Issue 80, 2017

Synthesis, crystallographic characterization and homogeneous catalytic activity of novel unsymmetric porphyrins

Abstract

Unsymmetric porphyrins, containing both pentafluorophenyl (PFP = A) and 3,4-dimethoxyphenyl (DMP = B) substituents at the meso positions, were prepared using Lindsey's methodology. The isomeric trans-A2B2 (P1) and cis-A2B2 (P2) porphyrins together with the tris(pentafluorophenyl)porphyrin A3B (P3) were isolated using chromatography. The porphyrins were characterized by UV-VIS, 1H NMR spectroscopy, mass spectrometry, elemental analysis (C, H, N) and cyclic voltammetry (CV), and their molecular structures were confirmed by single crystal XRD. Their manganese complexes, MnP1, MnP2 and MnP3, were also synthesised and used as catalysts in cyclooctene and cyclohexane oxidation reactions under homogeneous conditions. The catalytic studies were supported by electrochemical measurements and showed that the number of electron-withdrawing substituents on the porphyrins rings influences the catalytic activity. These porphyrins may be used as precursors for the design of new materials, such as Polymers of Intrinsic Microporosity (PIMs).

Graphical abstract: Synthesis, crystallographic characterization and homogeneous catalytic activity of novel unsymmetric porphyrins

Supplementary files

Article information

Article type
Paper
Submitted
07 avq 2017
Accepted
23 okt 2017
First published
31 okt 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 50610-50618

Synthesis, crystallographic characterization and homogeneous catalytic activity of novel unsymmetric porphyrins

A. R. Antonangelo, K. C. M. Westrup, L. A. Burt, C. G. Bezzu, T. Malewschik, G. S. Machado, F. S. Nunes, N. B. McKeown and S. Nakagaki, RSC Adv., 2017, 7, 50610 DOI: 10.1039/C7RA08734A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements