A new application for bis­(cyclometalated) iridium­(III) species containing ancillary acyclic diaminocarbene ligands, viz. for sensing of mercury­(II) ions, is disclosed. A family of bis­(cyclometalated) iridium­(III) species supported by both parent isocyanide and acyclic diaminocarbene ligands was prepared, and their electrochemical and photophysical properties were evaluated, revealing efficient blue-green phosphorescence in solution with quantum yields of up to 55%. We uncovered that the photophysical properties of these complexes are dramatically altered by the presence of metal ions and that the complex [Ir­(ppy)2(CN)­{C­(NH2)­(NHC6H4-4-X)}] with an ADC ligand reacts selectively with Hg2+ ions, enabling its use for sensing of mercury­(II) ions in solution. The limit of detection was as low as 2.63 × 10–7 M, and additional mechanistic studies indicated the formation of an unusual dinuclear iridium­(III) cyclometalated intermediate, bridged by a mercury dicyano fragment as a driving force of mercury sensing.

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Nuclearity control of nickel(ii)–azole systems for the generation of well-defined (azolate)2NiIIspecies.

The present paper reports data on the biological activity of nanocompositions based on a C60-L-threonine (C60-Thr) derivative. These nanocompositions promote the nonspecific resistance of plants to the action of stress factors (ultraviolet radiation, pesticides, and phytopathogens). Additionally, we determined the perspectives of the C60-Thr adduct application in the cultivation of plants due to the decrease of the pesticide load on the environment. The biological study of C60-Thr revealed the plant growth-stimulating ability due to its influence on the photosynthetic apparatus activity and antioxidant properties.

Fabrication of conductive copper structures on the surface of various dielectric materials is quite important in many fields of science.

Nickel(II)‐mediated coupling between the cyanamide Me2NCN and the ketoximes Me(R)C=NOH (R = Me, Ph) gives chelates of the general formula [NiClx(H2O)y{HN=C(NMe2)(ON=C(R)Me)}2]n+ ([1]+: R = Me; x = 1, y = 0; salts with both Cl– and [NiCl4]2– were isolated; [2]2+: R = Me; x = 0, y = 2; salt with Cl– was isolated; [3]+: R = Ph; x = 1, y = 1; salt with Cl– was isolated) and the iminium salts [H2N=C(NMe2)ON=C(R)Me]+ ([4]+: R = Me; salt with [NiCl4]2– was isolated; [5]+: R = Ph; salt with Cl– was isolated). This reaction demonstrates the difference in the reactivity between conventional nitriles and dialkylcyanamides: whereas nitriles RCN (R = Alk, Ar) react with NiII/ketoxime systems to afford (1,3,5‐triazapentadiene)NiII species, formed by postulated nitrile–oxime coupling intermediates, cyanamides under the same conditions give either stable cyanamide–oxime coupling products or the Busch‐type complex [Ni{HN=C(Me)CH2C(Me2)NH2}2]Cl2 ([6]Cl2). The reason for the different stability of the coupling products was interpreted theoretically on the basis of quantum chemical calculations (M06‐L/6‐31G* level of theory). The NMe2 moiety in the chelate ligands leads to an increase in electron‐density delocalization and also stabilizes the systems in terms of electrostatic factors.

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