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99% 2N 99.9% 3N     99.99% 4N   99.999% 5N     99.9999% 6N 

ORGANO-METALLICS INFORMATION CENTER
AE OrganoMetallics ™

32.4 (A)/00.022


Hydrogen                                Helium  
Lithium Beryllium                     Boron Carbon Nitrogen Oxygen Fluorine Neon
Sodium Magnesium                     Aluminum Silicon Phosphorus Sulfur Chlorine Argon
Potassium Calcium Scandium Titanium Vanadium Chromium Manganese Iron Cobalt Nickel Copper Zinc Gallium Germanium Arsenic Selenium Bromine Krypton
Rubidium Strontium Yttrium Zirconium Niobium Molybdenum Technetium Ruthenium Rhodium Palladium Silver Cadmium Indium Tin Antimony Tellurium Iodine Xenon
Cesium Barium Lanthanum Hafnium Tantalum Tungsten Rhenium Osmium Iridium Platinum Gold Mercury Thallium Lead Bismuth Polonium Astatine Radon
Francium Radium Actinium Rutherfordium Dubnium Seaborgium Bohrium Hassium Meitnerium Darmstadtium Roentgenium Copernicium Ununtrium Ununquadium Ununpentium Ununhexium Ununseptium Ununoctium
                                   
    Cerium Praseodymium Neodymium Promethium Samarium Europium Gadolinium Terbium Dysprosium Holmium Erbium Thulium Ytterbium Lutetium    
    Thorium Protactinium Uranium Neptunium Plutonium Americium Curium Berkelium Californium Einsteinium Fermium Mendelevium Nobelium Lawerencium      

(click on an element to view our products)



American Elements
is a manufacturer and supplier specializing in organo-metallic compounds of Cerium, Lanthanum, Erbium, Ytterbium, Neodymium, Yttrium and other Rare Earth elements, Palladium, Hafnium, Scandium, Niobium, Tungsten, Ruthenium, Platinum as well as other advanced elements and more common catalytic metals, such as copper, tin and nickel in the form of acetylacetonates, cyclohexanebutyrates, 2-ethylhexanoates, trifluoroacetates, trifloromethanesulfonates, hexafloro- and trifloroacetylacetonates and Tris(2,2,6,6-tetramethyl-3,5-heptanedionate).

Organo-Metallic compounds are metallic cations bound to carbon-based anions making the compound soluble in organic rather than aqueous solvents so the elemental metal can serve as a catalyst in organic synthesis reactions.

For example, 2-Ethylhexanoates are carboxylates with many commercial applications They are commonly used in various catalysts for oxidation, hydrogenation and polymerization and as an adhesion promoter. The High Purity acetylacetonate anion complexes by bonding each oxygen atom to the metallic cation to form a chelate ring. Because of this property, Metallic Acetylacetonates are commonly used in various catalysts and catalytic reagents for organic synthesis such as hydrogenation and polymerization.


Organo-Metallics are marketed under the trade name and trademark AE OrganoMetallics™. American Elements can produce a variety of purities including 99%, 99.9%, 99.99%, 99.999% and 99.9999% which are sometimes referred to as 2N, 3N, 4N, 5N and 6N. Specific impurities, such as iron, calcium and silica can be reduced to customer specified levels.

Please select from the table an AE OrganoMetallics™ products:



Acetylacetonate  2-Ethylhexanoate Trifluoromethanesulfonate Other
Aluminum Acetylacetonate
Aluminum 2-Ethylhexanoate
Barium Acetylacetonate
Beryllium Acetylacetonate
Cadmium Acetylacetonate
Calcium Acetylacetonate
Cerium Acetylacetonate
Chromium Acetylacetonate
Cobalt Acetylacetonate
Copper Acetylacetonate
Dysprosium Acetylacetonate
Erbium Acetylacetonate
Europium Acetylacetonate
Gadolinium Acetylacetonate
Gallium Acetylacetonate
Hafnium Acetylacetonate
Holmium Acetylacetonate
Indium Acetylacetonate
Iridium Acetylacetonate
Iron Acetylacetonate
Lanthanum Acetylacetonate
Lead Acetylacetonate
Lithium Acetylacetonate
Lutetium Acetylacetonate
Magnesium Acetylacetonate
Manganese Acetylacetonate
Neodymium Acetylacetonate
Nickel Acetylacetonate
Palladium Acetylacetonate
Platinum Acetylacetonate
Praseodymium Acetylacetonate
Rhodium Acetylacetonate
Ruthenium Acetylacetonate
Samarium Acetylacetonate
Scandium Acetylacetonate
Sodium Acetylacetonate
Strontium Acetylacetonate
Terbium Acetylacetonate
Thallium Acetylacetonate
Thorium Acetylacetonate
Thulium Acetylacetonate
Tin Acetylacetonate
Vanadium Acetylacetonate
Ytterbium Acetylacetonate
Yttrium Acetylacetonate
Zinc Acetylacetonate
Zirconium Acetylacetonate
Aluminum 2 Ethylhexanoate
Barium 2-Ethylhexanoate
Beryllium 2-Ethylhexanoate
Bismuth 2-Ethylhexanoate
Calcium 2-Ethylhexanoate
Cadmium 2-Ethylhexanoate
Cerium 2-Ethylhexanoate
Chromium 2-Ethylhexanoate
Cobalt 2-Ethylhexanoate
Cobalt(II) 2-ethylhexanoate Solution
Copper 2-Ethylhexanoate
Dysprosium 2-Ethylhexanoate
Erbium 2-Ethylhexanoate
Europium 2-Ethylhexanoate
Gadolinium 2-Ethylhexanoate
Gallium 2 - Ethylhexanoate
Hafnium 2-Ethylhexanoate
Holmium 2-Ethylhexanoate
Indium 2-Ethylhexanoate
Iridium 2 - Ethylhexanoate
Iron 2 - Ethylhexanoate
Lanthanum 2-Ethylhexanoate
Lead 2 - Ethylhexanoate
Lithium 2 - Ethylhexanoate
Lutetium 2-Ethylhexanoate
Magnesium 2-Ethylhexanoate
Manganese 2-Ethylhexanoate
Molybdenum 2-Ethylhexanoate
Neodymium 2-Ethylhexanoate
Nickel 2-Ethylhexanoate
Niobium 2-Ethylhexanoate
Palladium 2 - Ethylhexanoate
Platinum 2 - Ethylhexanoate
Potassium 2 - Ethylhexanoate
Praseodymium 2 - Ethylhexanoate
Rhenium 2-Ethylhexanoate
Ruthenium 2 - Ethylhexanoate
Samarium 2-Ethylhexanoate
Scandium 2-Ethylhexanoate
Silicon 2-Ethylhexanoate
Silver 2-Ethylhexanoate
Sodium 2 - Ethylhexanoate
Strontium 2 - Ethylhexanoate
Tellurium 2-Ethylhexanoate
Terbium 2-Ethylhexanoate
Thalium 2-Ethylhexanoate
Thallium 2 - Ethylhexanoate
Thorium 2 - Ethylhexanoate
Tin 2-Ethylhexanoate
Tin(II) 2-ethylhexanoate
Vanadium 2-Ethylhexanoate
Ytterbium 2-Ethylhexanoate
Yttrium 2-Ethylhexanoate
Yttrium(III) 2-ethylhexanoate
Zinc 2-Ethylhexanoate
Aluminum Trifluoromethanesulfonate
Barium Trifluoromethanesulfonate
Beryllium Trifluoromethanesulfonate
Bismuth Trifluoromethanesulfonate
Cadmium Trifluoromethanesulfonate
Calcium Trifluoromethanesulfonate
Cerium Trifluoromethanesulfonate
Cerium Trifluoromethanesulfonate Hydrate
Chromium Trifluoromethanesulfonate
Cobalt Trifluoromethanesulfonate
Copper Trifluoromethanesulfonate
Dysprosium Trifluoromethanesulfonate
Erbium Trifluoromethanesulfonate
Europium Trifluoromethanesulfonate
Gadolinium Trifluoromethanesulfonate
Gallium Trifluoromethanesulfonate
Hafnium Trifluoromethanesulfonate
Holmium Trifluoromethanesulfonate
Indium Trifluoromethanesulfonate
Iridium Trifluoromethanesulfonate
Iron Trifluoromethanesulfonate
Lanthanum Trifluoromethanesulfonate
Lead Trifluoromethanesulfonate
Lithium Trifluoromethanesulfonate
Lutetium Trifluoromethanesulfonate
Magnesium Trifluoromethanesulfonate
Manganese Trifluoromethanesulfonate
Neodymium Trifluoromethanesulfonate
Nickel Trifluoromethanesulfonate
Palladium Trifluoromethanesulfonate
Platinium Trifluoromethanesulfonate
Praseodymium Trifluoromethanesulfonate
Rhodium Trifluoromethanesulfonate
Ruthenium Trifluoromethanesulfonate
Samarium Trifluoromethanesulfonate
Scandium Trifluoromethanesulfonate
Scandium Trifluoromethanesulfonate
Silver Trifluoromethanesulfonate
Sodium Trifluoromethanesulfonate
Strontium Trifluoromethanesulfonate
Terbium Trifluoromethanesulfonate
Thalium Trifluoromethanesulfonate
Thorium Trifluoromethanesulfonate
Thulium Trifluoromethanesulfonate
Tin Trifluoromethanesulfonate
Ytterbium Trifluoromethanesulfonate
Yttrium Trifluoromethanesulfonate
Zinc Trifluoromethanesulfonate
Zirconium Trifluoromethanesulfonate
Tris[N,N-bis(trimethylsilyl)amide]cerium(III)
Tris[N,N-bis(trimethylsilyl)amide]europium(III)
Tris[N,N-bis(trimethylsilyl)amide]gadolinium(III)
Tris[N,N-bis(trimethylsilyl)amide]holmium(III)
Tris[N,N-bis(trimethylsilyl)amide]lanthanum(III)
Tris[N,N-bis(trimethylsilyl)amide]neodymium(III)
Tris[N,N-bis(trimethylsilyl)amide]praseodymium(III)
Tris[N,N-bis(trimethylsilyl)amide]samarium(III)
Tris[N,N-bis(trimethylsilyl)amide]terbium(III)
Tris[N,N-bis(trimethylsilyl)amide]yttrium

Aluminum Tris(2,2,6,6-tetramethyl-3,5-heptanedionate)
Calcium Bis(2,2,6,6-tetramethyl-3,5-heptanedionate)
Chromium Tris(2,2,6,6-tetramethyl-3,5-heptanedionate)
Cobalt Tris(2,2,6,6-tetramethyl-3,5-heptanedionate)
Copper Bis(2,2,6,6-tetramethyl-3,5-heptanedionate)
Dimethylcadmium
Iron Tris(2,2,6,6-tetramethyl-3,5-heptanedionate)
Nickel Bis(2,2,6,6-tetramethyl-3,5-heptanedionate)
Scandium Tris(2,2,6,6-tetramethyl-3,5-heptanedionate) Hydrate
Terbium Tris(2,2,6,6-tetramethyl-3,5-heptanedionate)
Thulium Tris(2,2,6,6-tetramethyl-3,5-heptanedionate)
Yttrium Tris(2,2,6,6-tetramethyl-3,5-heptanedionate)
Zirconium Diisopropoxidebis(2,2,6,6-tetramethyl-3,5-heptanedionate)

Iron p-toluenesulfonate Hexahydrate
Silver p-toluenesulfonate
Zinc p-toluenesulfonate Hydrate

Tris(cyclopentadienyl)erbium
Tris(cyclopentadienyl)gadolinium
Tris(cyclopentadienyl)lanthanum
Bis(cyclopentadienyl)nickel
Tris(cyclopentadienyl)yttrium

Tris(tetramethylcyclopentadienyl)cerium(III)
Tris(tetramethylcyclopentadienyl)europium(III)
Tris(tetramethylcyclopentadienyl)gadolinium(III)
Tris(tetramethylcyclopentadienyl)lanthanum(III)

Erbium Tris(2,2,6,6-tetramethyl-3,5-heptanedionate)
Tris(isopropylcyclopentadienyl)erbium

Europium Tris[3-(trifluoromethylhydroxymethylene)-(+)-camphorate]
Tris(benzoylacetonato) mono(phenanthroline)europium
Tris(dibenzoylmethane) mono(1,10-phenanthroline)europium

Gadolinium Octanoate

Neodymium(III) Tris(2,2,6,6-tetramethyl-3,5-heptanedionate)
Neodymium(III) Hexafluoro-2,4-pentanedionate

Praseodymium(III) Tris[3-(trifluoromethylhydroxymethylene)-d-camphorate]
Praseodymium(III) Tris[3-(heptafluoropropylhdroxymethylene)-d-camphorate]

Yttrium Trifluoroacetate Hydrate

Zinc Acrylate
Zinc Citrate Dihydrate
Zinc Stearate
Zinc Undecylenate
Zinc Trifluoroacetate Hydrate



Chloride, Nitrate, etc. Oxide & Metal Price Quote Submicron & Nanopowder Tolling Foil Sputtering Target Crystal Growth Advanced Materials Information Center

 

Recent Research & Development for Organometallics

  • Rearrangement/Fragmentation Reactions of Oligosilanes with Aluminum Chloride. Wagner H, Baumgartner J, Marschner C, Poelt P. Organometallics. 2011 Aug 8;30(15):3939-3954. Epub 2011 Jul 11. PMID: 21818171 [PubMed] Free PMC Article

  • Conformational Control of Polysilanes: Use of CH(2) Spacers in the Silicon Backbone. Wallner A, Hlina J, Wagner H, Baumgartner J, Marschner C. Organometallics. 2011 Aug 8;30(15):3930-3938. Epub 2011 Jul 11. PMID: 21818170 [PubMed] Free PMC Article

  • Coordination Driven Self-Assembly and Anticancer Activity of Molecular Rectangles Containing Octahedral Ruthenium Metal Centers. Vajpayee V, Song YH, Yang YJ, Kang SC, Kim H, Kim IS, Wang M, Stang PJ, Chi KW. Organometallics. 2011 Jun 27;30(12):3242-3245. PMID: 21779140 [PubMed]

  • Molecular Hume-Rothery Compounds [M(ZnR)(n)] and [M(ZnR)(a)(GaR)(b)] (a + 2b = n = 8): Relations of Coordination Polyhedra and Electronic Structure. Molon M, Gemel C, von Hopffgarten M, Frenking G, Fischer RA. Inorg Chem. 2011 Jul 12. [Epub ahead of print] PMID: 21749048 [PubMed - as supplied by publisher]

  • d(0) organometallics in catalysis. Arnold J, Scott P. Dalton Trans. 2011 Aug 14;40(30):7665. Epub 2011 Jul 6. No abstract available. PMID: 21734996 [PubMed - in process]

  • Solvothermal growth of a ruthenium metal-organic framework featuring HKUST-1 structure type as thin films on oxide surfaces. Kozachuk O, Yusenko K, Noei H, Wang Y, Walleck S, Glaser T, Fischer RA. Chem Commun (Camb). 2011 Aug 14;47(30):8509-11. Epub 2011 Jun 29. PMID: 21716991 [PubMed - in process]

  • Room Temperature Z-Selective Homocoupling of a Olefins by Tungsten Catalysts. Marinescu SC, Schrock RR, Müller P, Takase MK, Hoveyda AH. Organometallics. 2011;30(7):1780-1782. No abstract available. PMID: 21686089 [PubMed]

  • Characterization of Tunable Radical Metal-Carbenes: Key Intermediates in Catalytic Cyclopropanation. Belof JL, Cioce CR, Xu X, Zhang XP, Space B, Woodcock HL. Organometallics. 2011 Apr 29;30(10):2739-2746. PMID: 21643517 [PubMed]

  • Novel Organometallic Reagents: Geminal Dianionic Derivatives of the Heavy Group 14 Elements. Lee VY, Sekiguchi A. Inorg Chem. 2011 Jun 1. [Epub ahead of print] PMID: 21630690 [PubMed - as supplied by publisher]

  • Screening for low aquatic bioaccumulation (2): physico-chemical constraints. Nendza M, Herbst T. SAR QSAR Environ Res. 2011 Jun;22(3):351-64. PMID: 21598198 [PubMed - in process]

  • Preparation of polyfunctional zinc organometallics using an Fe- or Co-catalyzed Cl/Zn-exchange. Melzig L, Diène CR, Rohbogner CJ, Knochel P. Org Lett. 2011 Jun 17;13(12):3174-7. Epub 2011 May 19. PMID: 21595435 [PubMed - in process]

  • Homoleptic hexa and penta gallylene coordinated complexes of molybdenum and rhodium. Bollermann T, Cadenbach T, Gemel C, Freitag K, Molon M, Gwildies V, Fischer RA. Inorg Chem. 2011 Jun 20;50(12):5808-14. Epub 2011 May 17. PMID: 21591639 [PubMed - in process]

  • Quantum-sized gold nanoclusters: bridging the gap between organometallics and nanocrystals. Jin R, Zhu Y, Qian H. Chemistry. 2011 Jun 6;17(24):6584-93. doi: 10.1002/chem.201002390. Epub 2011 May 17. PMID: 21590819 [PubMed - in process]

  • Driving Catalyst Reoxidation in Wacker Cyclizations with Acetal-Based Metal-Hydride Abstractors. Cochrane NA, Brookhart MS, Gagné MR. Organometallics. 2011 May 9;30(9):2457-2460. PMID: 21572581 [PubMed]

  • Hydrosilation of Carbonyl-Containing Substrates Catalyzed by an Electrophilic ?-Silane Iridium(III) Complex. Park S, Brookhart M. Organometallics. 2010 Oct;29(22):6057-6064. PMID: 21572562 [PubMed]

  • Synthesis of Highly Stable 1,3-Diaryl-1H-1,2,3-triazol-5-ylidenes and their Applications in Ruthenium-Catalyzed Olefin Metathesis. Bouffard J, Keitz BK, Tonner R, Lavallo V, Guisado-Barrios G, Frenking G, Grubbs RH, Bertrand G. Organometallics. 2011 Mar 9;30(9):2617-2627. PMID: 21572542 [PubMed]

  • N-Heterocyclic Carbene Bound Nickel(I) Complexes and Their Roles in Catalysis. Zhang K, Conda-Sheridan M, Cooke S, Louie J. Organometallics. 2011 May 9;30(9):2546-2552. PMID: 21572533 [PubMed]

  • Physicochemical Studies and Anticancer Potency of Ruthenium ?-p-Cymene Complexes Containing Antibacterial Quinolones. Kljun J, Bytzek AK, Kandioller W, Bartel C, Jakupec MA, Hartinger CG, Keppler BK, Turel I. Organometallics. 2011 May 9;30(9):2506-2512. Epub 2011 Apr 6. PMID: 21552495 [PubMed] Free PMC Article

  • Conjugate additions to alkylidene bis(sulfoxides). Brebion F, Vincent G, Chelli S, Kwasnieski O, Najera F, Delouvrié B, Marek I, Derat E, Goddard JP, Malacria M, Fensterbank L. Chem Asian J. 2011 Jul 4;6(7):1825-33. doi: 10.1002/asia.201000904. Epub 2011 Mar 11. PMID: 21400664 [PubMed - in process]

  • Chelate-Assisted Oxidative Coupling Reaction of Arylamides and Unactivated Alkenes: Mechanistic Evidence for Vinyl C-H Bond Activation Promoted by an Electrophilic Ruthenium-Hydride Catalyst. Kwon KH, Lee DW, Yi CS. Organometallics. 2010 Oct 21;29(22):5748-5750. PMID: 21344062 [PubMed]

PRODUCT LIST




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