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891.
892.
2,6-二氨基吡啶与苦基氯的反应历程研究 总被引:2,自引:0,他引:2
对2,6-二氨基吡啶与苦基氯的反应历程进行了研究。通过二氨基吡啶与几种多硝基卤代苯的反应、溶剂效应、NaF的促进作用和紫外光谱吸收,证实该反应属于芳香族亲核取代反应类型,按加成-消除历程进行,反应过渡态涉及一个Mcisenheimer络合物。 相似文献
893.
894.
B. Hu Y. Song L. Wang Q. Zhang J. Li K. Wei Y. Chen L. Zhang 《Journal of Radioanalytical and Nuclear Chemistry》2006,269(1):231-233
Summary Electronic stopping power of 19F in Ni, Pd and Gd was measured and compared to Mstar and SRIM calculation as well as experimental results published in literature.
It turns out that the present electronic stopping power agrees reasonably well with them. 相似文献
895.
杂多酸的固载化─关于制备负载型酸催化剂的一般原理 总被引:10,自引:0,他引:10
杂多酸同时具有酸和氧化-还原的催化特性,有着很广泛的应用前景.这类化合物在一系列精细合成中取代硫酸作为催化剂以满足环保的要求,显示出了很大的潜力.杂多酸固载化后,不仅能在液相氧化和酸催化反应中把催化剂从反应介质中很方便地分离出来,而且还为这类均相催化反应的多相化,甚至利用催化蒸馏新工艺等创造了应有的条件,可以使生产工艺大大简化,获得更广泛的应用.本文以很好表征过的多种孔性材料,包括氧化物,如Al_2O_3、SiO_2、TiO_2、硅藻土、膨润土和来源不同的活性炭为载体,考察了负载杂多酸催化剂的催化活性.在大量前期工作的基础上,通过总结载体对固载杂多酸催化活性的影响等,探讨载体的内在性质在杂多酸固载、吸附和催化反应中的作用本质,为由吸附法制备各种负载型固体酸催化剂在液相中的应用提供可资参考的模型. 相似文献
896.
Summary Three -Cyclodextrin derivatives (-CDs) were synthesized by substituting the 2,6-OH groups of -CD with allyl groups and the 3-OH groups with three different acyl groups (valeryl, heptanonyl, octanoyl). The chromatographic properties of these -CDs as stationary phases for capillary gas chromatography (CGC) were studied. The test results showed that the three -CDs possessed good coating properties and that the capillary columns coated with them exhibited high column efficiency. These -CDs can separate not only the disubstituted benzene isomers but also some racemic compounds. 相似文献
897.
In the present paper, on the basis of our work. advances in study of the catalysts of polyacid-type hydrotalcite-like are reported and reviewed. Using polyoxometalates (POM) as pillaring species and layered double hydroxides (LDH) as host matter, a new class of catalytic materials, LDHPOM, has been synthesized by five different methods. Their acidic and oxidative catalytic properties have been investigated by several research groups. The above mentioned information is given in this review. 相似文献
898.
Reaction of copper powder with 2-thenoyltrifluoroacetone and PPh3 yielded the complex [Cu(C8H4O2F3S)(PPh3)2], which have been characterized by elemental analysis and IR spectra. The crystal is monoclinic, space group P21/n , a=1.0584(1), b=1.6738(1), c=2.2728(9) nm; β =94.22(2); V =4.0152 nm 3; Z=4; Dc=1.299 g·cm-3; R=0.048, RW=0.054. Copper (Ⅰ) ion is coordinated by two O and two P atoms forming distorted tetrahedron. 相似文献
899.
Pan L Woodlock EB Wang X Lam KC Rheingold AL 《Chemical communications (Cambridge, England)》2001,(18):1762-1763
Structurally distinct coordination polymers [Ag(bpp)]ClO4 1 and [Ag(bpp)]PF6 2 [bpp = 1,3-bis(4-pyridyl)propane] have been assembled; the conversion of 1 into 2 on treatment with NaPF6 is driven by argentophilic interactions and is the first such transformation reported for silver(I)-organic coordination polymers. 相似文献
900.
Guan X Lin X Kwok WM Du Y Li YL Zhao C Wang D Phillips DL 《The journal of physical chemistry. A》2005,109(6):1247-1256
Ultraviolet photolysis of low concentrations of CH2I2 in methanol solution found that CH2I2 is converted into dimethoxymethane and some H+ and I- products. Picosecond time-resolved resonance Raman (ps-TR3) experiments observed that the isodiiodomethane (CH2I-I) photoproduct decayed faster as the concentration of methanol increases, suggesting that isodiiodomethane is reacting with methanol. Ab initio calculations indicate isodiiodomethane is able to react with methanol via an O-H insertion/HI elimination to form an iodoether (ICH2-O-CH3) and HI products. The iodoether can then further react via another O-H insertion/HI elimination reaction to form the dimethoxymethane (CH3-O-CH2-O-CH3) observed in the photochemistry experiments. A reaction mechanism consistent with these experimental and theoretical observations is proposed. 相似文献