C, C‐ and N, C‐Coupled Dimers of 2‐Aminotetraphenylporphyrins: Regiocontrolled Synthesis, Spectroscopic Properties, and Quantum‐Chemical Calculations. Issue 14 (26th February 2014)

• Record Type: Journal Article
• Authors: Bruhn, Torsten; Witterauf, Franziska; Götz, Daniel C. G.; Grimmer, Carina T.; Würtemberger, Max; Radius, Udo; Bringmann, Gerhard
• Is Part Of: Chemistry. Volume 20:Issue 14(2014)
• Page Start: 3998
• Page End: 4006
• Publication Date: 2014-02-26
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/chem.201304169
• Languages: English
• ISSNs: 0947-6539

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>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.</p> </abstract>