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Perovskite solar cells have made significant strides in recent years. However, there are still challenges in terms of photoelectric conversion efficiency and long-term stability associated with perovskite solar cells. The presence of defects in perovskite materials is one of the important influencing factors leading to subpar film quality. Adopting additives to passivate defects within perovskite materials is an effective approach. Therefore, we first discuss the types of defects that occur in perovskite materials and the mechanisms of their effect on performance. Then, several types of additives used in perovskite solar cells are discussed, including ionic compounds, organic molecules, polymers, etc. This review provides guidance for the future development of more sustainable and effective additives to improve the performance of solar cells.

The present research paper details the synthesis of novel ionic compounds based on triterpene acids (betulinic, oleanolic and ursolic), with these acids acting both as anions and connected through a spacer with various nitrogen-containing compounds (pyridine, piperidine, morpholine, pyrrolidine, triethylamine and dimethylethanolamine) and acting as a cation. Based on the latter, a large number of ionic compounds with various counterions (BF4-, SbF6-, PF6-, CH3COO-, C6H5SO3-, m-C6H4(OH)COO- and CH3CH(OH)COO-) have been synthesized. We studied the cytotoxicity of the synthesized compounds on the example of various tumor (Jurkat, K562, U937, HL60, A2780) and conditionally normal (HEK293) cell lines. IC50 was determined, and the influence of the structure and nature of the anion and cation on the antitumor activity was specified. Intracellular signaling, apoptosis induction and effects of the most active ionic compounds on the cell cycle and mitochondria have been discussed by applying modern methods of multiparametric enzyme immunoassay and flow cytometry.

Metal borohydrides are the ionic compounds which have attracted significant recent attention due to their potential applications as materials for hydrogen storage and solid electrolytes. The ammine borohydride compounds Y(BH 4 ) 3 · x NH 3 belong to the emerging class of materials, where the application-relevant properties can be tuned by introducing neutral NH 3 ligands. To study the dynamical properties of Y(BH 4 ) 3 · 3NH 3 and Y(BH 4 ) 3 · 7NH 3 , we have measured the 1 H and 11 B nuclear spin–lattice relaxation rates and nuclear magnetic resonance (NMR) spectra in these compounds over a wide temperature range (6–298 K). Our measurements have revealed that both compounds retain the unusually high reorientational mobility of BH 4 − anions down to low temperatures. In particular, for the fastest BH 4 reorientational process, the corresponding H jump rate is of the order of 10 8  s −1 near 96 K in Y(BH 4 ) 3 · 3NH 3 and near 33 K in Y(BH 4 ) 3 · 7NH 3 . The fast reorientational motion of BH 4 − anions is discussed in terms of the coordination environment of BH 4 groups in Y(BH 4 ) 3 · x NH 3 .

The development of a methodology for the synthesis of new compounds with antitumor activity represents a significant and priority task within the field of medicinal chemistry. As a continuation of our research group’s earlier studies on the antitumor activity of ionic derivatives of natural compounds, we have synthesized a series of previously undescribed pyrazole ionic compounds through a series of transformations of lithocholic acid methyl ester. To investigate the biological activity of the newly synthesized lithocholic acid derivatives, a series of modern flow cytometry techniques were employed to assess their cytotoxic activity, effects on the cell cycle, and induction of apoptosis. This included the analysis of alterations in the mitochondrial potential, accumulation of ROS ions in mitochondria, and loss of cytochrome c. These compounds demonstrate promising antitumor activity through their effects on mitochondrial oxidation and phosphorylation processes. These compounds, which we have designated as “soft dissociators”, exhibit enhanced biopharmacological properties relative to the original lithocholic acid molecule.

According to the WHO, the secondary form of hematopoietic-depressive status increases the risk of death in people with oncological, infectious, and hormonal diseases. The choice of drugs that stimulate the hematopoietic activity of B-lymphopoiesis is limited. The current leucopoiesis drugs have a number of side effects: thymic preparations stimulate the production of PGE2, which causes chronic inflammation and various autoimmune diseases through the differentiation of T helper 1 (Th1) cells, the proliferation of Th17 cells, and the production of IL-22 from Th22 cells through EP2 and EP4 receptors; cytokine preparations can cause uncontrolled immune reactions and impaired contractility of smooth and cardiac muscles; drugs based on nucleic acids can stimulate the division of all cells, including bacterial and cancerous ones. The use of oligonucleotides such as ribozymes and antisense oligodeoxynucleotides (AS-ODNs) shows promise as therapeutic moieties, but faces a number of challenges such as nuclease sensitivity, off-target effects, and efficient delivery. The search for substances that stimulate B-lymphopoiesis among ionic compounds was motivated by the discovery of the unique properties of lidocaine docusate, one of the first ionic liquid forms of the known drugs. The lidocaine docusate (protonated form of lidocaine (2-(diethylamino)-N-(2,6-dimethylphenyl) acetamide + docusate-anion (dioctylsulfosuccinate))) suppresses the division of pheochromocytoma cells and activates immunity in rats. The trimecaine-based ionic compound (TIC) demonstrates high B-lymphopoiesis-stimulating activity. The TIC compound stimulates an increase in the volume of transitional B cells, which play an important role for further differentiation and formation of a sufficient number of mature B1 cells and mature B2 cells, where mature B2 cells make up the bulk of the functional population of B lymphocytes. The TIC compound most strongly stimulated the restoration of the number of marginal zone B cells, follicular B cells, and activated germinal center B cells after the cytotoxic emptying of the follicular centers of the spleen induced cyclophosphamide. It significantly exceeds the activity of the comparison drug methyluracil. The TIC compound does not affect the level of pro-B, pre-B-I, or pre-B-II bone marrow cells, which prevents the risk of the formation of immature functionally defective cells.

Freshwater fish Cirrhinus mrigala were exposed to tris(2-chloroethyl) phosphate (TCEP) with three different concentrations (0.04, 0.2, and 1 mg/L) for a period of 21 days. During the study period, thyroid-stimulating hormone (TSH), triiodothyronine (T3), and thyroxine (T4) levels were significantly ( p < 0.05) inhibited. The superoxide dismutase (SOD), catalase (CAT), glutathione S-transferase (GST), and lipid peroxidation (LPO) levels were increased significantly ( p < 0.05) in gills, liver, and kidney tissues, whereas glutathione (GSH) and glutathione peroxidase (GPx) (except liver tissue) activities were inhibited when compared to the control group. Likewise, exposure to TCEP significantly ( p < 0.05) altered the biochemical (glucose and protein) and electrolyte (sodium, potassium, and chloride) levels of fish. Light microscopic studies exhibited series of histopathological anomalies in the gills, liver, and kidney tissues. The present study reveals that TCEP at tested concentrations causes adverse effects on fish and the studied biomarkers could be used for monitoring the ecotoxicity of organophosphate esters (OPEs).

Phosphonate ligands demonstrate strong affinity for metal ions. However, there are several cases where the phosphonate is found non-coordinated to the metal ion. Such compounds could be characterized as salts, since the interactions involved are ionic and hydrogen bonding. In this paper we explore a number of such examples, using divalent metal ions (Mg2+, Ca2+, Sr2+ and Ni2+) and the phosphonic acids: p-aminobenzylphosphonic acid (H2PABPA), tetramethylenediamine-tetrakis(methylenephosphonic acid) (H8TDTMP), and 1,2-ethylenediphosphonic acid (H4EDPA). The compounds isolated and structurally characterized are [Mg(H2O)6]·[HPABPA]2·6H2O, [Ca(H2O)8]·[HPABPA]2, [Sr(H2O)8]·[HPABPA]2, [Mg(H2O)6]·[H6TDTMP], and [Ni(H2O)6]·[H2EDPA]·H2O. Also, the coordination polymer [Ni(4,4’-bpy)(H2O)4]·[H2EDPA]·H2On was synthesized and characterized, which contains a bridging 4,4’-bipyridine (4,4’-bpy) ligand forming an infinite chain with the Ni2+ cations. All these compounds contain the phosphonate anion as the counterion to charge balance the cationic charge originating from the metal cation.

This study investigated the contributions of particulate matter (PM) from various emission sources during the dry season, which resulted from frequent fires occurring in degraded forests and peatlands in Indonesia. Samples of fine (PM 2.5 ) and coarse (PM 2.5-10 ) particles collected during the dry season in Riau, Indonesia were analyzed to determine the mass concentrations of metallic trace elements, ionic compound, black carbon (BC), and organic carbon (OC). The average concentrations of PM 2.5 and PM 2.5-10 at Riau, Indonesia were 63.85 ± 3.22 µg m −3 and 27.72 ± 2.40 µg m −3 , respectively. The positive matrix factorization (PMF) model was adopted to identify possible PM sources and their contributions to the ambient PM level. The PMF results identified six major PM 2.5 sources, including biomass burning (BB) (28.7%), secondary aerosols (SA) (26.9%), vehicle exhaust (VE) (12.8%), industrial emissions (IE) (12.3%), soil dust (SD) (11.9%), and sea salt (SS) (7.5%). Moreover, there were five primary PM 2.5-10 sources, including VE (28.6%) and BB (24%), followed by IE (19.9%), SD (17.2%), and SA (15.3%). A conditional probability function (CPF) analysis revealed that the southeast sector dominated among source direction-dependent contributions. The noncarcinogenic health risks for both adults and children resulting from exposure to PM 2.5 were mainly contributed by Co, Ni, and Mn, and carcinogenic risks were caused by the toxic metals Cr and Co. Both noncarcinogenic and carcinogenic health risks resulting from cumulative multielement exposure for both adults and children exceeded acceptable levels. Clearly, more attention should be devoted to reducing the noncarcinogenic and carcinogenic health risks caused by particulate-bound toxic elements through inhalation exposure.

The computed electrostatic potentials on C,H,N,O molecular solids and nitrogen-rich C,H,N,O salts are used in analyzing and comparing intralattice attractive forces and crystal densities in these two categories of compounds. Nitrogen-rich C,H,N,O salts are not an assured path to high densities. To increase the likelihood of high densities, small cations and large anions are suggested. Caution is recommended in predicting benefits of nitrogen-richness for explosive compounds.

The influence of non-ionic compounds in combination with sodium oleate on the contrast behavior of flotation response of calcium minerals is investigated theoretically and experimentally. The flotation and adsorption analyses are carried out with monomineral fractions of calcite and scheelite, while the flotation process analysis is conducted with an ore material screened into size grades of -44 and -15 urn. The process conditions of the highest difference in adsorption of oleate and contrast in extraction of scheelite and calcite are found. The conditions of the maximum depression of calcite in the rougher flotation circuit are determined.