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Synthesis, Structure and Catalysis of Organometallic Porphyrin-Pincer Hybrids: A Review


Porphyrins are tetrapyrrolic conjugated aromatic macrocycles with 18 π electrons. These Nature’s favourite molecules are present in the active sites of several important biomolecules. Porphyrins can be structurally manipulated at their core, meso and β positions to get desired electronic properties. Pincers are monoanionic, tridentate meridional ligands and their metal complexes have proven to be robust, efficient and reliable catalysts in several organic transformations. Like porphyrins, pincers too can be structurally manipulated to obtain desired properties. The amalgamation of these two molecules leads to a new class of hybrid molecules called porphyrin-pincer complexes which offer two different metal binding sites, viz., core and periphery of porphyrin ring. Also, these hybrid molecules offer researchers to study the possible electronic interplay between the metals present in two binding sites, which is expected to perturb their electronic property. This dedicated review focusses on the developments that have taken place in last two decades in the area of porphyrin-pincer hybrid organometallic compounds in which porphyrin acts as anionic aromatic ligand providing a stable carbon-metal σ-bond.

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Publication details

The article was received on 14 Aug 2017, accepted on 13 Sep 2017 and first published on 14 Sep 2017

Article type: Perspective
DOI: 10.1039/C7DT03009F
Citation: Dalton Trans., 2017, Accepted Manuscript
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    Synthesis, Structure and Catalysis of Organometallic Porphyrin-Pincer Hybrids: A Review

    G. S. Ananthnag and D. V. S. Shetti, Dalton Trans., 2017, Accepted Manuscript , DOI: 10.1039/C7DT03009F

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