Department Chemie, Lehrstuhl für Anorganische Festkörperchemie, Ludwig-Maximilians-Universität München, Butenandtstraße 5-13 (D), 81377 München, Germany.
Chemistry. 2012 Feb 6;18(6):1811-9. doi: 10.1002/chem.201101885. Epub 2012 Jan 5.
Pyrolysis of prominent precursor compounds for the synthesis of carbon nitride type materials (e.g., melamine, thiourea) have been studied in detail. Molecular adducts containing monoprotonated melamium C(6)N(11)H(10)(+) and melaminium HC(3)N(3)(NH(2))(3)(+) ions, respectively, have been identified as intermediates. The adduct C(6)N(11)H(10)Cl·0.5NH(4)Cl was obtained by the reaction of melamine C(3)N(3)(NH(2))(3) with NH(4)Cl at 450 °C. During the pyrolysis of thiourea, guanidinium thiocyanate was initially formed and subsequently the melamium thiocyanate melamine adduct C(6)N(11)H(10)SCN·2C(3)N(3)(NH(2))(3) was isolated at 300 °C. A second melaminium thiocyanate melamine adduct with the formula HC(3)N(3)(NH(2))(3)SCN·2C(3)N(3)(NH(2))(3) represents an intermediary reaction product that is best accessible at low pressures. The crystal structures of the compounds were solved by single-crystal XRD. Unequivocal proton localization at the C(6)N(11)H(10)(+) ion was established. A typical intramolecular and interannular hydrogen bridge and other characteristic hydrogen-bonding motifs were identified. Additionally, the adducts were investigated by solid-state NMR spectroscopy. Our study provides detailed insight into the thermal condensation of thiourea by identifying and characterizing key intermediates involved in the condensation process leading to carbon nitride type materials. Furthermore, factors promoting the formation of melamium adduct phases over melem are discussed.
对用于合成碳氮化物材料的突出前体化合物(例如三聚氰胺、硫脲)的热解进行了详细研究。分别鉴定出含有单质子化三聚氰胺 C(6)N(11)H(10)(+)和三聚氰胺 HC(3)N(3)(NH(2))(3)(+)离子的分子加合物作为中间体。加合物 C(6)N(11)H(10)Cl·0.5NH(4)Cl 是通过在 450°C 下使三聚氰胺 C(3)N(3)(NH(2))(3)与 NH(4)Cl 反应得到的。在硫脲的热解过程中,最初形成了胍基硫氰酸盐,随后在 300°C 下分离出三聚氰胺硫氰酸盐三聚氰胺加合物 C(6)N(11)H(10)SCN·2C(3)N(3)(NH(2))(3)。具有化学式 HC(3)N(3)(NH(2))(3)SCN·2C(3)N(3)(NH(2))(3)的第二个三聚氰胺硫氰酸盐三聚氰胺加合物代表了一种中间反应产物,在低压下最容易获得。通过单晶 XRD 解决了化合物的晶体结构。在 C(6)N(11)H(10)(+)离子处确立了质子的明确定位。鉴定并确定了典型的分子内和环间氢键以及其他特征氢键模式。此外,还通过固态 NMR 光谱对加合物进行了研究。我们的研究通过鉴定和表征参与导致碳氮化物材料的缩合过程的关键中间体,提供了对硫脲热缩合的详细了解。此外,还讨论了促进三聚氰胺加合物相而不是 melem 形成的因素。