Study of the Mechanisms of Flux Pinning in Type 2 Superconductors

Flux pinning mechanisms in type-2 semiconductors and specific heat measurements on annealed and deformed pure niobium sample

Three-coordinate iron(II) expanded ring N-heterocyclic carbene complexes

A sterically demanding seven-membered expanded ring N-heterocyclic carbene (NHC) ligand allows access to rare examples of three-coordinate iron(II)-NHC complexes incorporating only halide coligands of the general formula [Fe(NHC)X 2 ] (NHC = 7-DiPP; X = Br (1) Cl (2)). Reducing the steric influence of the ancillary NHC ligand through modulation of the N-aryl substituents leads to either four- or three-coordinate complexes of the general formula [Fe(NHC)Br 2 (THF)] (3) or [Fe(NHC)Br 2 ] (4) (NHC = 7-Mes), dependent upon the solvent of recrystallization. The further reduction of NHC steric influence results in four-coordinate geometries at iron in the form of the dimeric species [Fe(NHC)Br(μ-Br)] 2 (5) or [Fe(NHC)Br 2 (THF)] (6) (NHC = SDiPP), again dependent upon the solvent of recrystallization. Compounds 1-6 have been analyzed by 1 H NMR spectroscopy, X-ray crystallography, elemental microanalysis, Mössbauer spectroscopy (for 1 and 3-5), and Evans method magnetic susceptibility. In addition to these measurements the three-coordinate species 1 and 4 have been further analyzed by SQUID magnetometry and CASSCF calculations, which show significant magnetic anisotropy that is extremely sensitive to the coordination geometry

Are interactions between epicardial adipose tissue, cardiac fibroblasts and cardiac myocytes instrumental in atrial fibrosis and atrial fibrillation?

Atrial fibrillation is very common among the elderly and/or obese. While myocardial fibrosis is associated with atrial fibrillation, the exact mechanisms within atrial myocytes and surrounding non-myocytes are not fully understood. This review considers the potential roles of myocardial fibroblasts and myofibroblasts in fibrosis and modulating myocyte electrophysiology through electrotonic interactions. Coupling with (myo)fibroblasts in vitro and in silico prolonged myocyte action potential duration and caused resting depolarization; an optogenetic study has verified in vivo that fibroblasts depolarized when coupled myocytes produced action potentials. This review also introduces another non-myocyte which may modulate both myocardial (myo)fibroblasts and myocytes: epicardial adipose tissue. Epicardial adipocytes are in intimate contact with myocytes and (myo)fibroblasts and may infiltrate the myocardium. Adipocytes secrete numerous adipokines which modulate (myo)fibroblast and myocyte physiology. These adipokines are protective in healthy hearts, preventing inflammation and fibrosis. However, adipokines secreted from adipocytes may switch to pro-inflammatory and pro-fibrotic, associated with reactive oxygen species generation. Pro-fibrotic adipokines stimulate myofibroblast differentiation, causing pronounced fibrosis in the epicardial adipose tissue and the myocardium. Adipose tissue also influences myocyte electrophysiology, via the adipokines and/or through electrotonic interactions. Deeper understanding of the interactions between myocytes and non-myocytes is important to understand and manage atrial fibrillation

Predicting the Detectability of Thin Gaseous Plumes in Hyperspectral Images Using Basis Vectors

This paper describes a new method for predicting the detectability of thin gaseous plumes in hyperspectral images. The novelty of this method is the use of basis vectors for each of the spectral channels of a collection instrument to calculate noise-equivalent concentration-pathlengths instead of matching scene pixels to absorbance spectra of gases in a library. This method provides insight into regions of the spectrum where gas detection will be relatively easier or harder, as influenced by ground emissivity, temperature contrast, and the atmosphere. Our results show that data collection planning could be influenced by information about when potential plumes are likely to be over background segments that are most conducive to detection

Exploring the coordination capabilities of a family of flexible benzotriazole-based ligands using Cobalt (II) sources

In this study we focus on the coordination chemistry of a family of three flexible benzotriazole-based ligands (L1-L3) using Cobalt(II) salts. Our efforts have resulted to the formation of ten novel compounds, formulated as [Co2(L1)2Cl4]·2MeCN (1·2MeCN), Co2(L1)2Br4 (2), [Co(L2)Cl2]·MeCN (3·MeCN), Co(L2)Cl2 (4), [Co2(L2)2Br4]·2MeCN (5·2MeCN), [Co(L2)2(NO3)2]·2MeCN (6·2MeCN), [Co2(L3)2Cl4]·2MeCN (7·2MeCN), Co2(L3)2Cl4 (8), Co2(L3)2Br4 (9), and Co(L3)2(NO3)2 (10). The structures have been well characterised through X-Ray crystallography, FT-IR, ESI-MS, PXRD, Elemental Analysis and TGA studies. The compounds show a large structural variety depending on synthetic parameters (ratio, temperature and metal salt) and the ligand selection (various conformations in each ligand). When tuned appropriately, these factors drastically affect dimensionality, metal geometry and the nuclearity of the final product, resulting in a range of 0D dimers (1, 3, 5, 8, 9), 1D (2, 7, 10) and 2D (4, 6) coordination polymers (CPs). A temperature-induced single-crystal to single-crystal transformation of compound 3 to 4 is additionally reported. The magnetic properties of representative compounds (4, 7, 9) are subject to large changes with only minor structural variations, suggesting that tetrahedral Co(II) nodes in CPs or MOFs could function as sensitive reporters of small changes in the local environment

Development of high energy batteries Final report

Development of battery systems with lithium anodes in nonaqueous electrolytes of propylene carbonate and potassium thiocyanat

Association of Fidaxomicin with C. difficile spores: Effects of Persistence on Subsequent Spore Recovery, Outgrowth and Toxin Production.

Background: We have previously shown that fidaxomicin instillation prevents spore recovery in an in-vitro gut model, whereas vancomycin does not. The reasons for this are unclear. Here, we have investigated persistence of fidaxomicin and vancomycin on C. difficile spores, and examined post-antibiotic exposure spore recovery, outgrowth and toxin production. Methods: Prevalent UK C. difficile ribotypes (n=10) were incubated with 200mg/L fidaxomicin, vancomycin or a non-antimicrobial containing control for 1 h in faecal filtrate or Phosphate Buffered Saline. Spores were washed three times with faecal filtrate or phosphate buffered saline, and residual spore-associated antimicrobial activity was determined by bioassay. For three ribotypes (027, 078, 015), antimicrobial-exposed, faecal filtrate-washed spores and controls were inoculated into broth. Viable vegetative and spore counts were enumerated on CCEYL agar. Percentage phase bright spores, phase dark spores and vegetative cells were enumerated by phase contrast microscopy at 0, 3, 6, 24 and 48 h post-inoculation. Toxin levels (24 and 48h) were determined by cell cytotoxicity assay. Results: Fidaxomicin, but not vancomycin persisted on spores of all ribotypes following washing in saline (mean=10.1mg/L; range= 4.0-14mg/L) and faecal filtrate (mean =17.4mg/L; 8.4-22.1mg/L). Outgrowth and proliferation rates of vancomycin-exposed spores were similar to controls, whereas fidaxomicin-exposed spores showed no vegetative cell growth after 24 and 48 h. At 48h, toxin levels averaged 3.7 and 3.3 relative units (RU) in control and vancomycin-exposed samples, respectively, but were undetectable in fidaxomicin-exposed samples. Conclusion: Fidaxomicin persists on C. difficile spores, whereas vancomycin does not. This persistence prevents subsequent growth and toxin production in vitro. This may have implications on spore viability, thereby impacting CDI recurrence and transmission rates