超强激光脉冲下等离子体块的整体加速研究

为了克服激光加速中强流离子束空间电荷效应对粒子输运的影响,提出一种利用两块不同密度的固体靶先后和一束强度约为1022 W/cm2、脉冲长度为5T(T为激光周期)的超强脉冲激光相互作用的方案,实现了中性等离子体块的加速。通过一维PIC数值模拟研究发现,在合适的参数下,加速后的电子与质子几乎以相同的速度共同飞行长达60λ(λ为激光波长)的距离,其中质子与电子的能量分别为GeV和100MeV量级。     

浙江新高考化学加试题难度研究*

在对已有试题难度量化工具进行改进的基础上,建构了化学加试题难度评估工具。对2015年至2019年国家新高考实验区浙江省的8次化学选考加试题的难度进行了量化评价。结果表明,8次化学加试题整卷难度变化较大,但同一学年、有相同学生可能参与的2次化学选考的整体难度相近;加试题能力特征和难度差异明显,“有机化学基础”加试题(第32题)难度相对稳定,而第30题(化学反应原理)与第31题(实验化学)加试题难度却表现出一定的波动性。在对8次化学加试题的难度及相关因素进行分析的基础之上,也对如何提高加试题的编制质量,提出了可行性建议。     

Synthesis and characterization of an unexpected mechanochromicbistricyclic aromatic ene

An unexpected bistricyclic aromatic ene AF was synthesized in a tin(II) chloride-mediated reductive aromatization reaction. The obtained AF showed a highly overcrowded structural conformation as revealed by X-ray crystallography. Interestingly, AF exhibited reversible high-contrast mechanochromism and thermochromism between pale and red color. The obvious chromism is likely ascribed to the conformation transformation and trace amount of diradical species formation upon stimulus.     

Metal-free synthesis of 1,2,3-benzotriazines

The recent molecular iodine catalyzed [1,2]-rearrangement of aryl amines and 3-amino-1H-indazolesfor the synthesis of 1,2,3-benzotriazines is highlighted.     

Enantioselective carboxylative cyclization of propargylic alcohol with carbon dioxide under mild conditions

An enantioselective carboxylative cyclization of propargylic alcohols and CO2 was realized under mild conditions,based on a kinetic resolution strategy,which enabled the synthesis of chiral cyclic carbonates and propargylic alcohols with promising yield and enantioselectivity simultaneously.     

Singlet relaxation dynamics and long triplet lifetimes of thiophene-coupled perylene diimides dyads: New insights for high efficiency organic solar cells

In the active layer of organic solar cells (OSCs), the lifetime of triplet excitons is one of the decisive factors in the diffusion length and therefore has important impact on the power conversion efficiency of the devices. Herein, we have investigated singlet excited state relaxation dynamics and their triplet exciton lifetimes of two thiophene-coupled perylene diimides (PDI) dyads (2PDI-Th and fused-2PDI-Th), in order to provide a unique explanation in depth on their different performances in OSC devices. From the transient absorption (TA) spectra, the singlet excitons of 2PDI-Th form excimers in the time scale of 1.5 ps. Then the excimers go into the triplet state via intersystem crossing (ISC). In fused-2PDI-Th, triplet excitons are generated directly from the singlet excited excitons via the efficient ISC. Density functional theory (DFT) calculations further support the formation of excimers. DFT results indicate that 2PDI-Th exhibits an H-typed molecular configuration which is beneficial to form the excimers, while fused-2PDI-Th gives a twisted X-shaped configuration in the optimized ground and excited state. In steady-state emission spectra, 2PDI-Th shows abroad and featureless spectral characteristics of the excimers with a decay time of 840 ps, which is much shorter than those of PDI (5.5 ns) and fused-2PDI-Th (3.3 ns). The triplet lifetime (67 μs) of fused-2PDI-Th is factor of 3 longer than that of 2PDI-Th (22 μs). These results demonstrate that ring-fused structure is an efficient strategy to eliminate excimer formation and prolong the lifetime of triplet excitons, which provides a new insight for design of optoelectronic molecules for high efficiency organic solar cells.     

品红褪色机理的实验探究

中学阶段常用于检验二氧化硫气体的品红溶液分为酸性品红和碱性品红2种。通过设计集演示、对比于一体的绿色环保二氧化硫性质实验装置,优化实验条件,探讨了酸性品红和碱性品红与SO2、酸碱反应的性质差异及褪色机理,并提出鉴别酸性品红和碱性品红的简便办法。     

铝与碱溶液反应的实验研究

铝与氢氧化钠溶液反应一直以来都是教学的难点,从定量角度证明了该反应的氧化剂,并解释了氢氧根离子在反应中的作用。在此基础上,结合实验表现出的铝与不同碱溶液反应的差异,进一步探讨了几种阳离子对铝与碱溶液反应的影响。     

Ordered Large-Pore MesoMOFs Based on Synergistic Effects of TriBlock Polymer and Hofmeister Ion

Ordered mesoporous metal–organic frameworks (mesoMOFs) were constructed with a uniform pore size up to about 10 nm and thick microporous walls, opening up the possibility for the mass diffusion of large-size molecules through crystalline MOFs. The synergistic effects based on triblock copolymer templates and the Hofmeister salting-in anions promote the nucleation of stable MOFs in aqueous phase and the in situ crystallization of MOFs around templates, rendering the generation of a microcrystal with periodically arranged large mesopores. The improved mass transfer benefiting from large-pore channels, together with robust microporous crystalline structure, endows them as an ideal nanoreactor for the highly efficient digestion of various biogenic proteins. This strategy could set a guideline for the rational design of new ordered large-pore mesoMOFs with a variety of compositions and functionalities and pave a way for their potential applications with biomacromolecules.     

Engineering the Charge-Transfer State to Facilitate Spin–Orbit Charge Transfer Intersystem Crossing in Spirobis[anthracene]diones

Spiro conjugation has been proposed to dictate the efficiency of charge transfer, which could directly affect the spin–orbit charge transfer intersystem crossing (SOCT-ISC) process. However, this process has yet to be exemplified. Herein, we prepared three spirobis[anthracene]diones, in which two benzophenone moieties are locked in close proximity and differentially functionalized to fine-tune the charge transfer state. Its feasibility for SOCT-ISC was theoretically predicted, then experimentally evaluated. Through fine-tuning the spiro conjugation coupling and varying the solvent dielectric constants, ISC rate constants were engineered to vary in a dynamic range of three orders of magnitude, from 7.8×10⁸ s⁻¹ to 1.0×10¹¹ s⁻¹, which is the highest ISC rate reported for SOCT-ISC system to our knowledge. Our findings substantiate the key factors for effective SOCT-ISC and offer a new avenue for the rational design of heavy atom free triplet sensitizers.