Photonic time‐stretch digitizer and its extension to real‐time spectroscopy and imaging

Real‐time wideband digitizers are the key building block in many systems including oscilloscopes, signal intelligence, electronic warfare, and medical diagnostics systems. Continually extending the bandwidth of digitizers has hence become a central challenge in electronics. Fortunately, it has been shown that photonic pre‐processing of wideband signals can boost the performance of electronic digitizers. In this article, the underlying principle of the time‐stretch analog‐to‐digital converter (TSADC) that addresses the demands on resolution, bandwidth, and spectral efficiency is reviewed. In the TSADC, amplified dispersive Fourier transform is used to slow down the analog signal in time and hence to compress its bandwidth. Simultaneous signal amplification during the time‐stretch process compensates for parasitic losses leading to high signal‐to‐noise ratio. This powerful concept transforms the analog signal's time scale such that it matches the slower time scale of the digitizer. A summary of time‐stretch technology's extension to high‐throughput single‐shot spectroscopy, a technique that led to the discovery of optical rouge waves, is also presented. Moreover, its application in high‐throughput imaging, which has recently led to identification of rogue cancer cells in blood with record sensitivity, is discussed.     

Discovery of 4,6-bis(2-((E)-benzylidene)hydrazinyl)pyrimidin-2-Amine with Antibiotic Activity

Robenidine (E)-N′-((E)-1-(4-chlorophenyl)ethylidene)-2-(1-(4-chlorophenyl)ethylidene)hydrazine-1-carboximidhydrazide displays methicillin-resistant Staphyoccoccus aureus (MRSA) and vancomycin-resistant Enterococci (VRE) MICs of 2 μg mL⁻¹. Herein we describe the structure-activity relationship development of a novel series of guanidine to 2-aminopyrimidine isosteres that ameliorate the low levels of mammalian cytotoxicity in the lead compound while retaining good antibiotic activity. Removal of the 2-NH₂ pyrimidine moiety renders these analogues inactive. Introduction of a central 2-NH₂ triazine moiety saw a 10-fold activity reduction. Phenyl to cyclohexyl isosteres were inactive. The 4-BrPh and 4-CH₃Ph with MIC values of 2 and 4 μg mL⁻¹, against MRSA and VRE respectively, are promising candidates for future development.     

New Cr,Mo, W,and Fe Metal Complexes with Potentially Heptadentate (S3N4) Tripodal Schiff Base Ligand: Synthesis,Characterization, and Antibacterial Activity

Russian Journal of General Chemistry - Reactions of Cr, Mo, W, and Fe metal carbonyls with potentially heptadentate (S3N4) tripodal Schiff base ligand, (thio)3tren, have been studied. The Schiff...     

Determination of stress intensity factors in half-plane containing several moving cracks

The dynamic stress intensity factors in a half-plane weakened by several finite moving cracks are investigated by employing the Fourier complex transformation. Stress analysis is performed in a half-plane containing a single dislocation and without dislocation. An exact solution in a closed form to the stress fields and displacement is ob- tained. The Galilean transformation is used to transform between coordinates connected to the cracks. The stress components are of the Cauchy singular kind at the location of dislocation and the point of application of the the influence of crack length and crack running force. Numerical examples demonstrate velocity on the stress intensity factor.     

Synthesis and Reactivity of Functionalized Binary and Ternary Thiometallate Complexes [(RT)4S6], [(RSn)3S4]2−, [(RT)2(CuPPh3)6S6], and [(RSn)6(OMe)6Cu2S6]4− (R=C2H4COOH,CMe2CH2COMe; T=Ge,Sn)

Caged chalcogens : A series of novel, functionalized T_nS_m cages (T=Ge, Sn; n/m=4:6, 3:4) with terminal COO(H) or COMe groups were synthesized and show further reactivity toward Cu^I complexes (an example of which is shown here) and to hydrazines. This led to the generation of functionalized Cu/T/S clusters or the formation of Schiff bases at the C?O groups, respectively, with or without further fragmentation of the T/S core.

     

A convenient two-step preparation of monodeuteriated tetramethylsilane

Purified partially mono-deuteriatedTMS was synthesized by preparing lithiomethyltrimethylsilane from chloromethyltrimethylsilane and reaction of the former with deuteriated water. Using this reference deuterium chemical shifts in parts per million can be reported with respect to [²H] resonance frequency of internalTMS in deuterium nmr spectroscopy.

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Eine einfache zweistufige Synthese von monodeuteriertem Tetramethylsilan (Kurze Mitteilung)

Zusammenfassung Es wird die Synthese von partiell monodeuteriertemTMS beschrieben. Dazu wurde Monochlormethyltrimethylsilan in Lithiomethyltrimethylsilan übergeführt und dieses mit D₂O weiter zum Zielprodukt umgesetzt.

     

The Casazza-Tremain conjecture in the infinite dimensional Hilbert spaces

In this paper, the proof of the Casazza-Tremain Conjecture in the infinite dimensional Hilbert spaces is given.     

A first-principle DFT study of solvent effects on metiamide tautomers and imaginary interactions with H<Subscript>2</Subscript>-receptors

Metiamide is a class of medications called H₂-receptor antagonist or H₂ blockers. It decreases the amount of acid made in the stomach. It is commonly used in the treatment for peptic ulcer disease and gastroesophageal reflux disease. In this study, the metiamide tautomer stability, structural data, HOMO and LUMO (energies and shapes), ΔΕ _HOMO–LUMO gaps, UV–visible data and graphs, dipole moments, Mulliken charges, and thermodynamic and kinetic stabilities in aqueous media as a biological solvent and some of the different media (vacuum, H₂O, Et-OH and DMSO) were investigated for the tautomers of metiamide by the density functional theory DFT-B3LYP/6-31G* method. The results presented that the probability of the adaptability and compatibility of which tautomer (T1–T6) are better than the other tautomers for interactions with the pattern and structural map of the H₂-receptor. The diversities of the interaction points and mosaic patterns of the T3 and T4 tautomers in H₂O media with the imaginary H₂-receptor were investigated.