卟啉
金属化
化学
金属有机化学
金属
组合化学
配位复合体
光化学
有机化学
催化作用
作者
B.M.J.M. Suijkerbuijk,Robertus J. M. Klein Gebbink
标识
DOI:10.1002/anie.200703362
摘要
Abstract The coordination chemistry of porphyrins has traditionally involved the ability of the porphyrin's tetrapyrrolic core to accommodate metal ions of varying charges and sizes, and on the organometallic chemistry of the resulting metalloporphyrins. However, the organometallic chemistry of porphyrins is not necessarily restricted to the metal bound in the porphyrin core, but can also be extended to the porphyrin periphery, be it through direct metalation of the porphyrin macrocycle at the meso or β position, or by attachment to or merger of the porphyrin skeleton with ligands, followed by metalation. This Review focuses on the synthetic strategies used for porphyrins with peripheral metal–carbon bonds. The exciting results that have been produced underscore the importance and future potential of this field.
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