Dipartimento di Chimica , Università di Roma Sapienza , P.le A. Moro 5 , I-00185 Rome , Italy.
Department of Chemistry , University of Houston , Houston , Texas 77204-5003 , United States.
Inorg Chem. 2019 Nov 18;58(22):15269-15282. doi: 10.1021/acs.inorgchem.9b02279. Epub 2019 Oct 30.
The autocyclotetramerization of the precursor 2,3-dicyano-5,6-di(2'-pyridyl)pyrazine [(CN)PyPyz] in the presence of MCl compounds (M = Al, Ga) leads to the formation of the new mononuclear porphyrazine complexes [PyTPyzPzMCl]·HO (PyTPyzPz = tetrakis-2,3-[5,6-di(2-pyridyl)pyrazino]porphyrazinato anion). From these species, the hydroxide analogues [PyTPyzPzMOH]·HO were obtained by contact with hot water, and their corresponding pentanuclear species [(PdCl)PyTPyzPzMCl]·HO could be easily formed by the reaction with PdCl. Physicochemical characterization of the mono- and pentanuclear macrocycles was based on elemental analysis, and mass, powder X-ray, and IR spectra. UV-vis spectral studies of the mononuclear species in solutions of DMF, DMSO, or pyridine ( ≈ 10-10 M) indicate (mainly in DMF and DMSO) the initial presence of aggregation, in some cases accompanied by the concomitant occurrence for the complex of a one-electron reduction. While disaggregation into a single species evolves spontaneously over time, the -1 charged species, eventually also found present, can be brought back to its neutral form by addition of a slight amount of HCl, the final spectrum showing the presence of the starting neutral species in its pure monomeric form. Similar aspects were faced also for the parent pentanuclear complexes. Cyclic voltammetry experiments, conducted for the mono-/pentanuclear complexes in DMF and DMSO ( ≈ 10 M), exhibit progressive one-electron reductions (1 → 4) characterized by values (V vs SCE) positioned to significantly less negative values than those known for the phthalocyanine (Pc) analogues, these data confirming the previously already proven higher electron-deficient character of the M derivatives of the PyTPyzPz macrocycle with respect to Pc. The role of the present new series of Al and Ga macrocyclic species to act as photosensitizers for the generation of singlet oxygen, O, the cytotoxic agent in the anticancer treatment known as photodynamic therapy (PDT), has been explored in DMF/HCl. Among the quantum yields Φ, the value found for the Ga complex [PyTPyzPzGaCl] (0.68), practically coincident with that observed for the TTDPz analogue (0.69), is well above those of most porphyrazines analogues (Φ = 0.4-0.6), a result encouraging further research work for potential applications in the biochemical field.
在 MCl 化合物(M = Al、Ga)存在下,前体 2,3-二氰基-5,6-二(2'-吡啶基)吡嗪((CN)PyPyz)的自动环三聚反应导致新的单核卟啉嗪配合物[PyTPyzPzMCl]·HO 的形成(PyTPyzPz = 四-2,3-[5,6-二(2-吡啶基)吡嗪基]卟啉嗪阴离子)。从这些物种中,通过与热水接触获得了相应的氢氧化物类似物[PyTPyzPzMOH]·HO,并且通过与 PdCl 的反应很容易形成相应的五核物种[(PdCl)PyTPyzPzMCl]·HO。单核和五核大环的物理化学性质是基于元素分析、质量、粉末 X 射线和 IR 光谱确定的。在 DMF、DMSO 或吡啶( ≈ 10-10 M)溶液中对单核配合物的紫外可见光谱研究表明(主要在 DMF 和 DMSO 中),最初存在聚集,在某些情况下,与配合物的单电子还原同时发生。虽然随着时间的推移,聚集物自发地解聚为单一物种,但最终也存在的-1 价物种可以通过添加少量 HCl 回到其中性形式,最终的光谱显示出起始中性物种以其纯单体形式存在。对于母体五核配合物也面临类似的方面。在 DMF 和 DMSO( ≈ 10 M)中进行的单/五核配合物的循环伏安实验显示出逐步的单电子还原(1→4),其特征为 值(相对于 SCE)显著小于已知的酞菁(Pc)类似物的值,这些数据证实了之前已经证明的 PyTPyzPz 大环的 M 衍生物相对于 Pc 具有更高的缺电子特性。在 DMF/HCl 中探索了本系列新型 Al 和 Ga 大环物质作为产生单线态氧(O)的光敏剂的作用,O 是光动力疗法(PDT)中已知的抗癌治疗中的细胞毒性剂。在量子产率Φ中,发现 Ga 配合物[PyTPyzPzGaCl](0.68)的值与 TTDPz 类似物(0.69)几乎相同,明显高于大多数卟啉嗪类似物(Φ=0.4-0.6)的值,这一结果鼓励进一步研究潜在应用于生化领域的工作。