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Until recently, melam, [C(3)N(3)(NH(2))(2)](2)NH, has been regarded as a short-lived intermediate in the condensation process of melamine that is only detectable under special reaction conditions owing to its high reactivity. A new synthetic approach has allowed a closer look at the formation and condensation behavior of melam by using elevated ammonia pressure in autoclaves. Whereas the thermal treatment of dicyandiamide at 450 °C and 0.2 MPa ammonia yielded melam in large amounts, prolonged treatment under these conditions (9 days) led to the formation of a melam-melem adduct, thus enabling the first insight into the condensation process of melam into melem. The hydrothermal treatment of melam at 300 °C (24 h) yields melam hydrate, [C(3)N(3)(NH(2))(2)](2)NH⋅2 H(2)O (space group P2(1)/c; a=676.84(2), b=1220.28(4), c=1394.24(4) pm; β=98.372(2)°; V=1139.28(6)×10(6) pm(3); Z=4), which crystallizes as a layered structure that is composed of almost-planar melam molecules, thereby forming ellipsoidal rosette-like motifs. The resulting voids are filled with four water molecules, thus forming a dense network of hydrogen bonds.
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Wirnhier et al. (2012) studied this question.
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