PtCl2 mediated peripheral transformation of carbatriphyrin(3.1.1) into a meso-fused β–β′ dimer and its monomer analogue
An unprecedented formation of a meso-fused β–β′ carbaporphyrin dimer and its monomer with a keto group was described. These analogues were synthesized from carbatriphyrin(3.1.1.) by a metal assisted strategy using PtCl2 salt in a single step without any prefunctionalized precursors. Upon dimerizatio...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2020-10, Vol.56 (84), p.12809-12812 |
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creator | Murugavel, M Adinarayana, B Das, Mainak Peruncheralathan, S Narasinga Rao Palepu Srinivasan, A |
description | An unprecedented formation of a meso-fused β–β′ carbaporphyrin dimer and its monomer with a keto group was described. These analogues were synthesized from carbatriphyrin(3.1.1.) by a metal assisted strategy using PtCl2 salt in a single step without any prefunctionalized precursors. Upon dimerization, the monomeric ligand with a dianionic core is transformed into a dimeric structure with unique trianionic cores. |
doi_str_mv | 10.1039/d0cc05309k |
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These analogues were synthesized from carbatriphyrin(3.1.1.) by a metal assisted strategy using PtCl2 salt in a single step without any prefunctionalized precursors. 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title | PtCl2 mediated peripheral transformation of carbatriphyrin(3.1.1) into a meso-fused β–β′ dimer and its monomer analogue |
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