Centro de Química Estrutural, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais 1, 1049-001 Lisboa, Portugal.
Molecules. 2021 Jul 14;26(14):4264. doi: 10.3390/molecules26144264.
The molecular interactions of anionic tetrasulfonate phenyl porphyrin (TPPS) with poly(amido amine) (PAMAM) dendrimers of generation 2.0 and 4.0 (G2 and G4, respectively) forming H- or J-aggregates, as well as with human and bovine serum albumin proteins (HSA and BSA), were reviewed in the context of self-assembly molecular complementarity. The spectroscopic studies were extended to the association of aluminum phthtalocyanine (AlPCS) detected with a PAMAM G4 dendrimer with fluorescence studies in both steady state and dynamic state, as well as due to the fluorescence quenching associated to electron-transfer with a distribution of lifetimes. The functionalization of TPPS with peripheral substituents enables the assignment of spontaneous pH-induced aggregates with different and well-defined morphologies. Other work reported in the literature, in particular with soft self-assembly materials, fall in the same area with particular interest for the environment. The microencapsulation of TPPS studies into polyelectrolyte capsules was developed quite recently and aroused much interest, which is well supported and complemented by the extensive data reported on the Imaging Microscopy section of the Luminescence of Porphyrins and Phthalocyanines included in the present review.
阴离子四磺基苯基卟啉(TPPS)与第二代和第四代聚(酰胺-胺)(PAMAM)树枝状大分子(分别为 G2 和 G4)形成 H-或 J-聚集物,以及与人血清白蛋白和牛血清白蛋白(HSA 和 BSA)的分子相互作用,在自组装分子互补性的背景下进行了综述。光谱研究扩展到了与 PAMAM G4 树枝状大分子检测到的铝酞菁(AlPCS)的缔合,以及在稳态和动态状态下的荧光研究,以及由于与寿命分布相关的电子转移而产生的荧光猝灭。TPPS 的外围取代基的功能化使得能够自发地分配具有不同且明确定义形态的 pH 诱导聚集物。文献中报道的其他工作,特别是与软自组装材料相关的工作,也属于同一领域,特别引起了人们对环境的兴趣。TPPS 的聚电解质胶囊微胶囊化研究最近才得到发展,并引起了广泛关注,这得到了包括在本综述中的卟啉和酞菁的发光部分的成像显微镜部分中广泛报道的大量数据的很好的支持和补充。