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  4. Host-guest chemistry in the hexanuclear (arene)ruthenium metalla-prismatic cage [Ru6(p-cymene)6(tpt)2(dhnq)3]6+

Host-guest chemistry in the hexanuclear (arene)ruthenium metalla-prismatic cage [Ru6(p-cymene)6(tpt)2(dhnq)3]6+

Author(s)
Barry, Nicolas P. E.
Therrien, Bruno  
Institut de chimie  
Date issued
2009
In
Eur. J. Inorg. Chem.
Vol
31
From page
4695
To page
4700
Subjects
hexanuclear ruthenium hydroxynaphthoquinonato pyridinyltriazine bridged cage carceplex prepn encapsulation
Abstract
A large cationic triangular metalla-prism, [Ru6(p-cymene)6(tpt)2(dhnq)3]6+ ([1]6+), incorporating (p-cymene)ruthenium building blocks, bridged by 5,8-dihydroxy-1,4-naphthoquinonato (dhnq) ligands, and connected by two 2,4,6-tri(pyridin-4-yl)-1,3,5-triazine (tpt) subunits, allows encapsulation of various guest mols. This cationic cage, isolated as its triflate salt, possesses a portal size smaller than its cavity, thus allowing both, permanent and temporary encapsulation of guest mols. The host-guest properties of [1]6+ have been studied in soln. in the presence of planar mols. [phenanthrene, pyrene, (pyren-1-ylmethyl)amine, Pt(acac)2, triphenylene]. The stability const. of assocn. (Ka) was estd. by NMR spectroscopy for the following host-guest systems: [pyrene1]6+, [phenanthrene1]6+ and [(pyren-1-ylmethyl)amine1]6+. All Ka values were found to be larger than 2.4 × 104 M-1 for these host-guest systems ([D3]acetonitrile, 21 °C). The other two synthesized complexes, [Pt(acac)21]6+ and [triphenylene1]6+, were shown to act as carceplexes only. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009). [on SciFinder(R)]
Publication type
journal article
Identifiers
https://libra.unine.ch/handle/20.500.14713/52568
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