We report on the influence of spin-orbit coupling (SOC) in Fe-based superconductors via application of circularly polarized spin and angle-resolved photoemission spectroscopy. We combine this technique in representative members of both the Fe-pnictides (LiFeAs) and Fe-chalcogenides (FeSe) with tight-binding calculations to establish an ubiquitous modification of the electronic structure in these materials imbued by SOC. At low energy, the influence of SOC is found to be concentrated on the hole pockets, where the largest superconducting gaps are typically found. This effect varies substantively with the k_{z} dispersion, and in FeSe we find SOC to be comparable to the energy scale of orbital order. These results contest descriptions of superconductivity in these materials in terms of pure spin-singlet eigenstates, raising questions regarding the possible pairing mechanisms and role of SOC therein.

No abstract

We described the first total syntheses of clausenapin, indizoline, claulansine M, and a novel synthetic route to clausenaline D via divergent method. Key steps involved TFAA-mediated intramolecular acylation to construct the carbazole core and subsequent Claisen rearrangement to generate key intermediates for further elaboration to target molecules.

No abstract

Nowadays, traditional sunscreen molecules face many adverse problems: single energy relaxation pathway, lack of adequate UVA light protection, and therefore no longer meeting the growing demand for UVA protection. In this work, we reported a novel sunscreen molecule (E)-3-(5-bromofuran-2-yl)-1-(2-hydroxyphenyl)­prop-2-en-1-one (hereinafter referred to as FPPO-HBr) which tackled adverse problems of traditional sunscreen molecules as single energy relaxation pathway, lacking effective UVA light protection. Various nonradiative pathways were proposed and verified by combining the steady-state and femtosecond transient absorption (FTA) spectroscopy and theoretical calculation. Upon UV excitation, the FPPO-HBr mainly decays via excited-state intramolecular proton transfer (ESIPT) followed by conformation twist in ultrafast manner. Importantly, 1H NMR spectra proved that the FPPO-HBr could not undergo trans–cis photoisomerization. Additionally, excellent photostability was also observed for newly synthesized FPPO-HBr. The current work could provide new perspectives for sunscreen molecules synthesis and mechanism.