鲁米诺—过氧化氢—奎宁化学发光体系测定微量奎宁

本文报导了鲁米诺—过氧化氢—奎宁化学发光体系,建立了测定微量奎宁的最佳条件。对6.6×10~(-6)mol/L奎宁测定的变异系数为1%。该法可用于测定药物中的奎宁,结果良好。     

饲育条件下Semisulcospiens decipiens的生长

在饲育温度条件下研究了Ｓ．ｄｅｃｉｐｉｅｎｓ的生长和产仔数及与饲育水温的关系。结果表明水温在上升期和下降期，新生贝和稚贝的生长速度较快，产仔数也较多．成体贝在水温１１℃～２９℃时，都可产出新生贝，以１８℃～２４℃时产出较多．在高温饲育条件下，成体贝的生长速度缓慢。     

多缩乙二醇双对甲苯磺酸酯的新合成法

本文报道了一种合成多缩乙二醇双对甲苯磺酸酯的新方法。该法收率明显提高,并能得到品状的三缩四乙二醇双对甲苯磺酸酯(文献为油状物)。     

7—氯—8—甲基喹啉氯化过程研究

本文用ＨＭＯ法对７－氯－８－甲基喹啉的电子密度、键级和自由价进行了计算，认为７－氯－８－甲基喹啉可以进行Ｃ３位亲电氯代反应。通过实验研究氯化过程，测定出六种氯化物，结果表明，在合适条件下，Ｃ３位的氯化伴随着甲基侧链的自由基氯代反应同时发生。     

平面桁架结构损伤的探测、定位与评估

利用参数识别技术描述了对平面桁架结构损伤的探测、定位与评估（ＤＬＥ）的一个新算法。这一概念始于精确＂健康＂模型，利用动力响应数据周期地更新这一＂健康＂模型，当损伤发生时，用一个识别算法（一个显式桁架损伤模型），以动力响应数据构造出一个桁架损伤模型，由此比较损伤模型与健康模型的参数，从而探测、定位及评估损伤的程度     

实验性脾虚证大鼠血清中微量元素含量的研究

用破气苦降药加饮食失节法复制了大鼠脾虚证模型。采用原子吸收光谱法检测了血清发Ｚｎ、Ｃｕ和Ｆｅ的含量。本研究证明，脾虚证大鼠血清Ｚｎ值明显降低（Ｐ＜０．００１）；Ｃｕ值、Ｆｅ值无明显差异（Ｐ＞００５）；Ｃｕ／Ｚｎ比值上升。用中药加味四君子汤治疗后，血清Ｚｎ值明显回升并高于正常水平（Ｐ＜００５），Ｃｕ值回升（Ｐ＜０．０５），但Ｆｅ值和Ｃｕ／Ｚｎ比值与自然恢复及对照组比较无显著性差异。这说明：１．脾虚组Ｚｎ的降低可能与消化吸收障碍有关；２．加味四君子汤对脾虚证时血清Ｚｎ及Ｃｕ／Ｚｎ比值的变化有明显的调整和恢复作用．     

Synthesis of optically active poly(N‐propargylsulfamides) with helical conformation

A novel chiral N‐propargylsulfamide monomer ( 1a ) and its enantiomer ( 1b ) were synthesized and polymerized with (nbd)Rh⁺B^?(C₆H₅)₄ as a catalyst providing poly(1) (poly( 1a ) and poly( 1b )) in high yields (≥99%). Poly(1) could take stable helices in less polar solvents (chloroform and THF), demonstrated by strong circular dichroism signals and UV–vis absorption peaks at about 415 nm and the large specific rotations; but in more polar solvents including DMF and DMSO, poly(1) failed to form helix. Quantitative evaluation with anisotropy factor showed that the helical screw sense had a relatively high thermal stability. These results together with the IR spectra measured in solvents showed that hydrogen bonding between the neighboring sulfamide groups is one of the main driving forces for poly(1) to adopt stable helices. In addition, copolymerization of monomer 1a and monomer 2 was conducted, the solubility of poly(1) was improved drastically. However, the copolymerization had adverse effects on the formation of stable helices in the copolymers. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 500–508, 2007     

应用测力—落刀装置对积屑瘤、鳞刺的研究

本文研制了一种测力—落刀装置,对积屑瘤和鳞剌的某些问题进行了试验研究。结果表明:在积屑瘤存在的区域内,由于刀具实际前角的增加,以及切屑与积屑瘤的接触长度小于自然接触长度,从而导致了切削力的降低。积屑瘤不是整体稳定不变的,也不是高频地整体脱落后再重新生长。而是基体比较稳定,头部产生高频的分裂、成长,其分裂的部分留在工件表面成为鳞剌,同时,引起了切削力的较大波动。切削力动态分量越大,相应的鳞剌高度越高。     

Synthesis and application as polymer electrolyte of hyperbranched polyether made by cationic ring‐opening polymerization of 3‐{2‐[2‐(2‐hydroxyethoxy)ethoxy]ethoxymethyl}‐3′‐methyl‐oxetane

A novel cyclic ether monomer 3‐{2‐[2‐(2‐hydroxyethoxy)ethoxy]ethoxy‐methyl}‐3′‐methyloxetane (HEMO) was prepared from the reaction of 3‐hydroxymethyl‐3′‐methyloxetane tosylate with triethylene glycol. The corresponding hyperbranched polyether (PHEMO) was synthesized using BF₃·Et₂O as initiator through cationic ring‐opening polymerization. The evidence from ¹H and ¹³C NMR analyses revealed that the hyperbranched structure is constructed by the competition between two chain propagation mechanisms, i.e. active chain end and activated monomer mechanism. The terminal structure of PHEMO with a cyclic fragment was definitely detected by MALDI‐TOF measurement. A DSC test implied that the resulting polyether has excellent segment motion performance potentially beneficial for the ion transport of polymer electrolytes. Moreover, a TGA assay showed that this hyperbranched polymer possesses high thermostability as compared to its liquid counterpart. The ion conductivity was measured to reach 5.6 × 10^?5 S/cm at room temperature and 6.3 × 10^?4 S/cm at 80 °C after doped with LiTFSI at a ratio of Li:O = 0.05, presenting the promise to meet the practical requirement of lithium ion batteries for polymer electrolytes. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3650–3665, 2006     

Double‐hydrophilic block copolymer for encapsulation and two‐way pH change‐induced release of metalloporphyrins

A double hydrophilic block copolymer composed of poly(acrylic acid) (PAA) and poly(4‐vinyl pyridine) (P4VP) was obtained through hydrolysis of diblock copolymer of poly(tert‐butyl acrylate) (PtBA) and P4VP synthesized using atom transfer radical polymerization. Water‐soluble micelles with PAA core and P4VP corona were observed at low (acidic) pH, while micelles with P4VP core and PAA corona were formed at high (basic) pH. Two metalloporphyrins, zinc tetraphenylporphyrin (ZnTPP) and cobalt tetraphenylporphyrin (CoTPP), were used as model compounds to investigate the encapsulation of hydrophobic molecules by both types of micelles. UV–vis spectroscopic measurements indicate that micelles with P4VP core are able to entrap more ZnTPP and CoTPP as a result of the axial coordination between the transition metals and the pyridine groups. The study found that metalloporphyrins encapsulated by the micelles with PAA core could be released on pH increase, while those entrapped by the micelles with P4VP core could be released on pH decrease. This behavior originates from the two‐way pH change‐induced disruption of PAA‐b‐P4VP micelles. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 1734–1744, 2006