Diferrocenylmercury diphosphine diastereomers with unique geometries: trans-chelation at Pd(ii) with short Hg(ii)⋯Pd(ii) contacts
Author:
Affiliation:
1. Department of Chemistry
2. Rutgers University-Newark
3. Newark
4. USA
5. Institut für Anorganische und Analytische Chemie
6. Technische Universität Braunschweig
7. 38106 Braunschweig
8. Germany
Abstract
Two isomeric diphosphine chelate ligands with divergent orientation of the ferrocenes were prepared independently and their complexation to Pd(ii) investigated.
Funder
Deutsche Forschungsgemeinschaft
Division of Chemistry
Publisher
Royal Society of Chemistry (RSC)
Subject
Inorganic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2019/DT/C9DT02728A
Reference68 articles.
1. J. A. Gillespsie , E.Zuidema , P. W. N. M.Leuwen and P. C. J.Kamer , Phosphorus Ligand Effects in Homogenous Catalysis and Rational Catalyst Design , in Phosphorus(III) Ligands in Homogeneous Catalysis: Design and Synthesis , ed. P. C. J. Kamer and P. W. N. M. Leuwen , Wiley , 1st edn, 2012
2. The bite angle makes the difference: a practical ligand parameter for diphosphine ligands
3. Ligand Bite Angle Effects in Metal-catalyzed C−C Bond Formation
4. Wide Bite Angle Diphosphines: Xantphos Ligands in Transition Metal Complexes and Catalysis
5. The Steric Nature of the Bite Angle
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Palladium(0) complexes of diferrocenylmercury diphosphines: synthesis, X-ray structure analyses, catalytic isomerization, and C–Cl bond activation;Dalton Transactions;2021
2. Metallophilic interactions: observations of the shortest metallophilicinteractions between closed shell (d10⋯d10, d10⋯d8, d8⋯d8) metal ions [M⋯M′ M = Hg(ii) and Pd(ii) and M′ = Cu(i), Ag(i), Au(i), and Pd(ii)];Dalton Transactions;2020
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