Use of a cyclo-P-4 building block - a way to networks of host-guest assemblies

Peresypkina, Eugenia and Bielmeier, Martin and Virovets, Alexander and Scheer, Manfred (2020) Use of a cyclo-P-4 building block - a way to networks of host-guest assemblies. CHEMICAL SCIENCE, 11 (34). pp. 9067-9071. ISSN 2041-6520, 2041-6539

Full text not available from this repository. (Request a copy)

Abstract

Despite the proven ability to form supramolecular assemblies via coordination to copper halides, organometallic building blocks based on four-membered cyclo-P-4 ligands find only very rare application in supramolecular chemistry. To date, only three types of supramolecular aggregates were obtained based on the polyphosphorus end-deck complexes (CpTa)-Ta-R(CO)(2)(eta(4)-P-4) (1a: Cp-R = Cp ''; 1b: Cp-R = Cp '''), with none of them, however, possessing a guest-accessible void. To achieve this target, the use of silver salts of the weakly coordinating anion SbF6- was investigated as to their self-assembly in the absence and in the presence of the template molecule P3Se4. The two-component self-assembly of the building block 1a and the coinage-metal salt AgSbF6 leads to the formation of 1D or 3D coordination polymers. However, when the template-driven self-assembly was attempted in the presence of an aliphatic dinitrile, the unprecedented barrel-like supramolecular host-guest assembly P3Se4@[{(Cp '' Ta(CO)(2)(eta P-4(4)))Ag}(8)](8+) of 2.49 nm in size was formed. Moreover, cyclo-P-4-based supramolecules are connected in a 2D coordination network by dinitrile linkers. The obtained compounds were characterised by mass-spectrometry, H-1 and P-31 NMR spectroscopy and X-ray structure analysis.

Item Type: Article
Uncontrolled Keywords: ;
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Anorganische Chemie
Chemistry and Pharmacy > Institut für Anorganische Chemie > Chair Prof. Dr. Manfred Scheer
Depositing User: Dr. Gernot Deinzer
Date Deposited: 11 Mar 2021 12:45
Last Modified: 11 Mar 2021 12:45
URI: https://pred.uni-regensburg.de/id/eprint/43805

Actions (login required)

View Item View Item