有机聚合物1×32波导热光开关阵列

研制出紧凑型树状分支结构马赫-曾德尔干涉(MZ I)型有机聚合物1×2热光开关以及1×32集成波导热 光开关阵列。利用旋转涂覆法、紫外固化工艺、接触曝光、反应离子刻蚀(RIE)、真空镀膜 、切割和抛光等传统 微加工工艺,成功完成了器件制备。通过优化刻蚀工艺,有效减小了刻蚀后波导的表面与侧 壁粗糙度。通过在 波导和金属掩膜层之间添加聚合物隔离层,进一步减小了波导的传输损耗。实验结果显示, 制备的1×2热 光开关插损仅为2.84dB,串扰为－31.13dB ,光开关的电功耗为4.1mW;制备的1×32波 导热光开关阵列插 损为11.8dB, 串扰为－25.3dB,电功耗小于5mW, 器件开关时间 为1.15ms。测试结果与数值模拟结果 吻合很好,研制的光开关有望应用于光交换器(OXC)、 光分插复用器(OADM)以及光 控相控阵天线的波束扫描控制系统中。     

高速相干光通信系统中水印辅助的低密度奇偶校验方案

为了研究水印辅助的低密度奇偶校验(LDPC)方 案在高速相干接收光通信系统 中的译码性能,提出了一种适用于相干光通信系统的水印符号辅助的LDPC前向纠错方案 ,与传统LDPC相比,可以大大提高相干接 收机的抗噪声能力。在100Gbit/s 16进制正 交幅度高制(16QAM)相干接收光通信系统上的仿真实验结果表明, 在误码率(BER)为10－9时, 所提出的前向纠错方案与传统LDPC相比 较,信噪比(SNR)增益提高了0.45dB ;同时,在相同BER下,水印符号辅助的LDPC方 案的译码迭代次数有很明显的降低。     

采用自适应归一化实数编码遗传算法优化鱼眼镜头系统

针对遗传算法(GA)优化超多参量光学系统时鲁棒性 较差的问题,在混入逃逸函数实数编码GA(MERCGA)的基础上,进一步结合参量归一化和自适 应变异概率的措施,提出了自适应归一化 实数编码GA(ANRCGA)。用ANRCGA对鱼眼镜头光学系统案例进行优化设计,并应用 评价函 数和Zemax光线追迹方法对MERCGA和ANRCGA的优化结果作比较。结果表明,应用本文的ANRCG A 比引自专利的参考设计及MERCGA优化得到光学系统的成像质量有明显提高,算法的鲁棒 性和计算效率也到了改善。     

650nm波长低功耗聚合物可变光衰减器的研制

为了有效改善基于无机材料的可变光衰减器(VO A)功耗大以及成本高的问题,设计并研制了一种基于有 机聚合物材料的低功耗马赫-曾德尔干涉仪(MZI)型VOA器件。为保证器件的单模传输,优 化了波导的结构和横截面 尺寸,同时对加热电极的热场分布进行了模拟分析。最后,采用紫外光刻和湿法刻蚀等半导 体工艺,制备出功耗较低、响应速 度较快的VOA器件。在650nm工作波长下,测得器件的衰减为14.6dB,驱动功率仅为12.3mW,器件的上升时间为 240μs, 下降时间为200μs。实验结果表明,采用聚合物材料,并通过对器 件的结构参数进行优化,可研制出工作在可见光波段的低功耗VOA器件。     

长距离光传播路径中大气相干长度的测量研究

基于大口径闪烁法和差分到达角起伏法开展了间距为3.95 km近水平路径的大气相干长度测量实验。测量结果表明:在同路径的上下行光传播方向上,闪烁法测量相干长度的相关系数为0.94,而到达角起伏法测量相干长度的相关系数为0.79。路径权重的理论分析揭示了闪烁法对路径中部的湍涡敏感,且路径权重函数关于路径中部呈对称分布;到达角起伏法对接收端附近的湍涡敏感,其路径权重函数从发射端到接收端呈单调递增趋势。因此,实际的长距离光传输实验中,在不能确定路径中湍流强度分布的情况下,采用闪烁法测量路径上的湍流效应更适宜。     

Synthesis and Stereochemistry of Optically Active Selenium and Tellurium Compounds

Abstract

The synthesis and stereochemistry of tricoordinated optically active selenium and tellurium compounds are described. Telluronium salts, telluronium imides, and seleninic acids were prepared and optically resolved by fractional recrystallization of diastereomeric mixtures or by chromatography using a chiral column of racemic mixtures. Diphenyl dichalcogenides also were optically resolved by chiral crystallization. Their absolute configurations were determined or estimated based on X-ray crystallographic analysis, specific rotations, and circular dichroism spectra. The kinetic studies and the mechanism for the racemization were also studied.     

SYNTHESIS AND CONFORMATIONAL STUDIES OF A NUMBER OF SATURATED BICYCLIC SIX-MEMBERED RING PHOSPHITES

Abstract

An ¹H NMR study of the conformation of the dioxaphosphorinane ring of a number of diastereoisomeric bicyclic saturated six-membered ring phosphites (3ab-10ab) has been performed. The dioxaphosphorinane ring of these phosphites is transannelated with a tetrahydrofuran, cyclopen-tane, tetrahydropyran or cyclohexane ring. The substituent on the phosphorus atom is a methoxy or phenoxy group. It is shown that the cis isomers 3a-10a prefer a chair conformation of the dioxaphosphorinane ring, independent of the substituent on the phosphorus atom and of the nature of the transannelated ring. In contrast, for the trans isomers 3b-10b a twist rather than a chair conformation of the dioxaphosphorinane ring is preferred. The fraction of the twist conformer in the trans isomers is mainly determined by the substituent on phosphorus. The size and composition of the transannelated ring are relatively unimportant in this respect. For both cis and trans isomers the preferred geometry is solvent-independent. The measured ^3JPOCH couplings of the cis isomers 3a-10a are used to formulate an expression for the dependence of such couplings upon dihedral angles in bicyclic phosphites.     

Thermal and optical properties of highly fluorinated copolymers of methacrylates

Copolymers of pentafluorophenylhexafluoroisopropyl methacrylate (FPPMA) with trifluoroethyl methacrylate (TFEMA) were prepared in THF solution and in bulk using azobisisobutyronitrile as a free radical initiator. The monomer reactivity ratios of TFEMA (M₁) and FPPMA (M₂) were calculated as r₁ = 0.55 and r₂ = 0.07. The refractive indices of poly(TFEMA) and poly(FPPMA) are very similar as 1.435 and 1.430, respectively, at 532 nm, and the copolymer films were transparent. The glass transition temperatures (T_g) of the copolymers were in the range of 80–90°C and showed a negative deviation from the Gordon–Taylor equation. The thermal decomposition temperature (T_d) was increased with the content of FPPMA in copolymers. Low water absorption for 1:1 FPPMA/TFEMA copolymer was detected. Copolymers of FPPMA with hexafluoroisopropyl methacrylate (HFPMA) were also prepared. The monomer reactivity ratios of HFPMA (M₁) and FPPMA (M₂) were calculated as r₁ = 0.43 and r₂ = 0.10. The T_gs of the copolymers were in the range of 88–95°C and showed also a negative deviation from the Gordon–Taylor equation. T_g and T_d of the copolymers were increased with the content of FPPMA. The refractive index of poly(HFPMA) (1.384 at 532 nm) is much lower than that of FPPMA homopolymer, but copolymer films obtained were clear and transparent. Copyright © 2013 John Wiley & Sons, Ltd.     

13C-NMR Sequence Analysis. XVIII. Tacticity of Poly(D,L-β-amino Acids)

D, L-Cis-2-aminocyclobutane-1-carboxylic acid NCA, D, L-cis-and trans-2-aminocyclohexane-1-carboxylic acid N-carboxyanhydride (NCA) and D, L-cis-2-aminocyclohexane-1-carboxylic acid NCA were polymerized under various conditions. The ¹³C-NMR spectra of the resulting β-polyamides measured in trifluoro-acetic acid show splittings of all signals reflecting diads and triads. Poly-D, L-3-aminobutyric acid obtained by anionic polymerization of D, L-4-methyl acetidinone does not display tacticity effects in its ¹³C-NMR spectrum. Hence it is concluded that tacticity effects are observable only if both α- and β-carbons have a substituent. Furthermore, it was found that the reaction conditions do not have a strong influence on the stereospecificity of the NCA-polymerization. In all cases nearly random sequences of D and L-units were obtained.     

中枢多巴胺系统正电子发射计算机断层扫描显像剂的研究进展

中枢多巴胺系统与多种神经行为障碍的病理生理学有关。一直以来,多巴胺系统正电子发射计算机断层扫描(PET)成像在研究活体大脑中多巴胺生物化学过程上有着重要价值。PET成像的基础是¹¹C、¹⁸F等发射正电子的放射性核素标记的显像剂,这些显像剂通过与多巴胺神经系统不同的靶点特异性结合从而反映多巴胺合成、囊泡储存、突触释放和受体结合以及再摄取过程,推动神经病学、精神病学、药物滥用和成瘾以及药物开发的研究进展。本文综述了以氨基酸脱羧酶、多巴胺转运体、多巴胺受体以及囊泡单胺转运体为靶点的¹¹C、¹⁸F标记的PET显像剂的研究进展。