OsB9 −: An Aromatic Osmium-Centered Monocyclic Boron Ring

Transition-metal-centered monocyclic boron wheels are important candidates in the family of planar hypercoordinate species that show intriguing structure, stability and bonding situation. Through the detailed potential energy surface explorations of MB9 − (M Fe, Ru, Os) clusters, we introduce herein OsB9 − to be a new member in the transition-metalcentered borometallic molecular wheel gallery. Previously, FeB9 − and RuB9 − clusters were detected by photoelectron spectroscopy and the structures were reported to have singlet D9h symmetry. Our present results show that the global minimum for FeB9 − has a molecular wheel-like structure in triplet spin state with Cs symmetry, whereas its heavier homologues are singlet molecular wheels with D9h symmetry. Chemical bonding analyses show that RuB9 − and OsB9 − display a similar type of electronic structure, where the dual σ + π aromaticity, originated from three delocalized σ bonds and three delocalized π bonds, accounts for highly stable borometallic molecular wheels

An unprecedented binodal (4,6)-connected Co(II) MOF as dual-responsive luminescent sensor for detection of acetylacetone and Hg2+ ions

A new Co(II) organic framework, {[Co2(L)(hfpd)(H2O)]·1.75H2O}n (1) (H4hfpd = 4,4′-(hexafluoroisopropylidene)diphthalic acid, L = 4,4′-bis(imidazol-1-yl)-biphenyl) was hydrothermally synthesized and characterized. 1 possesses an unusual (4,6)-connected layered network architecture. Fluorescence titration results present that 1 is rarely dual-responsive probe to detect acetylacetone and Hg2+ ions by luminescence quenching.publishe

Mixed adsorption and surface tension prediction of nonideal ternary surfactant systems

To deal with the mixed adsorption of nonideal ternary surfactant systems, the regular solution approximation for nonideal binary surfactant systems is extended and a pseudo-binary system treatment is also proposed. With both treatments, the compositions of the mixed monolayer and the solution concentrations required to produce given surface tensions can be predicted based only on the gamma-LogC curves of individual surfactants and the pair interaction parameters. Conversely, the surface tensions of solutions with different bulk compositions can be predicted by the surface tension equations for mixed surfactant systems. Two ternary systems: SDS/Hyamine 1622/AEO7, composed of homogeneous surfactants, and AES/DPCl/AEO9, composed of commercial surfactants, in the presence of excess NaCl, are examined for the applicability of the two treatments. The results show that, in general, the pseudo-binary system treatment gives better prediction than the extended regular solution approximation, and the applicability of the latter to typical anionic/cationic/nonionic nonideal ternary surfactant systems seems to depend on the combined interaction parameter, $${\mathop {(\beta }\nolimits_{an}^s } + {\mathop \beta \nolimits_{cn}^s })/2 - {\mathop \beta \nolimits_{ac}^s }/4$$ : the more it deviates from zero, the larger the prediction difference. If $${\mathop {(\beta }\nolimits_{an}^s } + {\mathop \beta \nolimits_{cn}^s })/2 - {\mathop \beta \nolimits_{ac}^s }/4$$ rarr0, good agreements between predicted and experimental results can be obtained and both treatments, though differently derived, are interrelated and tend to be equivalent

Genomic epidemiology of Vibrio cholerae reveals the regional and global spread of two epidemic non-toxigenic lineages

Non-toxigenic Vibrio cholerae isolates have been found associated with diarrheal disease globally, however, the global picture of non-toxigenic infections is largely unknown. Among non-toxigenic V. cholerae, ctxAB negative, tcpA positive (CNTP) isolates have the highest risk of disease. From 2001 to 2012, 71 infectious diarrhea cases were reported in Hangzhou, China, caused by CNTP serogroup O1 isolates. We sequenced 119 V. cholerae genomes isolated from patients, carriers and the environment in Hangzhou between 2001 and 2012, and compared them with 850 publicly available global isolates. We found that CNTP isolates from Hangzhou belonged to two distinctive lineages, named L3b and L9. Both lineages caused disease over a long time period with usually mild or moderate clinical symptoms. Within Hangzhou, the spread route of the L3b lineage was apparently from rural to urban areas, with aquatic food products being the most likely medium. Both lineages had been previously reported as causing local endemic disease in Latin America, but here we show that global spread of them has occurred, with the most likely origin of L3b lineage being in Central Asia. The L3b lineage has spread to China on at least three occasions. Other spread events, including from China to Thailand and to Latin America were also observed. We fill the missing links in the global spread of the two non-toxigenic serogroup O1 V. cholerae lineages that can cause human infection. The results are important for the design of future disease control strategies: surveillance of V. cholerae should not be limited to ctxAB positive strains

A new understanding of nuclei spectra properties with propagation model

The AMS-02 experiment has observed new properties of primary cosmic rays (CRs) categorized into two groups: He-C-O-Fe and Ne-Mg-Si-S, which are independent of CR propagation. In this study, we investigate the unexpected properties of these nuclei using a spatial propagation model. All nuclei spectra are accurately reproduced and separated into primary and secondary contributions. Our findings include: 1. Primary CR spectra are identical. 2. Our calculations align with AMS-02 results for primary-dominated nuclei within a 10\% difference, but show significant discrepancies for the secondary-dominated nuclei. 3. The primary element abundance is presented for the first time. We anticipate that the DAMPE and future HERD experiments will provide observations of nuclei spectra above TeV energy.Comment: 8 pages, 8 figures. accepted by PR

Poly[bis­[μ-1,3-bis­(diphenyl­phosphan­yl)propane-κ2 P:P′]-di-μ-thio­cyanato-κ2 S:N;κ2 N:S-disilver(I)]

In the title coordination polymer, [Ag2(NCS)2(C27H26P2)2]n, two centrosymmetrically related Ag+ cations are linked by two thio­cyanate anions into binuclear eight-membered macrocycles. The Ag⋯Ag separation within the macrocycle is 5.4400 (6) Å. The distorted tetra­hedral coordination about each metal atom is completed by the P atoms of two bridging 1,3-bis­(diphenyl­phosphan­yl)propane ligands, forming polymeric ribbons parallel to the a axis