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81.
82.
相转移催化合成对甲氧基肉桂酸-2-乙基己酯的研究 总被引:5,自引:1,他引:5
对甲氧基肉桂酸 2 乙基己酯是一种有效的UVB防晒剂[1 ,2 ] ,一般采用Claisen Schmidt缩合反应制得[3] ,但由于催化剂KOH处于水相 ,对反应物不能充分起到催化作用导致产率较低[4] 。我们利用乙二醇 (PEG)为相转移催化剂合成立体专一的反式对甲氧基肉桂酸 2 乙基己酯 ,产率提高到 72 .5 %。合成路线如下 :1 实验部分1 .1 仪器与试剂BIO RAPFT45 0红外光谱仪 ,用液膜法测试 ;Brurer AM 30 0超导核磁共振仪 (溶剂DC Cl3) ;MAT/44S ,GC MS型色质联用谱仪 ;试剂均为分析纯 ,上海化学试剂… 相似文献
83.
84.
[reaction: see text] The palladium-catalyzed cross-coupling reaction of cyclopropylboronic acids with acyl chlorides was achieved by the combination of Ag(2)O and K(2)CO(3) as the base. Highly enantiomerically enriched cyclopropyl ketones (ee >90%) were also obtained by the reaction of corresponding chiral cyclopropylboronic acids. 相似文献
85.
光同时诱导水中Cr(Ⅵ)的还原与橙黄Ⅱ的氧化;染料;橙黄Ⅱ;Cr(Ⅵ);光还原;光降解 相似文献
86.
α-亚甲基-γ-丁内酰胺衍生物具有细胞毒性、抗肿瘤等生理活性, 有关这些化合物的合成方法一直是人们感兴趣的课题之一。本文拟就(1)含必要官能团的开链前体的成环反应, (2)现成的γ-丁内酰胺的α-亚甲基化反应等两个方面对α-亚甲基-γ-丁内酰胺的合成方法进行综述。 相似文献
87.
The diffusiophoretic motion of a polyelectrolyte molecule or charged floc in an unbounded solution of a symmetrically charged electrolyte with a uniform prescribed concentration gradient is analytically studied. The model used for the particle is a porous sphere in which the density of the hydrodynamic frictional segments, and therefore also that of the fixed charges, is constant. The electrokinetic equations which govern the electrostatic potential profile, the ionic concentration distributions (or electrochemical potential energies), and the fluid velocity field inside and outside the porous particle are linearized by assuming that the system is only slightly distorted from equilibrium. Using a regular perturbation method, these linearized equations are solved for a charged porous sphere with the density of the fixed charges as the small perturbation parameter. An analytical expression for the diffusiophoretic mobility of the charged porous sphere in closed form is obtained from a balance between its electrostatic and hydrodynamic forces. This expression, which is correct to the second order of the fixed charge density of the particle, is valid for arbitrary values of kappaa and lambdaa, where kappa is the reciprocal of the Debye screening length, lambda is the reciprocal of the length characterizing the extent of flow penetration inside the particle, and a is the particle radius. Our result to the first order of the fixed charge density agrees with the corresponding solution for the electrophoretic mobility obtained in the literature. In general, the diffusiophoretic mobility of a porous particle becomes greater as the hindrance to the diffusive transport of the solute species inside the particle is more significant. 相似文献
88.
Yongcheng Liu Xin Chen Jianghong Qian Haiying Liu Zhengzhong Shao Jiaqi Deng Tongyin Yu 《Applied biochemistry and biotechnology》1997,62(2-3):105-117
The structure and properties of the blend of regenerated silk fibroin (RSF) and poly(vinyl alcohol) (PVA) were investigated.
The two polymers in the blend are in the state of phase segregation. Infrared (IR) spectra indicate that the RSF in the blend
maintains its intrinsic properties, thus, ethanol treatment can transfer silk I structure of RSF to silk II structure. The
water absorption property and mechanical property of the blend are improved in comparison with those of RSF. The blend maintains
the major merit of RSF, that is, it can immobilize glucose oxidase on the basis of the conformational transition from silk
I structure to silk II structure. The properties of the immobilized enzyme are examined. Moreover, the second generation of
glucose sensor based on the immobilized enzyme is fabricated and it has a variety of advantages including easy maintenance
of enzyme, simplicity of construction, fast response time and high stability. 相似文献
89.
A highly sensitive and selective catalytic adsorptive cathodic striping procedure for the determination of trace germanium is presented. The method is based on adsorptive accumulation of the Ge(IV)‐gallic acid (GA) complex onto a hanging mercury drop electrode, followed by reduction of the adsorbed species. The reduction current is enhanced catalytically by addition of vanadium(IV)‐EDTA. The optimal experimental conditions include the use of 0.03 mol/L HClO4 (pH1.6), 6.0×10?3 mol/L GA, 3.0×10?3 mol/L V(IV), 4.0×10?3 mol/L EDTA, an accumulation potential of ?0.10 V(vs. Ag/AgCl), an accumulation time of 120 s and a differential pulse potential scan mode. The peak current is proportional to the concentration of Ge(IV) over the range of 3.0×10?11 to 1.0×10?8 mol/L and the detection limit is 2×10?11 mol/L for a 120 s adsorption time. The relative standard deviation at 5.0×10?10 mol/L level is 3.1%. No serious interferences were found. The method was applied to the determination of germanium in ore, mineral water and vegetable samples with satisfactory results. 相似文献
90.
为建立一种快速、简便、灵敏测定葡萄糖酸锌含量的方法,在非离子型表面活性剂聚氧乙烯异辛基苯基醚(TritonX-100)存在下,用2-(3,5-二溴-2-吡啶偶氮)-5-二甲氨基酚(3,5-diBr-DM-PAP)作显色剂,直接光度法测定了葡萄糖酸锌。结果表明,该法显色络合物最大吸收波长为560 nm,线性范围为0~1.5μg.mL-1,表观摩尔吸光系数为1.10×105L.mol-1.cm-1,回收率为98.7%~102.2%,具有操作快速、简便,结果灵敏可靠等优点,应用该法直接测定补锌口服液葡萄糖酸锌含量,结果满意。 相似文献