Fluorocarbon- containing hydrophobically modified poly(N-isopropylacrylamide)

A fluorocarbon-modified poly(N-isopropylacrylamide) has been synthesized by copolymerization of N-isopropyl acrylamide with a small amount of acrylate or methacrylate containing a perfluoroalkyl group. It was found that the hydrophilicity of macromolecular backbone is an important factor to the solution properties of the copolymers and that hydrophobic association between fluorocarbon groups is stronger than that between the corresponding hydrocarbon analogies. The viscosity of some of the copolymer solutions was very sensitive to temperature. It was dilatant at higher fluorocarbon comonomer content ( > 0.20-1.0 mol%) and was Newtonian at very low fluorocarbon comonomer content (0.03-0.2 mol% ) . Evidence for hydrophobic association of the fluorocarbon groups was obtained from the effects of adding Nad and surfactants on the solution viscosity. The LC-ST properties of these copolymers were studied by DSC method and this was also found to be consistent with hydrophobic association between the fluorocarbo     

On Mixed Pressure-Velocity Regularity Criteria to the Navier-stokes Equations in Lorentz Spaces,Part Ⅱ:The Non-slip Boundary Value Problem

This paper is a continuation of the authors recent work [Beir?o da Veiga, H.and Yang, J., On mixed pressure-velocity regularity criteria to the Navier-Stokes equations in Lorentz spaces, Chin. Ann. Math., 42(1), 2021, 1–16], in which mixed pressure-velocity criteria in Lorentz spaces for Leray-Hopf weak solutions of the three-dimensional NavierStokes equations, in the whole space R~3 and in the periodic torus T~3, are established. The purpose of the present work is to extend the result of mentio...     

A new proposal for the discretization of the Griffin—Wheeler—Hartree—Fock equations

A polynomial expansion is proposed as a new way to discretize the Griffin-Wheeler-Hartree-Fock equations of the Generator Coordinate Hartree-Fock method. The implementation of the polynomial expansion in the Generator Coordinate Hartree-Fock method discretizes the Griffin-Wheeler-Hartree-Fock equations through a numerical mesh which is not equally spaced. This procedure makes the optimization of Gaussian exponents in the Generator Coordinate Hartree-Fock method more flexible and more efficient. The results obtained with the polynomial expansion for atomic Hartree-Fock energies show this technique is very powerful when employed in the design of compact and high accurate Gaussian basis sets used in ab initio non-relativistic (Hartree-Fock) and relativistic (Dirac-Fock) calculations.     

利用浅海声场干涉条纹反演海底参数方法研究

浅海频散特性导致声场在距离-频率平面形成干涉条纹,该干涉条纹蕴含着声源以及海底信息。本文通过降噪、滤波等方法,提取船舶辐射噪声干涉条纹中距离域干涉准周期、波导不变量以及去扩展衰减系数(不考虑扩展损失后接收到噪声级随距离的衰减程度)三种特征量的观测值,基于无限均匀沉积层海底模型,采用简正波计算程序理论计算上述三种特征量作为拷贝,提出一种以模拟退火法作为搜索寻优策略的新的匹配反演海底参数的方法。海试数据处理结果表明,该方法反演估计所得海底密度、声速、衰减系数三参数用于浅海负跃层条件下的声场预报效果比较良好。     

浅海环境中矢量水听器角度谱特性

为探明远场舰船噪声和近场平台噪声声能流相互作用的机制对矢量水听器角度谱特性的影响,基于简正波矢量场理论,构建舰船平台噪声声场模型,获得与海上实验结果相符的声能流角度谱特性,声能流方向均随频率变化。对远场舰船噪声声能流和近场平台噪声声能流相互作用进行仿真,两者声能流强度的此消彼长使角度谱出现4种条纹,与海上实验获得的角度谱特性一致,导致目标方位估计出现误差,且不同频带上的结果不一致。说明两个声能流相互作用时,影响合成能流角度谱特性的主要因素是两者的声压级之差,为浅海中同时存在多个声源时的目标方位估计提供参考。     

采用可见光源和分划板快速装调激光光路

 分析了激光测量光路的特点和装校要求,给出了采用可见光源、分划板装校激光光路的原理。以预放测量模块为例,介绍了装校的流程及装校中的注意事项,分析了装校所能达到的精度,并用内调焦望远镜进行了装校精度检查。结果表明,采用可见光源、分划板装校的激光光路透镜光轴正过心的偏心极限误差小于等于0.07 mm,光轴倾斜极限误差小于等于25″。     

2,2-亚戊基-1,3-二氧六环-4,6-二酮与原甲酸三乙酯和芳香胺的反应

剂,在有机合成中已有一定应用。开展Meldrum's 酸系列化合物的研究,旨在:1.寻找有结构特点的新试剂,2.合成一系列新化合物,3.研究新化合物的应用。本文通过控制反应温度(28～29℃)催化剂用量(比文献用量多近一倍),提高了2,2-亚戊基-1,3-二氧六环-4,6-二酮(PDDO,3)的制备得率(由15%     

[5-(芳亚甲基氨基)-1,3,4-噻二唑-2-基]硫乙酰芳胺的合成及 生物活性研究

在K2CO3存在下利用聚乙二醇-400 (PEG-400)作相转移催化剂, 于固-液相转移催化条件下, 通过5-芳亚甲基氨 基-2-巯基-1,3,4-噻二唑与氯乙酰芳胺的硫烷基化反应, 合成了16个未见文献报道的[5-(芳亚甲基氨基)-1,3,4-噻二唑-2-基]硫乙酰芳胺衍生物. 经元素分析, FT-IR,1H NMR和13C NMR确证了其结构. 生物活性实验结果表明, 部分化合物对小麦幼苗的生长具有明显的植物生长调节活性, 并对枯草杆菌具有一定的抑制活性.     

Reaction of vinyl chloride with late transition metal olefin polymerization catalysts

The reactions of vinyl chloride (VC) with representative late metal, single-site olefin dimerization and polymerization catalysts have been investigated. VC coordinates more weakly than ethylene or propylene to the simple catalyst (Me(2)bipy)PdMe(+) (Me(2)bipy = 4,4'-Me(2)-2,2'-bipyridine). Insertion rates of (Me(2)bipy)Pd(Me)(olefin)(+) species vary in the order VC > ethylene > propylene. The VC complexes (Me(2)bipy)Pd(Me)(VC)(+) and (alpha-diimine)Pd(Me)(VC)(+) (alpha-diimine = (2,6-(i)Pr(2)[bond]C(6)H(3))N[double bond]CMeCMe[double bond]N(2,6-(i)Pr(2)[bond]C(6)H(3))) undergo net 1,2 VC insertion and beta-Cl elimination to yield Pd[bond]Cl species and propylene. Analogous chemistry occurs for (pyridine-bisimine)MCl(2)/MAO catalysts (M = Fe, Co; pyridine-bisimine = 2,6-[(2,6-(i)Pr(2)[bond]C(6)H(3))N[double bond]CMe](2)-pyridine) and for neutral (sal)Ni(Ph)PPh(3) and (P[bond]O)Ni(Ph)PPh(3) catalysts (sal = 2-[C(H)[double bond]N(2,6-(i)Pr(2)-C(6)H(3))]-6-Ph-phenoxide; P[bond]O = [Ph(2)PC(SO(3)Na)[double bond]C(p-tol)O]), although the initial metal alkyl VC adducts were not detected in these cases. These results show that the L(n)MCH(2)CHClR species formed by VC insertion into the active species of late metal olefin polymerization catalysts undergo rapid beta-Cl elimination which precludes VC polymerization. Termination of chain growth by beta-Cl elimination is the most significant obstacle to metal-catalyzed insertion polymerization of VC.