Division of Structural Studies, Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90-363, Łódź, Poland.
Chemistry. 2020 Oct 15;26(58):13264-13273. doi: 10.1002/chem.202002238. Epub 2020 Sep 11.
A well-defined and stable "AB" binary system in the presence of "C" a crystalline synthon ground in a ball mill undergoes selective transformation in the solid state according to the equation AB+C→AC+B. When the amount of C is increased two times then the equation AB+2C→AC+BC is valid. The other variants are more complex. The pathway BC+A is allowed and leads to the AC and B products. The pathway AC+B is not preferred, and no transformation is observed. These non-obvious correlations were observed for cocrystal of barbituric acid (BA):thiobarbituric acid (TBA) recently reported by Shemchuk et al. (Chem. Commun. 2016, 52, 11815-11818) in the presence of 1-hydroxy-4,5-dimethyl-imidazole 3-oxide (HIMO). This synthon shows high affinity for the BA TBA cocrystal as well for its individual components, BA and TBA. Single-quantum, double-quantum (SQ-DQ) 2D H very fast MAS NMR with a spinning rate of 60 kHz was employed as a basic and most diagnostic tool for the study of cocrystals transformations. Analysis of the experimental data was supported by theoretical calculations, including computation of the stabilization energy, E , defined as the energy difference between the energy of a co-crystal and the sum of the energies of particular components in the respective stoichiometric ratios. Two mechanisms of synthon replacement have been proposed. Pathway 1 assumes a concerted mechanism of substitution. In this approach, synthon attack is synchronized in time with the departure of one of the components of the binary system. Pathway 2 implies a non-concerted process, with an intermediate stage in which three separate components are present. Evidence suggesting a preference for Pathway 2 is shown.
在研磨机中研磨形成的结晶合成子“C”存在的情况下,具有明确和稳定“AB”二元体系会根据方程式 AB+C→AC+B 在固态中进行选择性转化。当 C 的量增加两倍时,方程式 AB+2C→AC+BC 成立。其他变体则更为复杂。允许路径 BC+A 发生,并导致生成 AC 和 B 产物。不优先选择路径 AC+B,且观察不到转化。这些不明显的相关性已在 Shemchuk 等人最近报道的巴比妥酸(BA):硫代巴比妥酸(TBA)共晶中观察到(Chem. Commun. 2016, 52, 11815-11818),该共晶存在于 1-羟基-4,5-二甲基-咪唑 3-氧化物(HIMO)中。该合成子对 BA-TBA 共晶及其各个组成部分 BA 和 TBA 都具有高亲和力。采用单量子、双量子(SQ-DQ)2D H 非常快的 MAS NMR(转速为 60 kHz)作为研究共晶转化的基本和最具诊断性工具。实验数据分析得到了理论计算的支持,包括计算稳定能 E,E 定义为共晶的能量与相应化学计量比中各个组成部分能量之和的能量差。提出了两种取代合成子的机制。途径 1 假设取代的协同机制。在这种方法中,合成子的攻击与二元体系中一种组成部分的离去同步进行。途径 2 意味着非协同过程,其中存在三个单独的中间阶段。显示出对途径 2 的偏好的证据。