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Tebbe's reagent, useful in organic chemistry, is an aluminium-containing derivative of titanocene that arises from the reaction of titanocene dichloride with trimethylaluminium. It is used for the "olefination" reactions. [17] Arenes, such as C 6 (CH 3) 6 react to give the piano-stool complexes [Ti(C 6 R 6)Cl 3] + (R = H, CH 3; see figure above).
Reagents are "substances or compounds that are added to a system in order to bring about a chemical reaction or are added to see if a reaction occurs." [1] Some reagents are just a single element. However, most processes require reagents made of chemical compounds. Some of the most common ones used widely for specific reactive functions are ...
Reagent Chemicals [a] is a publication of the American Chemical Society (ACS) Committee on Analytical Reagents, [1] detailing standards of purity for over four hundred of the most widely used chemicals in laboratory analyses and chemical research. Chemicals that meet this standard may be sold as "ACS Reagent Grade" materials.
In metallurgy, Keller's reagent is a mixture of nitric acid, hydrochloric acid, and hydrofluoric acid, used to etch aluminum alloys to reveal their grain boundaries and orientations. [1] It is also sometimes called Dix–Keller reagent , after E. H. Dix, Jr., and Fred Keller of the Aluminum Corporation of America , who pioneered the use of this ...
Dotmatics is an R&D scientific software company used by scientists in the R&D process that help them be more efficient in their efforts to innovate. Founded in 2005, the company's primary office is in Boston with 14 offices around the globe. [1]
The reagent used can be any substance that gives S 2− ions in such solutions; most commonly used are hydrogen sulfide (at 0.2-0.3 M), thioacetamide (at 0.3-0.6 M), addition of hydrogen sulfide can often prove to be a lumbersome process and therefore sodium sulfide can also serve the purpose. The test with the sulfide ion must be conducted in ...
Samarium(II) iodide is a reagent for carbon-carbon bond formation, for example in a Barbier reaction (similar to the Grignard reaction) between a ketone and an alkyl iodide to form a tertiary alcohol: [9] R 1 I + R 2 COR 3 → R 1 R 2 C(OH)R 3 Barbier reaction using SmI 2. Typical reaction conditions use SmI 2 in THF in the presence of ...