Albina Y. Ziganshina

Self-assembly of an aminoalkylated resorcinarene in aqueous media: host–guest properties

A new water-soluble resorcinarene, with a negatively-charged lower rim and a positively-charged upper rim self-assembles into supramolecular oligomers to bind 1,5-diaminonaphthalene in water.

Synthesis and structural peculiarities of homeomorphic phosphorus bridgehead macrobicyclic compounds and novel dioxaphospha[3.1.1.]p, m, p-cyclophanes

The double-capping reaction of p,m,p-trinuclear diphenol 4 with PCl3 affords the three homeomorphic isomers 5-7 of a phosphite macrobicyclic compound in low yields. X-ray structures of out, out-isomer 5 and in, in-isomer 6 show very flat macrobicyclic structures with P-P distances of 4.9 A and 4.5/5.3 A (two conformers), respectively. The main product of the reaction, however, appears to be diphosphite 8, which contains two dioxaphospha[3.1.1.]p,m,p-cyclophane subunits. The structural peculiarities of 8 were studied after subsequent oxidation to the corresponding phosphate 12. At room temperature the free rotation either of the para-phenylene rings and the meta-phenylene ring in the macrocyclic moieties are hindered as could be demonstrated by means of NOESY measurements. The latter occupies an angled position in respect to the macrocyclic plane. This leads to the existence of conformational isomers due to different relative positions of the meta-phenylene ring to the P-OR substituent (cis,trans). We could isolate the cis,cis-isomer of 12 and establish its structure by X-ray diffraction.

The Synergistic Extraction of Lanthanide Ions by a Mixture of Calix[4]resorcinarene or its Dimethylamino-, Piperidyl- or Trimethylammoniummethylated Derivatives and 1,10-Phenanthroline in n-Heptanol

The alkylaminomethylatedcalix[4]resorcinarene derivatives, modified bydimethylamino-, piperidyl- and trimethylammoniummoieties, have been synthesised to investigate theirextractability towards lanthanide ions and to comparewith the extractability of calix[4]resorcinarene. Both calix[4]resorcinarene and its derivatives have beenshown to synergistically affect lanthanide ionextraction from neutral aqueous solutions by1,10-phenanthroline through outer-sphere interactionof lanthanide bis-phenanthrolinate cations withdeprotonated forms of calix[4]resorcinarene. Thederivatives with dimethylamino- andpiperidylmethylated moieties are shown to be moreeffective extractants in comparison with theunsubstituted one.

Controlling the Size and Morphology of Supramolecular Assemblies of Viologen–Resorcin[4]arene Cavitands

A novel class of self-assembling nanoparticles is formed with viologen-resorcin[4]arene cavitands; the association model is strongly controlled by their hydrophobicity. Interestingly, the cavitand assemblies are designed through click chemistry to form self-assembled noncovalently connected aggregates through counterion displacement. The iodide and benzoate ions are utilized as strongly polarizable counterions to induce cavitand self-assembly. The counterion-mediated decrease in hydrophilicity of the viologen-resorcin[4]arenes is the underlying trigger to induce particle formation. These particles can be used as nanocontainers and find their applications in delivery systems.

Controlling the release of hydrophobic compounds by a supramolecular amphiphilic assembly

Here, we report a novel approach of using a supramolecular system based on calix[4]resorcinarene and surfactant to facilitate the release of hydrophobic compounds. This finding is an important step towards the development of controlled-release formulations for water-insoluble drugs.

pH-controlled photoinduced electron transfer in the [(Mo6Cl8)L6]-calix[4]resorcine-dimethylviologen system.

A pH-controlled photoinduced electron transfer in the supramolecular system [(Mo(6)Cl(8))L(6)]-calix[4]resorcine-dimethylviologen is reported.

Aminoalkylated Calix[4]resorcinarenes as pH Sensitive “hosts” for Charged Metallocomplexes

On the basis of RCA, pH-potentiometry and EPR-spectroscopy data aminoalkylated derivatives were proved to bind metal ion complexes both in alkaline and in acidic media. Outer-sphere coordination is the only interaction mode in these host-guest complexes.

Highly active Pd–Ni nanocatalysts supported on multicharged polymer matrix

In this article, we report the synthesis of mono- and bimetallic Pd–Ni nanocomposites supported on a multicharged polymeric matrix for catalytic applications. The morphology and catalytic properties of the composites depend on the Pd–Ni ratio. In the Suzuki–Miyaura coupling reaction, the composite with an equal amount of palladium and nickel is the most active and the reaction occurs within six hours in water at room temperature.

Application of ferrocene-resorcinarene in silver nanoparticle synthesis

An amphiphilic resorcinarene with ferrocene groups at the lower rim has been applied as both reductant and stabilizer in the synthesis of colloidal silver nanoparticles. The structure of the nanocomposite obtained was investigated by transmission electron microscopy, atomic force microscopy, X-ray powder diffraction, dynamic light scattering, and UV and IR spectroscopy. In the nanocomposite, the silver nanoparticles are stabilized by the multi-layers formed by ferrocene-resorcinarene. The diameter of the nanoparticles is 20–30 nm while the size of the nanocomposite is about 45 nm. The nanoparticles demonstrate good catalytic activity for p-nitrophenol reduction. 40 nanomoles of the silver nanoparticles is sufficient to complete the reduction of p-nitrophenol over ten minutes.

Closed polymer containers based on phenylboronic esters of resorcinarenes

Novel polymer nanospheres (p(SRA-B)) were prepared by cross-linking a sulfonated resorcinarene (SRA) with phenylboronic acid. p(SRA-B) shows good stability in water and can be used as a nanocontainer for the pH- and glucose-controlled substrate release. Fluorescent dyes (fluorescein, pyrene and 1,3,6,8-pyrenetetrasulfonic acid tetrasodium salt) were successfully loaded into p(SRA-B). The release of dye is achieved by lowering the pH value to 3 or by adding glucose.