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2.
A new series of thiophene‐ and furan‐containing chromophores with a chiral prolinol donor and a sulfone acceptor has been synthesized. The UV‐vis absorptions, second‐order nonlinear optical properties, and X‐ray crystal structures are described. 相似文献
3.
The three new lignanoids 1 – 3 and the five new phyllocladane diterpenoids 7 – 11 were isolated from the leaves of Callicarpa furfuraceae, together with two known lignanoids, lariciresinol ( 4 ) and (+)‐sesamin ( 5 ), and five known diterpenoids, 17‐norphyllocladane‐3,16‐dion ( 6 ), calliterpenone ( 12 ), calliterpenone 17‐acetate ( 13 ), (3β,16α)‐phyllocladane‐3,16,17‐triol ( 14 ), and (3β,16α)‐phyllocladane‐3,16,17‐triol 17‐acetate ( 15 ). Their structures were established by spectral‐data interpretation. 相似文献
4.
牛血清白蛋白与有机小分子偶氮磺Ⅲ、溴偶氮磺Ⅲ相互作用的研究 总被引:1,自引:0,他引:1
本文研究了在不同酸度下.偶氮磺、溴偶氮磺Ⅲ与牛血清白蛋白的作用情况,用光度法求出了不同条件下偶氮磺Ⅲ、溴偶氮磺Ⅲ与牛血清白蛋白的结合个数,并用三种不同的方法相互对照.证明偶氮磺Ⅲ、溴偶氮磺Ⅲ在牛血清白蛋白上有两类不同接合部位。利用Forster非幅射转移理论确定了有机小分子在牛血清白蛋白上的结合位置并对反应机理作了初步讨论。 相似文献
5.
Czechoslovak Mathematical Journal - We characterize the Choquet integrals associated to Bessel capacities in terms of the preduals of the Sobolev multiplier spaces. We make use of the boundedness... 相似文献
6.
Meng-Kiat Chuah 《Proceedings of the American Mathematical Society》1996,124(11):3481-3491
Let be a compact semi-simple Lie group, and let be a maximal unipotent subgroup of the complexified group . In this paper, we classify all the -invariant Kaehler structures on . For each Kaehler structure , let be the line bundle with connection whose curvature is . We then study the holomorphic sections of , which constitute a -representation space.
7.
Ali Mohammad Akbar Mirza Aminul Huq Keng See Tho Wai Butcher Raymond J. 《Transition Metal Chemistry》2003,28(2):241-245
Condensation of 2,6-diacetylpyridine (dap) with S-methyldithiocarbazate (smdtc) in a 1:2 molar ratio yields a bicondensed pentadentate Schiff base (H2dapsme) which reacts with K2MCl4 (M = PdII, PtII) giving stable complexes of empirical formula, [M(dapsme)] · 0.5Me2CO. These complexes have been characterized by a variety of physico-chemical techniques. Condensation of dap with smdtc in a 1:1 molar ratio also yields the bicondensed Schiff base (H2dapsme) as the major product, but a mono-condensed one-armed Schiff base (Hmdapsme) is also obtained as a minor product. The latter reacts with K2PdCl4 in an EtOH–H2O mixture yielding a crystalline complex of empirical formula, [Pd(mdapsme)Cl], the crystal structure of which has been determined by X-ray diffraction. The complex has a distorted square-planar structure in which the ligand is coordinated to the palladium(II) ion as a uninegatively charged tridentate chelating agent via the pyridine nitrogen atom, the azomethine nitrogen atom and the thiolate sulfur atom; the oxygen atom of the acetyl group does not participate in coordination. 相似文献
8.
Mohammed A. Suliman Mohammed A. Gondal Mohamed A. Dastageer Gaik‐Khuan Chuah Chanbasha Basheer 《Photochemistry and photobiology》2019,95(6):1485-1494
An efficient method of photocatalytic degradation of methylparaben in water using Ag nanoparticles (NPs) loaded AgBr‐mesoporous‐WO3 composite photocatalyst (Ag/AgBr@m‐WO3), under visible light is presented. In this process, quantification of methylparaben in water was carried out by high‐performance liquid chromatography (HPLC) and the HPLC results showed a significant reduction of methylparaben in water due to the enhanced of photocatalytic degradation efficiency of Ag/AgBr@m‐WO3. For the material synthesis, highly ordered mesoporous‐WO3 (m‐WO3) was initially synthesized by sol–gel method and AgBr nanoparticles (NPs) were subsequently introduced in the pores of m‐WO3, and finally, the Ag nanoparticles were introduced by light irradiation. The enhanced photocatalytic degradation of methylparaben in water is attributed to the formation of surface plasmonic resonance (SPR) due to the introduction of Ag NPs on the surface of the catalyst. Also, the formation of heterojunction between AgBr and mesoporous‐WO3 in Ag/AgBr@m‐WO3 significantly inhibited the recombination of light‐induced electron‐hole pairs in the semiconductor composite. The morphological and optical characterizations of the synthesized photocatalysts (Ag/AgBr@m‐WO3) were carried out using SEM, TEM, XDR, N2 adsorption–desorption, UV‐VIS diffuse reflectance spectroscopy (DRS). Also, the photocatalytic studies using radical scavengers were carried out and the results indicated that is the main reactive species. 相似文献
9.
Keng Lung Lee Joey Feld Dr. Paul Hume Prof. Tilo Söhnel Dr. Erin Leitao 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(2):815-824
A series of ammonium monosubstituted H-phosphonate salts were synthesized by combining H-phosphonate diesters with amines in the absence of solvent at 80 °C. Variation of the ester substituent and amine produced a range of ionic liquids with low melting points. The products and by-products were analyzed by spectroscopic and spectrometric techniques in order to get a better mechanistic picture of the dealkylation and formal dearylation observed. For dialkyl H-phosphonate diesters, (RO)2P(O)H (R=alkyl), the reaction proceeds via direct dealkylation with the reactivity increasing in the order R=iPr<Et<Me corresponding to DFT calculated activation enthalpies of 22.6, 20.8, and 17.9 kcal mol−1. For the diphenyl H-phosphonate diesters, (PhO)2P(O)H, the dearylation was found to proceed via phenol-assisted formation of a 5-coordinate intermediate, (PhO)3PH(OH), from which P(OPh)3 and water were eliminated. The presence of an equivalent of water then facilitated the formation of P(OH)2OPh and the amine, R'NH2, subsequently abstracted a proton from it to yield [(PhO)PH(O)O]-[R'NH3]+. 相似文献
10.
Geoffrey Cottenet Carine Blancpain Véronique Sonnard Poh Fong Chuah 《Analytical and bioanalytical chemistry》2013,405(21):6831-6844
Considering the increase of the total cultivated land area dedicated to genetically modified organisms (GMO), the consumers’ perception toward GMO and the need to comply with various local GMO legislations, efficient and accurate analytical methods are needed for their detection and identification. Considered as the gold standard for GMO analysis, the real-time polymerase chain reaction (RTi-PCR) technology was optimised to produce a high-throughput GMO screening method. Based on simultaneous 24 multiplex RTi-PCR running on a ready-to-use 384-well plate, this new procedure allows the detection and identification of 47 targets on seven samples in duplicate. To comply with GMO analytical quality requirements, a negative and a positive control were analysed in parallel. In addition, an internal positive control was also included in each reaction well for the detection of potential PCR inhibition. Tested on non-GM materials, on different GM events and on proficiency test samples, the method offered high specificity and sensitivity with an absolute limit of detection between 1 and 16 copies depending on the target. Easy to use, fast and cost efficient, this multiplex approach fits the purpose of GMO testing laboratories. Figure
A broad multiplex real‐time PCR method for the detection and identification of GMOs 相似文献