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Updated: Jan 7, 2026

Preparation of Enantiopure Non-Activated Aziridines and Synthesis of Biemamide B, D, and epiallo-Isomuscarine
Published on: June 13, 2022
Resolving a Nearly Two-Centuries-Old Mystery: On the Structural Chemistry and Physicochemical Properties of Compounds
Thaddäus J Koller1, Kristian Witthaut1, Reinhard M Pritzl1
1Department of Chemistry, University of Munich (LMU), Munich, Germany.
Abstract:
Ammelide, also known as melanuric acid, is a simple molecular compound, which can be regarded as the double hydrolysis product of the industrially relevant compound melamine. Within this work, the first structural description of ammelide was provided almost 200 years after its discovery. This not only gave the first unambiguous evidence that ammelide's preferred tautomeric form in the solid is 6-amino-1,3,5-triazine-2,4(1H,3H)-dione, but also showed that ammelide adopts a layered structure similar to the closely related ammeline. Moreover, the crystal structures of three modifications of the 1:1 adduct between ammeline and ammelide were elucidated, which form layers with a honeycomb motif and hexagonal voids analogous to melamine cyanurate. Differential thermal analysis and thermogravimetric analysis demonstrated that both pure ammelide and its adduct with ammeline have exceptionally high thermal stabilities, resulting from their dense hydrogen bonding networks. Finally, the synthesis and structural characterization of the ammelide's nitrate and perchlorate salts were carried out to examine the potential of ammelide as part of insensitive high-energy-density materials through sensitivity measurements and theoretical calculations.
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Physical Properties of Amines
Structures of Carboxylic Acid Derivatives
Carboxylic acid derivatives contain an acyl group attached to a heteroatom such as chlorine, oxygen, or nitrogen. The carbonyl carbon and oxygen are both sp2-hybridized with an unhybridized p orbital.
The three sp2 orbitals of the carbonyl carbon form three σ bonds, one each with the carbonyl oxygen, the α carbon, and the heteroatom, whereas the other two sp2 orbitals of the carbonyl oxygen are occupied by the lone pairs. Further, the unhybridized p...
Structure of Amines
Preparation of Amides
The DCC-promoted synthesis of amides begins with the protonation of DCC by carboxylic acid. The protonation makes it a better acceptor. Next, the addition of carboxylate to the protonated carbodiimide gives a reactive acylating agent.
Subsequently, the amine acts as a nucleophile that attacks the acylating agent to form a tetrahedral intermediate. In the...
Nomenclature of Carboxylic Acid Derivatives: Amides and Nitriles
The IUPAC and common names of amides are derived from the parent carboxylic acid, by replacing the suffix “oic acid” and “ic acid,” respectively, with “amide.” In the following example, the IUPAC name ethanamide is derived from ethanoic acid, and the common name, acetamide, is obtained from acetic acid.
Basicity of Heterocyclic Aromatic Amines