Axial Coordinated Manganese(III) Porphyrin/Tetraazaporphyrin - 4-(10-phenylanthracen-9-yl)Pyridine Dyads: Self-Assembly, Structure and Spectral Properties in Ground and Excited States.

Self-assembly of new donor-acceptor systems based on (5,10,15,20-tetraphenylporphinato)manganese(III)/(5,10,15,20-tetra-4-tert-butylphenylporphinato)manganese(III)/(octakis(4-tert-butylphenyl)tetraazaporphinato)manganese(III) acetate ((AcO)MnTPP/(AcO)MnTBPP/(AcO)MnTAP) and 4-(10-phenylanthracen-9-yl)pyridine (PyAn) was studied using fluorescence spectroscopy and mass spectrometry. It was found that the coordination complexes of 1 : 1 composition (dyads) are formed in toluene. The spectral properties, the chemical structures and redox behavior of the dyads were described using H NMR, IR, ESR spectroscopy and cyclic voltammetry, respectively.

Alkylimidazolium Protic Ionic Liquids: Structural Features and Physicochemical Properties.

We focus on a series of protic ionic liquids (PILs) with imidazolium and alkylimidazolium (1R3HIm, R=methyl, ethyl, propyl, and butyl) cations. Using the literature data and our experimental results on the thermal and transport properties, we analyze the effects of the anion nature and the alkyl radical length in the cation structure on the above properties. DFT calculations in gas and solvent phase provide further microscopic insights into the structure and cation-anion binding in these PILs.

Dendritic Iron(III) Carbazole Complexes: Structural, Optical, and Magnetic Characteristics.

This paper focuses on the synthesis, structural characterization, and study of the optical, magnetic, and thermal properties of novel architectures combining metal ions as magnetoactive centers and photoactive blocks formed by carbazole units. For this purpose, a series of azomethine complexes of the composition [Fe(L)]X (L = 3,6-bis[(3',6'-di--butyl-9-carbazol)-9-carbazol]benzoyloxy-4-salicylidene-N'-ethyl-N-ethylenediamine, X = NO, Cl, PF) were synthesized by the reaction of metal salts with Schiff bases in a mixture of solvents. The UV-Vis absorption properties were studied in dichloromethane and rationalized via time-dependent density functional theory (DFT) calculations.

Polymorphic forms of antiandrogenic drug nilutamide: structural and thermodynamic aspects.

Attempts to obtain new cocrystals of nonsteroidal antiandrogenic drug nilutamide produced alternative polymorphic forms of the compound (Form II and Form III) and their crystal structures were elucidated by single-crystal X-ray diffraction. Apart from the cocrystallization technique, lyophilization was found to be an effective strategy for achieving polymorph control of nilutamide, which was difficult to obtain by other methods. The physicochemical properties and relative stability of the commercial Form I and newly obtained Form II were comprehensively investigated by a variety of analytical methods (thermal analysis, solution calorimetry, solubility, and sublimation), whereas for Form III, only a handful of experimental parameters were obtained due to the elusive nature of the polymorph.

Triethylamine-Based Salts: Protic Ionic Liquids or Molecular Complexes?

Amines can interact with protic acids with different degrees of proton transfer, which can lead to the formation of both hydrogen-bonded complexes and protic ionic liquids (PILs) in which the hydrogen bond between the cation and anion contributes to the formation of ion pairs. This work is devoted to studying the degree of proton transfer from different acids (hydrochloric, nitric, phosphoric, acetic, propionic, benzoic, and salicylic) to triethylamine (TEA). The results of quantum-chemical calculations based on the density functional theory (DFT) and thermal (phase transition and destruction temperatures) and physicochemical (conductivity, viscosity) characteristics of the compounds show that TEA interaction with acetic and propionic acids leads to the formation of hydrogen-bonded complexes.