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41.
Hai-Bin Tian Duan-Zhi Yin Lan Zhang Li-Hua Wang Chun-Fu Zhang Jun-Ling Li Wei Zhou Chun-Ying Wu Yong-Xian Wang 《Journal of Radioanalytical and Nuclear Chemistry》2004,262(2):383-389
The compound 3-{[4-(4-[18F]fluorophenyl)methyl]piperazin-1-yl}-methyl-1H-pyrrolo[2,3-b]pyridine ([18F]3), which is an analogue of L-745,870 binding D4
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
42.
钙黄绿素蓝荧光法测定食品中的微量锌(Ⅱ) 总被引:5,自引:0,他引:5
本文研究了在CTMAB存在下,用钙黄绿素蓝荧光法测定食品中的微量锌(Ⅱ)的实验条件。在本实验条件下,Zn(Ⅱ)与钙黄绿素蓝生成1:1的配合物使钙黄绿素蓝的荧光增强,最大激发波长和最大发射波长分别为353nm和440nm。 相似文献
43.
The development of highly active and stable reversible oxygen electrocatalysts is crucial for improving the efficiency of metal-air battery devices. Herein, an efficient liquid exfoliation strategy was designed for producing silk-like FeS2/NiS2 hybrid nanocrystals with enhanced reversible oxygen catalytic performance that displayed excellent properties for Zn-air batteries. Because of the unique silk-like morphology and interface nanocrystal structure, they can catalyze the oxygen evolution reaction (OER) efficiently with a low overpotential of 233 mV at j = 10 mA cm?2. This is an improvement from the recently reported catalysts in 1.0 M KOH. Meanwhile, the oxygen reduction reaction (ORR) activity of the silk-like FeS2/NiS2 hybrid nanocrystals showed an onset potential of 911 mV and a half-wave potential of 640 mV. In addition, the reversible oxygen electrode activity of the silk-like FeS2/NiS2 hybrid nanocrystals was calculated to be 0.823 V, based on the potential of the OER and ORR. Further, the homemade rechargeable Zn-air batteries using FeS2/NiS2 hybrid nanocrystals as the air-cathode displayed a high open-circuit voltage of 1.25 V for more than 17 h and an excellent rechargeable performance for 25 h. The solid Zn-air batteries exhibited an excellent rechargeable performance for 15 h. This study provided a new method for designing interface nanocrystals with a unique morphology for efficient multifunctional electrocatalysts in electrochemical reactions and renewable energy devices. 相似文献
44.
[reaction: see text] Bi(NO(3))(3).5H(2)O was used as an efficient nitrating reagent in the nitration of phenolic compounds to give nitrated phenols in good to high yields. The nitration reaction proceeded smoothly by grinding 1 equiv of phenol, 2-methylphenol, 4-methylphenol, or 4-chlorophenol and Bi(NO(3))(3).5H(2)O, and the nitration of other phenolic compounds could be performed in acetone at ambient temperature (22-30 degrees C). 相似文献
45.
An efficient palladium-catalyzed amination of aromatic bromides with hindered N-alkyl-substituted anilines is described, either using the combination of Pd(OAc)(2) and P(t-Bu)(3) or a palladium(I) tri-tert-butylphosphine bromide dimer, [Pd(mu-Br)(t-Bu(3)P)](2), a new, commercially available, and easily handled catalyst. 相似文献
46.
本文首次利用碳基钴簇合物PhPCo_3(CO)_9催化剂,在常压和-20℃-0℃,用苯乙烯和重氮乙酸乙酯进行环丙烷化反应,合成了菊酸酯,重氮乙酸乙酯可全部转化,酯的选择性可达85%。产物经减压分馏后,由IR和 ̄1HNMR分析,确证了产物为菊酸酯,表明了羰基钴簇合物对苯乙烯的环丙烷化反应有良好的催化性能,为四面体异核簇合物用于不对称催化反应打下了基础。 相似文献
47.
48.
Guo Jin-xin Sun Si-xiu Zhu Rong-xiu Yin Zhi-lei Yu Hai-yun Li Da-zhi Zhang Wei-min Xu Xian-gang Sun Xuan Shao Hua 《Journal of Radioanalytical and Nuclear Chemistry》2004,261(1):221-224
The 222Rn emanation fraction (EF) released from the technically enhanced naturally occurring radioactive material (TE-NORM) wastes
at certain sites of petroleum and gas production was determined. The samples were analyzed by γ-ray spectrometry to determine
the activity concentration of the 226Ra content, of which the 222Rn emanation fraction was calculated. The results showed that the 222Rn emanation fraction differs in the oil and gas production sites and it is independent of the activity concentration of 226Ra.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
49.
The styrene-butadiene rubber (SBR) cured by dicumyl peroxide was reinforced by magnesium methacrylate [Mg(MAA)2], which was added into SBR directly or prepared in situ in SBR through the neutralization of magnesium oxide (MgO) and methacrylic acid (MAA). The experimental results show that the SBR vulcanizates reinforced by Mg(MAA)2 prepared in situ have better mechanical properties than those reinforced by Mg(MAA)2 added directly. The SBR vulcanizates with Mg(MAA)2 prepared in situ are semi-transparent, but those with Mg(MAA)2 added directly are opaque. The Fourier transform infrared analysis shows that the polymerization conversion of Mg(MAA)2 in the SBR vulcanizates with Mg(MAA)2 prepared in situ is much higher than that in the SBR vulcanizates with Mg(MAA)2 added directly. The scan probe microscopy photographs show that the particles in the SBR vulcanizates with Mg(MAA)2 prepared in situ are much finer and disperse more evenly than that in the SBR vulcanizates with Mg(MAA)2 added directly. 相似文献
50.
The liquid chromatographic enantiomer separation of N-fluorenylmethoxycarbonyl (FMOC) protected alpha-amino acids and their ethyl ester derivatives was performed on polysaccharide-derived chiral stationary phases, Chiralcel OD, Chiralpak AD, and Chiralpak AS. In general, Chiralcel OD and Chiralpak AD showed good performance for resolution of N-FMOC alpha-amino acids and their ethyl esters, respectively. All investigated N-FMOC alpha-amino acid enantiomers were baseline separated on Chiralcel OD or Chiralpak AD, whereas N-FMOC alpha-amino acid ethyl ester enantiomers were baseline resolved (alpha = 1.15-3.03) on Chiralpak AD, except for two analytes. The L-enantiomers of all examined FMOC alpha-amino acid ethyl ester derivatives are preferentially retained on Chiralpak AD, while the elution orders of the other enantiomer separations are not consistent. 相似文献