卟啉
化学
阳离子聚合
超分子化学
自催化
离子键合
离子强度
金属
水溶液中的金属离子
自组装
动力学
离子
光化学
无机化学
结晶学
高分子化学
物理化学
有机化学
水溶液
催化作用
晶体结构
物理
量子力学
作者
Roberto Zagami,Maria Angela Castriciano,Andrea Romeo,Luigi Monsù Scolaro
标识
DOI:10.1142/s1088424623500153
摘要
Under acidic conditions and at high ionic strength or in the presence of templating species, 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrin (TPPS[Formula: see text] self-organizes into J-aggregates. In these species, the porphyrins align in a general edge-to-edge geometry, responsible for their peculiar optical properties. The self-assembling process is hierarchical, and the kinetics are strongly dependent on the mixing protocols. In the case of sigmoidal profiles, the kinetic data have been treated using a model proposed in the literature by R.F. Pasternack. Accordingly, an autocatalytic growth with the formation of an [Formula: see text]-mer of porphyrin units is the rate-determining step (RDS) leading to the eventual J-aggregates whose size spans from nano- up to the micro-scale. The impact of different experimental parameters, together with inorganic counter-anions, and various cationic and anionic species (organic anions, metal ions, porphyrins, and metal complexes) will be reviewed.
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