ON THE CAUCHY PROBLEM FOR AW-RASCLE SYSTEM WITH LINEAR DAMPING

The existence of global BV solutions for the Aw-Rascle system with linear damping is considered.In order to get approximate solutions we consider the system in Lagrangian coordinates,then by using the wave front tracking method coupling with and suitable splitting algorithm and the ideas of[1]we get a sequence of approximate solutions.Finally we show the convergence of this approximate sequence to the weak entropic solution.     

How do molecular interactions affect fluorescence behavior of AIEgens in solution and aggregate states?

Molecular interactions are crucial in diverse fields of protein folding,material science,nanotechnology,and life origins.Although mounting experimental research controls luminescent behavior by adjusting molecular interactions in light-emitting materials,it remains elusive to correlate microscopic molecular interactions with macroscopic luminescent behavior directly.Here,we synthesized three red luminogens with subtle structural variation and investigated the influence of molecular interactions on their luminescent behavior in solution and aggregate states.Our results indicate that strongπ-πand D-A interactions in both dilute solution(between luminogen and solvent molecules)and aggregate(between luminogens)states cause the redshift in emission,while weak interactions(e.g.,Van der Waals,C–H…π,and C–H…F interactions)enhance the quantum yield.This work provides a thoughtful investigation into the complicated influence of various molecular interactions on luminescent behavior.     

Molecular-level Engineering of S-scheme Heterojunction: the Site-specific Role for Directional Charge Transfer

The promising S-scheme heterojunction photocatalysts are considered as a novel frontier due to their superiority in various solar-driven energy-related applications. Recently, a novel atom-specific tailoring strategy has been introduced on the construction of S-scheme heterojunction for promoting the electronic transferability. The S-scheme heterojunction is regulated by integrating high-crystalline carbon nitride with Co-doped Ce O₂. Specifically, this atom-specific regulation of S-s...     

Stereoselective interactions of chiral dipeptides on amylose based chiral stationary phases

Dipeptides are stereo-specifically involved in several biological functions that are challenging to separate enantiomerically. Elution order of enantiomers is an important issue in chiral chromatography. Amylose tris-(3,5-dimethylphenylcarbamate) chiral stationary phase(CSP) is the best and most-widely-used CSP in chiral separations, but experimental data of enantiomeric separation of dipeptides on this CSP is lacking. Simulation studies were conducted to determine the order of elution and the chiral recognition mechanism of didpetides on this CSP. Results indicated that the docking energy of SR-enantiomers were higher than SS-antipodes. The range of docking energies for SR-enantiomers was -7.44 to -5.92 kcal/mol with CSP, but -7.15 to -5.87 kcal/mol for SS-stereoisomers. Therefore it is predicted that SS-enantiomer will elute first, followed by SR-antipode. Furthermore, hydrogen bondings, van der Waal’s interactions and electrostatic interactions were observed among SR- and SSenantiomers and chiral grooves of CSP. The number of hydrogen bonds was one in each enantiomer binding except S-Ala-R-Tyr, which contained two hydrogen bonds. No hydrogen bond was found in S-Ala-R-Trp, S-Leu-S-Trp, and S-Leu-S-Tyr dipeptides bindings. The chiral recognition mechanisms dictate different strengths of stereoselective bindings of the enantiomers on CSP.     

CR Geometry in 3-D

CR geometry studies the boundary of pseudo-convex manifolds.By concentrating on a choice of a contact form,the local geometry bears strong resemblence to conformal geometry.This paper deals with the role conformally invariant operators such as the Paneitz operator plays in the CR geometry in dimension three.While the sign of this operator is important in the embedding problem,the kernel of this operator is also closely connected with the stability of CR structures.The positivity of the CR-mass under the natural sign conditions of the Paneitz operator and the CR Yamabe operator is discussed.The CR positive mass theorem has a consequence for the existence of minimizer of the CR Yamabe problem.The pseudo-Einstein condition studied by Lee has a natural analogue in this dimension,and it is closely connected with the pluriharmonic functions.The author discusses the introduction of new conformally covariant operator P-prime and its associated Q-prime curvature and gives another natural way to find a canonical contact form among the class of pseudo-Einstein contact forms.Finally,an isoperimetric constant determined by the Q-prime curvature integral is discussed.     

Recovery of Immersions from Their Metric Tensors and Nonlinear Korn Inequalities: A Brief Survey

The authors discuss the existence and uniqueness up to isometries of Enof immersions φ : Ω  R~n→ E~n with prescribed metric tensor field(g ij) : Ω→ S~n, and discuss the continuity of the mapping(gij) →φ defined in this fashion with respect to various topologies. In particular, the case where the function spaces have little regularity is considered. How, in some cases, the continuity of the mapping(gij) →φ can be obtained by means of nonlinear Korn inequalities is shown.     

新型哌啶-查尔酮类衍生物的设计、合成及抗宫颈癌和逆转顺铂耐药活性

本文采用活性亚结构拼接原理,设计并合成了15个新型含哌啶的查尔酮类衍生物,利用¹H NMR、¹³C NMR和HR-MS对结构进行表征,并初步评价了其抗宫颈癌和抗顺铂耐药宫颈癌活性作用。结果表明,化合物6g具有一定的抗肿瘤活性和逆转顺铂耐药作用;并采用Elisa法、联合顺铂用药、Western Blot和分子对接对化合物6g与VEGFR-2和P-gp靶点进行了初步的研究。本研究为基于VEGFR-2和P-gp双靶点新型分子靶向查尔酮类衍生物的设计提供了一条思路。     

Comonotone approximation with interpolation at the ends on an interval

Let a function f ∈ C[-1, 1], changes its monotonisity at the finite collection Y := {y1,… ,ys} of s points yi ∈ (-1, 1). For each n ≥ N(Y), we construct an algebraic polynomial Pn, of degree ≤ n, which is comonotone with f, that is changes its monotonisity at the same points yi as f, and |f(x)-Pn(x)|≤c(s)ω2(f,(√1-x2)/n), x∈[-1,1],where N(Y) is a constant depending only on Y, c(s) is a constant depending only on s and ω2 (f, t) is the second modulus of smoothness of f.     

Restriction of Intramolecular Motion(RIM): Investigating AIE Mechanism from Experimental and Theoretical Studies

Mechanistic studies promote scientific development from phenomena to theories.Aggregation-induced emission(AIE),as an unusual photophysical phenomenon,builds the bridge between molecular science and aggregate mesoscience.With the twenty-year development of AIE,restriction of intramolecular motion(RIM)has been verified as the working mechanism of AIE effect.In this review,these mechanistic works about RIM are summarized from experimental and theoretical perspectives.Thereinto,the experimental studies are introduced from three parts:external rigidification,structural modification and structural characterization.In the theoretical part,calculations on the low-frequency motion of AIEgens have been performed to prove the RIM mechanism.By virtue of the theoretical calculations,some new mechanisms are proposed to supplement the RIM,such as restriction of access to conical intersection,suppression of Kasha transition,restriction of access to dark state,etc.It is foreseeable that the RIM mechanism will unify the photophysical theories for both molecules and aggregates,and inspire more progress in aggregate science.