卟啉
超分子化学
材料科学
四吡咯
共轭体系
四苯基卟啉
非线性光学
酞菁
发色团
纳米技术
纳米材料
光化学
组合化学
分子
化学
有机化学
聚合物
非线性系统
酶
复合材料
物理
量子力学
作者
Mathias O. Senge,Marijana Fazekas,E.G.A. Notaras,Werner J. Blau,Monika Zawadzka,Oliver B. Locos,Éimhín M. Ní Mhuircheartaigh
标识
DOI:10.1002/adma.200601850
摘要
Abstract Porphyrins and phthalocyanines have outstanding chemical and thermal stability. The macrocyclic structure and chemical reactivity of tetrapyrroles offers architectural flexibility and facilitates the tailoring of chemical, physical and optoelectronic parameters. The specific optical properties of the tetrapyrrole macrocycle combined with the synthetic methodologies now available and the already available theoretical and spectroscopic knowledge on their optical behavior make porphyrins a target of choice for this area. They are versatile organic nanomaterials with a rich photochemistry and their excited state properties are easily modulated through conformational design, molecular symmetry, metal complexation, orientation and strength of the molecular dipole moment, size and degree of conjugation of the π‐systems, and appropriate donor‐acceptor substituents. Here we review the structural chemistry and optical properties of recently synthesized porphyrin derivatives that offer potential for nonlinear optical (NLO) applications and complement existing studies on phthalocyanines. Classes of interest include the classic A 4 symmetric tetrapyrroles, while optimized systems include push‐pull porphyrins, oligomeric and supramolecular self‐assembled systems, films and nanoparticle systems, and highly conjugated porphyrin arrays.
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