In this manuscript, we designed and synthesized three core cross-linked micelles (M-5L, P-5L, and P-5D) with redox-responsive disulfide bonds in the core and carrying optically active helical polyisocyanide arms. Their arms were different in the helicity of the main chain and the chirality of the side groups. These micelles showed excellent redox-responsiveness to reducing agent. However, because of the different chiralities of the arms, the three micelles exhibited different performances in drug delivery and controlled release. The M-5L micelle carrying left-handed helical arms showed better therapeutic effect than the other two due to the rapid cell membrane permeability.
One novel bisferrocene pyrazole derivative, bis [2-(5-trifluoromethyl-3-ferrocenyl) pyrazolyl] methane (abbreviated as (3)), was synthesized and fully characterized. A single crystal of (3) was obtained and solved by X-ray diffraction analysis. The bisferrocene derivative exhibits MLCT (metal to ligand charge transfer) and π→π* transitions in the UV-visible range, which have been verified by density functional theory (DFT) calculations. Its electrochemical properties were studied with the aid of cyclic voltammetry (CV), differential pulse voltammetry (DPV) and rapid scan time-resolved Fourier transform infrared spectroscopy (RS-TRS FT-IR) analysis. Furthermore, the electrochemical mechanism was elucidated based on the results from the cyclic voltabsorptometry (CVA) determination technique. (3) apparently shows a single wave in the cyclic voltammetric experiments which indicates there is no intermediate, however, the intermediate of (3) was observed by employing the RS-TRS FT-IR spectroelectrochemistry technique. The detailed investigation brought us safely to the conclusion that the methylene can also act as a linker, leading to electronic communication in either D-π-D and A-π-A systems.
We present the frequency dependence of microwave-absorbing properties of La 1Ϫx Sr x MnO 3 ͑xϭ0.4, 0.5, 0.6, and 0.7͒ powders at room temperature. The absorbing properties change gradually with x in the frequency range of 8-12 GHz. The optimal absorption can be achieved for a xϭ0.4 sample and its microwave loss peak value is about 25 dB. Further experimental results show that the absorption can be attributed to magnetic and dielectric losses and the microwave loss peak corresponds to the maximum dielectric loss tangent tan ␦ e near 10.5 GHz. Furthermore, the absorbing properties of the oxides mixed with carbonic fiber and Y-type planar hexagonal ferrite have been rudimentarily studied. Results show that these additives greatly enhance the microwave-absorbing properties of the oxides.
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