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1.10- phenanthroline cyanide

FIA methods based on ferric reducing power similar to the FRAP principle reaction have been used for the determination of ascorbic acid, vitamin E, and total iron. Table 30.1 summarizes most of these studies. Spectrophotometric detection is also used in many of these studies because of the chromogenic effect from Fe oxidation, which changes with complex ligands, such as TPTZ, o-phenanthroline, cyanide, and DPPH. Different FIA manifolds have also been investigated and proposed, from single to multiple lines. Therefore, like other chromogenic antioxidant tests, the FRAP assay has the potential for several flow injection adaptations. [Pg.587]

Cu, Ni, Co, Cr, Fe, or Al, even in traces, must be absent when conducting a direct titration of the other metals listed above if the metal ion to be titrated does not react with the cyanide ion or with triethanolamine, these substances can be used as masking reagents. It has been stated that the addition of 0.5-1 mL of 0.001 M o-phenanthroline prior to the EDTA titration eliminates the blocking effect of these metals with solochrome black and also with xylenol orange (see below). [Pg.317]

These are thermodynamically relatively weak oxidants (Table 18) and their action is relatively restricted, for example, to inorganic ions of moderate reducing power such as iodide, to polyfunctional organic compounds such as hydroxy-acids, and, in the cases of Ag(I) and Cu(II), to CO and H2. Fe(III) is particularly affected by hydrolysis and all these oxidants form complexes with suitable ligands. Cyanide ion and 1,10-phenanthroline form strong complexes with Fe(III) which greatly affect its behaviour. Tris-l,10-phenanthrolineiron(III) (ferriin) displays... [Pg.407]

Table XVI shows a selection of stability constants and redox potentials for iron(II) and iron(III) complexes. This Table covers a wide range of the latter, showing how the relative stabilities of the iron(II) and iron(III) complexes are refiected in. B (Fe /Fe ) values. A more detailed illustration is provided by the complexes of a series of linear hexadentate hydroxypyridinonate and catecholate ligands, where again high stabilities for the respective iron(III) complexes are refiected in markedly negative redox potentials (213). The combination of the high stabilities of iron(III) complexes of hydrox5rpyridinones, as of hydroxamates, catecholates, and siderophores, and the low stabilities of their iron(II) analogues is also apparent in Fig. 8. Here redox potentials for hydroxypyranonate and hydroxypyridinonate complexes of iron are placed in the overall context of redox potentials for iron(III)/iron(II) couples. The -(Fe /Fe ) range for e.g., water, cyanide, edta, 2,2 -bipyridyl, and (substituted) 1,10-phenanthrolines is... Table XVI shows a selection of stability constants and redox potentials for iron(II) and iron(III) complexes. This Table covers a wide range of the latter, showing how the relative stabilities of the iron(II) and iron(III) complexes are refiected in. B (Fe /Fe ) values. A more detailed illustration is provided by the complexes of a series of linear hexadentate hydroxypyridinonate and catecholate ligands, where again high stabilities for the respective iron(III) complexes are refiected in markedly negative redox potentials (213). The combination of the high stabilities of iron(III) complexes of hydrox5rpyridinones, as of hydroxamates, catecholates, and siderophores, and the low stabilities of their iron(II) analogues is also apparent in Fig. 8. Here redox potentials for hydroxypyranonate and hydroxypyridinonate complexes of iron are placed in the overall context of redox potentials for iron(III)/iron(II) couples. The -(Fe /Fe ) range for e.g., water, cyanide, edta, 2,2 -bipyridyl, and (substituted) 1,10-phenanthrolines is...
SDS), and indeed SDS-catalysis of Hg " -catalyzed replacement of cyanides in [Fe(C1 6]" 1 1,10-phenanthroline has been proposed as an analytical method for the determination of mercury. ... [Pg.422]

The standard electrode potentials, E°(V) for some chelates of the Fe /Fe redox couple areas follows o-phenanthroline, 1.20 2,2 -bipyridyl 1.096 water, 0.77 cyanide, 0.10 oxalate, -0.01 and 8-hydroquinone, -0.15 (Latimer, 1952). In the case of bipyridyl... [Pg.192]

The chlorine groups in 4-chloro-1,10-phenanthroline and 4,7-dichloro-1,10-phenanthroline are replaced by cyano groups on fusion with potassium cyanide342 while 2-cyano- and 5-cyano- 1,10-phenanthrolines have been obtained from 2-chloro and 5-bromo-l,10-phenanthrolines, respectively, by reaction with cuprous cyanide.267... [Pg.53]

Metal-binding agents (118-120) Oxalate, citrate, 1,10-phenanthroline, azide, diethyldithiocarbamate, cyanide, and 8-hydroxyquinoline inhibit, suggesting the metalloenzyme nature of the catalyst... [Pg.580]

NMO NMP Nu PPA PCC PDC phen Phth PPE PPTS Red-Al SEM Sia2BH TAS TBAF TBDMS TBDMS-C1 TBHP TCE TCNE TES Tf TFA TFAA THF THP TIPBS-C1 TIPS-C1 TMEDA TMS TMS-C1 TMS-CN Tol TosMIC TPP Tr Ts TTFA TTN N-methylmorpholine N-oxide jV-methyl-2-pyrrolidone nucleophile polyphosphoric acid pyridinium chlorochromate pyridinium dichromate 1,10-phenanthroline phthaloyl polyphosphate ester pyridinium p-toluenesulfonate sodium bis(methoxyethoxy)aluminum dihydride (3-trimethylsilylethoxy methyl disiamylborane tris(diethylamino)sulfonium tetra-n-butylammonium fluoride f-butyldimethylsilyl f-butyldimethylsilyl chloride f-butyl hydroperoxide 2,2,2-trichloroethanol tetracyanoethylene triethylsilyl triflyl (trifluoromethanesulfonyl) trifluoroacetic acid trifluoroacetic anhydride tetrahydrofuran tetrahydropyranyl 2,4,6-triisopropylbenzenesulfonyl chloride 1,3-dichloro-1,1,3,3-tetraisopropyldisiloxane tetramethylethylenediamine [ 1,2-bis(dimethylamino)ethane] trimethylsilyl trimethylsilyl chloride trimethylsilyl cyanide tolyl tosylmethyl isocyanide meso-tetraphenylporphyrin trityl (triphenylmethyl) tosyl (p-toluenesulfonyl) thallium trifluoroacetate thallium(III) nitrate... [Pg.1319]

It is worthwhile to analyze why co-existing soft ligands assist low oxidation numbers. If we want to make a copper(I) compound, it is very difficult to try the aqua ion, the fluoride or the anhydrous sulphate because they disproportionate to the metallic element and a higher oxidation state, here Cu(II). However, as seen in Eq. (7) it is easier to make the ammonia complex Cu(NH3)2 under anaerobic conditions, and even easier to make copper(I) complexes of pyridine and of conjugated bidentate ligands such as 2,2 -dipyridyl and 1.10-phenanthroline. The experimental problems are reversed in the case of iodides and cyanides, where it is easy to precipitate Cul or CuCN or to prepare solutions in an excess of the ligand containing Cul J,... [Pg.20]

It is of interest to note that the adduct Fe(phen)2(CN)2(BH3)2 (phen = 1,10-phenanthroline) has been prepared 87>. Cyanide bridges exist between the transition metal and BH3 groups. [Pg.26]

Although simple copper(n) cyanides cannot be prepared, stable complexes can be obtained with o-phenanthroline [Cu(phen)2CN]Y,nH20 Y = Cl, Br, I, N03, C104, or [Cu(phen)CN2]. The i.r. and electronic spectra of these compounds are consistent with trigonal-bipyramidal copper with an equatorial CN group. A square-planar [Cu(phen)(CN)2] was also prepared.680... [Pg.311]


See other pages where 1.10- phenanthroline cyanide is mentioned: [Pg.463]    [Pg.439]    [Pg.135]    [Pg.691]    [Pg.189]    [Pg.109]    [Pg.149]    [Pg.232]    [Pg.243]    [Pg.252]    [Pg.41]    [Pg.440]    [Pg.447]    [Pg.1140]    [Pg.45]    [Pg.132]    [Pg.294]    [Pg.22]    [Pg.1483]    [Pg.10]    [Pg.12]    [Pg.439]    [Pg.173]    [Pg.709]    [Pg.48]    [Pg.351]    [Pg.30]    [Pg.247]    [Pg.248]    [Pg.48]    [Pg.49]    [Pg.291]   
See also in sourсe #XX -- [ Pg.1219 ]

See also in sourсe #XX -- [ Pg.4 , Pg.1219 ]




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1 : 10-Phenanthroline

1 : 10-phenanthrolin

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