场景轮廓的动态规划立体匹配算法

立体匹配算法是三维重建的关键步骤。由于实际场景中经常存在大片灰度相近的区域,稠密三维重建存在计算时间长、实时性差的问题。采用了场景的轮廓来重建场景的方法。基于场景中相邻点之间的视差应当是连续的假设,解决了轮廓在匹配时存在的"噪点"的问题,利用动态规划法对轮廓上各个点的视差进行约束以及求解最优解。由于提取轮廓后需要匹配的点数大为减少,用时可减少为原来的10%,得到与场景一致的轮廓视差图。     

Sesquiterpene lactones from Saussurea alata

Two new guaianolides, namely, 3beta,8alpha-dihydroxy-13-methoxyl-4(14),10(15)-dien-(1alphaH,5alphaH,6beta H,11betaH)-12,6-olide (1) and 3beta,8alpha-dihydroxy-13-methoxyl-4(14),10(15)-dien-(1alphaH,5alphaH,6beta H,11alphaH)-12,6-olide (2), together with six known guaianolides, 8-hydroxyzaluzanin C, austricin, chlorojanerin, cynaropicrin, chlorohyssopifolin E and chlorohyssopifolin A were isolated from the aerial parts of Saussurea alata. The structures were established mainly based on spectral analysis, especially 2D NMR techniques.     

非化学配比锰基钙钛矿输运特性研究

本文报道了用溶胶凝胶法并经过低温(900℃)后处理制备的具有非化学配比的La2/3Ca1/3Mn1-xO3(x=0～0.10)多晶样品的电输运和磁性质的实验研究.结果表明,随x的增加,样品呈现出明显增强的非本征磁电阻效应,同时其本征磁电阻效应减弱.实验还观察到样品的颗粒尺寸随x的增加而减小的现象.基于样品的结构特征,本文讨论了其独特输运性能的形成原因.     

一类超线性Duffing方程的Aubry-Mather集

本文通过引进适当的作用-角变量变换并结合新的估计方法,对超线性Duffing方程的Poincaré映射应用推广的Aubry-Mather定理,获得了一类超线性Duffing方程的Aubry-Mather集存在的充分性条件.     

Tunable microlens arrays using polymer network liquid crystal

A tunable-focus microlens array based on polymer network liquid crystal (PNLC) is demonstrated. The PNLC was prepared using an ultraviolet (UV) light exposure through a patterned photomask. The photocurable monomer in each of the UV exposed spot forms an inhomogeneous centro-symmetrical polymer network which acts as a lens when a homogeneous electric field is applied to the cell. The focal length of the microlens arrays is tunable with the applied voltage.     

Dynamic relaxation process of a 3D super crystal structure in a Cu:KTN crystal

In this Letter,we report the existence and relaxation properties of a critical phenomenon on called a 3D super crystal that emerges at T=TC?3.5℃,that is,in the proximity of the Curie temperature of a Cu:KTN sample.The dynamics processes of a 3D super crystal manifest in its formation containing polarized nanometric regions and/or polarized clusters.However,with strong coupling and interaction of microcomponents,the characteristic relaxation time measured by dynamic light scattering demonstrates a fully new relaxation mechanism with a much longer relaxation time.As the relaxation mechanism of a relaxator is so-far undetermined,this research provides a novel perspective.These results can help structure a fundamental theory of ferroelectric relaxation.     

FeCo2(CO)9(μ3-S)簇合物羰基取代衍生物的合成与表征

Mono-、 di- and tri-substituted derivatives of FeCo₂(CO)₉(μ₃-S) with P(OR)₃ were synthesized. They have the following formular, FeCo₂(CO)_9-n(μ₃-S)［P(OR)₃］_n ［n=1, R=CH₂CH₂CH₃(a); n=1,2,3, R=CH₂CH₂CH₂CH₃(b); n=1,2,R=CH(CH₃)(CH₂)₂CH₃(c)］. The six new compounds were characterized by elemental analysis, IR, ¹H NMR and MS spectra and their molecular structures were deduced.     

Understanding the electronic energy transfer pathways in the trimeric and hexameric aggregation state of cyanobacteria phycocyanin within the framework of Förster theory

In the present study, the electronic energy transfer pathways in trimeric and hexameric aggregation state of cyanobacteria C‐phycocyanin (C‐PC) were investigated in term of the Förster theory. The corresponding excited states and transition dipole moments of phycocyanobilins (PCBs) located into C‐PC were examined by model chemistry in gas phase at time‐dependent density functional theory (TDDFT), configuration interaction‐singles (CIS), and Zerner's intermediate neglect of differential overlap (ZINDO) levels, respectively. Then, the long‐range pigment‐protein interactions were approximately taken into account by using polarizable continuum model (PCM) at TDDFT level to estimate the influence of protein environment on the preceding calculated physical quantities. The influence of the short‐range interaction caused by aspartate residue nearby PCBs was examined as well. Only when the protonation of PCBs and its long‐ and short‐range interactions were properly taken into account, the calculated energy transfer rates (1/K) in the framework of Förster model at TDDFT/B3LYP/6‐31+G* level were in good agreement with the experimental results of C‐PC monomer and trimer. Furthermore, the present calculated results suggested that the energy transfer pathway in C‐PC monomer is predominant from β‐155 to β‐84 (1/K = 13.4 ps), however, from α‐84 of one monomer to β‐84 (1/K = 0.3–0.4 ps) in a neighbor monomer in C‐PC trimer. In C‐PC hexamer, an additional energy flow was predicted to be from β‐155 (or α‐84) in top trimer to adjacent β‐155 (or α‐84) (1/K = 0.5–2.7 ps) in bottom trimer. © 2013 Wiley Periodicals, Inc.     

High-spin- and low-spin-state structures of [Fe(chloroethyltetrazole)6](ClO4)2 from synchrotron powder diffraction data

The spin-crossover complex [Fe(teec)(6)](ClO(4))(2) (teec = chloroethyltetrazole) exhibits a 50 % incomplete spin crossover in the temperature range 300-30 K. Time-resolved synchrotron powder diffraction experiments have been carried out to elucidate its structural behavior. We report crystal structure models of this material at 300 K (high spin) and 90 K (low spin), as solved from synchrotron powder diffraction data by using Genetic Algorithm and Parallel Tempering techniques and refined with Rietveld refinement. During short synchrotron powder diffraction experiments (five minutes duration) two distinguishable lattices were observed the quantities of which vary with temperature. The implication of this phenomenon, that is interpreted as a structural phase transition associated with the high-to-low spin crossover, and the structural characteristics of the high-spin and low-spin models are discussed in relation to other compounds showing a similar type of spin-crossover behavior.     

1-(α-萘乙酰基)-4-芳酰基氨基硫脲及3-(α-萘亚甲基)-4-芳酰基-1,2,4-三唑琳-5-硫酮的合成

许多酰氨基硫脲类衍生物有抗病毒、抗细菌、抗肿瘤等功效,我们曾经通过5-(α-萘)-2H-四唑-2-乙酰肼与芳酰异硫氰酸酯缩合得一系列新的酰氨基硫脲和相关的杂环衍生物,观察到它们在很低的浓度下就有调节小麦芽鞘生长的功能。Kothari等用α-萘乙酰肼与芳基异硫氰酸酯缩和制得一系列1-(α-萘乙酰基)-4-芳基氨基硫脲及