Herein, we aim to raise awareness of the capabilities and accessibility of advanced in vitro CNS technologies. We provide an overview of some of the main recent developments (since 2015) in in vitro CNS models. In particular, we focus on engineered in vitro models based on cell culture systems combined with microfluidic platforms (e.g. 'organ-on-a-chip' systems). We delve into the fundamental principles underlying these systems and review several applications of these platforms for the study of the CNS in health and disease. Our discussion further addresses the challenges that hinder the implementation of advanced in vitro platforms in personalized medicine or in large-scale industrial settings, and outlines the existing differentiation protocols and industrial cell sources. We conclude by providing practical guidelines for laboratories that are considering adopting organ-on-a-chip technologies.The ruthenium(ii)-catalyzed cross-coupling reaction between 2-aryl quinazolinones and activated aldehydes is described. This method enables the site-selective hydroxyalkylation under redox-neutral conditions. Moreover, this protocol provides a facile access to various tetracyclic isoindoloquinazolinones by using Cu(OAc)2 as an external oxidant via C-H addition and subsequent intramolecular cyclization. A wide substrate scope and a high level of chemoselectivity as well as broad functional group tolerance are observed.Contactless thermometry with the requirements of high accuracy and high efficiency is an extremely acute need in many fields. Optical thermometers based on the fluorescence intensity ratio (FIR) of the thermally coupled energy levels of Er3+ have been demonstrated to be excellent candidates to afford that due to their advantages of high spatial resolution, rapid response, anti-jamming capability, etc. In this paper, we summarize the recent developments in optical thermometry based on the FIR of the electronic levels Er3+2H11/2/4S3/2 and the Stark sublevels of Er3+4F9/2 and Er3+4I13/2 manifolds, including physical mechanism, improvement of thermometric sensitivity, biological application and so on. Moreover, the challenges in creating novel Er3+-based optical thermometers and potentially new research directions for future work are discussed in detail. Overall, the Er3+-based optical thermometers have exhibited outstanding advantages for non-contact temperature sensing, but great efforts are still needed to improve their key performance indicators for meeting the demands of practical applications.Recently, a new class of lithium chlorides and bromides (e.g., Li3YCl6 and Li3YBr6) were reported to be promising solid-state electrolytes with high ionic conductivity in all-solid-state battery cells. However, their response under mechanical loading is not known which is critical as mechanical properties can play a pivotal role in reducing interfacing resistance between electrolytes and electrodes. To address this issue, herein, we report the thermo-physical properties of these lithium chlorides and bromides using density functional theory calculations. It was found that the new structures possess relatively larger shear moduli than those of thio-phosphate-type solid-state electrolytes and smaller Young's moduli than those of Garnet-type solid-state electrolytes. This suggests that the new halide materials can be more effective in suppressing the formation of lithium dendrites, accommodating volumetric changes of electrode materials and preventing their own degradation. Meanwhile, Poisson's ratio and Pugh's indicator calculations showed that Li3YCl6 and Li3ScCl6 possess improved ductility than other halide candidates, and thus hold promise as solid-state electrolytes. On the other hand, owing to their relatively high thermal conductivities, lithium bromides were found to be more advantageous in conducting heat which is important to ensure safety. These results provide fundamental insights into the mechanical properties of lithium chlorides and bromides and contribute to the rational mechanical design of solid-state electrolytes and the development advanced all-solid-state batteries.A new method for calculating internal conversion rate constants (k[combining low line]IC), including anharmonic effects and using the Lagrangian multiplier technique, is proposed. The deuteration effect on k[combining low line]IC is investigated for naphthalene, anthracene, free-base porphyrin (H2P) and tetraphenylporphyrin (H2TPP). The results show that anharmonic effects are important when calculating k[combining low line]IC for transitions between electronic states that are energetically separated (ΔE) by more than 20 000-25 000 cm-1. Anharmonic effects are also important when ΔE less then 20 000-25 000 cm-1 and when the accepting modes are X-H stretching vibrations with a frequency larger than 2000 cm-1. The calculations show that there is mixing between the S1 and S2 states of naphthalene induced by non-adiabatic interactions. The non-adiabatic interaction matrix element between the S1 and S2 states is 250 cm-1 and 50 cm-1 for the normal and fully deuterated naphthalene structure and this difference significantly affects the estimated fluorescence quantum yield. Besides aromatic hydrocarbons H2P and H2TPP, the k[combining low line]IC rate constant is also calculated for pyrometene (PM567) and tetraoxa[8]circulene (4B) with a detailed analysis of the effect of the vibrational anharmonicity.The volume change and concurrent stress evolution of electrode materials during the cycling of lithium-ion batteries can cause severe mechanical issues such as the fracture of active materials and electrodes, thus leading to safety issues and capacity fading. https://www.selleckchem.com/products/ml323.html Recent years have witnessed a thriving interest to gain a complete understanding of battery electrode materials from the viewpoint of mechanics. This review paper aims at discussing battery electrode materials from a mechanical perspective to provide an overview of the recent innovative efforts in this field. On the one hand, we introduce the mechanical issues of active materials and electrodes in the electrochemical processes, along with a focus on the strategies developed for enhancing the mechanical strength of electrode materials and constructing mechanically robust electrodes. On the other hand, experimental and theoretical studies on the stress-regulated effects on electrochemical processes are discussed to demonstrate the intriguing role of mechanical stress as an enabler in electrochemistry.