium(II) and platinum(II) organometallic complexes with the model nucleobase anions of thymine, uracil, and cytosine antitumor activity and interactions with DNA of the platinum compounds. Inorg Chem 45 6347-6360... [Pg.54]

Somewhat more loosely related to platinum antitumor drugs were EHMO calculations performed on heterobimetallic Pt-Pd complexes with a bridging methylcytosinate anion by Mealli, Randaccio, Lippert, and coworkers [31][32], The calculations served to elucidate the metal-metal and metal-ligand binding interactions, and yielded a qualitative interpretation of the 195Pt-NMR chemical shifts. [Pg.539]


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See also in sourсe #XX -- [ Pg.194 ]




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