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181.
本文建立了2,2’-二羟基联苯(DHP)和4-羟基联苯(HP)的胶束增敏导数-可变角同步荧光同时分析方法,可变角同步扫描所得到的DHP和HP的谱峰位置均对应于常规光谱中的最佳激发-发射位置,经二阶求导后,消除分析谱带干扰,所得的二阶导数-可变角同步光谱即可用于两物质的同时测定,方法快速灵敏,DHP测定范围为0.05~0.5mg/L,HP测定范围为0.07~2mg/L。 相似文献
182.
Synthesis,photophysical and electrochemical studies of di-2-pyridyl ketone complexes of rhodium(III)
Huang Wen Liang Lee Jen Rong Shi Sheu Yuan Tsai Cheng Yuan 《Transition Metal Chemistry》2003,28(4):381-387
Complexes of rhodium(III) with di-2-pyridyl ketone (dpk), Rh(dpk)(MeCN)Cl3
(1) and cis-[Rh(dpk)2Cl2]+
(2), have been successfully prepared and characterized. At low temperature (77 K), complex (2) in EtOH/MeOH (4:1, v/v) shows a broad, symmetric and structureless red emission with a microsecond lifetime and, hence, is assigned as the dd* phosphorescence. Electrochemical data, including cyclic voltammetry, normal pulse voltammetry, triple pulse voltammetry and controlled potential electrolysis, have been obtained for the two dpk complexes of rhodium(III) in MeCN. On the basis of analysis of the electrochemical (1,2) and luminescence data (2), electron transfer mechanisms are proposed. For complex (1), two reduction processes occur at the metal-localized orbitals with elimination of chlorides during the first reduction step. This is followed by a one-electron reduction at the metal. For complex (2), three electrons are transferred to the metal in two successive reduction steps accompanied by elimination of two chlorides. After these two reduction steps another one-electron reduction occurs at the dpk ligand. 相似文献
183.
In the presence of [Ru(terpyridine)(2,6‐pyridinedicarboxylate)], aliphatic and benzylic alcohols are oxidized to the corresponding aldehydes or ketones with high selectivity by using hydrogen peroxide as the oxidant. There is no need for the addition of co‐catalysts or organic solvents. By applying an optimized reaction protocol, high catalyst productivity (turnover number>10 000) and activity (turnover frequency up to 14 800 h?1) has been achieved. 相似文献
184.
风毛菊化学成分研究(Ⅰ) 总被引:6,自引:0,他引:6
从风毛菊中分离得到16种化合物,经光谱方法鉴定为山奈素-3-O-(6"-O-巴豆酰)-β-D-葡萄糖甙(1)、槲皮素-3-O-(6"-O-巴豆酰)-β-D-葡萄糖甙(2)、丁香甙甲醚(3))、山奈素-3-O-β-D-葡萄糖甙、槲皮素-3-O-β-D-葡萄糖甙、丁香甙、α-香树脂醇棕榈酸酯、β-香树酯醇棕榈酸酯、羽扇豆醇棕榈酸酯、羽扇豆醇乙酸酯、羽扇豆醇、β-谷甾醇、棕榈酸、二十四烷酸、二十六烷酸、二十五烷烃,其中(1)、(2)和(3)为新化合物。 相似文献
185.
186.
Ai Jun HOU Hui YANG Bei JIANG Qin Shi ZHAO Yan Ze LIU Zhong Wen LIN Han Dong SUN Laboratory of Phytochemistry Kunming Institute of Botany Chinese Academy of Sciences Kunming Department of Phytochemistry Henan College of Traditional Chinese 《中国化学快报》2000,11(9)
In continuation of our research on diterpenoids in the Isodon species, several newcompounds"' were obtained from the leaves oflsodon xerophilus (C. Y. Wu et H. W. Li)H. Hara (Labiatae), a perennial shrub native to Yunnan province. Further fractionation ofthe EtOAc extract led to the isolation of tWo new enl-kauranoids, xerophilusin E (l) andxerophilusin F (2). This paper deals with the structUral elucidation of the newcompounds.Xerophilusin E (l), a minor constitUent, was obtained as p… 相似文献
187.
Shi Liang HUANG Yi LUO Zhi Shu HUANG Xian Zhang BU Pei Qing LIU Lin MA Yue Ming LI Albert S. C. CHAN Lian Quan GU 《中国化学快报》2006,17(6):769-772
Mansonone compounds represent a series of naturally occurring o-quinones mainly isolated from the heartwood of Mansonia Altissima1 and Ulmus Glabra2. Mansonone F contained oxaphenalene skeleton which was a relatively novel structure and rarely existed in … 相似文献
188.
稀土金属作用下芳香醛、酮的还原偶联反应 总被引:4,自引:1,他引:4
由Ln/ROH/TMSCl组成的体系能选择性地使芳香族醛、酮还原偶联形成频哪醇, 产率优良, 而对脂肪族醛酮呈惰性。 相似文献
189.
[reaction: see text] OSW saponins, featuring a 16beta,17alpha-dihydroxycholest-22-one aglycon and an acylated beta-D-xylopyranosyl-(1-->3)-alpha-L-arabinopyranosyl residue attached to the 16-hydroxyl group, have recently been discovered from a group of lily plants, which show potent antitumor activities with a novel mechanism of action. This paper describes an aldol approach to the stereoselective construction of the 16alpha,17alpha-dihydroxycholest-22-one structure from 16alpha-hydroxy-5-androsten-17-ones and propionates. Elaboration of the aldol adducts toward OSW-1, involving installation of the isoamyl ketone side chain, inversion of the 16-hydroxyl configuration, and selective protection of the C22-oxy function, has been explored and accomplished. In particular, the present route was found convenient for the synthesis of OSW saponin analogues with a C22-ester side chain. Thus, the 23-oxa-analogue of OSW-1 (40) was prepared starting from the industrial dehydroisoandrosterone (1) in a linear eight-step sequence and in 26% overall yield. Analogues with a variety of modified side chains were prepared, via aldol condensation with propionates of varying length, thiopropionate, and acetate (for preparation of 68-75) or via aminolysis of the 22,16-lactone 26 (for preparation of the 23-N-analogues). Cross metathesis (CM) reaction was also found feasible for modification at the final stage from C22-allyl ester 70. Valuable structure-activity relationships (SAR), together with the practical synthetic approach, have thus been provided to set a new stage for further studies on this new type of antitumor structures. 相似文献
190.
Jingcheng Hao Hanqing Wang Shuo Shi Runhua Lu Taotao Wang Ganzuo Li Haiying Sun 《中国科学B辑(英文版)》1997,40(3):225-235
By the orthogonal design, the optimal formation conditions for the middle-phase microemulsions in the system dioctadecyldimethylammonium
chloride (DODMAC)/ sodium dodecyl sulfate (SDS)/n-butanol/n-hep-tane/brine were obtained as follows: WDODMAC: WSDS = 1:4-1:5,C
π-butanol (%) = 11.0-12.0, andC
NaCl (%) = 3.25
Investigations have been made on the effects of the concentrations of NaCl and n-butanol (l.0%-14.0%), the ratios ofWDODMAC: to WSDS, and the kinds of alcohols (n-propanol, n-butanol, and n-pentanol) on the formation, the phase behaviour, the ultralow interfacial
tensions, the optimal salinity (S*), and the length of salinity (δS). Some rules and data were worked out about the formation and characteristics of the middle-phase
microemulsions. The mi-crostructures of the middle-phase microemulsions were also studied by using FT-IR, ESR, and freeze
fracture electron microscopy techniques. The results from the three methods show that the microstructures of the middlephase
mi-croemulsions undergo the change from O/W to bicontinuous (B.C.) and to W/O. The distribution rule of the orga-nized molecule
assemblies in the middle-phase microemulsions is conducible to constructing the model of microemulsion systems, to recognizing
the microstructures of the middle-phase microemulsions, and to setting forth the relationship between the microstructures
and macro-properties of rnicroemulsions.
Project supported by the Niltional Natural Science Foundation of China and the Chinese Postdoctoral Science Foundation. 相似文献