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951.
Direct trimethylsilylation1) of phenanthrene in different molar ratio of phenanthrene/sodium/trimethylchlorosilane is reported and discussed. Instead of the aromatic silyl compounds, such as 9-trimethylsilylphenanthrene (V), the hydroaromatic silyl compounds, such as 9, 10–bis (trimethylsilyl)-9, 10-dihydrophenanthrene (I) were obtained preferentially. Structure of these compounds are characterized and discussed. These silylated products have a general trend to change their properties during long time storage in the atmosphere under exposure to light. A significant difference of chemical shifts between silylated aromatic compound (V) and silylated hydroaromatic compound (I-IV) was observed. 相似文献
952.
Determination of 1-aminocyclopropane-1-carboxylic acid in apple extracts by capillary electrophoresis with laser-induced fluorescence detection 总被引:1,自引:0,他引:1
A rapid and sensitive method for the determination of 1-aminocyclopropane-1-carboxylic acid (ACC) in apple tissues has been described. This method is based on the derivatization of ACC with 3-(2-furoyl)quinoline-2-carboxaldehyde (FQ), and separation and quantification of the resulting FQ-ACC derivative by capillary electrophoresis coupled to laser-induced fluorescence detection (CE-LIF). Our results indicated that ACC derivatized with FQ could be well separated from other interfering amino acids using 20 mM borate buffer (pH 9.35) containing 40 mM sodium dodecyl sulfate and 10 mM Brij 35. The linearity of ACC was determined in the range from 0.05 to 5 microM with a correlation of 0.9967. The concentration detection limit for ACC was 10 nM (signal-to-noise = 3). The sensitivity and selectivity of this described method allows the analysis of ACC in crude apple extracts without extra purification and enrichment procedure. 相似文献
953.
954.
流动注射在线共沉淀预富集火焰原子吸收法测定痕量铜 总被引:3,自引:0,他引:3
研究了以Ni^2+-DDTC为共沉淀载体,流动注射在线共沉淀预富集-火焰原子吸收光谱法测定痕量铜的体系,在0.3mol.L^-1的硝酸介质中,铜离子在编织反应器中与Ni^2+-DDTC(产生共沉淀,并被收集在编织器内壁上,用甲基异丁基酮(MIBK)在线洗脱沉积物并引入火争原子化器中测定。当富集时间为40s时,40μg.L^-1的铜10次测定的相对标准偏差为3.0%,灵敏度提高60倍,检出限(3σ) 相似文献
955.
Simmonds等报道异戊烯基化的查耳酮和黄烷酮对昆虫具有拒食活性[1],Echeverri等发现,从植物Passiflorafoetida树脂中分离到的4,7-二甲氧基莰非醇(1)在很低的浓度下(40μg/g)对昆虫Dionejuno的幼虫也具有... 相似文献
956.
957.
The localized molecular orbitals and their energy levels for the clusters [Fe3S4(SH)3]2–, [(HS)3Fe3S4·Ni(PH3)]2–, [Mo3S4(OH2)9]4+, and [Mo3S4·Ni]4+ have been calculated by mean of the Edmiston-Ruedenberg energy localization technique under the CNDO/2 approximation in order to reveal the resemblance between [Fe3S4]+ and [Mo3S4]4+ in the geometrical configurations and the addition reactivities with heterometal atoms. It is shown that in these two cluster species with core {M
3(3-S)(-S)3} of similar structure (M = Mo, Fe) there exist three synergically connected three-centered two-electron (M-S-M) -bonds around the puckered six-membered {M3S3} rings on account of delocalization of a lone electron pair on each bridging S atom; these (M-S-M) -bonds are thus capable of forming cubane-like heterometal clusters with intruder metal atoms through the ( M) bonding. It is therefore seen that unlike the [Mo3S4]4+ with appreciable bonding between the Mo atoms, the extra d-electrons on the metal atoms in the [Fe3S4]+ cluster are localized on the Fe atoms, exhibiting an electronic structure significantly different from that of the [Mo3S4]4+ cluster. 相似文献
958.
Tao Liu Yong-Gang Wei Qi-Hua Wu Qing-Xiang Guo 《Research on Chemical Intermediates》2005,31(9):833-844
A series of adamantanamine-(OCH2CH2)n-phenothiazine (n = 0, 1, 2, 3) electron donors was synthesized. Photoinduced electron transfer was observed in the supramolecular complex
of the phenothiazine derivatives with p-nitrobenzoyl-β-cyclodextrin (NBCD) through binding of the adamantyl group by the NBCD cavity, which is stabilized clearly via hydrophobic interactions in aqueous solution. Detailed Stern–Volmer constants were measured and they were partitioned into
dynamic Stern–Volmer quenching constants and static binding constants. The results revealed an efficient electron transfer
process inside the supramolecular systems compared to that controlled by diffusion. This observation also indicates that the
chain length will influence the electron transfer efficiency of a supramolecular donor–acceptor system. 相似文献
959.
As bio‐inspired chemical model of the oxygen‐evolving complex (OEC) in photosystem II, a new tyrosine‐modified corrole ligand 3 and its high‐valent copper and manganese complexes 3a and 3b were synthesized and characterized. The copper complexes 1a and 2a of corrole 1 and 2 were also prepared for comparison. The emission property indicates that the emission of ligands 2 and 3 is located at 670 nm, but no emission is observed for their metal complexes due to its suppression by the metal center. The electrochemical study shows that 3a might dimerize at the first two reversible oxidations, a behavior which was not observed in the case of 1a and 2a . The corrolato manganese(IV) complex 3b shows one reversible reduction and one quasireversible oxidation at ?0.17 and 0.77 V vs. Ag/Ag+, respectively. 相似文献
960.
Nd-Fe-B磁体烧结过程晶粒长大行为的研究 总被引:4,自引:0,他引:4
定量描述了Nd-Fe-B磁体烧结过程晶粒长大行为,分析了烧结温度、烧结时间、合金粉末粒度及其分布对烧结过程晶粒长大的影响,讨论了烧结过程晶粒长大机制。在Nd-Fe-B磁体烧结过程开始之后的0—1h时间区段,晶粒长大迅速;随着烧结时间的延长,晶粒长大速度减小。合金粉末平均粒度增大,或者合金粉末粒度分布范围增宽,显著促进Nd-Fe-B磁体烧结过程中晶粒的长大。在Nd-Fe-B磁体的烧结过程中,存在两类晶粒长大机制,即Nd2Fe14B颗粒的溶解与析出、Nd2Fe14B颗粒的并合与长大。Nd2Fe14B颗粒的并合与长大不仅使磁体的平均晶粒尺寸增大,也使晶粒尺寸分布范围增宽,是烧结Nd-Fe-B磁体显微组织中出现异常大晶粒的根本原因。 相似文献