PtCl 2 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 PtCl 2 salt in a single step without any prefunctionalized precursors. Upon dimerizat...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2020-10, Vol.56 (84), p.12809-12812 |
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container_title | Chemical communications (Cambridge, England) |
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creator | Murugavel, M. Adinarayana, B. Das, Mainak Peruncheralathan, S. Palepu, Narasinga Rao 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 PtCl
2
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 |
format | Article |
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2
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-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 PtCl
2
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
title | PtCl 2 mediated peripheral transformation of carbatriphyrin(3.1.1) into a meso -fused β–β′ dimer and its monomer analogue |
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