Brothers Penelope J
Department of Chemistry, The University of Auckland, Private Bag 92019, Auckland, New Zealand.
Chem Commun (Camb). 2008 May 14(18):2090-102. doi: 10.1039/b714894a. Epub 2008 Feb 5.
The coordination of boron to a range of polypyrrole-containing ligands is explored in this feature article. The boron dipyrromethenes are well-known as laser dyes and fluorescent labels in biology. Subphthalocyanine and subporphyrin macrocycles containing only three pyrrole rings can exist only when templated by a central boron atom. Boron complexes of expanded porphyrins (six or eight pyrroles) can complex boron in dipyrromethene (but not bipyrrole) sites. The primary focus of the article is on boron porphyrin and corrole complexes, where the tight fit of two boron atoms within the very constrained coordination site gives rise to unexpected chemistry at both boron and the porphyrin ligand. These unusual features are described and reasons for their occurrence postulated.
在这篇专题文章中,我们探讨了硼与一系列含聚吡咯配体的配位情况。硼二吡咯亚甲基作为激光染料和生物学中的荧光标记物而广为人知。仅含三个吡咯环的亚酞菁和亚卟啉大环只有在以中心硼原子为模板时才能存在。扩展卟啉(六个或八个吡咯)的硼配合物可以在二吡咯亚甲基(而非联吡咯)位点络合硼。本文的主要重点是硼卟啉和咕啉配合物,其中两个硼原子在非常受限的配位位点内紧密配合,导致硼和卟啉配体都出现了意想不到的化学性质。文中描述了这些不寻常的特征,并推测了其出现的原因。