American Elements specializes in producing Tellurium Bromide in an ultra dry form for use as a compound in semiconductors and other high purity applications. Ultra Dry Tellurium Bromide is generally immediately available in most volumes. High purity, submicron and nanopowder forms may be considered.American Elements produces to many standard grades when applicable, including Mil Spec (military grade); ACS, Reagent and Technical Grade; Food, Agricultural and Pharmaceutical Grade; Optical Grade, USP and EP/BP (European Pharmacopoeia/British Pharmacopoeia)and follows applicable ASTM testing standards.Typical and custom packaging is available. Additional technical, research and safety (MSDS) information is available as is a Reference Calculator for converting relevant units of measurement.
Tellurium Bromide is a highly water soluble crystalline Tellurium source for uses compatible with Bromides and lower (acidic) pH. Metallic Bromides are marketed under the trade name AE Bromides™. Most metal bromide compounds are water soluble for uses in water treatment, chemical analysis and in ultra high purity for certain crystal growth applications. Bromide in an aqueous solution can be detected by adding Tellurium disulfide (CS2) and chlorine. Tellurium Bromide is generally immediately available in most volumes. Ultra high purity and high purity compositions improve both optical quality and usefulness as scientific standards. Nanoscale (See also Nanotechnology Information and Quantum Dots) elemental powders and suspensions, as alternative high surface area forms, may be considered.American Elements produces to many standard grades when applicable, including Mil Spec (military grade); ACS, Reagent and Technical Grade; Food, Agricultural and Pharmaceutical Grade; Optical Grade, USP and EP/BP (European Pharmacopoeia/British Pharmacopoeia)and follows applicable ASTM testing standards.Typical and custom packaging is available. Additional technical, research and safety (MSDS) information is available as is a Reference Calculator for converting relevant units of measurement.
Tellurium is a Block P, Group 16, Period 5 element. The number of electrons in each of Tellurium's shells is 2, 8, 18, 18, 6 and its electronic configuration is [Kr] 4d10 5s2 5p4. In its elemental form tellurium's CAS number is 13494-80-9. The tellurium atom has a radius of 143.2.pm and it's Van der Waals radius is 206.pm. Tellurium is a p-type semiconductor, and shows greater conductivity in certain directions, depending on alignment of the atoms. It is grown in crystalline form with other elements such as indium telluride. Its conductivity increases slightly with exposure to light which makes many tellurides candidates for solar energyapplications. Tellurium improves the machinability of copper and stainless steel, and its addition to lead decreases the corrosive action of sulfuric acid on lead and improves its strength and hardness. Tellurium is used as a basic ingredient in blasting caps, and is added to cast iron for chill control. Tellurium is used in ceramics. Bismuth telluride has been used in thermoelectric devices. Iron is available as metal and compounds with purities from 99% to 99.999% (ACS grade to ultra-high purity); metals in the form of foil, sputtering target, and rod, and compounds as submicron and nanopowder. Tellurium was first discovered by Franz Muller von Reichenstein in 1782. The name Tellurium originates from the Greek word 'Tellus' meaning Earth. See Tellurium research below.
Multi-metal(loid) methylation in methanoarchaea is linked to central intermediates of methanogenesis.
Thomas F, Diaz-Bone RA, Wuerfel O, Huber B, Weidenbach K, Schmitz RA, Hensel R.
Appl Environ Microbiol. 2011 Oct 14. [Epub ahead of print]
PMID:
22003009
[PubMed - as supplied by publisher]
Synthesis, structure, and bonding of orthorhombic r(5)au(2)te(2) (R = lu, ho, dy, y). Electronic structure of the binary parent valence compound eu(5)as(4).
Chai P, Corbett JD.
Inorg Chem. 2011 Nov 7;50(21):10949-55. Epub 2011 Oct 12.
PMID:
21991925
[PubMed - in process]
Glucose-6-Phosphate Dehydrogenase Protects Escherichia coli from Tellurite-Mediated Oxidative Stress.
Sandoval JM, Arenas FA, Vásquez CC.
PLoS One. 2011;6(9):e25573. Epub 2011 Sep 30.
PMID:
21984934
[PubMed - in process]
Microbial processing of tellurium as a tool in biotechnology.
Turner RJ, Borghese R, Zannoni D.
Biotechnol Adv. 2011 Sep 1. [Epub ahead of print]
PMID:
21907273
[PubMed - as supplied by publisher]
Measurement of the ?? Decay Half-Life of ^{130}Te with the NEMO-3 Detector.
Arnold R, Augier C, Baker J, Barabash AS, Basharina-Freshville A, Blondel S, Bongrand M, Broudin-Bay G, Brudanin V, Caffrey AJ, Chapon A, Chauveau E, Durand D, Egorov V, Flack R, Garrido X, Grozier J, Guillon B, Hubert P, Hugon C, Jackson CM, Jullian S, Kauer M, Klimenko A, Kochetov O, Konovalov SI, Kovalenko V, Lalanne D, Lamhamdi T, Lang K, Liptak Z, Lutter G, Mamedov F, Marquet Ch, Martin-Albo J, Mauger F, Mott J, Nachab A, Nemchenok I, Nguyen CH, Nova F, Novella P, Ohsumi H, Pahlka RB, Perrot F, Piquemal F, Reyss JL, Richards B, Ricol JS, Saakyan R, Sarazin X, Simard L, Simkovic F, Shitov Y, Smolnikov A, Söldner-Rembold S, Stekl I, Suhonen J, Sutton CS, Szklarz G, Thomas J, Timkin V, Torre S, Tretyak VI, Umatov V, Vála L, Vanyushin I, Vasiliev V, Vorobel V, Vylov Ts, Zukauskas A; NEMO-3 Collaboration.
Phys Rev Lett. 2011 Aug 5;107(6):062504. Epub 2011 Aug 4.
PMID:
21902318
[PubMed - in process]
Synthesis and characterization of wurtzite ZnTe nanorods with controllable aspect ratios.
Zhang J, Jin S, Fry HC, Peng S, Shevchenko E, Wiederrecht GP, Rajh T.
J Am Chem Soc. 2011 Oct 5;133(39):15324-7. Epub 2011 Sep 12.
PMID:
21899348
[PubMed - in process]
A homometallic tricapped cubane cluster: [(Cp*Mo)4B4H4(?4-BH)3] (Cp* = ?5-C5Me5).
Thakur A, Sahoo S, Ghosh S.
Inorg Chem. 2011 Sep 5;50(17):7940-2. Epub 2011 Aug 11.
PMID:
21834507
[PubMed - in process]
Selective antimicrobial activity associated with sulfur nanoparticles.
Schneider T, Baldauf A, Ba LA, Jamier V, Khairan K, Sarakbi MB, Reum N, Schneider M, Röseler A, Becker K, Burkholz T, Winyard PG, Kelkel M, Diederich M, Jacob C.
J Biomed Nanotechnol. 2011 Jun;7(3):395-405.
PMID:
21830480
[PubMed - indexed for MEDLINE]
Bioactivity of the conjugation of green-emitting CdTe quantum dots with a carborane complex.
Wu C, Shi L, Li Q, Zhao J, Selke M, Yan H, Wang X.
J Nanosci Nanotechnol. 2011 Apr;11(4):3091-9.
PMID:
21776675
[PubMed - indexed for MEDLINE]
Isolation and characterization of an environmental cadmium- and tellurite-resistant Pseudomonas strain.
Chien CC, Jiang MH, Tsai MR, Chien CC.
Environ Toxicol Chem. 2011 Oct;30(10):2202-7. doi: 10.1002/etc.620. Epub 2011 Aug 10.
PMID:
21766319
[PubMed - in process]
An ultrasensitive hydrogen peroxide biosensor based on electrocatalytic synergy of graphene-gold nanocomposite, CdTe-CdS core-shell quantum dots and gold nanoparticles.
Gu Z, Yang S, Li Z, Sun X, Wang G, Fang Y, Liu J.
Anal Chim Acta. 2011 Sep 2;701(1):75-80. Epub 2011 Jul 4.
PMID:
21763811
[PubMed - indexed for MEDLINE]
Synchronous determination of mercury (II) and copper (II) based on quantum dots-multilayer film.
Ma Q, Ha E, Yang F, Su X.
Anal Chim Acta. 2011 Sep 2;701(1):60-5. Epub 2011 Jun 17.
PMID:
21763809
[PubMed - indexed for MEDLINE]
Procedure-Controlled Selective Synthesis of 5-Acyl-2-iminothiazolines and their Selenium and Tellurium Derivatives by Convergent Tandem Annulation.
Wang Y, Zhang WX, Wang Z, Xi Z.
Angew Chem Int Ed Engl. 2011 Jul 14. doi: 10.1002/anie.201101948. [Epub ahead of print] No abstract available.
PMID:
21761522
[PubMed - as supplied by publisher]
Synthesis, structures and ab initio studies of selenium and tellurium bis(carbodithioates and carbothioates).
Kato S, Tani K, Ishida M, Nonogaki J, Ebihara M, Hayashi S, Nakanishi W, Niyomura O, Ando F, Koketsu J.
Dalton Trans. 2011 Aug 28;40(32):8156-69. Epub 2011 Jul 13.
PMID:
21750832
[PubMed - in process]
Electrical bistability in self-assembled hybrid multilayers of phospholipid and nanoparticles.
Yuan B, Hu SX, Lu NY, Xu F, Zhou K, Ma YQ, Li M.
Nanotechnology. 2011 Aug 5;22(31):315303. Epub 2011 Jul 12.
PMID:
21747161
[PubMed - indexed for MEDLINE]
Organomercury(II) and tellurium(II) compounds with the "pincer" ligand 2,6-[O(CH2CH2)2NCH2]2C6H3--stabilization of an unusual organotellurium(II) cationic species.
Beleaga A, Bojan VR, Pöllnitz A, Rat CI, Silvestru C.
Dalton Trans. 2011 Sep 21;40(35):8830-8. Epub 2011 Jul 11.
PMID:
21743935
[PubMed - in process]
Differentiation between the motor and sensory fascicles of the peripheral nerves from adult rats using annexin V-CdTe-conjugated polymer.
Meng X, Lu L, Wang H, Liu B.
Neurol India. 2011 May-Jun;59(3):333-8.
PMID:
21743158
[PubMed - indexed for MEDLINE]
Tellurium tetrachloride and diphenyl ditelluride cause cytotoxicity in rat hippocampal astrocytes.
Roy S, Hardej D.
Food Chem Toxicol. 2011 Oct;49(10):2564-74. Epub 2011 Jul 1.
PMID:
21742007
[PubMed - in process]
Recent Research & Development for Bromides
Synthesis of Enol Lactones via Cu(I)-Catalyzed Intramolecular O-Vinylation of Carboxylic Acids.
Sun C, Fang Y, Li S, Zhang Y, Zhao Q, Zhu S, Li C.
Org Lett. 2010 Jan 5. [Epub ahead of print]
PMID: 19689116 [PubMed - as supplied by publisher]
Formation of ArF from LPdAr(F): Catalytic Conversion of Aryl Triflates to Aryl Fluorides.
Watson DA, Su M, Teverovskiy G, Zhang Y, García-Fortanet J, Kinzel T, Buchwald SL.
Science. 2009 Aug 13. [Epub ahead of print]
PMID: 19679769 [PubMed - as supplied by publisher]
(2-Pyridyl)acetone-Promoted Cu-Catalyzed O-Arylation of Phenols with Aryl Iodides, Bromides, and Chlorides.
Zhang Q, Wang D, Wang X, Ding K.
J Org Chem. 2009 Aug 12. [Epub ahead of print]
PMID: 19673481 [PubMed - as supplied by publisher]
Ni-Catalyzed Sonogashira Coupling of Nonactivated Alkyl Halides: Orthogonal Functionalization of Alkyl Iodides, Bromides, and Chlorides.
Vechorkin O, Barmaz D, Proust V, Hu X.
J Am Chem Soc. 2009 Aug 11. [Epub ahead of print]
PMID: 19670863 [PubMed - as supplied by publisher]
Zn-mediated electrochemical allylation of aldehydes in aqueous ammonia.
Huang JM, Dong Y.
Chem Commun (Camb). 2009 Jul 14;(26):3943-5. Epub 2009 May 28.
PMID: 19662260 [PubMed - in process]
Practical Catalytic Asymmetric Synthesis of Diaryl-, Aryl Heteroaryl-, and Diheteroarylmethanols.
Salvi L, Kim JG, Walsh PJ.
J Am Chem Soc. 2009 Aug 4. [Epub ahead of print]
PMID: 19653691 [PubMed - as supplied by publisher]
Direct Palladium-Catalyzed Arylations of Aryl Bromides with 2/9-Substituted Pyrimido[5,4-b]indolizines.
Jiang M, Li T, Meng L, Yang C, Xie Y, Ding J.
J Comb Chem. 2009 Jul 31. [Epub ahead of print]
PMID: 19645499 [PubMed - as supplied by publisher]
Versatile chemoselectivity in Ni-catalyzed multiple bond carbonylations and cyclocarbonylations in CO(2)-expanded liquids.
del Moral D, Banet Osuna AM, Córdoba A, Moretó JM, Veciana J, Ricart S, Ventosa N.
Chem Commun (Camb). 2009 Aug 21;(31):4723-5. Epub 2009 Jun 29.
PMID: 19641822 [PubMed - in process]
Highly Selective Biaryl Cross-Coupling Reactions between Aryl Halides and Aryl Grignard Reagents: A New Catalyst Combination of N-Heterocyclic Carbenes and Iron, Cobalt, and Nickel Fluorides.
Hatakeyama T, Hashimoto S, Ishizuka K, Nakamura M.
J Am Chem Soc. 2009 Jul 29. [Epub ahead of print]
PMID: 19639999 [PubMed - as supplied by publisher]
Hexacationic Dendriphos Ligands in the Pd-Catalyzed Suzuki-Miyaura Cross-Coupling Reaction: Scope and Mechanistic Studies.
Snelders DJ, van Koten G, Klein Gebbink RJ.
J Am Chem Soc. 2009 Jul 29. [Epub ahead of print]
PMID: 19639941 [PubMed - as supplied by publisher]
Can One Predict Changes from S(N)1 to S(N)2 Mechanisms?
Phan TB, Nolte C, Kobayashi S, Ofial AR, Mayr H.
J Am Chem Soc. 2009 Jul 27. [Epub ahead of print]
PMID: 19634906 [PubMed - as supplied by publisher]
A General Copper-Catalyzed Coupling of Azoles with Vinyl Bromides.
Liao Q, Wang Y, Zhang L, Xi C.
J Org Chem. 2009 Jul 15. [Epub ahead of print]
PMID: 19603753 [PubMed - as supplied by publisher]
Kinetics of Bromine-Magnesium Exchange Reactions in Heteroaryl Bromides.
Shi L, Chu Y, Knochel P, Mayr H.
Org Lett. 2009 Jul 14. [Epub ahead of print]
PMID: 19601592 [PubMed - as supplied by publisher]
C5-Modified nucleosides exhibiting anticancer activity.
Lee YS, Park SM, Kim HM, Park SK, Lee K, Lee CW, Kim BH.
Bioorg Med Chem Lett. 2009 Aug 15;19(16):4688-91. Epub 2009 Jun 21.
PMID: 19596579 [PubMed - in process]
Palladium-Catalyzed Coupling of Ammonia with Aryl Chlorides, Bromides, Iodides, and Sulfonates: A General Method for the Preparation of Primary Arylamines.
Vo GD, Hartwig JF.
J Am Chem Soc. 2009 Jul 10. [Epub ahead of print]
PMID: 19591470 [PubMed - as supplied by publisher]
New One-Pot Synthesis of (E)-beta-Aryl Vinyl Halides from Styrenes.
Pawluc´ P, Hreczycho G, Szudkowska J, Kubicki M, Marciniec B.
Org Lett. 2009 Jul 2. [Epub ahead of print]
PMID: 19572730 [PubMed - as supplied by publisher]
The Scope and Limitation of Nickel-Catalyzed Aminocarbonylation of Aryl Bromides from Formamide Derivatives.
Jo Y, Ju J, Choe J, Song KH, Lee S.
J Org Chem. 2009 Jul 2. [Epub ahead of print]
PMID: 19572571 [PubMed - as supplied by publisher]
Electroencephalographic and behavioral convulsant effects of hydrobromide and hydrochloride salts of bupropion in conscious rodents.
Henshall DC, Dürmüller N, White HS, Williams R, Moser P, Dunleavy M, Silverstone PH.
Neuropsychiatr Dis Treat. 2009;5:189-206. Epub 2009 Apr 8.
PMID: 19557114 [PubMed - in process]
A facile route to C2-substituted imidazolium ionic liquids.
Ennis E, Handy ST.
Molecules. 2009 Jun 19;14(6):2235-45.
PMID: 19553895 [PubMed - in process]
Synthesis of 1,3-amino alcohol derivatives via a silicon-mediated ring-opening of substituted piperidines.
McCall WS, Comins DL.
Org Lett. 2009 Jul 2;11(13):2940-2.
PMID: 19552467 [PubMed - indexed for MEDLINE]