Antimicrobial prospect of newly synthesized 1,3-thiazole derivatives

A new series of 1,3-thiazole and benzo[d]thiazole derivatives 10-15 has been developed, characterized, and evaluated for in vitro antimicrobial activity at concentrations of 25-200 μg/mL against Gram+ve organisms such as methicillin-resistant Staphylococcus aureus (MRSA), Gram-ve organisms such as Escherichia coli (E. coli), and the fungal strain Aspergillus niger (A. niger) by the cup plate method. Ofloxacin and ketoconazole (10 μg/mL) were used as reference standards for antibacterial and antifungal activity, respectively. Compounds 11 and 12 showed notable antibacterial and antifungal activities at higher concentrations (125-200 μg/mL), whereas benzo[d]thiazole derivatives 13 and 14 were found to display significant antibacterial or antifungal activity (50-75 μg/mL) against the Gram+ve, Gram-ve bacteria, or fungal cells used in the present study. In addition, a correlation between calculated and determined partition coefficient (log P) was established which allows future development of compounds within this series to be carried out based on calculated log P values. Moreover, compounds 13 and 14 show that the optimum logarithm of partition coefficient (log P) should be around 4.     

The impact of scaling on single event upset in 6T and 12T SRAMs from 130 to 22 nm CMOS technology

ABSTRACT

As transistor sizes scale down to nanometres dimensions, CMOS circuits become more sensitive to radiation. High-performance static random access memory (SRAM) cells are prone to radiation-induced single event upsets (SEU) which come from the natural space environment. The SEU generates a soft error in the transistor due to the strike of an ionizing particle. Thus, this paper compares the endurance of 12T SRAM and 6T SRAM circuit on 130 up to 22?nm CMOS technology towards SEU. Besides that, this paper discusses the trend of critical linear energy transfer (LET) and collected charge due to technology scaling for the respective circuit. The critical LET (LETcrit) and critical charge (Qcrit) of 6T are approximately 50% lower compared with 12T SRAMs.     

Optimizing nozzle convergent angle using central composite design on the particle velocity and acoustic power level for single-hose dry ice blasting nozzle

Journal of Thermal Analysis and Calorimetry - One of the important parameters in developing dry ice blasting nozzle is the high-speed dry ice pellets. However, many studies focus primarily only on...     

Soil depth profile of 137Cs, 210Pb and 40K in Algeria

ABSTRACT

Three soil depth profiles of ²¹⁰Pb, ¹³⁷Cs and ⁴⁰K at different areas of Algeria were studied. The soil sampling areas are near the location where the French nuclear tests took place at 1960–1966. The two depth soil profiles were collected at Ghardaia region and the third one at Reggane region. The vertical distributions of radionuclides at the two soil depth profiles from Ghardaia region are different, probably due to the different soil composition. The soil depth profile from sandy soil show uniformity in the distribution of radionuclides without a clear maximum (peak). The soil depth profile that characterised by silty sand show a clear peak at 20–50?cm depth for all studied radioactive nuclides, while the observed activities are two times higher than the corresponding values in sandy soil samples. More specifically in Ghardaia region the ²¹⁰Pb, ¹³⁷Cs, ⁴⁰K activity concentrations ranged between 27 and 50?Bq?kg^?1, 0.2 and 3?Bq?kg^?1 and 75 and 90?Bq?kg^?1 respectively in sandy soil type and between 37 and 75?Bq?kg^?1, 4 and 6?Bq?kg^?1 and 140 and 180?Bq?kg^?1 respectively in silty sand soil type. Finally, the third depth soil profile collected from Reggane site presents a completely different distribution of the studied radionuclides. The activity concentrations of ²¹⁰Pb, ¹³⁷Cs, ⁴⁰K ranged between 37 and 51?Bq?kg^?1, 0.16 and 0.39?Bq?kg^?1 and 120 and 309?Bq?kg^?1 respectively. Three peaks in the ¹³⁷Cs distribution revealed, were most probably, Chernobyl related ¹³⁷Cs accounts for the surface peak, while the deeper peaks are connected to the weapons fallout.     

Synthesis, characterization, and antimicrobial evaluation of oxadiazole congeners

A series of 1,3-oxazole, 1,3-thiazole, isomeric 1,2,4-oxadiazole, 1,3,4-oxadiazole, and 1,2,3,4-tetrazole heterocycles was synthesized. All the compounds shared as a common feature the presence of a 4-hydroxyphenyl substituent. The structures of the synthesized compounds were confirmed by MS, 1H-NMR, and elemental analysis. In vitro antimicrobial activity for all the newly synthesized compounds at concentrations of 200-25 μg/mL was evaluated against Gram+ve organisms such as methicillin-resistant Staphylococcus aureus (MRSA), Gram-ve organisms such as Escherichia coli (E. coli), and the fungal strain Aspergillus niger (A. niger) by the cup plate method. Ofloxacin and ketoconazole (10 μg/mL) were used as reference standards for antibacterial and antifungal activity, respectively. Compounds 15, 16, and 20 showed notable antibacterial and antifungal activities at higher concentrations (200 μg/mL), whereas 17-19 were found to display significant antibacterial or antifungal activity (25-50 μg/mL) against the Gram+ve, Gram-ve bacteria, or fungal cells used in the present study.     

Kupfer(I)-Komplexe mit 1-Azadien-Chelatliganden und ihre Reaktion mit Sauerstoff

Copper(I) Complexes with 1-Azadiene Chelate Ligands and Their Reaction with Oxygen The reaction of the bidendate 1-azadiene ligands Me₂N? (CH₂)_n? N?CH? CH?CH? Ph with CuX results in the formation of the dimeric compounds [ A CuX]₂ and [ B CuX]₂ ( A : n = 2, B : n = 3, X: I, Cl). The structure of complex 1 [ A CuI]₂ was determined by X-ray crystal structure analysis. 1 consists of two tetrahedrally coordinated Cu atoms connected by two iodo bridges. (Cu? Cu bond length: 261 pm). The ligand Me? N(CH₂CH₂N?CH? CH?CH? Ph)₂ ( C ) reacts with CuX to form the monomeric complexes [ C CuX] ( 5 : X?I, 6 : X?Cl). The crystal structure of 5 shows that the ligand acts as a tridendate ligand. The bond lengths of the CuN(sp²) bonds are significantly shorter than the Cu? N(sp³) distance. Reacting the podand-type ligands N(CH₂CH₂? N?CH? R)₃ ( D : R?Ph, E : R?-CH?CH? Ph) with CuX yields the ionic complexes 7 [ D Cu][CuCl₂] and 8 [ E Cu][CuCl₂]. 7 was characterized by X-ray analysis which confirmed that D acts as a four-dendate podand ligand. The compounds 1 ? 8 are unreactive towards CO₂ but take up O₂ even at deep temperatures. At ?78°C the orange-red complex 4 [ B CuCl]₂ reacts with O₂ in CH₂Cl₂ to form a deep violet solution, but the primary product of the oxidation could not be isolated. It reacts at room temperature to form the green complex 9 [μ-Cl, μ-OH][ B CuCl]₂. The X-ray structure analysis of 9 confirms that a dimeric Cu^II complex is formed in which both a chloro- and a hydroxo group are bridging the monomeric units. The Cu^II centers exhibit a distorted tetragonal-pyramidal coordination. The pathway of the reaction with O₂ will be discussed.