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排序方式: 共有1458条查询结果,搜索用时 15 毫秒
31.
32.
Lu W Mi BX Chan MC Hui Z Che CM Zhu N Lee ST 《Journal of the American Chemical Society》2004,126(15):4958-4971
The synthesis and structural, photophysical, electrochemical, and electroluminescent properties of a class of platinum(II) complexes bearing sigma-alkynyl ancillary ligands, namely [(C/N/N)Pt(C[triple bond]C]nR] [H(C/N/N) = 6-aryl-2,2'-bipyridine; n = 1-4; R = aryl, alkyl, or trimethylsilyl], have been studied. Substituents with different steric and electronic properties were introduced into the tridentate cyclometalating and arylacetylide ligands, and the pi-conjugation length of the oligoynyl moiety was homologously extended from ethynyl to octatetraynyl. The X-ray crystal structures of several derivatives confirm the Pt-(CC) ligation and reveal various intermolecular interactions, such as pi-pi, Pt...Pt, and C-H...F-C. The complexes display good thermal stability and intense phosphorescence in fluid and glassy solutions with high quantum yields and microsecond lifetimes. Their emission energies are sensitive to solvent polarity, the electronic affinities of the substituents on both the cyclometalating and arylacetylide groups, and the length of the oligoynyl ligand. By choosing appropriate cyclometalating and sigma-alkynyl ligands, the emission color of this class of platinum(II) complexes can be tuned from green-yellow to saturated red. In addition to (3)MLCT [Pt(5d) --> pi*(C/N/N)] and (3)IL(C/N/N), intriguing (3)IL(alkynyl) excited states localized on -(C[triple bond]C)(4)- and -(C[triple bond]Cpyrenyl-1) moieties that afford narrow-bandwidth emissions have been observed. Selected Pt(II) complexes were doped into the emissive region of multilayer, vapor-deposited organic light-emitting diodes. The tunable electrophosphorescence energy resembles that recorded in fluid solutions for these emitters, and the devices exhibit high luminance and efficiencies (up to 4.2 cd A(-1)). 相似文献
33.
The interactions of [Pt(CNN)(4-dpt)]PF(6), (1; 4-dpt=2,4-diamino-6-(4-pyridyl)-1,3,5-triazine, HCNN=6-phenyl-2,2'-bipyridine) with double-stranded DNA, poly(dA-dT)(2), and poly(dG-dC)(2) were examined by spectroscopic, electrophoretic, and hydrodynamic methods. The spectroscopic data were analyzed with McGhee, van't Hoff, and Gibbs-Helmholtz equations. In a comparative study, [Pt(CNN)(py)]PF(6) (2; py=pyridine) was prepared and the nature of its binding towards DNA was investigated [preliminary results: ChemBioChem 2003, 4, 62-68]. For reactions with calf thymus DNA at 20 degrees C, the intrinsic binding constants for 1 and 2 are (4.6+/-0.2)x10(5) and (2.3+/-0.3)x10(4) mol(-1) dm(3), respectively. Results of DNA-binding reactions revealed that 1 and 2 preferentially bind to the AT sequence of duplex DNA. Intercalation is the preferred binding mode for 2, whereas both intercalation and minor-groove binding are observed for 1. Complex 1 is cytotoxic against a number of carcinoma cell lines, including KB-3-1, CNE-3, and HepG2, and remains potent against multidrug- or cisplatin-resistant KB-V-1 and CNE1 cell lines, for which the resistance ratios are 1.6 and 1.5, respectively. Importantly, 1 is almost an order of magnitude less toxic to the normal cell line CCD-19Lu (IC(50)=176+/-1.7 microM) and it selectively induced apoptosis leading to cancer cell death with less than 5 % detectable necrosis. 相似文献
34.
Diode-pumped Nd:LGS intracavity-doubled green laser at 532 nm 总被引:1,自引:0,他引:1
It is reported that efficient continuous-wave (CW) green laser generation at 532 nm in a KTP crystal at type-II phase matching
direction performed with a diode-pumped Nd:LGS laser. With incident pump power of 18.2 W, output power of 2.68 W at 532 nm
has been obtained using a 5 mm-long KTP crystal. The optical conversion efficiency was up to 14.7%. At the output power level
of 2.68 W, the output stability is better than 3.5%. The beam quality M
2 values were equal to 1.33 and 1.19 in X and Y directions, respectively. 相似文献
35.
为了解决运动参数光电探测过程中的相机标定问题,制作一种两端及中间各安装一个红外反光标记球的一维标定物.不需要其它复杂标定装置,只要将这种特制的一维标定物在测量空间内多次随意移动并摄取其图像,即可实现标定.算法首先假定主点位于像面中心附近的某个位置,再求出焦距、旋转矩阵、平移向量和比例因子,最后通过评价函数将相机标定转换成寻找两相机最佳主点对的非线性最小化问题.在传统进化策略中引进个体的自我改进系数、个体间距离等概念,提出了求取子代个体间的欧式距离并排序的方法,设计了搜索最佳主点对的改进型进化策略算法.与传统标定方法相比,基于一维标定物的方法克服了多相机场合的遮挡问题,改进进化策略的引入打破了一维标定物需做某种特殊运动的限制,使一维标定物自由运动时相机内、外参数的同时求解成为可能,改进的模拟退火进化策略改善了算法的全局收敛性能并加快了收敛速度. 相似文献
36.
We develop a model of CA3 neurons embedded in a resistive array to mimic the effects of electric fields from a new perspective. Effects of DC and sinusoidal electric fields on firing patterns in CA3 neurons are investigated in this study. The firing patterns can be switched from no firing pattern to burst or from burst to fast periodic firing pattern with the increase of DC electric field intensity. It is also found that the firing activities are sensitive to the frequency and amplitude of the sinusoidal electric field. Different phase-locking states and chaotic firing regions are observed in the parameter space of frequency and amplitude. These findings are qualitatively in accordance with the results of relevant experimental and numerical studies. It is implied that the external or endogenous electric field can modulate the neural code in the brain. Furthermore, it is helpful to develop control strategies based on electric fields to control neural diseases such as epilepsy. 相似文献
37.
利用光纤布拉格光栅方程和光纤基模有效折射率随纤芯半径和环境折射率的函数关系, 建立了微纳光纤布拉格光栅(MNFBG)反射波长随环境折射率变化的数学模型, 给出了波长灵敏度函数, 并指出MNFBG反射波长的变化规律决定于有效折射率随纤芯半径和环境折射率变化的关系. 详细探究了有效折射率及其灵敏度的变化规律, 结果表明: 有效折射率随纤芯半径和环境折射率的减小而非线性减小, 其对环境折射率变化的灵敏度随环境折射率的增大而非线性增加, 而且随纤芯半径减小, 有效折射率的灵敏度、线性度以及线性响应范围均呈递增规律. 通过对纤芯半径为0.5 μm的MNFBG在1.20–1.30和1.33–1.43 环境折射率范围内的波长响应关系拟合, 分别获得了477.33 nm/RIU和856.30 nm/RIU的波长灵敏度以及99.58 %和99.7%的高线性度, 论证了分析结论以及折射率区间划分测量方案的正确性, 为MNFBG折射率传感器的设计、优化以及应用提供了参考依据.
关键词:
微纳光纤
光纤布拉格光栅
折射率传感
数值模拟 相似文献
38.
Dr. Yungen Liu Dr. Chun-Wai Tse Dr. Kar-Yee Lam Dr. Xiao-Yong Chang Dr. Xiangguo Guan Meng-Yao Chao Dr. Jie-Sheng Huang Prof. Dr. Chi-Ming Che 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(46):10828-10833
Ruthenium(II) complexes bearing a tridentate bis(N-heterocyclic carbene) ligand reacted with iminoiodanes (PhI=NR) resulting in the formation of isolable ruthenium(III)–amido intermediates, which underwent cleavage of a C−N bond of the tridentate ligand and formation of an N-substituted imine group. The RuIII–amido intermediates have been characterized by 1H NMR, UV/Vis, ESI-MS, and X-ray crystallography. DFT calculations were performed to provide insight into the reaction mechanism. 相似文献
39.
40.
Hsu‐Feng Lee Po‐Hsun Wang Yi‐Chiang Huang Wen‐Hung Su Ram Gopal Chun Che Lee Steven Holdcroft Wen‐Yao Huang 《Journal of polymer science. Part A, Polymer chemistry》2014,52(18):2579-2587
A series of sterically‐encumbered, sulfonated, poly(arylene ether) copolymers were synthesized and their proton conductivity examined. The series was prepared by copolymerizing a novel monomer, 2″,3″,5″,6″‐tetraphenyl‐[1,1′:4',1″:4″,1″':4″',1″″‐quinquephenyl]‐4,4″″‐diol, with 4,4'‐difluorobenzophenone and bisphenol A. Subsequent sulfonation and solution casting provided membranes possessing ion exchange capacities of 1.9 to 2.7 mmol/g and excellent mechanical properties (Young's modulus, 0.2–1.2 GPa; tensile strength, 35–70 MPa; elongation at break, 62–231%). Water uptake ranged from 34 to 98 wt% at 80 °C/100% RH. Proton conductivities ranged between 0.24 to 16 mS/cm at 80 °C/60% RH, and 3 to 167 mS/cm at 80 °C/95% RH. TEM analysis of the polymers, in the dehydrated state, revealed isolated spherical aggregates of ions, which presumably coalesce when hydrated to provide highly conductive pathways. The strategy of using highly‐encumbered polymer frameworks for the design of mechanically‐robust and dimensionally‐stable proton conducting membranes is demonstrated. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 2579‐2587 相似文献