C,C‐ and N,C‐Coupled Dimers of 2‐Aminotetraphenylporphyrins: Regiocontrolled Synthesis,Spectroscopic Properties,and Quantum‐Chemical Calculations |
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| Authors: | Dr. Torsten Bruhn Dipl.‐Chem. Franziska Witterauf Dr. Daniel C. G. Götz Carina T. Grimmer Dipl.‐Chem. Max Würtemberger Prof. Dr. Udo Radius Prof. Dr. Gerhard Bringmann |
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| Affiliation: | 1. Institute of Organic Chemistry, University of Würzburg, Am Hubland, 97074 Würzburg (Germany), Fax: (+49)?931‐31‐84755;2. Present address: Bayer Pharma AG, Process Research & Chemical Development, Friedrich‐Ebert‐Str. 217‐333, 42117 Wuppertal (Germany);3. Institute of Inorganic Chemistry, University of Würzburg, Am Hubland, 97074 Würzburg (Germany) |
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| Abstract: | β,β′‐Bisporphyrins are intrinsically chiral porphyrin dimers with fascinating properties. The configurational stability at their axes can be directed by variation of the central metal atoms. Herein, we present a regioselective functionalization of the monomeric 2‐amino‐tetraphenyl‐porphyrin as a versatile substrate for dimerization by oxidative coupling. By simple variation of the reaction conditions (solvent and oxidant), the oxidation selectively gave either the axially chiral C,C‐coupled diaminobisporphyrin in high yields or, under Ullmann conditions, the twofold N,C‐linked achiral dimer, also in good yields. A generalized mechanism for the coupling reaction is proposed based on DFT calculations. The axially chiral β,β′‐coupled porphyrin dimers were isolated as racemic mixtures, but can be resolved by HPLC on a chiral phase. TDDFT and coupled‐cluster calculations were used to explain the spectroscopic properties of the aminoporphyrins and their dimers and to elucidate the absolute configurations of the C,C‐coupled bisporphyrins. |
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| Keywords: | atropisomerism configuration determination oxidative coupling porphyrins quantum‐chemical calculations |
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