LYVE-1 在甲状腺乳头状癌的表达和意义

目的 观察淋巴管透明质酸受体1（LYVE-1）的表达和癌周组织中淋巴管的生成情况在甲状腺恶性肿瘤的变化及转 移中的作用。方法 应用免疫组织化学和real-time PCR方法检测45 例甲状腺乳头状癌中央区、癌周边区和正常甲状腺组织中的LYVE-1及其mRNA 表达情况,并计算淋巴管密度（LVD）。结果 甲状腺乳头状癌周边区LVD 高于甲状腺乳头状癌中央区,而正常组织中很少见LYVE-1 阳性的微淋巴管;甲状腺乳头状癌周边区LVD 与淋巴结转移有密切关系（P＜0.05）。结论 LYVE-1是一种特异性较高的淋巴管内皮特异性标志物,对淋巴管生成促进甲状腺乳头状癌的淋巴结转移。     

生态平衡制约下离散尺度结构种群的最优收获

研究基于扩展Leslie投影矩阵的离散尺度结构种群模型的最优收获问题,约束条件包括生态平衡和开发成本等.运用凸优化理论证明了最优收获策略的存在性,导出了最优收获模式,应用模型参数给出了收获比率.结论显示:最优策略具有两阶段结构.     

涉及差分算子的亚纯函数的唯一性

本文研究涉及差分算子的亚纯函数的唯一性问题,得到一个唯一性定理:设f是一个级不小于2的有限级整函数,η是非零复数,a(z)是不恒等于0的整函数,满足ρ(a)ρ(f)和λ(f-a)ρ(f).若f-a与Δnηf-a(n=1或2)CM分担0,则f(z)是整数级的,且ρ(a)=1或ρ(a)≥ρ(f)-1,f(z)=a(z)+[Δnηa(z)-a(z)]eA(z),其中A(z)是一个次数和ρ(f)相等的多项式.     

NEW CYCLIC AND POLYMERIC PHOSPHAZENES DERIVED FROM N-SILYLPHOSPHORANIMINES

Silicon-nitrogen-phosphorus compounds of the type Me ₃ SiN═PR(R′)X(X= Cl, Br, OCH₂CF ₃ , OPh), known as N-silylphosphoranimines,are useful precursors to both cyclic and polymeric phosphazenes.Depending on the leaving group (X), thermolysis reactions afford either cyclic trimers, [N═PR(R′)] ₃ (when X = Cl, Br), or linear polymers,[N═PR(R′)]_n (when X = OCH ₂ CF ₃ or OPh). Treatment of the P-trifluoroethoxy and P-phenoxy derivatives, Me ₃ SiN═PR(R′)X (X = OCH ₂ CF ₃ , OPh), with alcohols at lower temperature usually results in the formation of cyclic phosphazene trimers via silyl ether elimination. Recently, we have applied these synthetic methods to the preparation of some new phosphazene systems including a series of 4-aryl-functionalized trimers and polymers and a variety of non-geminal, mixed-substituent cyclic trimers. Representative examples of the synthesis, structural characterization, and reactivity of these new phosphazenes and their Si─N─P precursors are reported here.     

Efficient One-Pot Synthesis of Naphthoquinone-Fused Phosphorous Heterocycles via Mannich-Type Reaction

A series of naphthoquinone-fused phosphorus heterocycles was synthesized via a three-component Mannich-type reaction. 2-Chloroethoxylphosphorodichloridite was used as a phosphorus substrate to explore the structure–activity relationships of the 2-position of the heterocycles. One spiral heterocycle compound was structurally characterized by a single-crystal X-ray diffraction analysis.     

Synthesis and Herbicidal Activities of Sodium Hydrogen 1-(Substituted Phenoxyacetoxy)Alkylphosphonates

Abstract

A series of sodium hydrogen 1-(substituted phenoxyacetoxy) alkylphosphonates was designed and synthesized. The test for herbicidal activity indicated that most of the phosphonates (8) possessed excellent postemergence herbicidal activities against broadleaf weeds. Especially, 8f and 8g showed the best herbicidal activity against rape and amaranth with more than 95% inhibitory rate.

Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.     

Synthesis and Herbicidal Activity of [(Substituted Phenoxyacetoxy) (Substituted Phenyl)Methyl](Methyl) Phosphinates Containing Fluorine

Abstract

A series of [(substituted phenoxyacetoxy)(substituted phenyl)methyl](methyl)phos- phinates containing fluorine were designed and synthesized. All the synthesized compounds were identified by elemental analysis, IR, ¹H NMR, mass spectrometry. O-methyl [(2-fluorophenoxyacetoxy)(2,4-dichlorophenyl)methyl](methyl)phosphinate was further analyzed by X-ray single-crystal diffraction. Their herbicidal activity against a set of weed species was examined. Some of the compounds showed potential herbicidal activity, which provided some indications for further studies on structure modification.

Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.     

Synthesis and Herbicidal Activities of 2-Methylpropan-2-Aminium Methyl 1-(Substituted Phenoxyacetoxy) Alkylphosphonates

Abstract

A series of 2-methylpropan-2-aminium methyl 1-(substituted phenoxyacetoxy) alkylphosphonates were selectively synthesized by reacting the corresponding dimethyl 1-(substitutedphenoxyacetoxy)alkylphosphonates with an excess of 2-methylpropan-2-amine. All the title compounds were identified by IR, ¹H NMR, and ³¹P NMR, some of them were further analyzed by ¹⁹F NMR and ¹³C NMR. Their herbicidal activity was investigated and the results showed that most of the demethylated aminium salts exhibited notable herbicidal activities against Brassica napus L. and Echinochloa crusgalli.

Supplementary materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfer, and Silicon and the Related Elements for the following free supplemental files: Additional text, figures and tables.     

Synthesis of novel poly(aminophosphonate ester)s flame retardants and their applications in EVA copolymer

Novel oligomeric intumescent flame retardants, poly(amino phosphonate ester)s (PAPEs), containing both phosphorous and nitrogen, were synthesized by reacting diethyl phosphite with two different polyschiff bases obtained from the reaction of diamines with dialdehyde. The target PAPEs (designated as PAPE‐d and PAPE‐e, respectively) were characterized by ¹H NMR, ³¹P NMR, Fourier Transform infrared spectroscopy, elemental analysis, gel permeation chromatography and thermogravimetric analysis (TGA) techniques. Thermal stability and flammability of ethylene‐vinyl acetate copolymer (EVA)/PAPE blends with various PAPE content were investigated by TGA, limited oxygen index (LOI), vertical burning test (UL‐94) and microscale combustion colorimeter (MCC). The results indicate that PAPEs effectively improve the flame retardancy of EVA. The EVA/30%PAPE‐e blend has a LOI value of 28, and its peak heat release rate (PHRR) value in MCC measurement is reduced by 36%. At the same time, the EVA/PAPE blends also have high yield of residual char, indicating that PAPEs are effective charring agents. Scanning electron microscopy observations of the residues of the EVA/PAPE blends show the existence of compact char layer on the surface of the residues, which is responsible for the improvement of the flame retardancy of EVA. Copyright © 2012 John Wiley & Sons, Ltd.