Issue 36, 2020

Ambidentate bonding and electrochemical implications of pincer-type pyridylidene amide ligands in complexes of nickel, cobalt and zinc

Abstract

Pincer-type tridentate pyridyl bis(pyridylidene amide) (pyPYA2) ligand systems were coordinated to the Earth-abundant first row transition metals nickel, cobalt and zinc. A one-pot synthesis in water/ethanol afforded octahedral homoleptic bis-PYA complexes, [M(pyPYA2)2](PF6)2, whereas five-coordinate mono-PYA dichloride complexes, [M(pyPYA2)Cl2], were obtained upon slow addition of the ligand to the metal chlorides in DMF. Electrochemical measurements further revealed a facile oxidation of the metal centers from Ni2+ to Ni4+ and Co2+ to Co3+, respectively, while the Zn2+ system was redox inactive. These experiments further allowed for quantification of the much stronger electron donor properties of neutral N,N,N-tridentate pyPYA2 pincer ligands as compared to terpy. Remarkably, ortho-PYA pincer ligands feature amide coordination to the metal center via oxygen or nitrogen. This ambidentate ligand binding constitutes another mode of donor flexibility of the PYA ligand system, complementing the resonance structure dynamics established previously. NMR spectroscopic and MS analysis reveal that the meta-PYA ligand undergoes selective deuteration when coordinated to cobalt. This reactivity suggests the potential of this ligand as a transient proton reservoir for HX bond activation and, moreover, indicates the relevance of several resonance structures and therefore supports the notion that meta-PYA ligands are mesoionic.

Graphical abstract: Ambidentate bonding and electrochemical implications of pincer-type pyridylidene amide ligands in complexes of nickel, cobalt and zinc

Supplementary files

Article information

Article type
Paper
Submitted
14 juil. 2020
Accepted
21 août 2020
First published
21 août 2020
This article is Open Access
Creative Commons BY license

Dalton Trans., 2020,49, 12662-12673

Ambidentate bonding and electrochemical implications of pincer-type pyridylidene amide ligands in complexes of nickel, cobalt and zinc

P. Melle, N. Ségaud and M. Albrecht, Dalton Trans., 2020, 49, 12662 DOI: 10.1039/D0DT02482A

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