Hydroxylamine ligands

Hydroxylamine, IV-benzoyl-lV-phenyl-in gravimetry, 1, 532 liquid-liquid extraction, 1, 544 Hydroxylamine, A -cinnamoyl-A -phenyl-liquid-liquid extraction, 1,544 Hydroxylamine, Ar,A -di-(-butyl-metal complexes, 2, 798 Hydroxylamine, Ay/V-diethyl-metal complexes, 2,798 Hydroxylamine, AAmethyl-metal complexes, 2,798 Hydroxylamine, A -2-naphthol-A -nitroso-ammonium salt — see Ncocupferron Hydroxylamine, A -nilrosophenyl-ammonium salt — see Cupferron Hydroxylamine ligands, 2, 101 Hydroxylamine oxido reductase, 6, 727 Hydroxylases molybdenum, 6,658,662 Hydroxylation arenes... 

A-Benzoylphenylhydroxylamine (BPHA) reacts with Nb20 in bioling acidic aqueous solutions to yield a monomeric seven-coordinated niobium compound [NbO(BPHA)3]. The hydroxylamine ligand could be displaced by tropolone or 8-quinolinol, and the ratedetermining step was shown to be associative (equation 38).427 Oxoniobium and tantalum(V) 8-quinolinolates have also been reported. The optimal conditions for the formation and extraction of the [Nb0(C6H402)3]3 ion formed in the niobium(V)-pyrocatechol system, have been investigated.428... 

The reaction of Mo02(MeNHOi2 in the presence of the hydroxylamine ligand and CS2 proceeds according to Scheme 4. 4 The resultant formally seven-coordinate complex has a distorted pentagonal bipyramidal structure with the lone oxo group in the apical position. The five equatorial positions are occupied by two formally bidentate 0,N hydroxylamido ligands of... 

Hydroxylamine, O-acetyl-N-benzoyl-N-phenyl-hydroxamic acids from, 506 Hydroxylamine ligands, 101 Hydrozirconation, 342 Hypoxanthines metal complexes, 93... 

An interesting facet of the molecular modelling studies [66] was that they suggested that one methyl group of the hydroxylamine ligand was in an orientation suitable for replacement by other functionality. This is potentially important because PTPase active site residues are highly conserved, and enzyme selectivity is conferred... 

Amines, hydrazines, and hydroxylamines. Amine complexes are known for tetravalent complexes of the earliest actinides (Th, U), particularly for the halides, nitrates, and oxalates. The complexes are generated either in neat amine, or by addition of amine to the parent compound in a nonaqueous solvent. Some of the known simple amine compounds are presented in Table 6. The molecular structure of ThCl4(NMe3)3 has been determined. The coordination environment about the metal is a chloride capped octahedron. A very limited number of adducts exist in which a tetravalent actinide is coordinated by a hydrazine or hydroxylamine ligand the parent compound is generally a halide or sulfate complex. Cationic metal hydrates coordinated with primary, secondary, or tertiary amines have also been isolated with acetylacetonate, nitrate, or oxalate as counterions. 

The monovalent Co chemistry of amines is sparse. No structurally characterized example of low-valent Co complexed exclusively to amines is known. At low potentials and in non-aqueous solutions, Co1 amines have been identified electrochemically, but usually in the presence of co-ligands that stabilize the reduced complex. At low potential, the putative monovalent [Co(cyclam)]+ (cyclam = 1,4,8,11-tetraazacyclotetradecane) in NaOH solution catalyzes the reduction of both nitrate and nitrite to give mixtures of hydroxylamine and ammonia.100 Mixed N-donor systems bearing 7r-acceptor imine ligands in addition to amines are well known, but these examples are discussed separately in Section 6.1.2.1.3. 

These reagents are required for proper color development. Hydroxylamine hydrochloride is a reducing agent, which is required to keep the iron in the +2 state. The o-phenanthroline is a ligand that reacts with Fe2+ to form an orange-colored complex ion. This ion is the absorbing species. In addition, since the reaction is pH dependent, sodium acetate is needed for buffering at the optimum pH. 

In our hands, base-activated phosphoramidite-Ir complexes were not suited for the allylation of hydroxylamine and hydrazine derivatives (R. Weihofen and G. Helmchen, unpublished results). However, interesting results were obtained by Takemoto and coworkers with Pybox type ligands (Scheme 9.30) [40]. Phosphates... 

Hydroxylamine can act as either a N-nucleophile or O-nucleophile, depending on which of the reactive centers is protected. For all reactions Ph-Pybox has been used as ligand, and moderate to high levels of selectivity have been achieved. Hydroxamic acid derivatives and oximes have also been probed as O-nucleophiles [63]. 

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