Uranyl-salophen based ditopic receptors for the recognition of quaternary ammonium halides

Uranyl-salophen complexes endowed with aromatic side arms behave as very efficient ditopic receptors towards tetralkylammonium halides as a result of a combination of Lewis acid-base and cation-pi interactions.     

Ammonium ion mediated resorcarene capsules: ESI-FTICRMS study on gas-phase structure and ammonium ion affinity of tetraethyl resorcarene and its per-methylated derivative

The ammonium ion binding affinities of tetraethyl resorcarene (1) and its per-methylated derivative (2) were studied by electrospray ionization Fourier transform ion cyclotron resonance (ESI-FTICR) mass spectrometry. Ten different ammonium ions were tested as guests for the resorcarenes. A strong tendency for complex formation was observed with all ammonium ions of size and charge distribution suitable for noncovalent interactions with the cavities of the resorcarene hosts 1 and 2. Although differences in ammonium ion affinities were observed between 1 and 2 due to the dissimilar conformations, the overall tendency was that increase in the degree of substitution and the length of carbon chain of the ammonium cation facilitated the complex formation until the sterical hindrance impeded the complexation. Dimeric as well as monomeric ammonium ion complexes were formed with resorcarene 1, but resorcarene 2 was unable to form the dimeric capsules because of the lack of H-bond donor possibilities. The nature of binding of the guest was further investigated with ion-molecule reactions and by determination of the single crystal X-ray structure of host 1 complexed with tetramethyl ammonium bromide.     

The Structural Diversity of Benzofuran Resorcinarene Leads to Enhanced Fluorescence

An unexpected and previously unknown resorcinarene mono‐crown with a fused benzofuran moiety in its macrocyclic core was obtained as a byproduct from a bridging reaction of tetramethoxy resorcinarene with tetraethylene glycol ditosylate. The formation of the fused benzofuran moiety in the resorcinarene macrocycle resulted in a unique rigid and puckered boat conformation, as shown by XRD studies in the solid state. Modification of the macrocycle was also observed to affect the photophysical properties in solution by enhancing the fluorescence brightness compared with a conventional resorcinarene macrocycle. The fluorescent properties enabled unique detection of structural features, that is, the rigid boat conformation with the conjugated benzofuran system and the more flexible crown bridge part, in solution.     

Fluorescent Probe ABM for Screening Gastrointestinal Patient’s Immune State

The fluorescent probe-aminoderivative of benzanthrone, ABM (developed at Riga Technical University, Riga, Latvia) was used to characterize the membranes of lymphocytes of cancer patients: 46 patients with gastrointestinal diseases, 13 patients having different primary localizations with massive metastases and intoxication. Patients were divided into three groups: (1) with decreased fluorescence intensity, (2) normal fluorescence intensity, (3) increased fluorescence intensity. The lymphocytes distribution among subsets differed between groups, in correspondence to the level of florescence intensity. Surgical treatment affected the main immunological parameters and elevated the functional activity of lymphocytes. In the advanced tumors group, fluorescence intensity correlates with the survival rate. Results suggest that determination of lymphocytes functional activity by ABM can aid evaluation of the immune status in cancer patients.     

Complexation of small molecules by open-ended resorcarene hosts

[structure: see text] Sterically hindered tetraaminomethylated resorcarenes form inclusion complexes in CDCl(3) with acetonitrile and acetaldehyde, which are kinetically stable on the NMR time scale at 233 K.     

Conformational study of methyl esters of some aliphatic erythro- and threo-dichlorocarboxylic acids

The average conformations of methyl esters of some aliphatic erythro- and threo-dichlorocarboxylic acids in dilute carbon tetrachloride solutions have been determined from the vicinal proton–proton coupling constants and ¹H NMR shifts. The ¹³C shift differences between the erythro and threo forms are compared and discussed with regard to the differences in the average conformations.     

A semiempirical MO study of the electronic structure and excited states of the Tris(2,2′-bipyridyl)Iron(II) and Tris(glyoxal-Bis-N-methylimine)iron(II)Ions

A semi-empirical SCF-MO method, the PEEL method, has been applied in an investigation of the electronic structure and excited states of two iron compounds, [Fe(II)-(GMI)₃]⁺⁺ and [Fe(II)-(bipy)₃]⁺⁺.The electronic absorption spectra have been recorded. The calculations show that it is necessary to account for the trigonal distortion and the covalency in order to explain these spectra quantitatively. Mössbauer measurements have also been performed. The calculated electronic population of the iron is in accord with Mössbauer isomer shift data, indicating that a realistic electron distribution has been obtained by the PEEL method.

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Zusammenfassung Eine semiempirische SCF-MO-Methode, die PEEL-Methode, wurde zur Untersuchung der Elektronenstruktur sowie von angeregten Zuständen der beiden Eisenverbindungen [Fe(II)-(GMI)₃]⁺⁺ und [Fe(II)-(bipy)₃]⁺⁺ angewendet.Die elektronischen Absorptionsspektren wurden aufgenommen. Die Berechnungen zeigen, daß die trigonale Verzerrung und die Kovalenz berücksichtigt werden müssen, um die Spektren quantitativ zu erklären. Mössbauer-Messungen wurden ebenfalls durchgeführt. Die berechnete Elektronenverteilung am Eisenatom ist in Übereinstimmung mit den Daten der Isomerenverschiebung der Mössbauer-Messungen, wodurch gezeigt wird, daß mit der PEEL-Methode eine realistische Elektronen-Verteilung erhalten wurde.

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Résumé Une méthode SCF-MO semi-empirique, la méthode PEEL, a été appliquée à une étude de la structure électronique et des états excités de deux composés ferreux: [Fe(II)-(bipy)₃]⁺⁺ et [Fe(II)-(GMI)₃]⁺⁺. Les spectres d'absorption électronique ont été enregistrés. Les calculs montrent qu'il est nécessaire de rendre compte de la distorsion trigonale et de la covalence pour expliquer ces spectres quantitativement.Des mesures de l'effet Mössbauer ont aussi été effectuées. La population électronique calculée du fer est en bon accord avec les données sur le déplacement isomérique de Mössbauer, ce qui indique que la méthode PEEL fournit une distribution électronique réaliste.

     

Magnetic Properties of Monocrystal 57Fe/V Multilayers Investigated by CEMS,Nuclear Resonance Reflectivity in the Time Domain and Polarized Neutron Scattering

Hyperfine Interactions - We have performed a depth selective investigation of monocrystalline samples with composition [57Fe(10 ML)/V(5 ML)]20 and [57Fe(7 ML)/V(10 ML)]29 by means of synchrotron...     

Non-centrosymmetric tetrameric assemblies of tetramethylammonium halides with uranyl salophen complexes in the solid state

Ditopic salophen-UO(2) receptors 1-4 and 7 co-crystallize with tetramethylammonium (TMA) chloride and fluoride salts producing good quality crystals amenable for X-ray diffraction characterization. The arrangement of the receptor and salt units in the crystal lattice is such that tetrameric ball-shaped assemblies are formed, where an inner cluster of four TMA cations are surrounded by an outer shell of four UO(2)-bound anions. These elaborate architectures, which occur in all cases, regardless of a certain degree of structural modification on the receptors, lead to lattices that belong to non-centrosymmetric (NCS) space groups. Interestingly, the tetragonal symmetry of the tetrameric ball-shaped assemblies is either retained (I4?) or lost (R3c and I4?3d) at the lattice level, without compromising the NCS nature of the crystal lattices. The principal X-ray investigation on TMAX (X = Cl/F) co-crystals, that is, 1-(TMA)Cl, 2-(TMA)Cl, 3-(TMA)Cl, 4-(TMA)Cl, 7-(TMA)Cl, and 7-(TMA)F, is accompanied by NMR and electrospray ionization (ESI) mass spectrometry studies to gather additional insight on the modality of formation of the solid state structures observed. The important role of cation-π interactions in the receptor-salt recognition process is renewed and strengthened by comparison with NMR titration data with a novel reference compound, the salophen-UO(2) complex 8. Given the importance of NCS and polar crystalline solids in the development of functional materials, this study shows that this property can be introduced into elaborate host-guest systems, as those which assemble in the architectures described here, thus expanding its field of applicability.