Issue 41, 2019

Phosphine-functionalised tris(pyrazolyl)methane ligands and their mono- and heterobimetallic complexes

Abstract

The synthesis, characterisation and reactivity of new phosphine-functionalised tris(pyrazolyl)methane ligands (TpmPR2, 2a–c, with R = Ph, nBu, iPr) are presented. The reaction of 2a–c with [Rh(CO)2Cl]2 furnished N,P-heterochelate carbonyl complexes (3a–c), which were used to quantify the donor abilities of the ligands via IR spectroscopy. The coordination flexibility was demonstrated by treating representative members of this new ligand class with [CpRu(acn)3][PF6] (acn = acetonitrile), [(tht)AuCl] (tht = tetrahydrothiophene) and [Pd(allyl)Cl]2 providing either a N,N,P-heteroscorpionate complex (4) or the P-coordinated complexes (5,6) without any involvement of the pyrazolyl entities. With 2a and [Pd(cod)Cl2], another P,N-heterochelate complex (7) was obtained, which served as a precursor for a heterobimetallic complex containing palladium and copper (8). Detailed NMR spectroscopic and X-ray crystallographic investigations have been performed on all new complexes.

Graphical abstract: Phosphine-functionalised tris(pyrazolyl)methane ligands and their mono- and heterobimetallic complexes

Supplementary files

Article information

Article type
Paper
Submitted
16 Тра 2019
Accepted
05 Чер 2019
First published
05 Чер 2019
This article is Open Access
Creative Commons BY-NC license

Dalton Trans., 2019,48, 15397-15407

Phosphine-functionalised tris(pyrazolyl)methane ligands and their mono- and heterobimetallic complexes

H. E. Wagner, S. Hohnstein, M. G. Schußmann, L. A. Steppe and F. Breher, Dalton Trans., 2019, 48, 15397 DOI: 10.1039/C9DT02057H

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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