Photoredox-Mediated Reaction of gem-Diborylalkenes: Reactivity Toward Diverse 1,1-Bisborylalkanes

The use of gem-diborylalkenes as radical-reactive groups is explored for the first time. These reactions provide an efficient and general method for the photochemical conversion of gem-diborylalkenes to rapidly access 1,1-bisborylalkanes. This method exploits a novel photoredox decarboxylative radical addition to gem-diborylalkenes to afford α-gem-diboryl carbon-centered radicals, which benefit from additional stability by virtue of an interaction with the empty p-orbitals on borons. The reaction offers a highly modular and regioselective approach to γ-amino gem-diborylalkanes. Furthermore, EPR spectroscopy and DFT calculations have provided insight into the radical mechanism underlying the photochemistry reaction and the stability of the bis-metalated radicals, respectively.     

Harmonic Mode-Locked Er-Doped Fiber Laser by Evanescent Field-Based MXene Ti3C2Tx (T = F,O, or OH) Saturable Absorber

MXenes, as a legendary family of 2D van der Waals nanosheets materials, are extensively studied due to their unique characteristics of broadband nonlinear optical response. In particular, MXenes have excellent nonlinear optical properties of very large nonlinear absorption coefficients and very large nonlinear refractive indexes, which have attracted people's great attentions to study the application of MXenes in photonics, electronics, and optoelectronics in recent years. However, the high-repetition-rate (HRR) ultrafast pulses are not explored based on these kinds of materials. MXene Ti₃C₂T_x saturable absorber (SA) based on micro-fiber is fabricated by optical deposition method. Here, MXene Ti₃C₂T_x SA is used to achieve 36th harmonic mode-locking with a repetition rate of 218.4 MHz, a central wavelength of 1566.9 nm, the pulse width of 850 fs, and the spectral width of 3.51 nm. The maximum average output power and pulse energy are 6.95 mW and 0.032 nJ, respectively. This research based on MXene Ti₃C₂T_x light modulator opens a bright avenue for advanced nonlinear photonics.     

n一Si霍耳样品的制备及其性能参数测试

本文介绍ｎ－Ｓｉ霍耳样品的制备及其主要性能参数的测试原理与测试方法，并给出部分测试结果。     

一种检测麻痹性贝毒的高效液相色谱法

提出了一种利用高效液相色谱法同时分析麻痹性贝毒GTX组分和NEO/dcSTX/STX组分的方法。本法仅使用了一种缓冲溶液作为流动相,在InertsilC8-3色谱柱(250mm×4.6mm,5μm)上,采用梯度改变乙腈在流动相中的比例和流速,一次进样可同时定性及定量待测试样中的上述全部毒素组分。该缓冲溶液为9.0mmol/L磷酸铵缓冲溶液(pH=7.2),含有2.8mmol/L的庚烷磺酸钠。色谱分离过程首先以纯水相缓冲溶液进行等度洗脱,在16.5~19min向流动相中梯度加入1.5%的乙腈,加速GTX3和GCX2的洗脱,以避免GTX2的色谱峰与乙腈的溶剂峰重叠,随后从19min开始加大流动相中乙腈的比例为8.5%,以缩短边缘组分的保留时间。荧光检测器的激发波长和发射波长分别设为330nm和390nm。用本方法分析染毒的华贵栉孔扇贝和近江牡蛎,证实了本方法对PSP毒素具有良好的分析测定效果。     

Protonation and deprotonation of hydroxamic acids. An MO ab initio study

Ab initio molecular orbital calculations with 4-31G//4-31G, 6-31G^*//4-31G and 6-31+G//4-31G basis sets have been used to examine the structure, relative energy, protonation and deprotonation of a series of seven hydroxamic acids in the gas phase. The results show that hydroxamic acids are predominantly in the E-TS form and that the most probable protonation site is the carbonyl oxygen atom, while deprotonation proceeds by loss of NH hydrogen.     

Supramolecular Vesicles Based on Water‐Soluble 2,6‐Helic[6]arene: High Affinity Binding,Stimuli Responsiveness and Delivery of Doxorubicin to Cancer Cells

Water‐soluble 2,6‐helic[6]arene was used to construct supramolecular vesicles via host‐guest interaction. Water‐soluble 2,6‐helic[6]arene was discovered to be high affinity host for suitable biomarkers. Supramolecular vesicles were responsive to multiple stimuli types, including temperature, pH, Ca²⁺, CO₂ bubbling and biomarker displacement. Supramolecular vesicles were used to load and deliver anti‐ tumor drug doxorubicin to HeLa cells in vitro.     

Alkyl-chain branched effect on the aggregation and photophysical behavior of polydiarylfluorenes toward stable deep-blue electroluminescence and efficient amplified spontaneous emission

Robust branched polydiarylfluorenes are constructed forstable deep-blue electroluminescence and efficient amplified spontaneous emission.     

Charge transport in photofunctional nanoparticles self-assembled from zinc 5,10,15,20-tetrakis(perylenediimide)porphyrin building blocks

Molecules designed to carry out photochemical energy conversion typically employ several sequential electron transfers, as do photosynthetic proteins. Yet, these molecules typically do not achieve the extensive charge transport characteristic of semiconductor devices. We have prepared a large molecule in which four perylene-3,4:9,10-tetracarboxydiimide (PDI) molecules that both collect photons and accept electrons are attached to a central zinc 5,10,15,20-tetraphenylporphyrin (ZnTPP) electron donor. This molecule self-assembles into ordered nanoparticles both in solution and in the solid-state, driven by van der Waals stacking of the PDI molecules. Photoexcitation of the nanoparticles results in quantitative charge separation in 3.2 ps to form ZnTPP(+)PDI(-) radical ion pairs, in which the radical anion rapidly migrates to PDI molecules that are, on average, 21 A away, as evidenced by magnetic field effects on the yield of the PDI triplet state that results from radical ion pair recombination. These nanoparticles exhibit charge transport properties that combine important features from both photosynthetic and semiconductor photoconversion systems.     

稀土对表面组装用Sn2.0Ag0.7CuRE钎料合金组织与性能的影响

对真空条件下制备的Sn2.0Ag0.7CuRE钎料合金显微组织、力学及物理性能进行了研究。结果表明:当稀土(RE)的添加量小于0.1%(质量分数)时,RE均匀地分布在钎料合金中,除铺展面积和延伸率与Sn37Pb钎料相当外,Sn2.0Ag0.7CuRE钎料合金的拉伸强度和导电性能均高于传统的Sn37Pb钎料;当RE添加量达到0.5%时,钎料合金中出现了明显的梅花状和点状RE化合相且弥散分布于晶界和相界附近,且拉伸强度、延伸率和铺展面积都出现了不同程度的下降。从综合性能和制造成本考虑,真空条件下制备Sn2.0Ag0.7CuRE钎料合金,RE的添加量应不大于0.1%。     

Magnetization dynamics in arrays of strongly interacting magnetic nanocrystals

Arrays of 6.6 nm iron oxide nanocrystals coated with fatty acid molecules were produced using the Langmuir-Blodgett technique. The arrays had a varying number of layers stacked together, going from two dimensional to three dimensional and two different in-plane interparticle separations. While temperature-dependent ac susceptibility measurements of the isolated nanocrystals obeyed the Neel-Brown relaxation law, the array relaxation deviated significantly from this simple law. This deviation together with the observed dc field influence on the susceptibility-temperature curves, the large shifts in blocking temperatures and reduction in susceptibility-temperature curve widths on going from isolated particles to the arrays indicated collective magnetization dynamics during magnetization freezing. A scaling law analysis of this freezing dynamics yielded different powers for the two different interparticle separations with no dependence on dimensionality. In spite of the spin-glass-like behavior, it is possible that small, magnetically ordered domains of nanocrystals form at low temperature.