Issue 33, 2021

Cationic tetra- and pentacoordinate complexes of nickel based on POCN- and POCOP-type pincer ligands: synthesis, characterization, and ligand exchange studies

Abstract

Stirring acetonitrile solutions of the charge-neutral pincer complexes (POCN)NiBr (1, POCN = κPCN-{2-(i-Pr)2PO,6-CH2{c-N(CH2)5}-C6H3) and (POCOP)NiBr (2, POCOP = κPCP′-2,6-(i-Pr2OP)2C6H3) with AgSbF6 facilitates Br abstraction to give the corresponding cationic acetonitrile adducts [(POCN)Ni(NCMe)]+, 1a, and [(POCOP)Ni(NCMe)]+, 2a. Treating 1a and 2a with pyridine (py), 2,2′-bipyridine (bipy), phenanthroline (phen), or 4,4′-bipyridine (bipy*) gave the corresponding monocationic adducts [(POCN or POCOP)Ni(ligand)]+ (ligand = py: 1b and 2b; κNN′-bipy: 1c and 2c; κNN′-phen: 1d and 2d) and the dicationic dinuclear adducts [(POCN or POCOP)2Ni2(μ-bipy*)]2+ (1e and 2e). The new adducts 1a–1d and 2b–2e have been characterized by NMR spectroscopy; complex 1e proved to be insoluble and could not be analyzed by NMR. Single crystal X-ray diffraction studies were used to establish the solid-state structures of 1a–1e, and 2b–2d. UV-vis spectra have also been recorded for the pentacoordinated complexes 1c, 1d, 2c, and 2d. Studying the equilibria that govern the displacement of halides in (pincer)NiX (X = Cl, Br) by the in-coming nucleophiles py, bipy, and phen has allowed us to determine the following order for the relative nucleophilicities of the ligands involved in the halide substitution equilibria: Cl > Br > phen > bipy ≫ py > MeCN. Similar Keq measurements showed that cationic species are better stabilized with the POCN platform compared to POCOP. This implies that POCN is a better net donor of electron density compared to POCOP, such that the relative Lewis acidity (electrophilicity) of the cationic fragments should follow the order [(POCOP)Ni]+ > [(POCN)Ni]+. Cyclic voltammetry measurements on the bipy adducts showed reversible, one-electron oxidation events occurring at a lower Image ID:d1nj01355f-t1.gif value for [(POCN)Ni(bipy)]+, implying a more electron-rich Ni(II) centre with POCN vs. POCOP. Consistent with these assertions, mixing (POCN)NiBr and [(POCOP)Ni(phen)]+ in acetonitrile gave [(POCN)Ni(phen)]+ and (POCOP)NiBr. Similarly, the Keq value of 0.19 for the equilibrium exchange (POCN)NiCl + (POCOP)NiBr ⇆ (POCN)NiBr + (POCOP)NiCl indicates that the [(POCOP)Ni]+ fragment is better stabilized by Clvs. Br. These exchange reactions do not occur in THF or CH2Cl2, implying that they are driven by the nucleophilic character of the solvent.

Graphical abstract: Cationic tetra- and pentacoordinate complexes of nickel based on POCN- and POCOP-type pincer ligands: synthesis, characterization, and ligand exchange studies

Supplementary files

Article information

Article type
Paper
Submitted
06 شعبان 1442
Accepted
28 رمضان 1442
First published
28 رمضان 1442

New J. Chem., 2021,45, 15063-15073

Cationic tetra- and pentacoordinate complexes of nickel based on POCN- and POCOP-type pincer ligands: synthesis, characterization, and ligand exchange studies

N. Rahimi and D. Zargarian, New J. Chem., 2021, 45, 15063 DOI: 10.1039/D1NJ01355F

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