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Therrien, Bruno

Nom
Therrien, Bruno
Affiliation principale
Fonction
Professeur titulaire
Email
bruno.therrien@unine.ch
Identifiants
https://libra.unine.ch/handle/123456789/382
_
0000-0002-0388-2745

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  • Publication
    Accès libre
    In- and Out-of-Cavity Interactions by Modulating the Size of Ruthenium Metallarectangles
    (2010)
    Barry, Nicolas P.E.
    ;
    Furrer, Julien
    ;
    Therrien, Bruno 
    Cationic (arene)ruthenium-based tetranuclear complexes of the general formula [Ru4(η6-p-cymene)4(μ-N∩N)2(μ-OO∩OO)2]4+ were obtained from the dinuclear (arene)ruthenium complexes [Ru2 (η6-p-cymene)2(μ-OO∩OO)2Cl2] (p-cymene=1-methyl-4-(1-methylethyl)benzene, OO∩OO=5,8-dihydroxy-1,4-naphthoquinonato(2−), 9,10-dihydroxy-1,4-anthraquinonato(2−), or 6,11-dihydroxynaphthacene-5,12-dionato(2−)) by reaction with pyrazine or bipyridine linkers (N∩N=pyrazine, 4,4′-bipyridine, 4,4′-[(1E)-ethene-1,2-diyl]bis[pyridine]) in the presence of silver trifluoromethanesulfonate (CF3SO3Ag) (Scheme). All complexes 4–12 were isolated in good yield as CF3SO3- salts, and characterized by NMR and IR spectroscopy. The host–guest properties of the metallarectangles incorporating 4,4′-bipyridine and (4,4′-[(1E)-ethene-1,2-diyl]bis[pyridine] linkers were studied in solution by means of multiple NMR experiments (1D, ROESY, and DOSY). The largest metallarectangles 10–12 incorporating (4,4′-[(1E)-ethene-1,2-diyl]bis[pyridine] linkers are able to host an anthracene, pyrene, perylene, or coronene molecule in their cavity, while the medium-size metallarectangles 7–9 incorporating 4,4′-bipyridine linkers are only able to encapsulate anthracene. However, out-of-cavity interactions are observed between these 4,4′-bipyridine-containing rectangles and pyrene, perylene, or coronene. In contrast, the small pyrazine-containing metallarectangles 4–6 show no interaction in solution with this series of planar aromatic molecules.
  • Publication
    Accès libre
    Designing the Host-Guest Properties of Tetranuclear Arene Ruthenium Metalla-Rectangles to Accommodate a Pyrene Molecule
    (2010)
    Barry, Nicolas P. E.
    ;
    Furrer, Julien
    ;
    Freudenreich, Julien 
    ;
    Süss-Fink, Georg 
    ;
    Therrien, Bruno 
    Cationic tetranuclear arene ruthenium complexes of the general formula [Ru4(p-cymene)4(N∩N)2(dhnq)2]4+ comprising rectangular structures are obtained in methanol from the reaction of the dinuclear arene ruthenium precursor [Ru2(p-cymene)2(dhnq)2Cl2] (dhnq = 5,8-dihydroxy-1,4-naphthoquinonato) with pyrazine or bipyridine linkers [N∩N = pyrazine, 1; 4,4-bipyridine, 2; 1,2-bis(4-pyridyl)ethylene, 3] in the presence of AgCF3SO3. All complexes 1-3, isolated in good yield as triflate salts, have been characterised by NMR and IR spectroscopy. The interaction of these rectangular complexes with pyrene as a guest molecule has been studied in solution by various NMR techniques (1D, DOSY, ROESY). In [D3]acetonitrile, the pyrazine-containing metalla-rectangle 1 shows no meaningful interactions with pyrene. On the other hand, the 4,4-bipyridine- and 1,2-bis(4-pyridyl)ethylene-containing metalla-rectangles 2 and 3 clearly interact with pyrene in [D3]acetonitrile. DOSY measurements suggest that, in the case of [Ru4p-cymene)4(4,4-bipyridine)2(dhnq)2]4+ (2), the interactions occur on the outside of the rectangular assembly, while in the case of [Ru4(p-cymene)4{1,2-bis(4-pyridyl)ethylene}2 (dhnq)2]4+ (3), the pyrene molecule is found inside the hydrophobic cavity of the metalla-rectangle, thus giving rise to a host-guest system.