Pharmacologically active nitrogen-containing silicon glycerolate

The new modified nitrogen-containing silicon glycerolate was synthesized. The experimental results showed, that obtained product is nontoxic, displayed high wound healing activity and could be recommended for further preclinical and clinical testings.Целью работы являлась модификация диметилглицеролатов кремния путем введения в их структуру фармакофорной азотсодержащей группировки, в частности, диметнлэтаноламинной. В результате этой модификации будет достигнут оптимальный гидрофильно-липофильный баланс, повышена пенетрирующая активность в ткани и расширен спектр фармакологической активности диметилглицеролатов кремния

Unexpected Supramolecular Induced Redox Switching in Sandwich Gd Bisphthalocyaninate

The redox state of the phthalocyanine in sandwich lanthanide complexes is crucial for their applications. In this work, we demonstrate that the cation-induced supramolecular assembly of crown-substituted phthalocyanine lanthanide complexes Ln[(15C5)4Pc]2 can be used to control the redox state of the ligand simultaneously with the coordination sphere of the central metal. We achieve unprecedented redox switching of phthalocyanine ligands in a double-decker Gd(III) complex, resulting from the intramolecular inclusion of potassium cations between the decks with simultaneous twisting of the ligands (the skew angle between them decreases from 44.61° to 0.21°). Such a structural change leads to an increase in the deck to deck distance and drastically facilitates ligand reduction. It was demonstated that this process is anion dependent. Thus, only potassium salts of weak acids (KOPiv, KOAc) induce intramolecular inclusion of cations with redox switching in contrast to salts of strong acids (KBr, KOPic, KSCN and KPF6), where such a redox process does not occur. This breakthrough opens new avenues for controlling the electrochromic properties of phthalocyanines, along with other properties, such as electrical conductivity, optics, etc

Cation-Induced Dimerization of Crown-Substituted Phthalocyanines by Complexation with Rubidium Nicotinate As Revealed by X‑ray Structural Data

The supramolecular dimeric complex [(μ-oxo)­bis­(tetra-15-crown-5-phthalocyaninato)­(nicotinato)­aluminum­(III)]­tetra­(rubidium) bis­(nicotinate) was prepared by addition of an excess of a methanol solution of rubidium nicotinate to a chloroform solution of the aluminum crown-phthalocyaninate, [(HO)­Al­(15C5)₄Pc]. A single-crystal X-ray diffraction study of {[Rb₄(NicAl­(15C5)₄Pc)₂(μ-O)]²⁺(Nic^–)₂}·2.36HNic·11H₂O demonstrated that two molecules of the aluminum crown-phthalocyaninate nicotinate are connected through an Al–O–Al bridge supported by sandwiching of crown ether moieties by Rb⁺ cations