Cation Binding Properties Research Articles

Synthesis, characterization, electrochemistry and ion-binding studies of ruthenium(II) bipyridine receptor molecules containing calix[4]arene-azacrown as ionophore

A number of molecular receptors containing ruthenium(II) bipyridine moiety as fluorophore and calix[4]arene-azacrown hybrid molecule as ionophore have been synthesized and characterized. These receptors (1-4) exhibit strong 3MLCT luminescence bands in the range 613-618 nm. The cation-binding property of these fluoroionophores have been investigated with the ions Na+, K+, Mg2+, Ca2+, Cs+, Zn2+, Cd2+, Hg2+ and Pb2+ and the recognition event monitored by luminescence, 1H NMR spectroscopy, the oxidation potential of metal ion and UV/Vis absorption studies. The luminescence study suggests complexation of all four receptors with Zn2+, Cd2+ and Hg2+ and for 2 and 3 also with Pb2+. The binding constants (Ks, except 4) and stoichiometries of the complexes have been calculated from the luminescence titration data, with values of Ks ranging from 2.53 x 10(5) to 6.27 x 10(3) M(-1). The 1H NMR spectroscopy study exhibits interactions of Na+ and K+ with 1 and 4, K+ and Cs+ with 2, and K+ with 3. Binding constants with these metal ions have been calculated from 1H NMR titrations using computer programs or by a direct method depending on the type of change in the chemical shifts observed upon addition of metal ions. Stoichiometry of the complexes has been determined from Job's plot. Electrochemical properties of 1-4 have been studied in the absence and also in the presence of selected metal ions and the shift of the oxidation potentials of the Ru(II) in the presence of guest ions suggests an interaction of Na+, Hg2+ and Pb2+ with 1 and 2 but not with 3 and 4, indicating a selective electrochemical response towards certain metal ions. The results obtained are presented and discussed in light of ion-binding properties and methods of detection.

Sulphur-enriched thiacalix[4]arenes in the cone conformation: synthesis, crystal structures and cation binding properties

The synthesis and crystal structure of p-tert-butylthia- and p-tert-butylcalix[4]arene derivatives 1–7 substituted at the narrow rim by diethylthiophosphate ester groups, -PS(OEt)2 are reported. In these compounds the phosphorus atoms are directly attached to the phenolic O atoms of the calix units and the S atoms of the thiophosphate may serve as a two-electron donor to a metal ion. Their crystal structures were solved, which revealed their cone conformation. Their cation-binding properties have been established by liquid-liquid extraction of metal picrates from water into dichloromethane and stability constant determination in acetonitrile using UV-absorption spectrophotometry. Quantitative extraction was achieved for Ag+ (%E = 99) with the tetra-substituted thiacalix[4]arene derivative. The complexes were found to be of 1:1 stoichiometry and the location of the metal cations was shown to be nearby the sulphur atoms by 1H NMR.

A Facile Approach to the Preparation of Bis-Crown Ethers Based on SET-Promoted Photomacrocyclization Reactions

A novel methodology for the synthesis of bis-crown ethers has been developed. The preparative route takes advantage of an efficient single electron transfer promoted photomacrocyclization reaction of polyether branched bisphthalimides which contain alpha-trimethylsilylmethyl groups at terminal positions. The generality of the methodology was demonstrated by its application to the synthesis of symmetric and unsymmetric bis-crown ethers of various ring sizes. Finally, the metal cation binding and fluorescence emission properties of the bis-crowns, prepared by using the developed procedure, were briefly explored.

Selective Templated Complexation of a Cylindrical Macrotricyclic Host with Neutral Guests: Three Cation-Controlled Switchable Processes

A novel triptycene-based cylindrical macrotricyclic host 1 containing an anthracene unit and two dibenzo [24]crown-8 moieties was synthesized, and its cation binding properties were studied. It was found that the host could not only form complex with the paraquat derivative 4, but also show selective templated complexation with pyromellitic diimide 2 and anthraquinone 3 in the presence of lithium and potassium ions, respectively. Consequently, two novel cascade complexes with neutral molecules as bridging species were formed in solution and in the solid state, which were structurally studied by NMR, MS spectra, and X-ray methods. Moreover, we also found that the association and dissociation of the complexes could be easily achieved by the addition and removal of lithium or potassium ions, which resulted in three cation-controlled switchable processes.

Importance of Leu99 in Transmembrane Segment M1 of the Na+,K+-ATPase in the Binding and Occlusion of K+

Twenty-six point mutations were introduced into the N-terminal and middle parts of transmembrane segment M1 of the Na+, K+ -ATPase and its cytosolic extension. None of the alterations to charged and polar residues in the N-terminal part of M1 and its cytosolic extension had any major effect on the cation binding properties, thus rejecting the hypothesis that these residues are involved in cation selectivity. By contrast, specific residues in the middle part of M1, particularly Leu(99), were found critical to K+ interaction of the enzyme. Hence, mutation L99A reduced the affinity for K+ activation of E2P dephosphorylation 17-fold, and L99F reduced the equilibrium level of the K+-occluded intermediate [K2]E2 and increased the rate of K+ deocclusion 39-fold, i.e. more than seen for mutation E329Q of the cation-binding glutamate in M4. L99Q affected K+ interaction in yet another way, the equilibrium level of [K2]E2 being slightly increased despite an increased rate of K+ deocclusion, suggesting that the K+ ions leave and enter the occlusion pocket more frequently than in the wild type. L99Q furthermore affected the ability to discriminate between Na+ and K+ on the extracellular side. Our findings can be explained by a structural model in which Leu(99) and Glu(329) interact and cooperate in K+ binding and gating of the K+ sites. The disturbance of K+ interaction in mutants with alteration to Leu(91), Phe(95), Ser(96), or Leu(98) could be a consequence of the roles of these residues in positioning the M1 helix optimally for the interaction between Leu(99) and Glu(329). Phe(95) may serve to stabilize the pivot for movement of M1 through interaction with Ile(287) in M3.

A New Thiophene‐Based Tripodal Ligand: Synthesis and Cation Binding Properties.

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Synthesis and Cation Binding Properties of a New Bipyrazolic Tripodal Ligands

in which acyclic pyrazoles extract only the transi-tion metal cationswhen the macrocyclic pyrazolic com-pounds are expected to form stable complexes both withtransition and alkali metals, we demonstrate also here anaffinity of these new acyclic tripods only with the transitionmetal cations, with no complexation being observed towardalkali cations.The affinity of these hosts is especially high for mercury.This is not surprising if the high donor properties of nitrogentowards this metal are considered. We also notice an affinity toward Cu

40 Years of Supramolecular Chemistry

40 Years of Supramolecular Chemistry

A New Thiophene-Based Tripodal Ligand: Synthesis and Cation Binding Properties

The synthesis of a new tripodal ligand based on a thiophene ring is reported. The complexation properties of this compound towards bivalent metal ions (Hg2+, Cd2+, Pb2+, Cu2+, Zn2+) and alkaline metal ions (Li+, Na+, K+) has been studied by a liquid–liquid extraction process and the extracted cation percentage was determined by atomic absorption measurements.

New functionalised C,C-bipyrazoles. Synthesis and cation binding properties

The synthesis of two new C,C-bipyrazoles ligands with a side-arm bearing a functionalised donor-group is reported. The complexation properties of these compounds towards bivalent metal ions (Hg2+, Cd2+, Pb2+, Cu2+, Zn2+) and alkaline metal ions (Li+, Na+, K+) was studied by a liquid–liquid extraction process and the extracted cation percentage was determined by atomic absorption measurements.

Synthesis, luminescence and ion-binding properties of palladium(ii) complexes with 1,2-bis[di(benzo-15-crown-5)phosphino]ethane (dbcpe)

A series of palladium(II) complexes with 1,2-bis[di(benzo-15-crown-5)phosphino]ethane ligand (dbcpe), [Pd(dbcpe)X2] (X = Cl 1, Br 2 and I 3), have been successfully synthesised and characterised. The X-ray crystal structure of dbcpe has also been determined. The cation-binding properties of the complexes have been studied and the stability constants with alkali metal cations determined. The crown-free analogue of dbcpe, 1,2-bis[bis(3,4-dimethoxyphenyl)phosphino]ethane (ddmppe), and the related complexes have also been prepared and comparison studies have been made.

Ultra-wide bore 900 MHz high-resolution NMR at the National High Magnetic Field Laboratory

Access to an ultra-wide bore (105 mm) 21.1 T magnet makes possible numerous advances in NMR spectroscopy and MR imaging, as well as novel applications. This magnet was developed, designed, manufactured and tested at the National High Magnetic Field Laboratory and on July 21, 2004 it was energized to 21.1 T. Commercial and unique homebuilt probes, along with a standard commercial NMR console have been installed and tested with many science applications to develop this spectrometer as a user facility. Solution NMR of membrane proteins with enhanced resolution, new pulse sequences for solid state NMR taking advantage of narrowed proton linewidths, and enhanced spatial resolution and contrast leading to improved animal imaging have been documented. In addition, it is demonstrated that spectroscopy of single site 17O labeled macromolecules in a hydrated lipid bilayer environment can be recorded in a remarkably short period of time. 17O spectra of aligned samples show the potential for using this data for orientational restraints and for characterizing unique details of cation binding properties to ion channels. The success of this NHMFL magnet illustrates the potential for using a similar magnet design as an outsert for high temperature superconducting insert coils to achieve an NMR magnet with a field >25 T.

A novel photochemical approach to the synthesis of naphthalene-containing lariat-type crown ethers and an evaluation of their metal cation binding and fluorescence sensing properties

A novel method has been developed for the synthesis of naphthalene chromophore containing, lariat-type crown ethers. The route employs SET-promoted photocyclization reactions of polyether-tethered 2,3-naphthalimides to generate the variously ring-sized crown ether cores and an allylsilane N-acyliminum ion addition process to install amino ether side chains. The metal cation binding properties of the lariat-crown ethers, prepared in this manner, were evaluated. In addition, the ability of the lariat-crown ethers to serve as SET-based, fluorescence sensors of metal cations was probed. The results show that although the novel lariat-crown ethers strongly complex alkali metal cations (Na, K, Rb, Cs), this complexation is not associated with enhanced fluorescence from the naphthalene chromophores as would be expected if cation binding impeded SET quenching by the tertiary amine donor in the side chains. In contrast, the novel lariat-crown ethers serve as sensitive sensors for the divalent metal cations of Mg and Cu and the monovalent cation of Ag.

Photochromic and Cation-Binding Properties of New Crowned Spiropyrans

ABSTRACT Spectral properties of new crowned spiropyrans and their cationic complexes are described.

Nitrogen Heterocyclic Carbon-Rich Materials: Synthesis and Spectroscopic Properties of Dehydropyridoannulene Macrocycles

A new series of nitrogen heterocyclic dehydroannulenes 1-3 have been synthesized and their macrocyclic structures assigned using spectroscopic methods. The chiral and planar ground state conformations of 1 and 3, respectively, were determined by semiempirical theoretical calculations. All dehydropyridoannulenes and precursors possessing four aromatic rings functioned as fluorescent chromophores. A detailed spectroscopic investigation into the cation-binding properties of 3 in dilute solution revealed a particularly selective photoluminescence quenching sensory response for Pd(II) ions. Cycle 3, as well as 1 and 2, also exhibited reversible proton-triggered luminescence quenching behavior. At higher concentrations, 3 afforded a coordination polymer precipitate with Ag(I) ions. Cycles 1 and 2 and precursors 15, 23, and 29 also undergo thermochemical reactions that may potentially lead to carbon-rich polymers. The physicochemical properties of 1-3 suggest that dehydropyridoannulenes may serve as a particularly versatile new class of ligands for the creation of novel heteroatom-containing carbon-rich materials with many potential applications in supramolecular materials science and nanotechnology.

Pyrazolic Tripods Synthesis and Cation Binding Properties.

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Pyrazolic tripods synthesis and cation binding properties

The synthesis of two new bipyrazolic tripods with different functionalised arms is described. The complexing properties of these compounds towards heavy metal ions (Hg2+, Cd2+, Pb2+) and alkaline metal ions (K+, Na+, Li+) were studied by a liquid–liquid extraction process and the extracted cation percentage was determined by atomic absorption measurements.

Designing Calcium-sensitizing Mutations in the Regulatory Domain of Cardiac Troponin C

Cardiac troponin C belongs to the EF-hand superfamily of calcium-binding proteins and plays an essential role in the regulation of muscle contraction and relaxation. To follow calcium binding and exchange with the regulatory N-terminal domain (N-domain) of human cardiac troponin C, we substituted Phe at position 27 with Trp, making a fluorescent cardiac troponin C(F27W). Trp(27) accurately reported the kinetics of calcium association and dissociation of the N-domain of cardiac troponin C(F27W). To sensitize the N-domain of cardiac troponin C(F27W) to calcium, we individually substituted the hydrophobic residues Phe(20), Val(44), Met(45), Leu(48), and Met(81) with polar Gln. These mutations were designed to increase the calcium affinity of the N-domain of cardiac troponin C by facilitating the movement of helices B and C (BC unit) away from helices N, A, and D (NAD unit). As anticipated, these selected hydrophobic residue substitutions increased the calcium affinity of the regulatory domain of cardiac troponin C(F27W) approximately 2.1-15.2-fold. Surprisingly, the increased calcium affinity caused by the hydrophobic residue substitutions was largely due to faster calcium association rates (2.6-8.7-fold faster) rather than to slower calcium dissociation rates (1.2-2.9-fold slower). The regulatory N-domains of cardiac troponin C(F27W) and its mutants were also able to bind magnesium competitively and with physiologically relevant affinities (1.2-2.7 mm). The design of calcium-sensitizing cardiac troponin C mutants presented in this work enhances the understanding of how to control cation binding properties of EF-hand proteins and ultimately their structure and physiological function.

New Tetrapyrazolic Macrocycle. Synthesis and Cation Binding Properties.

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Influence of monovalent cation identity on parvalbumin divalent ion-binding properties.

Rat alpha- and beta-parvalbumins have distinct monovalent cation-binding properties [Henzl et al. (2000) Biochemistry 39, 5859-5867]. Beta binds two Na(+) or one K(+), and alpha binds one Na(+) and no K(+). Ca(2+) abolishes these binding events, suggesting that the monovalent ions occupy the EF-hand motifs. This study compares alpha and beta divalent ion affinities in Na(+) and K(+) solutions. Solvent cation identity seriously affects alpha. In Hepes-buffered NaCl, at 5 degrees C, the macroscopic Ca(2+)-binding constants are 2.6 x 10(8) and 6.4 x 10(7) M(-1) and the Mg(2+) constants, 1.8 x 10(4) and 4.3 x 10(3) M(-1). In Hepes-buffered KCl, the Ca(2+) values increase to 2.9 x 10(9) and 6.6 x 10(8) M(-1) and the Mg(2+) values to 2.2 x 10(5) and 3.7 x 10(4) M(-1). Monte Carlo simulation of alpha binding data-employing site-specific constants and explicitly considering Na(+) binding-yields a K(Na) of 630 M(-1) and indicates that divalent ion-binding is positively cooperative. NMR data suggest that the lone Na(+) ion occupies the CD loop. Solvent cation identity has a smaller impact on beta. In Na(+), the Ca(2+) constants for the EF and CD sites are 2.3 x 10(7) and 1.5 x 10(6) M(-1), respectively; the Mg(2+) constants are 9.2 x 10(3) and 1.7 x 10(2) M(-1). In K(+), these values shift to 3.1 x 10(7) and 3.8 x 10(6) M(-1) and the latter to 1.4 x 10(4) and 2.9 x 10(2) M(-1). These data suggest that parvalbumin divalent ion affinity, particularly that of rat alpha, can be significantly attenuated by increased intracellular Na(+) levels.