Raman spectroscopy is an important tool to understand the structural and molecular behaviour of the liquid crystals when they undergo through different temperatures. It also helps to understand the different phase changes of the liquid crystal material as temperature changes. In this work, the structural properties of two nematic liquid crystals having relatively high clearing temperature namely 4 butylcyclohexyl-3, 5-difluoro-4- isothiocyanato biphenyl and 4-pentylcyclohexyl-3, 5-difluoro-4-isothiocyanato biphenyl are studied. The study is done using temperature dependent Raman spectroscopy. From the studies of the two compounds it has been found that the experimental values are agree well with the various functional groups and different bond assignments recorded in literature. This agreement validates the presence of different functional groups and different stretching bonds in the two studied liquid crystal compounds. Deformations of some of the peak positions of the two liquid crystal compounds have been observed with the change in phase at different temperature. Also to understand the behaviour of the Raman peak near the clearing temperatures of the liquid crystal compounds the linewidth of the different peak values at different temperature have also been studied. From the line width study, the various phase transition temperatures of the two liquid crystalline compounds can be confirmed.
- MeSH
- bifenylové sloučeniny chemie MeSH
- kapalné krystaly * chemie MeSH
- Ramanova spektroskopie metody MeSH
- teplota MeSH
- Publikační typ
- časopisecké články MeSH
Current neuroscience research on neurosteroids and their synthetic analogues - neuroactive steroids - clearly demonstrate their drug likeness in a variety of neurological and psychiatric conditions. Moreover, research on neurosteroids continues to provide novel mechanistic insights into receptor activation or inhibition of various receptors. This mini-review will provide a high-level overview of the research area and discuss the various classes of potential physiological and pathological implications discovered so far.
- MeSH
- iontové kanály řízené ligandy metabolismus MeSH
- lidé MeSH
- neuroplasticita účinky léků MeSH
- neuroprotektivní látky farmakologie MeSH
- neurosteroidy analogy a deriváty metabolismus farmakologie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
We report as a proof-of-concept the first application of circularly polarized luminescence (CPL) measured with a Raman optical activity (ROA) spectrometer to differentiate several DNA structures without need of sensitizing complexes. The ROA/CPL approach provides sufficiently high CPL intensity to use hydrated Eu3+ ions, thus avoiding DNA structural changes associated with binding of sensitizers and overcoming the sensitizer quenching issue. We showed that deoxyguanosine monophosphate (dGMP), single- and double-stranded DNA provide different CPL spectra, which could be used for their discrimination. Our results demonstrate that ROA/CPL method is a promising approach to measure CPL spectra of complex biomolecules when the use of sensitizers is not possible. The method can be extended to other biomolecules, such as proteins, lipids, sugars, etc.
A unified strategy for the total synthesis of the methyl esters of all phytoprostane (PhytoP) classes bearing two ring-oxygen atoms based on an orthogonally protected common precursor is described. Racemic 16-F1t-, 16-E1-PhytoP and their C-16 epimers, which also occur as racemates in Nature, were successfully obtained. The first total synthesis of very sensitive 16-D1t-PhytoP succeeded, however, it quickly isomerized to more stable, but so far also unknown Δ13-16-D1t-PhytoP, which may serve as a more reliable biomarker for D-type PhytoP. The dioxygenated cyclopentane ring carrying the ω-chain with the oxygen functionality in the 16-position was approached by a radical oxidative cyclization mediated by ferrocenium hexafluorophosphate and TEMPO. The α-chain was introduced by a new copper-catalyzed alkyl-alkyl coupling of a 6-heptenyl Grignard reagent with a functionalized cyclopentylmethyl triflate.