Nickel-Cornered Molecular Rectangles as Polycyclic Aromatic Hydrocarbon Receptors.

Two nickel-cornered organometallic metalla-rectangles containing a pyrene-linked-di-N-heterocyclic carbene have been prepared. The dimensions of one side of the rectangle were modulated by either using pyrazine or 4,4'-bipyridine. The two molecules were tested as hosts for the recognition of seven small polycyclic aromatic hydrocarbons (PAHs) in [D6 ]acetone. By using 1 H NMR spectroscopy titrations, it could be established that the host-guest stoichiometries of the inclusion complexes formed were 1:1 for the pyrazine-based host, and 1:2 for the host containing bipyridine, in accordance with the larger dimensions of the latter. The molecular structure of the inclusion complex consisting of the bipyridine-containing host and pyrene was determined by X-ray crystallography, which confirms the 1:2 host-guest stoichiometry of this species. The determination of the association constants indicate that the binding strengths are in the order: Perylene

Rim, Side Arms, and Cavity: Three Sites for the Recognition of Anions by Tetraazolium Resorcinarene Cavitands.

Two tetrabenzoimidazolium-resorcinarene cavitands were prepared and used for the recognition of chloride, bromide, iodide, cyanide, nitrate, perchlorate, hexanoate, benzenesulfonate, and p-toluenesulfonate. Binding affinities of the two cavitands were determined by 1 H NMR titration and computational analysis. The observed spectral changes were related to specific interaction sites, which were supported by the computational studies. In the case of the C2-H tetrabenzoimidazolium-resorcinarene, the recognition region of the inorganic anions and hexanoate was located at the rim of the cavitand, although chloride and bromide also interacted with the aromatic C-H bonds located between adjacent arms of the cavitand. By contrast, the recognition of the two anions with an aromatic ring (benzenesulfonate and p-toluenesulfonate) results from encapsulation of the aromatic part of the anions inside the hydrophobic cavity of the host. In the case of the C2-Me tetrabenzoimizazolium-resorcinarene receptor, the ability of the molecule to bind all inorganic anions and hexanoate was suppressed, but the receptor maintained its ability to strongly bind benzenesulfonate and p-toluenesulfonate. This is interpreted in terms of suppression of the ability of the cavitand to form hydrogen bonds at the rim of the molecule due to replacement of the C2-H proton by a methyl group, while the hydrophobic pocket of the molecule maintains its binding abilities.

Unveiling the Importance of π-Stacking in Borrowing-Hydrogen Processes Catalysed by Iridium Complexes with Pyrene Tags.

This work describes the preparation of a series of pyrene-tagged N-heterocyclic carbene complexes of iridium, and their use in two benchmark borrowing hydrogen reactions: the reduction of ketones by transfer hydrogenation and the ß-alkylation of secondary alcohols with primary alcohols. The detailed study of these homogeneously catalysed reactions reveals several important implications regarding the strong influence of the pyrene tags in the catalysts. First, the catalytic activity is partially inhibited by addition of an external amount of pyrene, but only when pyrene-tagged catalysts and aromatic substrates are used. Second, the rate order of the reaction is highly dependent on the nature of the substrates and the ligand. When pyrene-tagged catalysts and aromatic substrates are used, the reaction follows a zero-order dependence on the concentration of the substrate. All other combinations afford a second-order rate in the substrates. And third, the presence or absence of the pyrene functionality in the catalyst also influences the reaction order with respect to the concentration of the catalyst. Pyrene-containing catalysts display a fractional rate order of below 1. Finally, two pyrene-tagged catalysts were supported onto reduced-graphene oxide (rGO), and used as heterogeneous catalysts. While the dimetallic catalyst was effectively recycled 12 times, the monometallic catalyst maintained its activity for only three runs.

A Tetraferrocenyl-Resorcinarene Cavitand as a Redox-Switchable Host of Ammonium Salts.

Tetraannulation of a resorcinarene-octaamino cavitand with ferrocenecarboxaldehyde allows the preparation of a tetrabenzimidazole-resorcinarene cavitand with four ferrocenyl moieties directly linked to the C2 atom of the imidazole units. Oxidation of the four ferrocenyl moieties produces important structural modifications of the molecule, as indicated by DFT calculations performed for the neutral and tetraoxidized forms of the cavitand. By means of (1) H NMR spectroscopic analysis, the encapsulating properties of the new tetraferrocenyl-resorcinarene cavitand toward a series of ammonium salts were evaluated, and a clear cutoff point in binding affinity with respect to size was observed. Cyclic voltammetric studies allowed us to estimate the relative association constants for the neutral and oxidized forms of the cavitand, thus indicating that the guest was bound to the neutral (reduced) state of the cavitand and was released from the oxidized form. These redox-addressable conformational and binding properties of the resorcinarene-tetraferrocenyl cavitand constitute all the necessary features of a redox-switchable molecular gripper. By means of mass-spectrometric analysis, we could unambiguously confirm the molar stoichiometry of the host-guest complex (1:1) and assess the strong guest encapsulation, as indicated by triggering the covalent coupling between host and guest in the gas phase.

A resorcinarene-based tetrabenzoimidazolylidene complex of rhodium.

A tetrabenzoimidazolium-resorcinarene cavitand was used for the preparation of a tetra-benzoimidazolylidene of rhodium, which is unprecedented in the field of poly-NHC metal complexes. Both the experimental and computational analyses of the molecule reveal a distorted vase conformation as the most stable one, although several non-interconverting conformational isomers due to the restricted rotation about the Rh-C(carbene) bond coexist in the product. There is a fluxional behaviour involving the vase-kite interconversion. The main interactions between the arms of the cavitand are mostly concentrated on the terminal organometallic fragments attached to NHC, along with those between -CH3 and a N-heterocyclic carbene ring from benzoimidazoles.