A classification of continuous wavelet transforms in dimension three

This paper presents a full catalogue, up to conjugacy and subgroups of finite index, of all matrix groups $H<\mathrm{GL}(3,\mathbb{R})$ that give rise to a continuous wavelet transform with associated irreducible quasi-regular representation. For each group in this class, coorbit theory allows to consistently define spaces of sparse signals, and to construct atomic decompositions converging simultaneously in a whole range of these spaces. As an application of the classification, we investigate the existence of compactly supported admissible vectors and atoms for the groups.     

Using block designs in crossing number bounds

The crossing number $\mathrm{\text{CR}}\left(G\right)$ of a graph $G=\left(V,E\right)$ is the smallest number of edge crossings over all drawings of $G$ in the plane. For any $k\ge 1$, the $k$‐planar crossing number of $G,{\mathrm{\text{CR}}}_k\left(G\right)$, is defined as the minimum of $\text{CR}\left(G_1\right)+\text{CR}\left(G_2\right)+?+\text{CR}\left(G_k\right)$ over all graphs $G_1,G_2,\dots ,G_k$ with ${\cup }_{i=1}^k{G}_i=G$. Pach et al [Comput. Geom.: Theory Appl. 68 (2018), pp. 2–6] showed that for every $k\ge 1$, we have ${\text{CR}}_k\left(G\right)\le (2/k^2?1/k^3)\text{CR}\left(G\right)$ and that this bound does not remain true if we replace the constant $2/k^2?1/k^3$ by any number smaller than $1/k^2$. We improve the upper bound to $(1/k^2)\left(1+o\left(1\right)\right)$ as $k\to \infty$. For the class of bipartite graphs, we show that the best constant is exactly $1/k^2$ for every $k$. The results extend to the rectilinear variant of the $k$‐planar crossing number.     

联保贷款中的策略性违约规避机制设计

针对联保贷款的策略性违约问题,通过对其产生原因的分析以及对现有文献中解决措施的探讨,设计了一个弹性联保贷款合约。该合约的特点在于,随着企业愿意承担的连带责任的增加,企业可获得的期望收益也随之增加,旨在从正面激励企业主动为同伴承担还款责任,达到规避策略性违约的目的。通过数值分析验证了该弹性合约的特性以及适用范围。并进一步在两企业模式基础上进行拓展,讨论了多于两企业的情况下该弹性合约的适用条件。     

Ligand Design to Acquire Specificity to Intended G-Quadruplex Structures

A G-quadruplex is a nucleic acid secondary structure that is adopted by guanine-rich sequences, and is considered to be relevant in various pharmacological and biological contexts. G-Quadruplexes have also attracted great attention in the field of DNA nanotechnology because of their extremely high thermal stability and the availability of many defined structures. To date, a large repertory of DNA/RNA G-quadruplex-interactive ligands has been developed by numerous laboratories. Several relevant reviews have also been published that have helped researchers to grasp the full scope of G-quadruplex research from its outset to the present. This review focuses on the G-quadruplex ligands that allow targeting of specific G-quadruplexes. Moreover, unique ligands, successful methodologies, and future perspectives in relation to specific G-quadruplex recognition are also addressed.     

X-ray photoelectron spectroscopy and Raman microscopy of a ferroan platinum crystal from the Kondyor Massif,Russian Far East

X-ray Photoelectron Spectroscopy was used to study a ferroan platinum crystal from the Kondyor Massif, Russian Far East. Prior to the X-ray Photoelectron Spectroscopic analyses, the nature of the crystal was confirmed by X-ray diffraction. The survey scan showed mainly the presence of Pt and Fe, with smaller amounts of O and Si. The high resolutions spectra of the Pt 4f and Fe 2p showed 18.3 atom% Fe in the crystal, which puts the composition on the lower boundary for ferroan platinum and confirms earlier analyses using other methods such as Scanning Electron Microscopy-Energy Dispersive X-ray analysis/microprobe. The binding energy of the Pt 4f5/2 was 74.0?eV and Pt 4f7/2 70.5?eV, while the Fe 2p3/2 for metallic Fe was observed at 707.2?eV. The Fe 2p3/2 for metallic Fe was significantly sharper than that of Fe 2p3/2 at 710.7?eV associated with surface material. The Raman spectrum was dominated by the Pt–Pt stretching mode at 253?cm^?1. Changed orientation resulted in the observation of two bands at 127 and 139?cm^?1, interpreted as being due to stretching modes of two Pt–Pt bonds with the third bond to Fe and Pt fixed. The presence of Ca-Fe-Al-Mg-Si-O on the surface was probably associated with the presence of a clinopyroxene. These minerals can be expected since the crystal came originally from a clinopyroxenite-dunite matrix. The spectra showed a variety of interferences, e.g. Al 2p with Pt 4f, Mg 2p with Fe 3p, and Ca 2p1/2 with Mg Auger, making exact determinations of the ratios of these elements difficult.     

Lipid Switches: Stimuli-Responsive Liposomes through Conformational Isomerism Driven by Molecular Recognition

Advancements in the field of liposomal drug carriers have culminated in greatly improved delivery properties. An important aspect of this work entails development of designer liposomes for release of contents triggered by environmental changes. The majority of these systems are driven by chemical reactions in the presence of different stimuli. However, a promising new paradigm instead focuses on molecular recognition events as the impetus for content release. In certain cases, these platforms exploit synthetic lipid switches designed to undergo conformational changes upon binding to target ions or molecules that perturb membrane assembly, thereby triggering cargo release. Examples of this approach reported thus far showcase how rational design of lipid switches can result in dramatic changes in lipid assembly properties. These strategies show great promise for opening up new pathophysiological stimuli that can be harnessed for programmed content release in drug delivery applications.     

Interaction between the end groups and the main chain of conjugated polymers by time-resolved EPR and fluorescence spectroscopy

ABSTRACT

Interaction between a zinc porphyrin (ZnPor) as the end-group and poly(9,9-di-n-octylfluorene-2,7-vinylene) (PFV) as the main chain in a porphyrin end-modified fluorescent conjugated polymer, ZnPFV, was studied by time-resolved electron paramagnetic resonance (EPR) and fluorescence spectroscopy. While fluorescence from the PFV part of ZnPFV showed a spectral profile almost identical to that of a PFV oligomer without end-modification, the emission spectrum of the ZnPor part exhibited a much broader profile compared to that of the reference zinc porphyrin monomer. Based on the analysis of lifetimes and quantum yields, it was found that radiative rate constant of the ZnPor part was enhanced by nearly three times. The observed unusual enhancement in the radiative rate constant was rationalised in terms of a partial π-conjugation between the end group and the main chain, as a result of co-planarisation in fluid solution. On the other hand, the time-resolved EPR spectrum of ZnPFV at 100?K basically showed a similar spectral pattern to that of the reference zinc porphyrin, but with significant differences in zero-field spitting parameters and initial population ratios. The π-system of the excited triplet state is deduced to deviate from D_4h symmetry in the end zinc porphyrin groups. The obtained results show that interaction of the porphyrin end group with the main chain of the polymer significantly influences the excited singlet state properties of the porphyrin, while its triplet state properties were affected to a lesser extent.