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In this reaction, the alkyl group is transferred (as an R− group) to the carbon atom of the coordinated carbonyl, and subsequent addition of carbocation reagent results in attachment of an R+ group to the oxygen.
Further increase in cross-linker reagent results in brittleness of buckypaper.
The use of the bifunctional chlorosilane as a silylating reagent results in dimethyl bis phenylethynyl) silane (20% yield).
Method that uses BF3/MeOH reagent produces small amounts of interfering compounds than the method using HCl/MeOH reagent, results reflected by the better statistical parameters.
The addition of Bi as modifier reagent results in lower cutting force and better surface roughness due to the formation of Bi compound and modifies the morphology of Mg2Si reinforcement particle.
Because of the inclusion of the synonym in the ontology, 135 additional reagent results are returned.
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Subsequent assembly and crosslinking using a bis-cyclooctyne reagent resulted in the formation of stable nanoparticles.
The assay is not specific for polyphenols; instead many interfering compounds may react with the reagent resulting in apparently elevated phenolic compounds concentrations.
This chlorination reaction involves the exothermic formation of a species called Vilsmeier reagent, resulting from a reaction between SOCl2 and DMAC.
Compounds 1 3 were obtained under mild conditions by reaction of the corresponding N,N′-phenylenebis(oxamate) analogues and Lawesson's reagent resulting in the formation of CS bonds at the carbonyl amide functions.
Subsequently, a polymer reaction, the ring-opening reaction of the epoxy groups of the grafted PGMA, was conducted with sodium 2,4-diaminobenzene sulfonate (SAS) as reagent, resulting in the functional grafted particles SAS-PGMA/SiO2.
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CEO of Professional Science Editing for Scientists @ prosciediting.com