Substituted pyridine coordinated N,N-trans and N,N-cis cyclopalladated complexes of (S)-4-tert-butyl-2-phenyl-2-oxazoline: Crystal structures, spectral study and catalysis of the decomposition of PS pesticides

Three pyridine coordinated cyclopalladated complexes: (S)-chloro{2-[2-(4-tert-butyl)oxazolinyl]phenyl-C,N}(4-R-pyridine)palladium(II) (R = H, 2; R = CF₃, 3; R = NMe₂, 4), have been synthesized and structurally characterized. While the crystal structure shows that 2 has a normal N,N-trans-conformation in the coordination sphere of palladium(II), 3 and 4 exhibit uncommon N,N-cis-conformations. From ¹H NMR measurements, the major coordination isomer in deuterated chloroform solution is N,N-trans configuration for three palladacycles. It was found that the three complexes catalyze effectively the methanolysis of the PS pesticides including chiral thiophosphates but show different activity depending on the substituents of co-coordinated pyridine ring in 2–4.     

Fluorescence sensing of theobromine by simple 2,6-diamino-pyridine and the novel cyclic chair-like hydrogen-bonded tetramer of its diacetyl derivative

2,6-Diaminopyridine is found to be a simple fluorescent sensor for theobromine and its diacetyl derivative 2 also effectively binds theobromine. The receptor-binding sites are based on the co-operative hydrogen-bonding abilities of secondary amides. An unprecedented hydrogen-bonded self-organised cyclic tetrameric supramolecular network is shown for one such small molecule 2 containing one heterocyclic ring in contrast to the binuclear substrates like guanine or pterin which usually form cyclic tetrameric structures.     

Comparison of Fracture Load of the Four Translucent Zirconia Crowns

Recently, translucent zirconia has become the most prevalent material used as a restorative material. This study aimed to compare the crown fracture load of the four most common different translucent zirconia brands available in the market at 1.5 mm thickness. Standardized tooth preparations for a full ceramic crown were designed digitally with software (AutoCAD) by placing a 1.0 mm chamfer margin and 1.5 mm occluso-cervical curvature for the crown sample manufacturing. Stylized crowns were chosen to control the thickness of the crown. The axial and occlusal thickness were standardized to 1.5 mm thickness except at the central pit, which was 1.3 mm thick. The STL file for the tooth dies was prepared using software (3Shape TRIOS^® Patient Monitoring, Copenhagen, Denmark). The tooth dies were printed with a resin material (NextDent Model 2.0, Vertex-Dental B.V., Soesterberg, The Netherlands) using a 3D printing software (3D Sprint^® Client Version 3.0.0.2494) from a 3D printer (NextDent™ 5100, Vertex-Dental B.V., Soesterberg, The Netherlands). The printing layer thickness was 50 µm. Then, a total of twenty-eight (N = 28) stylized crowns were milled out of AmannGirrbach (Amann Girrbach GmbH, Pforzheim, Germany) (n = 7), Cercon HT (Dentsply Sirona, Bensheim, Germany) (n = 7), Cercon XT (Dentsply Sirona, Bensheim, Germany) (n = 7), and Vita YZ XT (Zahnfabrik, Bäd Sackingen, Germany) (n = 7). Following sintering the crowns, sandblasting was performed and they were bonded to the tooth dies with the resin cement (RelyX U-200, 3M ESPE, Seefeld, Germany) and permitted to self-cure under finger pressure for 6 min. The crowns were loaded on the occlusal surface in a universal testing machine (MTS Centurion) with a stainless-steel ball indenter (7 mm radius) with a loading rate of 1 mm/min to contact the stylized crowns on each of the four cusps until failure. A rubber sheet (1.5 mm thickness) was positioned between the crown and indenter, which helped with the load distribution. Statistical analysis was done using SPSS version 20 (IBM Company, Chicago, USA). The fracture loads were analyzed using Dunnett’s T3 test, and the number of cracks was analyzed using the Mann–Whitney U test among the groups. The significant level was set at p value = 0.05. The mean fracture loads were 3086.54 ± 441.74 N, 4804.94 ± 70.12 N, 3317.76 ± 199.80 N, and 2921.87 ± 349.67 N for AmannGirrbac, Cercon HT, Cercon XT, and Vita YZ XT, respectively. The mean fracture loads for the surfaces with the greatest number of cracks (excluding the occlusal surfaces) were on the lingual surface for AmannGirrbach and Cercon HT, on the distal and mesial for Cercon XT, and on the buccal for Vita YZ XT. We found that the AmannGirrbach had the most overall cracks. Cercon XT had the greatest number of occlusal cracks and appeared to be the most shattered. Cercon HT had the least number of cracks. In conclusion, Cercon HT presented the best strength properties, the highest fracture load, and no visible cracks. AmannGirrbach presented the lowest strength properties.     

Non-covalent synthesis of ionic and molecular complexes of benzoic acid and substituted 2-aminopyrimidines by varying aryl/alkyl substituents and their supramolecular chemistry

The non-covalent synthesis of ionic and molecular complexes of substituted 2-aminopyrimidines with benzoic acid in crystalline solid phase is reported. The nature of supramolecular architecture varied with the substituents in the 2-aminopyrimidine ring. Two complexes have been synthesised from two differently substituted 2-aminopyrimidines and benzoic acid. In one case, proton transfer takes place and an ionic organic salt is formed, whereas in the other, there is no proton transfer and a hydrogen-bonded molecular complex is formed.     

Acridone Derivatives from Atalantia monophyla Inhibited Cancer Cell Proliferation through ERK Pathway

The present study aimed to investigate the effect of acridone alkaloids on cancer cell lines and elucidate the underlying molecular mechanisms. The ten acridone alkaloids from Atalantia monophyla were screened for cytotoxicity against LNCaP cell lines by a WST-8 assay. Then, the most potential acridone, buxifoliadine E, was evaluated on four types of cancer cells, namely prostate cancer (LNCaP), neuroblastoma (SH SY5Y), hepatoblastoma (HepG2), and colorectal cancer (HT29). The results showed that buxifoliadine E was able to significantly inhibit the proliferation of all four types of cancer cells, having the most potent cytotoxicity against the HepG2 cell line. Western blotting analysis was performed to assess the expression of signaling proteins in the cancer cells. In HepG2 cells, buxifoliadine E induced changes in the levels of Bid as well as cleaved caspase-3 and Bax through MAPKs, including Erk and p38. Moreover, the binding interaction between buxifoliadine E and Erk was investigated by using the Autodock 4.2.6 and Discovery Studio programs. The result showed that buxifoliadine E bound at the ATP-binding site, located at the interface between the N- and C-terminal lobes of Erk2. The results of this study indicate that buxifoliadine E suppressed cancer cell proliferation by inhibiting the Erk pathway.     

Ethyl (6aRS,8RS,12bRS)‐6‐oxo‐8‐phenyl‐6a,7,8,12b‐tetra­hydro‐6H‐benzo­[b]naphtho­[1,2‐d]­pyran‐6a‐carboxylate

In the title compound, C₂₆H₂₂O₄, the pyran­one ring adopts a twisted boat conformation, while the cyclo­hexane ring is close to an envelope conformation. The dihedral angle between the mean planes of the coumarin and naphthalene systems is 78.8 (1)°. The attached phenyl ring is in an equatorial position with respect to the cyclo­hexane ring.     

A ternary complex of aqua(18‐crown‐6)bis(o‐nitrophenolato)barium(II), the triaqua(18‐crown‐6)(o‐nitrophenolato)barium(II) cation and the o‐nitrophenolate anion

In the title compound [systematic name: tri­aqua(1,4,7,10,13,16‐hexaoxa­cyclo­octa­decane‐κ⁶O)(2‐nitro­phenolato‐κO)­barium(II)–aqua(1,4,7,10,13,16‐hexaoxa­cyclo­octa­decane‐κ⁶O)‐ bis(2‐nitro­phenolato‐κ²O,O′)­barium(II)–2‐nitro­phenolate (1/1/1)], [Ba(C₁₂H₂₄O₆)(C₆H₄NO₃)(H₂O)₃][Ba(C₁₂H₂₄O₆)(C₆H₄NO₃)₂(H₂O)](C₆H₄NO₃), the two Ba^II atoms encapsulated by the 18‐crown‐6 rings have different coordinations. Although both Ba^II atoms are coordinated to the six O atoms of the crowns, in the neutral moiety, the Ba^II atom is coordinated to one terminal O atom from a water mol­ecule, two phenolate O atoms and two nitro‐group O atoms, while in the cationic moiety, the Ba^II atom is coordinated to three terminal O atoms from water mol­ecules and one phenolate O atom. Both the crowns are eclipsed and translated along the b direction. In the asymmetric unit, the three components are interconnected by four O—H?O interactions. The packing is stabilized by two intermolecular C—H?O interactions and by one O—H?O interaction.     

Pulcherrins D-R, potential anti-inflammatory diterpenoids from the roots of Caesalpinia pulcherrima

Bioactivity-guided isolation and purification of the dichloromethane extract from the roots of Caesalpinia pulcherrima yielded 15 new cassane-type diterpenes, named pulcherrins D-R (1-15) together with eight known compounds. The structures of the new metabolites were determined on the basis of spectroscopic analyses including 1D- and 2D-NMR and mass spectroscopy. The anti-inflammatory activity of isolated compounds was investigated with the lipopolysaccharide (LPS)-induced murine macrophage RAW 264.7 cell lines. Compounds 8, 9, 11-15, and 17-23 showed potent NO inhibitory activity.     

The ternary complex 4‐(2‐pyridyl)pyridinium–3,5‐di­nitro­benzoate–3,5‐di­nitro­benzoic acid (1/1/1)

In the title ternary complex, C₁₀H₉N₂⁺·C₇H₃N₂O₆^?·C₇H₄N₂O₆, the pyridinium cation adopts the role of the donor in an intermolecular N—H?O hydrogen‐bonding interaction with the carboxyl­ate group of the 3,5‐di­nitro­benzoate anion. The mol­ecules of the ternary complex form molecular ribbons perpendicular to the b direction, which are stabilized by one N—H?O, one O—H?O and five C—H?O intermolecular hydrogen bonds. The ribbons are further interconnected by three intermolecular C—H?O hydrogen bonds into a three‐dimensional network.