Precision measurements of kaonic atoms at DA ΦNE and future perspectives

The DAΦNE electron-positron collider at the Frascati National Laboratories has made available a unique “beam" of negative kaons providing unprecedented conditions for the study of the low-energy kaon-nucleon interaction, a field still largely unexplored. The DEAR (DAΦNE Exotic Atom Research) experiment at DAΦNE and its successor SIDDHARTA (SIlicon Drift Detector for Hadronic Atom Research by Timing Application) aim at a precision measurement of the strong-interaction shift and width of the fundamental 1s level, via the measurement of the X-ray transitions to this level, for kaonic hydrogen and kaonic deuterium. The aim is to extract the isospin-dependent antikaon-nucleon scattering lengths and to contribute to the understanding of aspects of chiral symmetry breaking in the strangeness sector.     

Short-lived metal clusters in aqueous solutions: formation, identification, and properties

The formation and properties of short-lived homo- and heteronuclear metal clusters in aqueous solutions were investigated by pulse radiolysis. These species arise in early stages of the aggregation of metal atoms and ions in unusual oxidation states. The conditions favoring the formation of positively charged “magic” clusters and intermediate heterometallic clusters were elucidated. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 1–15, January, 1999.     

Evolution of IPv6 Internet topology with unusual sudden changes

The evolution of Internet topology is not always smooth but sometimes with unusual sudden changes. Consequently, identifying patterns of unusual topology evolution is critical for Internet topology modeling and simulation. We analyze IPv6 Internet topology evolution in IP-level graph to demonstrate how it changes in uncommon ways to restructure the Internet. After evaluating the changes of average degree, average path length, and some other metrics over time, we find that in the case of a large-scale growing the Internet becomes more robust; whereas in a top-bottom connection enhancement the Internet maintains its efficiency with links largely decreased.     

增强吸收型光双稳的耦合动力学方程及动态分析

本文从唯象的角度首次提出了增强吸收到光双稳的耦合动力学方程，利用计算机模拟，描述了增强吸收型光双稳的静态和动态特性。     

A facile approach for the construction of the oxetane ring from 5α-acyloxy-Δ~(4(20)) - taxoids

An oxetane ring can be constructed from 5α-acyloxy-Δ4(20)-taxoids. Hie facile intramolecular acyl migration from 5- to 20-position under slightly basic conditions enabled the construction of the oxetane ring in a convenient short cut, whereas the acyl migration from 2- to 20-position left the 2-hydroxyl accessible to a later benzoylation. An unexpected five-mem-bered 4-O, 20- O sulfite ring was formed in the attempted construction of the oxetane ring with 5α-triflate as a leaving group. After the construction of the oxetane ring, treatment with strong base LiHMDS and acetyl chloride gave the expected 4-O-acetate while treatment with acetic anhydride and DMAP gave a 4-O-acetoacetate.     

Time-evolution of cascade processes of muonic atoms in hydrogen-helium mixtures

The time-dependence of the population of muonic hydrogen states in hydrogen-helium mixtures is calculated for principal quantum number n. The number of muons transferred to helium nuclei is also determined. The dependence of the population of the ground state of muonic hydrogen on time and target density and the helium concentration is also considered. The results are in agreement with recent experimental data. The comparison of the calculated yield of K lines of X-ray in pure hydrogen and deuterium with experimental data indicates the essential role of the Coulomb deexcitation process. Possible Stark mixing is also analysed. Received 17 February 1999 and Received in final form 9 June 1999     

Dynamic phase transition behavior and unusual hydration process in poly(ethylene oxide)‐b‐poly(N‐vinylcaprolactam) aqueous solution

Dynamic phase transition and self‐assembly mechanism of thermosensitive poly(ethylene oxide)‐b‐poly(N‐vinylcaprolactam) (PEO‐b‐PVCL) copolymer are explored deeply. A gradual dehydration process with predominated hydrophobic interactions among copolymer chains in the phase transition process distinguishes the copolymer from homopolymer. PVCL in the inner zone is restricted and counter‐balanced by the PEO segments based on the sequence order of representative groups during the heating‐cooling cycles. Remarkably, PEO shell experiences unusual hydration process, which is first discovered. This hydrophilic shell plays as water absorption sponge layer and captures expelled water from PVCL core, accompanied by gradient distribution of water existed in the assembly structures. Peculiarly, pseudo‐linear changes of the integral area of free C?O are presented compared with inflection point in the hydrated C?O integral area, which propose that a part of hydrated C?O forms incomplete dehydrated states. During the cooling process, perfect reversibility is observed without obvious hysteresis. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 385–396     

Carbon Monoxide Coupling Reactions: A New Concept for the Formation of Hexahydroxybenzene

For linear and cyclic coupling reactions of CO, among other products, the formation of the hexapotassium salt of hexahydroxybenzene is of particular interesting. The interaction of metallic potassium and CO offers, via the assumed K[OC≡CO]K as the result of several carbon monoxide coupling reactions, the formation of C₆(OK)₆ among other products. To date, only speculations exist about the reaction pathway for these products, which were first described by Liebig in 1834. A novel concept is suggested here, which consists of the single steps (i) reductive coupling of CO, (ii) formation of dihetero-metallacyclopentynes (cis-2,5-diheterobutatriene as formal ethylenedione O=C=C=O complexes), (iii) formation of its dinuclear 1-metalla-2,5-dioxo-cyclopentyne complexes by external coordination of the triple bond, (iv) insertion of CO into the M−C bond of the formed metallacyclopropene, and (v) the reductive elimination of C₆(OK)₆. The novel aspect of this concept is the formation of dihetero-metallacyclopentynes (in analogy to the well characterized all-C-metallacyclopentynes), which have not been considered in the mechanism of reductive CO coupling reactions. It is expected that the presence of transition-metal impurities would promote the reaction.     

Unusual Photopolymerization Behavior of Amino Acid‐Derived Polydiacetylene Supramolecules

UV‐irradiation of aqueous suspensions of amino acid‐derived amphiphilic diacetylene supramolecules promotes a process that involves initial formation of species that absorb at 640 nm followed by the generation of polymers that have longer wavelength (686 nm) absorbance. The initially formed intermediate polydiacetylenes display substantial colorimetric reversibility while the long wavelength absorbing polymers show irreversible thermochromism during heating and cooling cycles. The long wavelength absorbing polydiacetylenes, formed from amino acid‐derived amphiphilic diacetylene supramolecules, are suggested to have more planer backbone structures that allow more efficient overlap of the conjugated p‐orbitals.