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Oxide ligands

The ranking is consistent with the three trends for determining A nature of the ligands, oxidation state of the metal, and position of the metal in the periodic table. [Pg.1457]

The well-known ambiguities in limiting descriptions of metal and ligand oxidation states are summarized below. [Pg.337]

It is interesting to note that orthometallation occurs preferentially at the aryl ring in the thiolactone 69 despite the availability of oxygen as a potential donor ligand oxidation of the dinuclear complex 70 by ceric ion gives the condensed isobenzothiophene derivative 71 in unspecified yield152 (Scheme 85). [Pg.357]

Figure 8.2. The metal-ion dependence of ligand oxidation in complexes of the reduced Curtis macrocycle. Figure 8.2. The metal-ion dependence of ligand oxidation in complexes of the reduced Curtis macrocycle.
Fig. 22. Remarkable activation-by-ligand-oxidation pathways for the reaction of ruthenium-arenes with thiolates. (a) Reaction of [Ru (r 6-bip)(en)(OH2)]+ with GSH (b) direct synthesis of ruthenium-arene sulfenato complexes (c) the air-stable thiolato complexes are oxidized in the presence of the antioxidant GSH. Fig. 22. Remarkable activation-by-ligand-oxidation pathways for the reaction of ruthenium-arenes with thiolates. (a) Reaction of [Ru (r 6-bip)(en)(OH2)]+ with GSH (b) direct synthesis of ruthenium-arene sulfenato complexes (c) the air-stable thiolato complexes are oxidized in the presence of the antioxidant GSH.
The results of Weiss field calculation on ferric ions at the surface metal ion sites are given in Figure 6 of ref 4, and the values for room temperature are shown in Figure 10. Since both ferric and pentavalent Sb ions can occupy octahedral or distorted octahedral sites with six ligand oxide ions and bulk hematite is considered to accommodate pentavalent Sb—119 ions in the metal ion sites (3 ), we can estimate STHF interactions on tetravalent Sn-119 ions at the surface metal ion sites of hematite. Using the magnetization of surface ferric ions at room temperature, the STHF magnetic fields on tetravalent Sn-119 ions at the surface sites are calculated to be... [Pg.416]

Group VI Donors. Oxygen and sulphur donor ligands. Oxidative addition of tetrachloro-l,2-benzoquinone to rrans-[Ir(CO)Cl(PR3)2] (R3 — Ph3 or Ph2Me) has been shown to give the Ir ° products [Ir(02CgCl4)(C0)Cl(PR3)2], whose structures (45) were confirmed from far-i.r. and H n.m.r. data. Comparison... [Pg.397]

The lowest energy excited triplet state of FePc is known to have a life time of about 45 nanoseconds (33) and we expect the life time of the lowest energy excited triplet state of FePc(Im )2 Also to be in the same time scale. Electrochemical oxidation at the phthalocycuiine ligand oxidation... [Pg.322]

Ligand (233) contains two 1,2-phenylenediamine domains that can be independently oxidized, and this is observed in the complex [(NH3)4Ru(/i-233)Ru(NH3)4] " " which undergoes two, two-electron ligand-oxidation processes further oxidation generates Ru -containing... [Pg.629]

Contents Formal Oxidation Numbers. Configurations in Atomic Spectroscopy. Characteristics of Transition Group Ions. Internal Transitions in Partly Filled Shells. Inter-Shell Transitions. Electron Transfer Spectra and Collectively Oxidized Ligands. Oxidation States in Metals and Black Semi-Conductors. Closed-Shell Systems, Hydrides and Back-Bonding. Homopolar Bonds and Catenation. Quanticule Oxidation States. Taxological Quantum Chemistry. [Pg.146]

Photoreduction of ammine complexes containing aliphatic amines instead of ammonia does not lead to production of molecular nitrogen instead, a variety of other ligand oxidation products are formed. Moeller and co-workers have studied three such systems in 3M HC1 solution 58 59 rather similar results have been obtained in more dilute acid solutions.55... [Pg.164]


See other pages where Oxide ligands is mentioned: [Pg.284]    [Pg.181]    [Pg.277]    [Pg.101]    [Pg.70]    [Pg.271]    [Pg.297]    [Pg.397]    [Pg.442]    [Pg.842]    [Pg.588]    [Pg.239]    [Pg.240]    [Pg.164]    [Pg.200]    [Pg.35]    [Pg.48]    [Pg.417]    [Pg.492]    [Pg.110]    [Pg.168]    [Pg.178]    [Pg.203]    [Pg.937]    [Pg.268]    [Pg.459]    [Pg.312]    [Pg.611]    [Pg.651]    [Pg.831]    [Pg.59]    [Pg.232]    [Pg.485]    [Pg.992]    [Pg.1031]    [Pg.128]    [Pg.284]    [Pg.5]   
See also in sourсe #XX -- [ Pg.398 , Pg.399 ]




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Allylic ligand oxidation

Aminyl radicals, ligand oxidation

Arene ligand reactivity oxidation

Aryl oxide ligands

Bispidine ligands iron oxidation

Bridging ligands oxides

Chelated organic ligands oxidation-reduction reactions

Cinchona Alkaloids as Chiral Ligands in Asymmetric Oxidations

Coordinated diimine ligands, oxidation

Coordinated diimine ligands, oxidation electron transfer

Coordinated diimine ligands, oxidation products

Coordinated diimine ligands, oxidation reaction products

Coordinated ligands oxidation

Coordination oxide ligands

Diaminophosphine oxide ligands

Ethylene ligands, oxidative coupling

Heteroatom-substituted secondary phosphine oxide ligands

Hydrogen oxide ligand

Iron bispidine ligands, oxidation chemistry

Iron complexes bispidine ligands, oxidation chemistry

Ligand Design for Oxidation

Ligand Effects for Transition Metal Oxides

Ligand properties lower oxides

Ligand properties oxidation states

Ligand properties oxides

Ligand substitution reactions high oxidation state complexes

Ligand synthesis Wacker oxidation

Ligand-centered oxidation-reduction

Ligand-transfer oxidations

Ligands imine from oxidation

Ligands substitution, nitric oxide

Ligands, transition-metal oxidation

Manganese Complexes for Alkene Oxidation Based on Pyridyl Ligands

Metal-ligand complexes, oxidation potentials

Monophosphine ligands aryl halide oxidative addition

Nitric Oxide A Non-Innocent Ligand

Nitric Oxide as a Paramagnetic Ligand

Nitric oxide ligand

Nitric oxide, ligand effects

Nitro ligands oxidation

Nitrogen oxide ligands

Nitrous oxide ligand

Oxidation Schiff base-type ligands

Oxidation and Reduction of Co-ordinated Ligands

Oxidation indole-based ligands

Oxidation ligand free metal catalysis

Oxidation ligand steric profile

Oxidation ligands

Oxidation of Coordinated Ligands

Oxidation of the porphyrin ligand

Oxidation phenolate ligands

Oxidation redox noninnocent” ligands

Oxidation states ligand characteristics

Oxidation-reduction reactions Bridging ligand

Oxidations, ligand-centered

Oxidative Additions Involving Ligand Bond Cleavage

Oxidative activation tridentate ligands

Oxidative addition bidentate diphosphine ligands

Oxidative addition monodentate ligands

Oxidative ligand-transfer reaction

Oxidative-addition donor ligands

Oxidative-addition ligand steric properties

Oxide ligand substitution

Water oxidation quinone ligands

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