The oxidation of cis-[Pt(NH3)2(OAc)2] with H2O2 yields a mixture of two isomers: ctc-[Pt(NH3)2(OH)2(OAc)2] and ctc-[Pt(NH3)2(OH)(OAc)(OH)(OAc)]. Following modification with 4-phenylbutyric (PhB) anhydride, two isomers were separated and characterized; the symmetric ctc-[Pt(NH3)2(PhB)2(OAc)2] ( 1 ) and the nonsymmetric ctc-[Pt(NH3)2(PhB)(OAc)(PhB)(OAc)] ( 2 ). They differ in their log P values and despite having similar cellular uptake and similar DNA platination levels, the symmetric ctc-[Pt(NH3)2(OH)2(OAc)2] is more than 4-fold more potent than the nonsymmetric isomer in a panel of 4 cancer cell lines. 相似文献
Plasma Chemistry and Plasma Processing - Non-thermal plasma has been a promising new cancer treatment modality in plasma oncology field. It generates extracellular and intracellular reactive... 相似文献
Methylammonium lead iodide (MAPbI3) perovskite has garnered significant interest as a versatile material for optoelectronic applications. The temperature-dependent photoluminescence (TDPL) and phase-transition behaviors revealed in previous studies have become standard indicators of defects, stability, charge carrier dynamics, and device performance. However, published reports abound with examples of irregular photoluminescence and phase-transition phenomena that are difficult to reconcile, posing major challenges in the correlation of those properties with the actual material state or with the subsequent device performance. In this paper, a unifying explanation for the seemingly inconsistent TDPL and phase-transition (orthorhombic-to-tetragonal) characteristics observed for MAPbI3 is presented. By investigating MAPbI3 perovskites with varying crystalline states, ranging from polycrystal to highly oriented crystal as well as single-crystals, key features in the TDPL and phase-transition behaviors are identified that are related to the extent of crystal domain-size-dependent residual stress and stem from the considerable volume difference (ΔV ≈ 4.5%) between the primitive unit cells of the orthorhombic (at 80 K) and tetragonal phases (at 300 K) of MAPbI3. This fundamental connection is essential for understanding the photophysics and material processing of soft perovskites. 相似文献
Today’s era is the era of smart and remote applications exploiting advancement in sensors, cloud, Internet of things etc. Major application is in healthcare monitoring and support using wireless body area network (WBAN) in which sensor nodes sense vital physiological parameters and send to server through sink i.e. smart phone nowadays for seamless monitoring. The most significant issue in such applications is energy efficiency which leads to enhanced network life time that ensures uninterrupted seamless services. From source to sink data transmission may occur considering three different scenarios: source to sink single hop direct data transmission irrespective of in-between node distance, source to sink multi hop data transmission in which transmission range of source node is fixed at a threshold to find next forwarder node and transmission range of source node is incremented by affixed value until data gets transmitted to sink. In this work WBAN having different network configurations based on fixed or random positions of nodes have been simulated. Different scenarios with fixed and varying number of nodes are framed and simulated using MATLAB 2020a for performance evaluation of proposed algorithm in terms of energy consumption, network lifetime, path loss etc. due to data transmission from source to sink. Experimental results show that incremental approach is better than direct one in terms of energy consumption, path loss and network lifetime. While selecting transmission range of a source node, it is considered to keep Specific Absorption Rate (SAR) lower to reduce impact on human tissue.
We investigate the nonlinear optical (NLO) polarizations for various geometric arrangements of the dipolar chromophores in a calix[n]arene geometry. The interactions were studied by using (HF)3 as model compounds both in parallel and frustrated orientations. The interdipolar angle between the monomer molecules is varied so that many different arrangements of the dipoles can be realized which is associated with the opening up of the calix[n]arene rings. Quantum-chemical calculations at both ab initio and semiempirical levels, show that the all-parallel arrangement of the dipoles exhibit the maximum magnitude for the nonlinear optical coefficients at small interdipolar angles for all interdipolar distances. In the frustrated orientations however, the NLO response is maximum at large interdipolar angles corresponding to the flattened calix[n]arene rings. The role of hydrogen bonding in stabilizing these assemblies in various conformations has been investigated. Crystallographic database analysis for calix[3]arenes shows that optical properties in real molecular systems can be modeled based on our simple interaction theory. 相似文献
Thermal plasma discharges have been widely used in the past for treatment of living human and animal tissue. However, extensive thermal damage and tissue desiccation occurs due to extreme temperatures. Some solutions have been offered where the temperature is lowered by short current pulses, addition of noble gases, or significant decrease in the size of treatment electrodes. We propose a method of direct treatment of living tissue that occurs at room temperature and pressure without visible or microscopic tissue damage. The presented Floating-Electrode Dielectric Barrier Discharge plasma is proven electrically safe to human subjects and our results show no gross (visual) or histological (microscopic) damage to skin samples in minutes, complete tissue sterilization from skin flora in seconds, and blood clot formation in seconds of electric plasma treatment. We also observe significant hastening of blood clot formation via electric plasma induced catalysis of “natural” processes occurring in human blood. A model describing these processes is offered.An erratum to this article can be found at 相似文献
Quantum chemical calculations on the linear and nonlinear electric polarizabilities of dipolar molecules separated by the alkyl spacers have been performed on O(2)N-Ph-N=N-Ph-(CH(2))(n)-Ph-N=N-Ph-NO(2), n = 1-12. These molecules exhibit a very strong odd-even behavior in the first hyperpolarizabilities (beta), with large (small) beta for n = odd (n = even). Such odd-even oscillations have been reported experimentally on similar systems, but the origin of such phenomena remains unclear. We propose it to be due to the role of the conformational orientation of the intervening alkyl spacers that leads to eclipsed orientation (parallel) of the dipoles for n = odd chains while staggered orientation (antiparallel) for n = even chains. The energy difference between the two extreme angular forms is approximately 6-8 kcal/mol, clearly more than the thermal fluctuations at room temperature. These conformational orientations will be preserved, leading to different packing arrangements at the macroscopic scale. We believe that it is this interaction at the molecular scale that controls such a macromolecular property. 相似文献