DIMERIZATION OF ALUMINUM PHTHALOCYANINE CHLORIDE IN ORGANIC AND AQUA-ORGANIC MEDIUM

I. Klimenko, T. Astakhova, E. Timokhina, A. Lobanov
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Abstract

Aluminum phthalocyanine chloride (AlClPc) is a photoactive macroheterocyclic compound, which, in its monomeric form, is used as a photosensitizer (PS) in photodynamic therapy and diagnostics. In this paper, its physicochemical properties were studied in organic (N, N-dimethylformamide, DMF) and aqua-organic (DMF-aqua) media. It has been shown that the hydrophobic properties of AlClPc prevent its widespread use in various pharmacological compositions due to its tendency to aggregate in aqueous solutions, which leads to the formation of non-fluorescent aggregates and a decrease in its photodynamic activity. The geometry and electronic structure of AlClPc in the monomeric and dimerized (H- and J-aggregates) states were studied using quantum-chemical calculations with the help of the electron density functional theory (DFT) method. Different types of orientation during the dimerization of AlClPc molecules are presented: “back to back”, “head to head”, “head to back”, as well as mixed-oriented types. It has been proven that both in DMF and DMF-aqua media, the preferred orientation is “back to back”, without sacrificing the monomeric geometry of the constituent molecules in the dimer. It is shown that in an aqueous organic solvent the AlClPc molecule is easily hydrated with the formation of a coordination bond between the Al atom of the AlClPc molecule and the O atom of the aqua molecule. The bond length is 2.23 Å, and the hydration energy is 16.84 kcal/mol. Hydration promotes the formation of dimers, in which two aqua molecules play the role of "bridges" between two AlClPc molecules. In such dimer, each aqua molecule has two bonds: one coordination bond between its O atom and the Al atom of one of the AlClPc molecules and one hydrogen bond between its H atom and the N atom of another AlClPc molecule. Based on the calculated data obtained, the AlClPc dimers in the DMF medium were assigned to H-aggregates, and in the DMF-water medium, to J-aggregates, respectively.
氯酞菁铝在有机和水-有机介质中的二聚化
酞菁氯化铝(AlClPc)是一种光活性大杂环化合物,其单体形式在光动力治疗和诊断中用作光敏剂(PS)。本文研究了其在有机(N, N-二甲基甲酰胺,DMF)和水-有机(DMF-aqua)介质中的理化性质。研究表明,AlClPc的疏水特性阻碍了其在各种药物组合物中的广泛应用,因为它倾向于在水溶液中聚集,从而导致非荧光聚集体的形成和光动力活性的降低。利用量子化学计算和电子密度泛函理论(DFT)方法研究了AlClPc在单体和二聚态(H-聚集体和j -聚集体)下的几何和电子结构。AlClPc分子在二聚化过程中呈现出不同的取向类型:“背对背”、“头对头”、“头对背”以及混合取向类型。已经证明,在DMF和DMF-水介质中,首选取向是“背对背”,而不牺牲二聚体中组成分子的单体几何形状。结果表明,在含水有机溶剂中,AlClPc分子的Al原子与水分子的O原子之间形成配位键,使AlClPc分子容易水化。键长为2.23 Å,水化能为16.84 kcal/mol。水合作用促进二聚体的形成,其中两个水分子在两个AlClPc分子之间起着“桥梁”的作用。在这种二聚体中,每个水分子有两个键:一个是它的O原子与其中一个AlClPc分子的Al原子之间的配位键,另一个是它的H原子与另一个AlClPc分子的N原子之间的氢键。根据得到的计算数据,在DMF介质中AlClPc二聚体分别归属于h聚集体,在DMF-水介质中归属于j聚集体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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