Comments on the evolving field of sonochemistry by a cavitation physicist

Sonochemistry is an evolving field that has shown recent rapid growth and increasing interest. Although this field concentrates on chemistry and uses acoustics principally as a tool, the basic mechanism that gives rise to sonochemistry — acoustic cavitation — is often ignored or given little attention. This paper addresses some of the relevant aspects of cavitation and physical acoustics that apply to sonochemistry.     

Microbubble-enhanced hemorrhage control using high intensity focused ultrasound

Our objective was to investigate whether hemorrhage control can be achieved faster when high-intensity focused ultrasound (HIFU) is applied in the presence of ultrasound contrast agents (UCA) as compared to HIFU only application. Incisions (3 cm long and 0.5 cm deep) were produced in the livers of anesthetized rabbits. UCA Optison (0.18 ml/kg) was injected into the mesenteric vein. A HIFU applicator (5.5 MHz, 6800 W/cm² in situ) was scanned at a rate of 1–2 mm/s in one direction over the incision (with multiple passes if needed), until hemostasis was achieved. Hemostasis times were 59 ± 23 s (n = 21) in the presence of Optison and 70 ± 23 s (n = 29) without Optison. The presence of Optison produced on average 37% reduction in hemostasis times normalized to initial bleeding rates (p < 0.05), as well as 60% faster formation of the coagulum seal over the incision (p < 0.05). Gross and histological observations showed similar appearance of HIFU lesions produced in the presence of Optison and HIFU lesions produced without Optison. Our results suggest potential utility of UCA for increasing efficiency of HIFU-induced hemostasis of solid organ injuries.     

Cosmic ray studies with the L3-cosmics program at CERN

The L3 detector at the CERN electron-positron collider had a muon spectrometer which was employed during the last years of LEP operation for cosmic ray studies. The results of this program include a precise muon spectrum and charge ratio between 20 GeV and 3 TeV, a limit on TeV primary antiprotons from a study of the Moon’s shadow, the (possible) observation of a are signal from a fixed position in the northern hemisphere through muons, a solar anisotropy of 200 GeV protons, and other results. Negative limits on muons associated with known H.E. gamma sources or gamma bursts, the search for anomalous H.E. interaction or decay events such as reported from the Kolar Gold Fields, and a search for muons correlated with a solar are are also noted.     

NMR Reveals That a Highly Reactive Nonheme FeIV=O Complex Retains Its Six-Coordinate Geometry and S=1 State in Solution

The [Fe^IV(O)(Me₃NTB)]²⁺ (Me₃NTB=tris[(1-methyl-benzimidazol-2-yl)methyl]amine) complex 1 has been shown by Mössbauer spectroscopy to have an S=1 ground state at 4 K, but is proposed to become an S=2 trigonal-bipyramidal species at higher temperatures based on a DFT model to rationalize its very high C−H bond-cleavage reactivity. In this work, ¹H NMR spectroscopy was used to determine that 1 does not have C₃-symmetry in solution and is not an S=2 species. Our results show that 1 is unique among nonheme Fe^IV=O complexes in retaining its S=1 spin state and high reactivity at 193 K, providing evidence that S=1 Fe^IV=O complexes can be as reactive as their S=2 counterparts. This result emphasizes the need to identify factors besides the ground spin state of the Fe^IV=O center to rationalize nonheme oxoiron(IV) reactivity.     

A Facile Method for the Separation of Methionine Sulfoxide Diastereomers,Structural Assignment,and DFT Analysis

Methionine (Met) oxidation is an important biological redox node, with hundreds if not thousands of protein targets. The process yields methionine oxide (MetO). It renders the sulfur chiral, producing two distinct, diastereomerically related products. Despite the biological significance of Met oxidation, a reliable protocol to separate the resultant MetO diastereomers is currently lacking. This hampers our ability to make peptides and proteins that contain stereochemically defined MetO to then study their structural and functional properties. We have developed a facile method that uses supercritical CO₂ chromatography and allows obtaining both diastereomers in purities exceeding 99 %. ¹H NMR spectra were correlated with X-ray structural information. The stereochemical interconversion barrier at sulfur was calculated as 45.2 kcal mol⁻¹, highlighting the remarkable stereochemical stability of MetO sulfur chirality. Our protocol should open the road to synthesis and study of a wide variety of stereochemically defined MetO-containing proteins and peptides.     

An Exceptionally Stable and Scalable Sugar–Polyolefin Frank–Kasper A15 Phase

“One-component” soft material Frank–Kasper (FK) phases are an intriguing structural form of matter that possess periodically ordered structures arising from the self-reconfiguration and close packing of an initial assembly of identical “deformable” spheres into two or more size- or shape-distinct sets of particles. Significant challenges that must still be addressed to advance the field of soft matter FK phases further, however, include their rare and unpredictable occurrence, uncertain mechanisms of solid-state assembly, and low thermodynamic stability. Here we show that a readily-accessible sugar–polyolefin conjugate quantitatively produces an exceptionally stable solid-state FK A15 phase through a rapid and irreversible thermotropic order–order transition, which contrary to other prevailing proposed mechanisms, does not require mass transfer between particles or large structural reorganization in the bulk to establish unit cell non-equivalency. Our results provide the basis for a realistic strategy for obtaining practical and scalable quantities of a diverse range of sugar–polyolefin FK A15 phases with unique intrinsic physical properties and chemical reactivities not previously seen in such systems.