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951.
2-氨基二甲基吡啶镉的单晶已被单晶定向的~(113)Cd核磁共振进行了研究。在CdCl_2+2-氨基二甲基吡啶中对于两个氯-四个氮的~(113)Cd的屏蔽张量元素分别是σ_(33)=368,σ_(22)=266,和σ_(11)=236×10~(-6)。 相似文献
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955.
Calculations of localized molecular orbitals (LMO) and their energy levels for the cluster cores [MO3O4]4+, [MO3SO3]4+, [MO3OS3]4+, [Mo3S4]4+ and [MO3OCl3]5+ have been made by the use of energy-localized CNDO/2-LMO. The results of these LMO calculations show that the six-membered closed and continuous π-conjugated systems around the [MO3Y3] rings, each of which is formed from three synergically connected three-centered two-electron
π bonds, is the most significant feature of the electronic structure for the quasi-aromatic clusters [Mo3(μ3-Y)(μ-X)3]4+ (X, Y = O, S), and the size and electronegativity of the bridging Y atoms exhibit significant effects on the degree of quasi-aromaticity of these cluster compounds. For the non-aromatic reference cluster [Mo3OCl3]5+, the results of our calculations also show a bonding scheme with only one isolated
π bond, thus leading to the loss of quasi-aromaticity; and meanwhile, there is a pair of extra electrons localized on the apical molybdenum atom of the Mo3 triangle, thus with three Mo---Mo single bonds. 相似文献
956.
Lin Jiacheng Li Qianqian Zeng Xiaodong Chen Ziyang Ding Qihang Li Yang Zhou Hui Meng Xianli Chen Deliang Deng Zixin Hong Xuechuan Xiao Yuling 《中国科学:化学(英文版)》2020,63(6):766-770
Osteosarcoma is the most common primary malignant tumor of bone, particularly among children and adolescents. Advances in imaging, surgical techniques, and implants have dramatically reduced the need for amputation in the past three decades.Recently, in vivo fluorescence imaging in the second near-infrared window(NIR-II, 1,000–1,700 nm) shows impressive advantages of deeper tissue penetration and higher spatial resolution, which makes it a promising tool for the early diagnosis and post-operative observation of Osteosarcoma. To the best of our knowledge, this paper is the first time to develop a novel NIR-II fluorescence probe conjugated with an osteosarcoma targeted oligopeptide for molecular tumor imaging in a xenograft orthotopic osteosarcoma mouse model. 相似文献
957.
Conjugated linoleic acids (CLA) have been a subject of extensive investigation for their anticarcinogenic, hypolipidemic, antiatherosclerotic and immune-enhancing activities. Stability of CLA in foods has not received much attention by both academics and industry. Although CLA has shown many beneficial effects, its decomposition must be prevented when CLA in foods is processed, stored and transported. However, no study to date has addressed the stability of CLA in foods. The present study was carried out further to examine the stability of CLA in egg yolk during the storage and frying, using gas liquid chromatography (GLC) and silver ion high-performance liquid chromatography (Agt-HPLC). The eggs, containing 4.0% CLA per gramme of egg yolk, were 40s. Either storage for 6 months or frying for 40 s did not significantly change the composition of CLA in egg yolk. However, the degradation of CLA was statistically significant when the CLA components of egg yolk protected CLA from degradation. It is concluded that CLA is well preserved in egg before it is consumed. 相似文献
958.
18-Crown-6-tetracarboxylic acid (18C6H4) is a chiral selector with high selectivity for the enantioseparation of solutes bearing the primary amine function. This work presents the simultaneous separation of positional enantiomers of methyl-DL-tryptophans by using 18C6H4 as an additive to the background electrolyte. Separation conditions such as pH, the concentration of 18C6H4, and the applied voltages have critical inference on the simultaneous separation. The addition of cyclodextrins as anionic surfactants to the background electrolyte did not improve the separation. The selector-selectand interactions between 18C6H4 and the positional enantiomers have been investigated. It was observed that both the position and type of substituents contribute to the enantioselectivity. The migration order and resolution depended on the distance from the substituents to the asymmetric carbon of the enantiomers. 相似文献
959.
Nitrogen-15 labeled pyrroles have been prepared from commercially available 15N glycine or sodium nitrite using the Barton-Zard, Knorr, and Kleinspehn approaches. These pyrroles were used as intermediates in the synthesis of per-15N labeled porphyrins needed for the analysis and assignment of vibrational spectra for sedimentary porphyrins. Etioporphyrin-I was prepared via pyrromethene intermediates, while etioporphyrins II-V and a related tetrahydrobenzoporphyrin were synthesized via stepwise routes involving the copper(II) mediated cyclization of a,c-biladienes as the key step. Detailed analyses of both the proton and carbon-13 NMR spectra provide nitrogen-15 coupling constants for these important structures. 相似文献
960.
Upon the electrochemical oxidation of tris(2,2′-bipyridyl) ruthenium(II) [Ru(bpy)2+3] and hydroxyl carboxylic acids, for instance, citric acid, tartaric acid, malic acid, and
-gluconic acid, bright electrochemiluminescences (ECLs) were observed. Different luminescent reactions were presented depending on the applied potential. The light emission was mainly caused by the reaction between alkoxide radical ion and Ru(bpy)3+3below the potential +1.80 V (vs Ag/AgCl). The luminescence intensity obviously increased because of the more complex reaction process. The luminescence wavelength of 608 nm, which could be found either at higher potential than +1.80 V or in the potential range from +1.30 to +1.80 V, confirmed that ECL was caused by Ru(bpy)2+3*. The factors which affect the determination and HPLC separation of the four acids were also investigated. 相似文献