Kahlfuss Christophe, Wytko Jennifer A, Weiss Jean
UMR 7177 CNRS-Université de Strasbourg, 1, rue Blaise Pascal, 67000, Strasbourg, France.
Chempluschem. 2017 Apr;82(4):584-594. doi: 10.1002/cplu.201600557. Epub 2017 Jan 16.
In nature, the various properties of tetrapyrrolic macrocycles are mostly due to their proteic environment and result from an evolutionary process that is difficult to reproduce during the lifetime of a synthetic chemist. Thus, the task of synthetic chemists attempting to reproduce the biological role of porphyrin architectures, which perform functions from catalysis to light harvesting, is complicated. This account describes how a phenanthroline-strapped porphyrin architecture initially designed to afford new hemoprotein models led, over the last two decades, to the preparation of highly linear self-assembled nano-objects inspired by light-harvesting architectures. The approach summarized herein mimics, in a very modest way, the polyvalence of tetrapyrrolic macrocycles found in nature.
在自然界中,四吡咯大环的各种性质主要归因于其蛋白质环境,是一个合成化学家在其职业生涯中难以重现的进化过程的结果。因此,试图重现卟啉结构生物功能(从催化到光捕获)的合成化学家的任务是复杂的。本文描述了一种最初设计用于提供新的血红蛋白模型的菲咯啉连接的卟啉结构如何在过去二十年中,促成了受光捕获结构启发的高度线性自组装纳米物体的制备。本文总结的方法以一种非常适度的方式模仿了自然界中四吡咯大环的多价性。