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Counterion Dynamics in an Interpenetrated Coordination Cage Capable of Dissolving AgCl
No full textIn solution, the eight BF4 counterions of a positively charged D4-symmetric interpenetrated [Pd4ligand8]8+ double cage (1) are localized in distinct positions. At low temperatures, one BF4 ion is encapsulated inside the central pocket of the supramolecular structure, two BF4 ions are bound inside the equivalent outer pockets, and the remaining five BF4 ions are located outside the cage structure (expressed by the formula [3BF4@1][BF4]5). On warming, the two BF4 ions in the outer pockets are found to exchange with the exterior ions in solution whereas the central BF4 ion stays locked inside the central cavity (here written as [BF4@1][BF4]7). The exchange kinetics were determined by exchange spectroscopy (EXSY) NMR experiments and line-shape fitting in different solvents. The tremendously high affinity of this double cage for the binding of two chloride ions inside the outer pockets allows for complete exchange of two BF4 ions by the addition of solid AgCl to give [2Cl+BF4@1][BF4]5. The uptake of the two chloride ions is allosteric and is thus accompanied by a structural rearrangement (compression along the Pd4 axis) of the double cage structure. An analysis by using 900MHz NOESY NMR spectroscopy shows that this compression of about 3.3% is associated with a helical twist of 8 degrees, which together resemble a screw motion. As a consequence of squeezing each of the outer two pockets by 53%, the volume of the central pocket is increased by 43%, which results in an increase of 36% in the 19F spin-lattice relaxation time (T1) of the central BF4 ion. The packing coefficients (PC) for the ions in the outer pockets (103% for BF4 and 96% for Cl) were calculated.DFG; Fonds der Chemischen Industri
Self-assembled coordination cages based on banana-shaped ligands
No full textThe combination of pyridyl ligands and square-planar Pd(II) or Pt(II) cations has proven to be a very reliable recipe for the realization of supramolecular self-assemblies. This tutorial review deals with the design, synthesis and host-guest chemistry of discrete coordination cages built according to this strategy. The focus is set on structures obeying the formula [PdnL2n] (n = 2-4). The most discussed ligands are bent, bis-monodentate bridges having their two donor sites pointing in the same direction. The structures of the resulting cages range from simple globules over intertwined knots to interpenetrated dimers featuring three small pockets instead of one large cavity. The cages have large openings that allow small guest molecules to enter and leave the cavities. Most structures are cationic and thus favour the uptake of anionic guests. Some examples of host-guest complexes are discussed with emphasis on coencapsulation and allosteric binding phenomena. Aside from cages in which the ligands have only a structural role, some examples of functional ligands based on photo-and redox-active backbones are presented
Reversible stabilization of transition-metal-binding DNA G-quadruplexes.
No full textYou can't top the CopperTop: Tetramolecular G-quadruplexes modified with terminal pyridine ligands exhibit metal-triggered stabilization as monitored by thermal denaturation studies, circular dichroism, and nondenaturing gel electrophoresis. Formation of the square-planar CuII(pyridine)4 complex was confirmed by EPR measurements. The metal complexation is fully reversible by removal of the transition metal with ethylenediaminetetraacetic acid (edta)
NMR-Based Structure Determination of an Intertwined Coordination Cage Resembling a Double Trefoil Knot
No full textDFG [IRTG 1422
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