Dimethyl Telluride
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Dimethyl Telluride
Dimethyl telluride is an organotelluride compound, formula ( CH3)2 Te, also known by the abbreviation DMTe. This was the first material used to grow epitaxial cadmium telluride and mercury cadmium telluride using metalorganic vapour phase epitaxy. Dimethyl telluride as a product of microbial metabolism was first discovered in 1939. It is produced by some fungi and bacteria (''Penicillium brevicaule'', ''P. chrysogenum'', and '' P. notatum'' and the bacterium ''Pseudomonas fluorescens''). The toxicity of DMTe is unclear. It is produced by the body when tellurium or one of its compounds are ingested. It is noticeable by the garlic smelling breath it gives those exposed, similar to the effect of DMSO. Tellurium is known to be toxic Toxicity is the degree to which a chemical substance or a particular mixture of substances can damage an organism. Toxicity can refer to the effect on a whole organism, such as an animal, bacterium, or plant, as well as the effect on a subst .... ...
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Chalcogen
The chalcogens (ore forming) ( ) are the chemical elements in group 16 of the periodic table. This group is also known as the oxygen family. Group 16 consists of the elements oxygen (O), sulfur (S), selenium (Se), tellurium (Te), and the radioactive elements polonium (Po) and livermorium (Lv). Often, oxygen is treated separately from the other chalcogens, sometimes even excluded from the scope of the term "chalcogen" altogether, due to its very different chemical behavior from sulfur, selenium, tellurium, and polonium. The word "chalcogen" is derived from a combination of the Greek word () principally meaning copper (the term was also used for bronze/brass, any metal in the poetic sense, ore or coin), and the Latinized Greek word , meaning ''born'' or ''produced''. Sulfur has been known since antiquity, and oxygen was recognized as an element in the 18th century. Selenium, tellurium and polonium were discovered in the 19th century, and livermorium in 2000. All of the chalcogens h ...
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Journal Of The Chemical Society
The ''Journal of the Chemical Society'' was a scientific journal established by the Chemical Society in 1849 as the ''Quarterly Journal of the Chemical Society''. The first editor was Edmund Ronalds. The journal underwent several renamings, splits, and mergers throughout its history. In 1980, the Chemical Society merged with several other organizations into the Royal Society of Chemistry. The journal's continuity is found in ''Chemical Communications'', ''Dalton Transactions'', ''Faraday Transactions'', and ''Perkin Transactions'', all of which are published by the Royal Society of Chemistry. History ;'' Proceedings of the Chemical Society'' * ''Memoirs of the Chemical Society of London'' (1841) * ''Proceedings of the Chemical Society of London'' (1842–1843) * ''Memoirs and Proceedings of the Chemical Society'' (1843–1848) * ''Proceedings of the Chemical Society, London'' (1885–1914) * Published as a supplement to ''Journal of the Chemical Society'' from 1914 to 1956 * ''Proc ...
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Organotellurium Compounds
Organotellurium chemistry describes the synthesis and properties of chemical compounds containing a carbon-tellurium chemical bond. Organotellurium chemistry is a lightly studied area, in part because of the few applications. Functional groups The Te analogues of common organosulfur and organoselenium functional groups are known. Tellurols are however unstable with respect to oxidation to the ditellurides. Commonly encountered organotellurium compounds are diorganomono- and ditellurides, R2Te and (RTe)2, respectively. Two other families of organoTe(IV) compounds are well developed: R4−xTeClx and the telluroxides (R2TeO). Synthesis and reactions Reduced organoTe compounds Reduced organoTe compounds are commonly obtained from NaHTe and lithium telluride: :Li2Te + 2 RBr → R2Te + 2 LiBr A direct route to organolithium compounds starts from reactions of organolithium or Grignard reagents and Te: :Te + ArLi → ArTeLi Butyl lithium gives the telluride similarly: :Te + ...
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Tellurides
The telluride ion is the anion Te2− and its derivatives. It is analogous to the other chalcogenide anions, the lighter O2−, S2−, and Se2−, and the heavier Po2−. In principle, Te2− is formed by the two-e− reduction of tellurium. The redox potential is −1.14 V. :Te(s) + 2 e− ↔ Te2− Although solutions of the telluride dianion have not been reported, soluble salts of bitelluride (TeH−) are known. Organic tellurides ''Tellurides'' also describe a class of organotellurium compounds formally derived from Te2−. An illustrative member is dimethyl telluride, which results from the methylation of telluride salts: :2 CH3I + Na2Te → (CH3)2Te + 2 NaI Dimethyl telluride is formed by the body when tellurium is ingested. Such compounds are often called telluroethers because they are structurally related to ethers with tellurium replacing oxygen, although the length of the C–Te bond is much longer than a C–O bond. C–Te–C angles tend to be clos ...
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Mycological Research
''Fungal Biology'' is a scientific journal that publishes peer-reviewed papers on all aspects of basic and applied research of the fungi, including lichens, yeasts, oomycetes, and slime moulds. A publication of the British Mycological Society, it was founded in 1896 as ''Transactions of the British Mycological Society'' (1896–1989) and was later titled ''Mycological Research'' (1989–2010). The founding editor was Carleton Rea (1896–1930). History The journal was established in 1896 under the title ''Transactions of the British Mycological Society''. The founding editor was Carleton Rea, who continued in the role until 1930. Rea was the sole editor until 1919, when he was joined by John Ramsbottom; subsequently there were two or three editors until 1967 when the group was expanded under a Senior Editor. The earliest issues contained reports on fungus-collecting expeditions and the first British sightings of fungal species; later, research papers and reviews were also publish ...
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Chemical Reviews
''Chemical Reviews'' is peer-reviewed scientific journal published twice per month by the American Chemical Society. It publishes review articles on all aspects of chemistry. It was established in 1924 by William Albert Noyes (University of Illinois). the editor-in-chief is Sharon Hammes-Schiffer. Abstracting and indexing The journal is abstracted and indexed in Chemical Abstracts Service, CAB International, EBSCOhost, ProQuest, PubMed, Scopus, and the Science Citation Index. According to the ''Journal Citation Reports'', the journal has a 2020 impact factor of 60.622. See also * Accounts of Chemical Research ''Accounts of Chemical Research'' is a semi-monthly peer-reviewed scientific journal published by the American Chemical Society containing overviews of basic research and applications in chemistry and biochemistry. It was established in 1968 and th ... References External links * American Chemical Society academic journals Review journals Monthly journals ...
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Toxic
Toxicity is the degree to which a chemical substance or a particular mixture of substances can damage an organism. Toxicity can refer to the effect on a whole organism, such as an animal, bacterium, or plant, as well as the effect on a substructure of the organism, such as a cell ( cytotoxicity) or an organ such as the liver (hepatotoxicity). By extension, the word may be metaphorically used to describe toxic effects on larger and more complex groups, such as the family unit or society at large. Sometimes the word is more or less synonymous with poisoning in everyday usage. A central concept of toxicology is that the effects of a toxicant are dose-dependent; even water can lead to water intoxication when taken in too high a dose, whereas for even a very toxic substance such as snake venom there is a dose below which there is no detectable toxic effect. Toxicity is species-specific, making cross-species analysis problematic. Newer paradigms and metrics are evolving to bypass ...
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Dimethyl Sulfoxide
Dimethyl sulfoxide (DMSO) is an organosulfur compound with the formula ( CH3)2. This colorless liquid is the sulfoxide most widely used commercially. It is an important polar aprotic solvent that dissolves both polar and nonpolar compounds and is miscible in a wide range of organic solvents as well as water. It has a relatively high boiling point. DMSO has the unusual property that many individuals perceive a garlic-like taste in the mouth after DMSO makes contact with their skin. In terms of chemical structure, the molecule has idealized Cs symmetry. It has a trigonal pyramidal molecular geometry consistent with other three-coordinate S(IV) compounds, with a nonbonded electron pair on the approximately tetrahedral sulfur atom. Synthesis and production Dimethyl sulfoxide was first synthesized in 1866 by the Russian scientist Alexander Zaytsev, who reported his findings in 1867. Dimethyl sulfoxide is produced industrially from dimethyl sulfide, a by-product of the Kraf ...
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Applied Organometallic Chemistry
''Applied Organometallic Chemistry'' is a monthly peer-reviewed scientific journal published since 1987 by John Wiley & Sons. The editor-in-chief is Cornelis J. Elsevier (University of Amsterdam). Contents The journal includes: * reviews * full papers * communications * working methods papers * crystallographic reports It also includes occasional reports on: * relevant conferences of applied work in the field of organometallics * including bioorganometallic chemistry * metal/organic ligand coordination chemistry. Abstracting and indexing The journal is abstracted and indexed in: * Biological Abstracts * BIOSIS Previews * Cambridge Structural Database * Chemical Abstracts Service * Ceramic Abstracts * ChemWeb * Compendex * Advanced Polymer Abstracts * Civil Engineering Abstracts * Mechanical & Transportation Engineering Abstracts * Current Contents/Physical * Chemical & Earth Sciences * Engineered Materials Abstracts * International Aerospace Abstracts * METADEX * PASCA ...
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Pseudomonas Fluorescens
''Pseudomonas fluorescens'' is a common Gram-negative, rod-shaped bacterium. It belongs to the ''Pseudomonas'' genus; 16S rRNA analysis as well as phylogenomic analysis has placed ''P. fluorescens'' in the ''P. fluorescens'' group within the genus, Text was copied from this source, which is available under Creative Commons Attribution 4.0 International License to which it lends its name. General characteristics ''Pseudomonas fluorescens'' has multiple flagella. It has an extremely versatile metabolism, and can be found in the soil and in water. It is an obligate aerobe, but certain strains are capable of using nitrate instead of oxygen as a final electron acceptor during cellular respiration. Optimal temperatures for growth of ''P. fluorescens'' are 25–30° C. It tests positive for the oxidase test. It is also a nonsaccharolytic bacterial species. Heat-stable lipases and proteases are produced by ''P. fluorescens'' and other similar pseudomonads. These enzymes cause m ...
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Penicillium Notatum
''Penicillium chrysogenum'' (formerly known as ''Penicillium notatum'') is a species of fungus in the genus ''Penicillium''. It is common in temperate and subtropical regions and can be found on salted food products, but it is mostly found in indoor environments, especially in damp or water-damaged buildings. It has been recognised as a species complex that includes ''P. notatum'', ''P. meleagrinum,'' and ''P. cyaneofulvum,'' but molecular phylogeny established that it is a distinct species and that ''P. notatum'' (its popular synonym) is '' P. rubens.'' It has rarely been reported as a cause of human disease. It is the source of several β-lactam antibiotics, most significantly penicillin. Other secondary metabolites of ''P. chrysogenum'' include roquefortine C, meleagrin, chrysogine, 6-MSA YWA1/melanin, andrastatin A, fungisporin, secalonic acids, sorbicillin, and PR-toxin. Like the many other species of the genus ''Penicillium'', ''P. chrysogenum'' usually repro ...
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