Synthesis,characterization, and in vitro antimicrobial activities of organotin(IV) complexes of Schiff bases with ONO‐type donor atoms

A new series of diorganotin complexes of the type R₂SnL (L¹: N‐(2‐hydroxy‐5‐chlorophenyl)‐ 3‐ethoxysalicylideneimine, R = Me, (Me₂SnL¹), R = n‐Bu, (n‐Bu₂SnL¹), R = Ph, (Ph₂SnL¹), L²: N‐(2‐hydroxy‐4‐nitro‐5‐chlorophenyl)‐3‐ethoxysalicylideneimine, R = Ph, Ph₂SnL², L³: N‐(2‐hydroxy‐4‐nitrophenyl)‐3‐methoxysalicylideneimine, R = Me, (Me₂SnL³), R = n‐Bu, (n‐Bu₂SnL³), L⁴: N‐(2‐hydroxy‐4‐nitrophenyl)‐3‐ethoxysalicylideneimine, R = Me, (Me₂SnL⁴), R = n‐Bu, (n‐Bu₂SnL⁴)) were synthesized and characterized by elemental analysis, infrared (IR), ¹H, and ¹³C NMR mass spectroscopic techniques, and electrochemical measurements. Ph₂SnL¹ and Ph₂SnL² were also characterized by X‐ray diffraction analysis and were found to show a fivefold C₂NO₂ coordination geometry nearly halfway between a trigonal bipyramidal and distorted square pyramidal arrangement. The C Sn C angles in the complexes were calculated using Lockhart's equations with the ¹J(^117/119Sn‐¹³C) and ²J(^117/119Sn‐¹H) values from the ¹H NMR and ¹³C NMR spectra. Biocidal activity tests against several micro‐organisms and some fungi indicate that all the complexes are mildly active against Gram (+) bacteria and the fungi, A. niger and inactive against Gram (−) bacteria. © 2010 Wiley Periodicals, Inc. Heteroatom Chem 21:373–385, 2010; View this article online at wileyonlinelibrary.com . DOI 10.1002/hc.20628     

Two-body Dirac equation versus KDP equation

A brief review of two-body Dirac and Kemmer-Duffin-Petiau approaches for the bound state problem of two fermions is presented from an algebraic point of view in a comparative manner. Reduction of the direct product of two Dirac spaces is discussed.Work supported by the T.B.T.A.K. under TBAG/CG-1.     

Thiuroniumderivate der Pyridoxingruppe

Ohne Zusammenfassung     

Generators for semigroup of Lipman

There is a correspondence between functions in the maximal ideal of the local ring of a rational singularity and certain positive divisors supported on the exceptional fiber of a resolution of the singularity. Here we give an algorithm to obtain a generating set over ℤ of these divisors.     

Tunable DNA Origami Motors Translocate Ballistically Over μm Distances at nm/s Speeds

Inspired by biological motor proteins, that efficiently convert chemical fuel to unidirectional motion, there has been considerable interest in developing synthetic analogues. Among the synthetic motors created thus far, DNA motors that undertake discrete steps on RNA tracks have shown the greatest promise. Nonetheless, DNA nanomotors lack intrinsic directionality, are low speed and take a limited number of steps prior to stalling or dissociation. Herein, we report the first example of a highly tunable DNA origami motor that moves linearly over micron distances at an average speed of 40 nm/min. Importantly, nanomotors move unidirectionally without intervention through an external force field or a patterned track. Because DNA origami enables precise testing of nanoscale structure‐function relationships, we were able to experimentally study the role of motor shape, chassis flexibility, leg distribution, and total number of legs in tuning performance. An anisotropic rigid chassis coupled with a high density of legs maximizes nanomotor speed and endurance.     

Oxygenation of a ruthenium(II) thiolate to a ruthenium(II) sulfinate proceeds via ruthenium(III)

Exposure of acetonitrile/methanol solutions of [PPN][Ru(DPPBT)3] [PPN = bis(triphenylphosphoranylidene); DPPBT = 2-diphenylphosphinobenzene thiolate] to oxygen initiates metal-centered oxidation, yielding the ruthenium(III) thiolate Ru(DPPBT)3. Ru(DPPBT)3 further reacts with oxygen, at sulfur, to give the ruthenium(III) sulfinate complex [Ru(DPPBT-O2)2(DPPBT)], which is reduced under ambient conditions to [PPN][Ru(DPPBT-O2)2(DPPBT)]. Ruthenium(II) sulfinate is the only product isolated from acetonitrile/methanol. Yellow crystals of [PPN][Ru(DPPBT-O2)2(DPPBT)] were obtained. Ruthenium(III) sulfinate was isolated as green prism-shaped crystals upon oxygenation of [PPN][Ru(DPPBT)3] in chlorobenzene/hexane. Electrochemical oxidation of ruthenium(II) sulfinate yields the ruthenium(III) derivative, which is rapidly reduced back to ruthenium(II) upon the addition of hydroxide.     

Synthesis,characterization, crystal structure and biological activity of the cobalt(IV) complex of 2,6-diacetylpyridine dioxime: [Co(dapdo)<Subscript>2</Subscript>]

The cobalt(IV) complex of 2,6-diacetylpyridine dioxime (dapdoH₂) was prepared and characterized by X-ray diffraction, elemental analysis and FT-IR. The titled complex was found to crystallize in the orthorhombic space group and was screened for antibacterial and antifungal activities by the disc diffusion and microtitter plate techniques using DMF as solvent. It has been found that the antimicrobial activity of the complex [Co(dapdo)₂] is slightly higher than the free ligand (dapdoH₂).     

Thiophosphate esters of cashew nutshell liquid derivatives as new antioxidants for poly(methyl methacrylate)

In this work, poly(methyl methacrylate) films 1% additivated with new thiophosphate esters antioxidants derived from technical Cashew Nutshell Liquid (CNSL), a byproduct of the cashew nut (Anacardium occidentale L.) industry, were investigated by thermogravimetry (TG/DTG) and differential scanning calorimetry (DSC) measurements under inert (N₂) and oxidative (synthetic air) atmospheres. Three new products were synthesized and characterized by GC/MS, ¹H and ³¹P NMR. The analyses were focused on the onset (T _e) and offset temperature (T _o) of degradation of the films, and on the maximum degradation temperature (T _MAX). It was observed that the thermal stability of the films increased with the addition of the thiophosphate ester antioxidants, which indicates that CNSL could be used as a natural source of phenolic material for the synthesis of antioxidants.