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In organic chemistry, an imide is a functional group consisting of two acyl groups bound to nitrogen. [1] The compounds are structurally related to acid anhydrides , although imides are more resistant to hydrolysis.
When R = H, the compound is a primary imine, when R is hydrocarbyl, the compound is a secondary imine. If this group is not a hydrogen atom, then the compound can sometimes be referred to as a Schiff base. [9] When R 3 is OH, the imine is called an oxime, and when R 3 is NH 2 the imine is called a hydrazone.
Acetone imine, or 2-propanimine is an organic compound and an imine with the chemical formula (CH 3) 2 CNH. It is a volatile and flammable liquid at room temperature . It is the simplest ketimine .
Heating magnesium amide to about 400 °C yields magnesium imide with the loss of ammonia. Magnesium imide itself decomposes if heated between 455 and 490 °C. [6] Beryllium imide forms from beryllium amide when heated to 230 °C in a vacuum. [7] When strontium metal is heated with ammonia at 750 °C, the dark yellow strontium imide forms. [8]
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The acid chloride functionality reacts with the aromatic amine to give the amide bond and hydrochloric acid (HCl) as a by-product. In the commercial preparation of polyamideimides, the polymerization is carried out in a dipolar, aprotic solvent such as N - methylpyrrolidone (NMP), dimethylacetamide (DMAC), dimethylformamide (DMF), or ...
Four logical operators allow atom and bond descriptors to be combined. The 'and' operator ; can be used to define a protonated primary amine as [N;H3;+][C;X4]. The 'or' operator , has a higher priority so [c,n;H] defines (aromatic carbon or aromatic nitrogen) with implicit hydrogen.
Chemical structure of Kapton, a polyimide. Polyimide (sometimes abbreviated PI) is a polymer containing imide groups belonging to the class of high-performance plastics.With their high heat-resistance, polyimides enjoy diverse applications in roles demanding rugged organic materials, such as high temperature fuel cells, displays, and various military roles.