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Il'ya A. Gural'skiy

Bio: Il'ya A. Gural'skiy is an academic researcher from Taras Shevchenko National University of Kyiv. The author has contributed to research in topics: Spin crossover & Spin transition. The author has an hindex of 21, co-authored 61 publications receiving 1624 citations. Previous affiliations of Il'ya A. Gural'skiy include Centre national de la recherche scientifique & University of Toulouse.


Papers
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TL;DR: The development of bilayer actuator devices using molecular spin crossover materials is reported on, demonstrating the versatility of this approach by fabricating actuators from four differentspin crossover materials and by using both thermal variation and light to induce motion in a controlled direction.
Abstract: Molecular actuators hold potential in a number of sensing applications but require careful design to ensure specific functionality. Shepherd et al. report a new platform for molecular actuators based on spin crossover materials, whose response can be controlled by various stimuli or chemical modification.

211 citations

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TL;DR: Laboratory and field tests with paint formulations containing 2 wt% of CeO2-x nanorods show a reduction in biofouling comparable to Cu2 O, the most typical biocidal pigment.
Abstract: CeO2-x nanorods are functional mimics of natural haloperoxidases. They catalyze the oxidative bromination of phenol red to bromophenol blue and of natural signaling molecules involved in bacterial quorum sensing. Laboratory and field tests with paint formulations containing 2 wt% of CeO2-x nanorods show a reduction in biofouling comparable to Cu2 O, the most typical biocidal pigment.

179 citations

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TL;DR: The spin state dependence of the electrical conductivity of the spin crossover compound [Fe(Htrz)(2)(trz)](BF(4)) (H Trz = 1H-1,2,4-triazole) is studied by means of dc electrical measurements.

137 citations

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TL;DR: The nanoscale manipulation and charge transport properties of the [Fe(Htrz)2(trz)](BF4) spin-crossover compound is demonstrated and are attractive building blocks for nanoelectronic switching and memory devices.
Abstract: The nanoscale manipulation and charge transport properties of the [Fe(Htrz)2(trz)](BF4) spin-crossover compound is demonstrated. Such 1D spin-crossover nanostructures are attractive building blocks for nanoelectronic switching and memory devices.

130 citations

Journal ArticleDOI
TL;DR: Results of high level ab initio calculations were in good agreement with experimental results, and were suggestive of the progressive enhancement of the pi-acidity by increasing the number of Ag(i) ions N-coordinated to tetrazine.
Abstract: A series of framework coordination polymers reveals the use of 1,2,4,5-tetrazines as efficient bridging ligands towards silver(I) and copper(I) ions. All four nitrogen atoms were functional as lone pair donors leading to an unprecedented μ4-coordination of the ligands (1,2,4,5-tetrazine, ttz; 3,6-dimethyl-1,2,4,5-tetrazine, Me2ttz) in [Ag(ttz)(X)] (X = NO3, 1; ClO4, 2), [Ag2(Me2ttz)(NO3)2] (3), [Ag2(Me2ttz)(H2O)2(ClO4)2] (4), [Ag3(Me2ttz)(H2O)2(CF3SO3)3] (5) and [Cu4Cl4(Me2ttz)] (6). In 1 and 2, μ4-tetrazines and silver ions (AgN4, Ag–N 2.42–2.53 A) compose a 3D framework of {42;84} topology. Structures 3 and 4 were based on disilver–tetrazine ribbons, while in 5μ4-tetrazines interconnect silver–triflate chains. In 6, μ4-ligands connect inorganic layers sustained by copper–chloride squares, hexa- and octagons (1.974(2) and 1.981(2) A). Multiple N-coordination to metal ions enhances the ability of the electron deficient tetrazine system for anion⋯π binding. Compounds 1 and 2 exhibit very short interactions of this type with corresponding O⋯C(N) separations down to a record value of 2.78 A and O⋯π 2.61 A. For 6, π-acidity of tetrazine was reflected by contacts Cl⋯π of 3.30 A. Results of high level ab initio calculations (RI-MP2/aug-cc-pVTZ) were in good agreement with experimental results, and were suggestive of the progressive enhancement of the π-acidity by increasing the number of Ag(I) ions N-coordinated to tetrazine.

122 citations


Cited by
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Journal ArticleDOI
10 Mar 1970

8,159 citations

Journal ArticleDOI
TL;DR: This review systematically introduces the classification, catalytic mechanism, activity regulation as well as recent research progress of nanozymes in the field of biosensing, environmental protection, and disease treatments, etc. in the past years.
Abstract: Because of the high catalytic activities and substrate specificity, natural enzymes have been widely used in industrial, medical, and biological fields, etc. Although promising, they often suffer from intrinsic shortcomings such as high cost, low operational stability, and difficulties of recycling. To overcome these shortcomings, researchers have been devoted to the exploration of artificial enzyme mimics for a long time. Since the discovery of ferromagnetic nanoparticles with intrinsic horseradish peroxidase-like activity in 2007, a large amount of studies on nanozymes have been constantly emerging in the next decade. Nanozymes are one kind of nanomaterials with enzymatic catalytic properties. Compared with natural enzymes, nanozymes have the advantages such as low cost, high stability and durability, which have been widely used in industrial, medical, and biological fields. A thorough understanding of the possible catalytic mechanisms will contribute to the development of novel and high-efficient nanozymes, and the rational regulations of the activities of nanozymes are of great significance. In this review, we systematically introduce the classification, catalytic mechanism, activity regulation as well as recent research progress of nanozymes in the field of biosensing, environmental protection, and disease treatments, etc. in the past years. We also propose the current challenges of nanozymes as well as their future research focus. We anticipate this review may be of significance for the field to understand the properties of nanozymes and the development of novel nanomaterials with enzyme mimicking activities.

1,549 citations

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TL;DR: This review describes a multidimensional treatment of molecular recognition phenomena involving aromatic rings in chemical and biological systems that facilitates the development of new advanced materials and supramolecular systems, and should inspire further utilization of interactions with aromatic rings to control the stereochemical outcome of synthetic transformations.
Abstract: This review describes a multidimensional treatment of molecular recognition phenomena involving aromatic rings in chemical and biological systems. It summarizes new results reported since the appearance of an earlier review in 2003 in host-guest chemistry, biological affinity assays and biostructural analysis, data base mining in the Cambridge Structural Database (CSD) and the Protein Data Bank (PDB), and advanced computational studies. Topics addressed are arene-arene, perfluoroarene-arene, S⋅⋅⋅aromatic, cation-π, and anion-π interactions, as well as hydrogen bonding to π systems. The generated knowledge benefits, in particular, structure-based hit-to-lead development and lead optimization both in the pharmaceutical and in the crop protection industry. It equally facilitates the development of new advanced materials and supramolecular systems, and should inspire further utilization of interactions with aromatic rings to control the stereochemical outcome of synthetic transformations.

1,221 citations

Journal ArticleDOI
TL;DR: The properties of Ladderlike Chains, and the role of Metal Cluster As Building Blocks for 1D CP 718, are described.
Abstract: 2.4.2. Interpenetrated Ladders 711 2.4.3. Unusual Motifs of Ladders 713 2.4.4. Properties of Ladderlike Chains 713 2.5. Rotaxane Polymers 714 2.5.1. 1D Polyrotaxanes 714 2.5.2. 2D Polyrotaxanes 715 2.5.3. 3D Polyrotaxanes 716 2.5.4. Hydrogen-Bonded Polyrotaxanes 716 2.6. Ribbon/Tape Polymers 717 2.7. Metal Cluster As Building Blocks for 1D CP 718 2.7.1. Metal Carboxylate Clusters 718 2.7.2. Metal Halide Clusters 719 2.7.3. Metal Chalcogenide Clusters 720 2.7.4. Polyoxometalate Clusters 721 2.7.5. Single Molecular Magnets as Building Blocks 722

967 citations

Journal ArticleDOI
TL;DR: This tutorial review provides an overview of the theoretical and experimental investigations that resulted in the recognition of anion-pi interactions, i.e., non-covalent forces between electron deficient aromatic systems and anions.
Abstract: This tutorial review provides an overview of the theoretical and experimental investigations that resulted in the recognition of anion-π interactions, i.e., non-covalent forces between electron deficient aromatic systems and anions. Several pioneering theoretical studies revealed that these interactions are energetically favorable (∼20–50 kJ mol–1). Anion-π interactions are gaining significant recognition, and their pivotal role in many key chemical and biological processes is being increasingly appreciated. The design of highly selective anion receptors and channels represent important advances in this nascent field of supramolecular chemistry.

926 citations