Issue 11, 2014

Synthesis, X-ray structure, spectral and electrochemical properties of a β-meso covalently linked BODIPY–Ru(ii) dipyrrin complex

Abstract

We synthesized the BODIPY–Ru(II) dipyrrin complex in decent yield by reacting β-dipyrromethanyl substituted BODIPY with [{(η6-C10H14)RuCl(μ-Cl)}2] under simple reaction conditions. The BODIPY–Ru(II) dipyrrin complex was characterized by 1D, 2D, 13C, 11B, 19F NMR, HR-MS, UV-vis, fluorescence and electrochemical techniques. The BODIPY–Ru(II) dipyrrin complex was further characterized by X-ray structure analysis, which showed that the Ru(II)-dipyrrin complex is in perpendicular orientation to the BODIPY plane in the BODIPY–Ru(II) dipyrrin complex. The ruthenium metal ion in the BODIPY–Ru(II) dipyrrin complex is bonded to dipyrrin nitrogens, one chloro group and arene ring (arene = C10H14) in an η6 manner resulting in a hexa coordination geometry around the Ru(II) ion. The absorption and steady-state fluorescence spectra of the BODIPY–Ru(II) dipyrrin complex showed a broad and hypsochromically shifted absorption and emission bands compared to that of β-dipyrromethanyl substituted BODIPY. The electrochemical studies indicated that the BODIPY–Ru(II) dipyrrin complex was easy to reduce compared to β-dipyrromethanyl substituted BODIPY supporting the electron deficient nature of the BODIPY–Ru(II) dipyrrin complex.

Graphical abstract: Synthesis, X-ray structure, spectral and electrochemical properties of a β-meso covalently linked BODIPY–Ru(ii) dipyrrin complex

Supplementary files

Article information

Article type
Paper
Submitted
04 Jul 2014
Accepted
10 Sep 2014
First published
11 Sep 2014

New J. Chem., 2014,38, 5551-5558

Synthesis, X-ray structure, spectral and electrochemical properties of a β-meso covalently linked BODIPY–Ru(II) dipyrrin complex

S. Madhu, S. Kumar, T. Chatterjee and M. Ravikanth, New J. Chem., 2014, 38, 5551 DOI: 10.1039/C4NJ01114G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements