Reaction control by a host-guest complexation method

Very successful stereo-, regio-, and enantio-controls of the photoreaction of a guest compound were achieved by irradiation of the host-guest complex in the solid state. In order to discover the reason for the successful control, the X-ray crystal structure of the complex was studied. The complexation method was also effective to freeze the equilibrium in solution and isolate the labile tautomeric isomer as an inclusion complex.     

Mechanism of host-guest complexation by cucurbituril

The factors affecting host-guest complexation between the molecular container compound cucurbit[6]uril (CB6) and various guests in aqueous solution are studied, and a detailed complexation mechanism in the presence of cations is derived. The formation of the supramolecular complex is studied in detail for cyclohexylmethylammonium ion as guest. The kinetics and thermodynamics of complexation is monitored by NMR as a function of temperature, salt concentration, and cation size. The binding constants and the ingression rate constants decrease with increasing salt concentration and cation-binding constant, in agreement with a competitive binding of the ammonium site of the guest and the metal cation with the ureido carbonyl portals of CB6. Studies as a function of guest size indicate that the effective container volume of the CB6 cavity is approximately 105 A(3). It is suggested that larger guests are excluded for two reasons: a high activation barrier for ingression imposed by the tight CB6 portals and a destabilization of the complex due to steric repulsion inside. For example, in the case of the nearly spherical azoalkane homologues 2,3-diazabicyclo[2.2.1]hept-2-ene (DBH, volume ca. 96 A(3)) and 2,3-diazabicyclo[2.2.2]oct-2-ene (DBO, volume ca. 110 A(3)), the former forms the CB6 complex promptly with a sizable binding constant (1300 M(-1)), while the latter does not form a complex even after several months at optimized complexation conditions. Molecular mechanics calculations are performed for several CB6/guest complexes. A qualitative agreement is found between experimental and calculated activation energies for ingression as a function of both guest size and state of protonation. The potential role of constrictive binding by CB6 is discussed.     

Dynamic aspects in host-guest complexation by coordination nanotubes

Rod-like guests accommodated in self-assemble coordination nanotubes are shown to stay in the tubes without flipping along its length at room temperature, but rapidly exchange intermolecularly at high temperature.     

Evidences for temperature-dependent mechanism of host-guest complexation

Summary High-performance liquid chromatography and ultraviolet spectroscopy methods were applied to the studies on the influence of temperature on the complexation of β-cyclodextrin with naphthalene and its derivatives. The strong nonlinearity of Van't Hoff plots suggests, that the retention mechanism of hydrocarbons investigated might be different in high and low temperature region. The total lack of correlation (r=−0.230) between chromatographic data (capacity factors ratio:k _PAH/k _PAH×CD) and spectrophotometric data (ΔA) at high temperature (60°) as well as a significant correlation (r=0.922) at subambient temperature (15°C) suggest, that the inclusion mechanism starts to be important at low temperature region and the predominant mechanism for chromatographic retention is the formation of an inclusion complexes in the mobile phase.     

Electrochemical sensor for cinchonine based on a competitive host-guest complexation

An electrochemical sensor for cinchonine (CCN) using the β-cyclodextrin (β-CD) modified poly(N-acetylaniline) (PAA) electrode has been developed, in which 1,4-hydroquinone (HQ) was chosen as a probe. Complexation of HQ with β-CD modified on the glassy carbon electrode (GCE) was examined by cyclic voltammetry (CV). HQ was included in the cavity of β-CD and reversible voltammograms were observed. In the presence of CCN, a competitive inclusion equilibrium with β-CD was established between HQ and CCN, lowering the peak current of HQ. The decrease in the peak current of HQ is directly proportional to the amount of CCN. Linear calibration plot was obtained over the range from 4.0 × 10⁻⁶ to 8.0 × 10⁻⁵ M with a detection limit (S/N = 3) of 2.0 × 10⁻⁶ M. From the inhibitory effect of CCN on the inclusion of HQ by β-CD, the apparent formation constant of CCN with the immobilized β-CD was estimated. This electrochemical sensor showed excellent sensitivity, repeatability, stability and recovery for the determination of CCN. The response mechanism of the sensor was discussed in detail. The optimum steric configuration of inclusion complex was presented by molecular dynamics simulation.     

On-off-on fluorescence detection for biomolecules by a fluorescent cage through host-guest complexation in water

Detection of nucleoside derivatives has paramount importance because they are the essential biomolecular units for all life. Herein, we report a host-guest approach by using a fluorescent tetraphenylethenebased octacationic cage as host and 8-hydroxypyrene-1,3,6-trisulfonic acid trisodium salt(HPTS) as guest and fluorescent indicator to form non-fluorescent 1:1:1 host-(endo-exo)guest complex in water. This new host-(endo-exo)guest complex can be successfully used for detecting nucleosides(e.g., ...     

Electrochemical and photochemical control of host-guest complexation at surfaces

The application of electrochemistry or photochemistry to modulate supramolecular interactions between host-guest systems in solution is a burgeoning field. In particular, the speed and reversibility associated with electrochemically or photochemically actuated supramolecular interactions has allowed the creation and modulation of novel solution-based devices. In recent years, great advances have been made in transferring these systems from the solution to the solid state, to facilitate the development of molecular-electronics components that can operate in unison under the influence of an externally applied stimulus. These studies pave the way for the creation of responsive surfaces with advanced materials and nanotechnology applications.     

Surface modification of polymeric vesicles via host-guest inclusion complexation

We have prepared a novel kind of building block (CD-PI-CD) of polyether imide (PI) with beta-cyclodextrin (beta-CD) at the both ends that self-assembles into vesicles in water. The vesicles are "reactive" in supramolecular chemistry because the host groups of beta-CD equally distribute on the inside and outside surfaces of the vesicles. Isothermal titration calorimetry (ITC) and static light scattering (SLS) studies demonstrate that both the inner and outer surfaces of the vesicles can be further modified noncovalently with adamantane-ended polyethlene glycol (Ada-PEG) via a host-guest inclusion interaction between beta-CD and adamantane.     

An AM1 semiempirical study of host-guest complexation in hemicarcerand complexes

Semiempirical AM1 calculations have been carried out on host-guest complexes of model hemicarcerands 1a and 2a. The justification for the choice of the AM1 Hamiltonian was based on a comparison between reported X-ray data for the smaller tetrabromocavitand 4a and computational results obtained using several different Hamiltonians. The complexation behavior of hemicarcerands 1a and 2a have been compared with experimental results reported by Cram et al. for the related hemicarcerands 1b and 2b. Based on this comparison, a criterion for predicting guest encapsulation was developed, E(complexation), which relies on the calculation of AM1 heats of formation for host, guest, and hemicarceplex. If E(complexation) is lower than 10 kcal/mol, then a guest will be encapsulated, while if it is greater than 30 kcal/mol, a guest will not be encapsulated. The use of constrained-path AM1 optimizations to determine the energy barriers to guest entry and exit from the host was found to be a useful tool for examining suitable host-guest combinations when the E(complexation) criteria does not hold. We have computed the barriers to exit of N, N-dimethylformamide (dmf) and furan from the hemicarcerand 1a, the former has been compared with the experiment and shows excellent agreement. Based on the success of the above computational methods in predicting which host-guest combinations will form stable hemicarceplexes we have synthesized a new target hemicarceplex 1b.furan.     

Chiral separations by host-guest complexation with cyclodextrin and crown ether in capillary zone electrophoresis

Summary Capillary zone electrophoresis using cyclodextrins and a chiral crown ether as buffer constituents was studied for the enantiomeric separation of drugs and amino acids. Based on results obtained from separation of racemic -amino acids both chiral selectors are compared with respect to resolution, efficiency and retention time. For (±)-Quinagolide effects of buffer composition and temperature are examined using -cyclodextrin as chiral agent. Optimum conditions were pH 2.5 at 30 mmol L^–1 -cyclodextrin. A linear dependence of retention on -cyclodextrin concentration allowed calculation of formation constants of the host-guest complexes. Buffer concentration and temperature also influence resolution. The application of a chiral crown ether to the separation of optical isomers in capillary zone electrophoresis is described for the first time. Chiral recognition of solutes depends on the formation of protonated alkyl amines and separation is attributed to the formation of diastereomeric host-guest complexes with different interactions for each enantiomer. The effects of crown ether concentration on resolution are presented.     

Determination of binding selectivities in host-guest complexation by electrospray/quadrupole ion trap mass spectrometry

The quantifiable relationship between the equilibrium solution composition and electrospray (ESI) mass spectral peak intensities of simple host-guest complexes was investigated. Specifically, host-guest complexes of simple crown ethers or glymes with alkali metals and ammonium ions were studied. Comparisons were made between the theoretical concentrations of host-guest complexes derived in solution from known stability constants and the peak intensities for the complexes observed by ESI mass spectrometry (ESI-MS). Two types of complexation experiments were undertaken. First, complexation of a single guest ion, such as an alkali metal, and two crown ethers was studied to evaluate the determination of binding selectivities. Second, complexation of two different guest ions by a single polyether host was also examined. In general, solvation was found to play an integral part in the ability to quantify binding selectivities by ESI-MS. The more similar the solvation energies of the two complexes in the mixture, the more quantifiable their binding selectivities by ESI-MS. In some cases, excellent correlation was obtained between the theoretically predicted selectivity ratios and the ESI mass spectral ratios, in particular when the ESI ratios were adjusted based on evaluation of ESI response factors for the various host-guest complexes.     

The use of FTICR-MS to detect chemical tags from a combinatorial library

The use of tagging in combinatorial chemistry permits tracking of the solid phase as it is taken through iterative split and mix cycles. Several analytical approaches to the identification of tags (and hence the chemical history of the support) have been described. We describe herein a novel chemical tagging strategy for combinatorial solid phase chemistry. The identities of the tags attached to a single bead are discovered by the high resolution, accurate mass technique of Fourier transform ion cyclotron resonance mass spectrometry (FTICR-MS).     

Configurational assignment of alpha-chiral carboxylic acids by complexation to dimeric Zn-porphyrin: host-guest structure,chiral recognition and circular dichroism

A circular dichroic (CD) excition chirality method based on host-guest chiral recognition has been developed to determine the absolute configuration of carboxylic acids with an alpha-stereogenic center; an amide C = O-->Zn coordination, identified by infrared spectroscopy and computations, is involved in this complexation.     

Zinc porphyrin tweezer in host-guest complexation: determination of absolute configurations of primary monoamines by circular dichroism

A nonempirical exciton chirality circular dichroic (CD) method for determining the absolute configurations of primary monoamines with amino group directly linked to the stereogenic center is described. Conventional exciton chirality CD method cannot be applied to these compounds since they lack the two sites for attaching the interacting chromophores. This was solved by covalently linking the monoamine to a trifunctional bidentate carrier moiety 1. Treatment of the carrier/monoamine conjugate with the porphyrin tweezer 4 consisting of two pentanediol-linked zinc porphyrins gives rise to 1:1 host-guest macrocyclic complexes that exhibit exciton-coupled CD spectra. The sign of the CD couplet can then be correlated with the absolute configuration of the monoamine as follows: a clockwise arrangement of the L, M, and S (large, medium, small) groups in the Newman projection of the monoamine with the amino group in the rear gives rise to a positive CD couplet, and vice versa; the assignments of L, M, S groups are based on conformational energies (A values). This method is applicable to cyclic and acyclic aliphatic amines, aromatic amines, amino esters, amides, and cyclic amino alcohols, and can be performed at the several microgram level.     

A systems approach to controlling supramolecular architecture and emergent solution properties via host-guest complexation in water

The assembly behavior of aryl/alkyl imidazolium ionic liquid salts in aqueous solution has been investigated. These salts undergo self-assembly into one-dimensional stacks via hydrophobic and π-π interactions upon increasing concentration, which led to a substantial increase in the solution viscosity in water. Addition of the macrocyclic host molecules cucurbit[n]urils (CB[n]) were found to effectively alter the supramolecular assemblies, as evidenced from the dramatic increase (by CB[7]) and decrease (by CB[8]) in solution viscosity and aggregation size in water, on account of the different binding stoichiometries, 1:1 complexation with CB[7] and 2:1 complexation with CB[8]. Furthermore, the aggregate architectures were controllably modified by competitive guests for the CB[n] hosts. This complex supramolecular systems approach has tremendous implications in the fields of molecular sensor design, nonlinear viscosity modification, and controlled release of target molecules from a defined supramolecular scaffold in water.     

Spectrofluorimetric study of host-guest complexation of ibuprofen with beta-cyclodextrin and its analytical application

The characteristics of host-guest complexation between beta-cyclodextrin (beta-CD) and two forms of ibuprofen (protonated and deprotonated) were investigated by fluorescence spectrometry. 1:1 stoichiometries for both complexes were established and their association constants at different temperatures were calculated by applying a non-linear regression method to the change in the fluorescence of ibuprofen that brought about by the presence of beta-CD. The thermodynamic parameters (deltaH, deltaS and deltaG) associated with the inclusion process were also determined. Based on the obtained results, a sensitive spectrofluorimetric method for the determination of ibuprofen was developed with a linear range of 0.1-2 microg ml(-1) and a detection limit of 0.03 microg ml(-1). The method was applied satisfactorily to the determination of ibuprofen in pharmaceutical preparations.     

1H NMR spectral evidence for a specific host-guest complexation induced charge localization in squaraine dyes

[reaction: see text]. Experimental support is provided for the charge localization in squaraines, a class of fundamentally and technologically important organic dyes, by (1)H NMR analysis through a host-guest complexation approach. Specific binding of Ca(2+) ions to the squaraine 2 with a podand sidearm resulted in a charge-localized structure 2a with dramatic shifts and resolution of the proton signals when compared to those of 2.     

Application of a rapid screening method to detect irradiated meat in Brazil

Based on the enormous potential for food irradiation in Brazil, and to ensure free consumer choice, there is a need to find a convenient and rapid method for detection of irradiated food. Since treatment with ionising radiation causes DNA fragmentation, the analysis of DNA damage might be promising. In this paper, the DNA Comet Assay was used to identify exotic meat (boar, jacaré and capybara), irradiated with ⁶⁰Co gamma rays. The applied radiation doses were 0, 1.5, 3.0 and 4.5 kGy. Analysis of the DNA migration enabled a rapid identification of the radiation treatment.