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Gold complexes,

The small amounts of gold contained in low-grade ores can be extracted using a combination of oxidation and complexation. Gold is oxidized to Au, which forms a very strong complex with cyanide anions Au ((2 q) + l CN(a q) [Au (CN)2] aq) K -lx 10 Suppose that a sample of ore containing 2.5 X 10 mol of gold is extracted with 1.0 L of 4.0 X 10 M aqueous KCN solution. Calculate the concentrations of the three species involved in the complexation equilibrium. [Pg.1324]

Cinellu, M.A. and Minghetti, G. (2002) Gold(l) and gold(lll) complexes with anionic oxygen donor ligands hydroxo, 0X0 and alkoxo complexes. Gold Bulletin, 35, 11. [Pg.80]

Shaw, C.F. Ill, Schaeffer, N.A., Elder, R.C., Eidsness, M.K., Trooster, J.M. and Calls, G.H.M. (1984) Bovine serum albumin-gold thiomalate complex gold-197 Moessbauer, EXAFS and XANES, electrophoresis, sulfur-35 radiotracer, and fluorescent probe competition studies. Journal of the American Chemical Society, 106, 3511-3521. [Pg.311]

Plaksin, I. N. Laskorin, B. N. Shivrin, G. N. Liquid extraction of complex gold and silver cyanides from cyanide solutions. Tsvetnye Metally 1961, 34, 20-23. [Pg.806]

Fig. 18. X-ray crystal structure of the injectable antiarthritic complex gold(I)-aurothiomalate 88 (side-chain on S omitted) showing the double helical chains. The right-handed helix shown contains thiomalate ligands with the R absolute configuration. Au-S bond lengths 2.283 and 2.286 A S-Au-S angles 178.88° and 169.41°. Adapted from (419). Fig. 18. X-ray crystal structure of the injectable antiarthritic complex gold(I)-aurothiomalate 88 (side-chain on S omitted) showing the double helical chains. The right-handed helix shown contains thiomalate ligands with the R absolute configuration. Au-S bond lengths 2.283 and 2.286 A S-Au-S angles 178.88° and 169.41°. Adapted from (419).
Localization energies of some isomeric proton addition complexes (Gold and Tye 1952c) ... [Pg.286]

In addition to the synthetic advances, the study of the optical properties of these species is a growing field. Many complexes which exhibit these interactions are luminescent. Other interesting points are the induction of rotator phases or the modulation of magnetic properties by designing the appropriate heterometallic complexes. Gold-gold interactions are still a hot topic in gold chemistry. This is evidenced in the observation that some complexes which exhibit these interactions, characterized some years ago, are revisited and modified in order to study their properties. [Pg.117]

Carbonyl Complexes of the Transition Metals Cluster Compounds Inorganometalhc Compounds Containing Transition Metal Main Group Elements Cyanide Complexes of the Transition Metals Dinuclear Organometallic Cluster Complexes Gold Inorganic Coordination Chemistry. [Pg.1472]

The presence of carbonaceous material in the ore precipitates the gold in cyanide solutions, thus resulting in an increase of gold content in the cyanidation residue. For such complex gold-bearing ores, a roasting operation oxidizes the carbonaceous matter and thereby makes the ore more amenable to cyanidation. However, the alteration of the associated minerals presents new dissolution problems which must be solved. [Pg.20]

Hydrido complexes, gold-osmium, 27 209 iridium, 26 117, 27 19 iron, 26 244, 27 168 iron-tungsten, 26 336 manganese, 26 226 mercury-molybdenum-ruthenium,... [Pg.357]

Taylor, A. (2013). Developments in the processing of refractory complex gold ores. Presented at AusIMM Bendigo Technical Meeting, 2013, Melbourne, Australia. [Pg.13]

Gold(lll) Complexes. Gold(m) is isoelectronic with Pt(n), and its complexes therefore show many structural similarities to those of Pt(n). [Pg.1053]

The formation of gold oligomers and, after a long time, of gold particles Au ,cn", that are also associated with complexed gold ions, is observed at 520 The... [Pg.1224]

The trans influence of a ligand is the ability of a ligand to weaken the bond trans to itself in a complex. Gold(I) and gold(III) complexes are, in the simplest treatment, considered to use sp and dsp hybrid orbitals in forming linear and square planar complexes respectively. A good o donor, L, tends to concentrate gold 6s character in the AuL bond and the trans bond must then overlap with an orbital of low s character. A weaker and more ionic bond is then formed. [Pg.5742]

The chemistry of gold is complex. Gold can exist in seven oxidation states -1,0, - -1, -1-2, +3, +4, and - -5. Apart fromAu in the colloidal and elemental forms, only Au+ and Au+ are known to form compounds that are stable in aqueous media and important in medical applications. The remaining oxidation states of -1, +2, +4, and +5 are not presently known to play a role in biochemical processes related to therapeutic uses of gold. Neither Au+ or Au+ forms a stable aquated ion ([Au(OH2)+ ] or [Au(OH2)4 ], respectively)... [Pg.325]


See other pages where Gold complexes, is mentioned: [Pg.386]    [Pg.233]    [Pg.357]    [Pg.298]    [Pg.41]    [Pg.382]    [Pg.546]    [Pg.386]    [Pg.869]    [Pg.40]    [Pg.340]    [Pg.43]    [Pg.233]    [Pg.618]    [Pg.147]    [Pg.392]    [Pg.298]    [Pg.210]    [Pg.99]    [Pg.228]    [Pg.233]    [Pg.237]    [Pg.248]    [Pg.250]    [Pg.256]    [Pg.693]    [Pg.225]    [Pg.99]    [Pg.228]   


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Absorption gold-silver complexes

Achiral gold complexes

Aldol reaction gold complex

Alkene-gold complexes

Alkene-gold complexes synthesis

Alkyl gold complexes

Alkynyl gold complexes

Anion complexes gold dithiocarbamates

Anti gold complexes

Anti-arthritic activity, gold complexes

Antimalarial gold complexes

Antitumor gold complexes

Aryl gold complexes

Asymmetric catalysis gold complexes

Benzene, pentafluoro-, gold complexes

Bis(diphenylphosphine)ethane Gold Complexes

Captopril—gold complexes

Carbene complexes gold adducts

Carbene complexes of gold

Carbene-gold complexes synthesis

Carbonyl complexes gold-osmium

Carbonyl complexes gold-ruthenium

Carbonyl complexes of gold

Carbonyl complexes, chromium gold-osmium

Carbonyl gold complexes

Catalysts gold complexes

Cationic complexes gold dithiocarbamates

Cationic gold complexes

Cationic gold complexes, enyne

Charge transfer gold complexes

Chiral gold complexes

Colloidal gold protein complexes

Complexes Blue Gold

Complexes gold amidinate

Complexes gold cyanide

Complexes gold-protein

Complexes of gold

Complexes pentafluorophenyl)gold

Complexes polyamine gold

Cyclic trinuclear gold complexes

Cyclohexene complexes with gold

Cyclometallated gold complexes

Cyclooctadiene complexes with gold

Cysteine-gold complexes

Cytotoxicity, gold complexes

Deposition of gold-phosphine complexes

Dimeric structures gold® complexes

Dimethyl gold complex

Dinuclear gold® complexes moieties

Dinudear gold complexes

Electrochemistry ferrocene-gold complexes

Ferrocene-gold complexes

Ferrocenylphosphine-gold complex

Four-coordinate gold complexes

Glyoxime, dimethylin analysis Gold complexes

Gold , macrocyclic complex

Gold -Schiff base complexes

Gold -alkyne complex

Gold -carbene complexes

Gold -ferrocenyl complex

Gold -porphyrin complex

Gold 5-coordinate complexes

Gold Complexes for Alkyne Activation

Gold Complexes in Asymmetric Catalysis

Gold Dicyanide Complexes

Gold allene complex

Gold anticancer complexes

Gold bimetallic complexes

Gold cluster complexes

Gold cluster complexes bonding

Gold cluster complexes mixed metal

Gold cluster complexes structure

Gold complex compounds, anions

Gold complex compounds, nonelectrolytes, with tertiary alkylphosphines or -arsines

Gold complex manganese

Gold complex molybdenum

Gold complex tantalum

Gold complex vanadium

Gold complexes 2,2 -bipyridyl

Gold complexes 2,3-dimercaptopropanol

Gold complexes Mossbauer spectra

Gold complexes This page has been reformatted by Knovel to provide easier navigation

Gold complexes acetylene

Gold complexes acetylide

Gold complexes amido

Gold complexes amines

Gold complexes ammines

Gold complexes anionic nitrogen donor ligands

Gold complexes antitumor activity

Gold complexes antitumor properties

Gold complexes antitumour activity

Gold complexes applications

Gold complexes arsenic donor ligands

Gold complexes arsenic-donors

Gold complexes arsenides

Gold complexes arsines

Gold complexes as antitumor agents

Gold complexes aurides

Gold complexes azides

Gold complexes bonding

Gold complexes boron bonds

Gold complexes bromides

Gold complexes carbenes

Gold complexes carbodiphosphoranes

Gold complexes carbon donor ligands

Gold complexes carbon-donors

Gold complexes carborane

Gold complexes carboranes

Gold complexes catalysis

Gold complexes cyano

Gold complexes cyclopentadienyl

Gold complexes decomposition

Gold complexes diamines

Gold complexes dinuclear

Gold complexes dithioacetates

Gold complexes dithiocarbamates

Gold complexes dithiolates

Gold complexes dithiophosphinates

Gold complexes electron-deficient

Gold complexes enantioselective aldol reaction

Gold complexes ether

Gold complexes five co-ordinate

Gold complexes fluorides

Gold complexes fulminates

Gold complexes halides

Gold complexes halogen-donors

Gold complexes homoleptic structures

Gold complexes hydrides

Gold complexes hydroarylation reactions

Gold complexes hydrolysis

Gold complexes imidazoles

Gold complexes iodides

Gold complexes isocyanates

Gold complexes labelled

Gold complexes ligand exchange reactions

Gold complexes ligands

Gold complexes linkage isomerism

Gold complexes luminescence properties

Gold complexes luminescent

Gold complexes main group metal bonds

Gold complexes maleonitriledithiolates

Gold complexes metathesis

Gold complexes mixed-valence compounds

Gold complexes mobilization

Gold complexes mono structures

Gold complexes monodentate arsines

Gold complexes monodentate stibines

Gold complexes nitriles

Gold complexes nitrogen donor ligands

Gold complexes nitrogen-donors

Gold complexes organic ligands

Gold complexes oxidation

Gold complexes oxygen donor ligands

Gold complexes oxygen donors

Gold complexes penicillamine

Gold complexes pentafluoride

Gold complexes phenanthroline

Gold complexes phosphides

Gold complexes phosphine methyls

Gold complexes phosphorus donor ligands

Gold complexes phosphorus-donors

Gold complexes photochemistry

Gold complexes phthalocyanine

Gold complexes phthalocyanines

Gold complexes pyrazoles

Gold complexes pyridines

Gold complexes pyrolysis

Gold complexes reaction intermediates

Gold complexes reactions

Gold complexes reactivity

Gold complexes rearrangement

Gold complexes redox properties

Gold complexes room temperature conductivity

Gold complexes selenides

Gold complexes selenium donor ligands

Gold complexes sensitizers

Gold complexes silyl

Gold complexes spectra

Gold complexes stabilizers

Gold complexes stibines

Gold complexes structure

Gold complexes substitution reactions

Gold complexes sulfides

Gold complexes sulfites

Gold complexes sulfur donor ligands

Gold complexes sulphur-donors

Gold complexes supported

Gold complexes syntheses

Gold complexes terms Links

Gold complexes thermodynamics of electroplating

Gold complexes thiazole

Gold complexes thioethers

Gold complexes thiolates

Gold complexes thiosulfates

Gold complexes thiourea

Gold complexes trans influence

Gold complexes trans-effect

Gold complexes transition metal bonds

Gold complexes unusual co-ordination numbers

Gold complexes utility

Gold complexes vibrational spectra

Gold complexes with alkenes

Gold complexes with alkynes

Gold complexes with captopril

Gold complexes with coordinated phosphorus atoms

Gold complexes with cysteine

Gold complexes with dithiocarbamates

Gold complexes with methyl iodide

Gold complexes with olefins

Gold complexes with phosphines

Gold complexes with thiolates

Gold complexes ylides

Gold complexes ylids

Gold complexes, attractive interactions

Gold complexes, oxidative

Gold complexes, oxidative addition reactions

Gold complexes, pyramidal

Gold compounds complexes

Gold cyclometalated complexes

Gold dithiocarbamate complexes

Gold halide complexes solubility

Gold isocyanide complexes

Gold metal complexes

Gold phosphine complexes, reactions with

Gold phosphine complexes, reactions with metal clusters

Gold phosphino complexes

Gold planar complexes

Gold sulfoxide complexes

Gold ylide complexes

Gold(I) Complexes with Monodentate Phosphines

Gold(I) Complexes with Polydentate Ligands

Gold(II) Complexes

Gold(III) Complexes

Gold(III) Square-Planar Complexes

Gold(IV) Complexes

Gold(V) Complexes

Gold(l) Complexes

Gold(ll) Complexes

Gold(lll) Complexes

Gold(lll) Complexes with Nitrogen and Oxygen Ligands

Gold(m) Complexes

Gold, olefin complexes

Gold, tetrakis -, complexes with

Gold, thiolate complexes

Gold, xanthate complexes

Gold-Protein Reactions and Complexes

Gold-chloride complexes

Gold-containing complexes

Gold-heterometal complexes

Gold-phosphine complex

Gold-rhenium complexes

Gold-silver supramolecular complexes

Gold-stibine complexes

Gold-thallium complexes

Gold-thallium supramolecular complexes

Gold-thio-complex

Gold-triflimide complexes

Gold-xenon complexes

Gold® I) complexes

Gold® isonitrile complexes

Group gold® complexes

Hexanuclear gold complex, structure

Hydrido complexes gold-osmium

Hydrido complexes gold-ruthenium

Isocyanides gold complexes

L-Cysteine, gold complex

Luminescence dinuclear gold complexes

Luminescence gold complexes

Luminescent gold alkynyl complexes

Luminescent gold complexes ligands

Luminescent gold phosphine complexes

Medical Applications of NHC-Gold and -Copper Complexes

Medicinally important gold complexe

Mesityl, gold complexes

Methanide-gold complexes

Methyl isocyanoacetate ferrocenylphosphine-gold complexes

Methylenomycin ferrocenylphosphine-gold complexes

Mixed-metal trinuclear complexes, gold

Mononuclear Gold(I) Complexes

Mononuclear Gold(II) Complexes

Mononuclear gold complexes

NHC-Copper, Silver and Gold Complexes in Catalysis

NHC-gold complex

NHC-gold complexe

NO2SC3H7, L-Cysteine, gold complex

Nucleophilic attack gold complexes

Oligomeric gold complexes

Orbital gold-copper complexes

Organometallic Gold(I) Complexes

Organometallic Gold(III) Complexes

Organometallic gold -alkynyl complexes

Organometallic gold complexes

Pentanuclear gold complex

Phosphine triethyl-, gold-osmium complex

Phosphine-gold® complexes luminescence

Phosphine-gold® complexes synthesis

Phosphines gold sulfide complexes

Photoinduced Electron Transfer Reactions of Gold Complexes

Photophysics of Gold Complexes

Photosensitivity, gold complexes

Polynuclear gold complex

Preparation of (Strept)avidin-Gold Complexes

Preparation of Antibody-Gold Complexes

Preparation of Lectin-Gold Complexes

Preparation of Protein A-Gold Complexes

Rhodium(I) and Gold(III) Complexes

Solid state gold-copper complexes

Solid state gold-lead complex

Solid state gold-platinum complexes

Solid state gold-silver complexes

Solid state gold-thallium complexes

Spectroscopic gold complexes

Square planar gold complexes

Square pyramidal gold cation complexes

Supported Gold Complex Catalysts

Synthesis of Gold-Containing Mixed-Metal Cluster Complexes

Thermal properties, gold complexes

Thiocyanate, gold complex

Thiolate-gold® complexes luminescence

Thiolato-gold complexes

Thiophene, tetrahydro-, gold complexes

Three and Four-Coordinate Gold(I) Complexes

Transition metal complexes, gold

Transition metal complexes, gold Au CH

Triphenylarsine, complex with gold

Ylide complexes of gold

Ylide-gold complexes synthesis

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