Assembly of cobalt-p-sulfonatothiacalix[4]arene frameworks with phosphate, phosphite and phenylphosphonate ligands

Three cobalt-calixarene coordination frameworks, namely, {[Co4Cl(H4TC4AS)]4(HPO3)8}4− (CIAC-253), {[Co4Cl(H4TC4AS)]4(PO4)8}12− (CIAC-254) and {[Co4Cl(H4TC4AS)]3(Ph-PO3)6}3− (CIAC-255) were obtained by solvothermal reaction of a cobalt salt, sodium p-sulfonatothiacalix[4]arene (Na4H4TC4AS) and phosphate, phosphite and phosphonate ligands. In CIAC-253 and CIAC-254, the shuttlecock-like Co4Cl-(TC4AS) secondary building units (SBUs) are bridged by HPO3 2− or PO4 3− anions into two quadrilateral frameworks while in CIAC-255, the Co4Cl-(TC4AS) SBUs are linked into a triangular framework by phenylphosphonate anions. The supramolecular interactions between the phenyl groups of phosphonate and TC4AS play a crucial role in the formation of the triangle. Magnetic measurements revealed that all the cobalt(II) centers exhibit antiferromagnetic interactions.

Biological functions of cobalt and its toxicology and detection in anti-doping control

Objectives. Over the last decade, hematopoietic stimulants have grown increasingly popular in elite sports. This is supported by the growing number of high-profile doping scandals linked to their use. A group of these stimulants includes cobalt salts, which cause an increase in the oxygen capacity of the blood as well as a powerful stimulation of metabolic processes, resulting innoticeable competitive advantages. The use of cobalt salts is regulated according to the Prohibited List of the World Anti-Doping Agency (WADA). Currently, only a few works have been dedicated to solving the problem of detecting the abuse of cobalt salts in anti-doping control. Only a few laboratories have included cobalt salt determination in their methodological bases. The purpose of this review is to attract the attention of the scientific community to the toxicity of cobalt compounds, consequences of their intake, and pharmacokinetics, as well as the problems in their detection methods due to their widespread availability in the modern market and the growing number of abuse cases.Results. The main biological functions of cobalt, cellular levels of exposure, toxicity, and symptoms of cobalt salt poisoning are presented in detail in this review article. The data from the literature on the main methods for detecting cobalt as a doping agent have been generalized and systematized. There is a major focus on the amount of cobalt in dietary supplements that could cause an athlete to test positive for cobalt when they are consumed.Conclusions. After analyzing promising cobalt detection approaches and methods, it was determined that high-performance liquid chromatography in combination with inductively coupled plasma mass spectrometry has an undeniable advantage for detecting cobalt as a doping agent. The lack of explicit WADA requirements for detection methods and the lack of its obligation to determine cobalt make it tempting for unscrupulous athletes to use its salts. Therefore, antidoping laboratories must implement the abovementioned method as soon as possible.

Intercalated 2D+2D hydrogen-bonded sheets in co-crystals of cobalt salt with 1H,1′H-[3,3′]bipyridinyl-6,6′-dione

Co-crystals of Co(II) salt and 1H,1′H-[3,3′]bipyridinyl-6,6′-dione 1 with the composition 1·Co(CHOO)2(H2O)4 were obtained by mixing both reactants. The single-crystal structure reveals that the metal salt and organic ratio is 1:1. The supramolecular organization of the two components in the co-crystal was mainly dictated by hydrogen bonds between 1 and Co(II) complex. Infrared and powder X-ray diffraction were used to confirm the homogeneity and the phase purity of the bulk crystalline sample of 1·Co(CHOO)2(H2O)4. TGA/DTA was recorded to evaluate the thermal stability of the co-crystals.

Cobalt Catalyzed C-P Bond Formation by Cross-Coupling of Boronic Acids with P(O)H Compounds in Presence of Zinc

In our current work, we have reported the first cobalt-catalyzed cross-coupling of arylboronic acid with alkyl/aryl phosphites under mild conditions. The reaction was carried out in the presence of zinc powder as an additive and ter-pyridine as a ligand. The use of non-precious cobalt salt makes the protocol advantageous, as it is inexpensive and more abundant than the previously used methods where precious metal salts (Pd and Pt) were used. The reaction has a wide substrate scope and the products were obtained in good yields.

Amplified vibrational circular dichroism as a manifestation of the interaction between a water soluble gold nanocluster and cobalt salt

Co2+ leads to the drastic enhancement of vibrational circular dichroism of a thiolate-protected gold cluster.