Zn2+ detection of a benzimidazole 8-aminoquinoline fluorescent sensor by inhibited tautomerization

A new fluorescent chemosensor based on 8-aminoquinoline L1 bearing a benzimidazole moiety was synthesized, which exists as two predominant tautomers L1A and L1B in diluted DMSO-d6 solution. Among various metal ions, L1 showed a highly selective and sensitive turn-on fluorescence response to the presence of Zn2+ ions in methanol. The detection limit for Zn2+ by L1 was calculated to be 1.76 x 10-7 M. The 1 : 1 complexation ratio of the L1–Zn complex was confirmed through Job plot measurements. Complexation studies were performed by FT-IR, NMR and HR-ESI MS measurements and DFT calculations. With the gained insight, it was possible to successfully apply L1 in water sample analysis

The rapidity structure of Mach cones and other large angle correlations in heavy-ion collisions

The pattern of angular correlations of hadrons with a (semi-)hard trigger hadron in heavy-ion collisions has attracted considerable interest. In particular, unexpected large angle structures on the away side (opposite to the trigger) have been found. Several explanations have been brought forward, among them Mach shockwaves and Cherenkov radiation. Most of these scenarios are characterized by radial symmetry around the parton axis, thus angular correlations also determine the rapidity dependence of the correlation. If the observed correlations are remnants of an away side parton after interaction with the medium created in the collision, pQCD allows to calculate the distribution $P(y)$ of the away side partons in rapidity. The measured correlation then arises as a folding of $P(y)$ and the rapidity structure of the correlation taking into account the detector acceptance. This places non-trivial and rather stringent constraints on the underlying scenario. We investigate these dependences and demonstrate that Mach shockwaves survive this folding procedure well whereas Cherenkov radiation scenarios face new challenges.Comment: 9 pages, 3 figures, version to appear in Phys. Lett.

1,3-thiazolium-4-aminides: syntheses and characterization of fluorescent mesoionic compounds

A series of mesoionic 1,3-thiazolium-4-aminides was synthesized starting from thioamides and chloroacetonitrile via cyanomethylbenzimidothioates which were cyclized by benzoylchloride. Depending on the reaction conditions 4-amino-1,3-thiazolium salts and 4-N-benzamido-1,3-thiazolium salts were obtained (X-ray structure analysis). Substitution of the amino groups with benzoyl chloride gave a series of the title mesoionic compounds (X-ray structure analysis) which were examined spectroscopically. Negative solvatochromism was found and temperature-dependent as well as time-resolved fluorescence measurements were made. Long lifetimes of the excited states (30–50 ns) were detected. Calculated frontier orbital profiles gain insight into the characteristics of 1,3-thiazolium-4-aminides as conjugated mesomeric betaines

Coherent control of the cooperative branching ratio for nuclear x-ray pumping

Coherent control of nuclear pumping in a three level system driven by x-ray light is investigated. In single nuclei, the pumping performance is determined by the branching ratio of the excited state populated by the x-ray pulse. Our results are based on the observation that in ensembles of nuclei, cooperative excitation and decay leads to a greatly modified nuclear dynamics, which we characterize by a time-dependent cooperative branching ratio. We discuss prospects of steering the x-ray pumping by coherently controlling the cooperative decay. First, we study an ideal case with purely superradiant decay and perfect control of the cooperative emission. A numerical analysis of x-ray pumping in nuclear forward scattering with coherent control of the cooperative decay via externally applied magnetic fields is presented. Next, we provide an extended survey of nuclei suitable for our scheme, and propose proof-of-principle implementations already possible with typical M\"ossbauer nuclear systems such as $^{57}\mathrm{Fe}$. Finally, we discuss the application of such control techniques to the population or depletion of long-lived nuclear states.Comment: 11 pages, 8 figures; updated to the published versio

Switchable mesomeric betaines derived from pyridinium-phenolates and bis(thienyl)ethane

Syntheses of push–pull substituted non-symmetric bis(thienyl)ethenes (BTEs) possessing a central perfluorocyclopentene core are described. The substituent effects of anisole, phenole, and phenolate as well as pyridine, pyridinium, and N-methylpyridinium substituents, joined through their 3- or 4-positions to the central BTE core, respectively, cover the range from very strongly electron-donating [σ(4-phenolate)=−1.00] to extremely strongly electron-withdrawing [σ(pyridinium-4-yl)=+2.57] in the title mesomeric betaines. The different isomers possessing 4-yl/4-yl, 4-yl/3-yl and 3-yl/3-yl substituents represent different combinations of conjugated and cross-conjugated partial structures and cause different spectroscopic properties. In addition, through-space conjugation between the 2- and 2′-position of the thiophenes can be observed which circumvents the charge-separation of through-bond cross-conjugation. The BTE possessing the push–pull chromophore consisting of 3-anisole and 4-pyridinium substituents (24) displays the best extinction coefficients within the series of compounds described here (ϵ=33.8/15.7 L/mol ⋅ cm), while the mesomeric betaine possessing an N-methylpyridinium-4-yl and a 4-phenolate substituent (29) displays considerable bathochromic shifts to λmax=724 nm in its closed form

Guiding Neutral Atoms with a Wire

We demonstrate guiding of cold neutral atoms along a current carrying wire. Atoms either move in Kepler-like orbits around the wire or are guided in a potential tube on the side of the wire which is created by applying an additional homogeneous bias field. These atom guides are very versatile and promising for applications in atom optics.Comment: 4 pages, 6 figures, submitted to PR

Octonionic representations of Clifford algebras and triality

The theory of representations of Clifford algebras is extended to employ the division algebra of the octonions or Cayley numbers. In particular, questions that arise from the non-associativity and non-commutativity of this division algebra are answered. Octonionic representations for Clifford algebras lead to a notion of octonionic spinors and are used to give octonionic representations of the respective orthogonal groups. Finally, the triality automorphisms are shown to exhibit a manifest \perm_3 \times SO(8) structure in this framework.Comment: 33 page

Atom Chips

Atoms can be trapped and guided using nano-fabricated wires on surfaces, achieving the scales required by quantum information proposals. These Atom Chips form the basis for robust and widespread applications of cold atoms ranging from atom optics to fundamental questions in mesoscopic physics, and possibly quantum information systems

Scientific Opportunities with an X-ray Free-Electron Laser Oscillator

An X-ray free-electron laser oscillator (XFELO) is a new type of hard X-ray source that would produce fully coherent pulses with meV bandwidth and stable intensity. The XFELO complements existing sources based on self-amplified spontaneous emission (SASE) from high-gain X-ray free-electron lasers (XFEL) that produce ultra-short pulses with broad-band chaotic spectra. This report is based on discussions of scientific opportunities enabled by an XFELO during a workshop held at SLAC on June 29 - July 1, 2016Comment: 21 pages, 12 figure