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排序方式: 共有492条查询结果,搜索用时 468 毫秒
41.
An effective method for achieving a room-temperature multiwavelength erbium-doped fiber ring laser is presented. Simultaneous multiwavelength lasing with 0.5-nm intervals is achieved both experimentally and theoretically by addition of sinusoidal phase modulation in the ring cavity to prevent single-wavelength oscillation. 相似文献
42.
A new butenolide, designated odoratinolide (1), was isolated from the bark of the Vietnamese medicinal plant Machilus odoratissima. Its structure was determined by spectroscopic analyses. 相似文献
43.
Christine Bressy Minh Ngoc NGuyen Brigitte Tanguy Van Giang Ngo André Margaillan 《Polymer Degradation and Stability》2010,95(7):1260-9117
Polymers containing hydrolytically labile trialkylsilyl ester side groups were synthesised via a conventional and a controlled radical polymerization. The trialkylsilyl methacrylate monomer unit was chosen for its capacity to hydrolyse into basic, acid or sea water varying the hydrophilic character of the resulting polymer backbone with time. The hydrolysis or saponification reaction of the ester bond of the trialkylsilyl methacrylate was monitored through a 1H NMR study showing the formation of siloxane side-products. Several copolymers and polymer blends were prepared as matrixes for controlled erodible systems. Their capacity to hydrolyse was demonstrated through SEM investigations with selective dissolution of free films containing hydrolysable copolymers and PMMA blends. Well-defined random and diblock copolymers with methyl methacrylate were investigated to show the effect of the microstructure on the erosion properties of the corresponding coatings. Poly(methyl methacrylate-b-tert-butyldimethylsilyl methacrylate) diblock copolymers synthesised through the RAFT process showed a better control of the erosion with a constant erosion rate over a long-time service in sea water at pH = 8.2. In addition, experiments showed that the erosion rate could be modulated by varying the molar proportion of hydrolysable side groups onto the copolymer backbone and the weight amount of copolymers mixed with PMMA in toluene solution. 相似文献
44.
The monoterpene (−)-isopulegol (7) has been used as a starting material for the total synthesis in eight/nine steps of two sesquiterpenes which were recently isolated from the medicinal plant Fabiana imbricata. Use of this approach has shown that a structure proposed as 3,11-amorphadiene (3) should be revised to that of 4,11-cadinadiene (18) and confirmed the structure proposed for the natural product 4-amorphen-1 1-ol (1). 相似文献
45.
Ngoc Binh Vo Le Anh Nguyen Tung Lam Pham Duy Tien Doan Thanh Binh Nguyen Quoc Anh Ngo 《Tetrahedron letters》2017,58(25):2503-2506
A procedure to exclusively obtain 3′S-cyanoanhydrovinblastine 12 from two naturally occurring vinca-alkaloids (catharanthine and vindoline) in one step with good yield is described. Stereoselective reductions of 12, providing straightforward access to three new vinca-alkaloids, including two diastereomers 3′S-cyano-(4′R,5′-dihydro)-anhydrovinblastine and 3′S-cyano-(4′S,5′-dihydro)-anhydrovinblastine as well as (3′S-aminomethyl)-(4′S,5′-dihydro)-anhydrovinblastine in good yields is also reported. 相似文献
46.
An efficient one-pot procedure for the synthesis of ionic liquids based on nitrogen-containing heterocycles, imidazolium or pyridinium under ‘green chemistry’ conditions has been described. Imidazolium salts and DBU have been found to catalyze efficiently the benzoin condensation giving good yields within very short reaction time using solvent-free microwave activation conditions. 相似文献
47.
48.
An oxacalix[2]arene[2]pyrimidine-bis(ZnII-porphyrin) conjugate was readily prepared via nucleophilic aromatic substitution of a phenolic AB3-Zn-porphyrin on the upper rim of a (1,3-alternate) 5,17-bis(methylsulfonyl)oxacalix[4]arene precursor. Efficient 1:1 complex formation between the ‘jaws’ bisporphyrin tweezer and fullerene C70 was evidenced by 1H NMR titrations (K = 3.0 × 104 M−1), while no detectable complexation could be observed with C60. On the other hand, an analogous oxacalix[4]arene-bis(Cu-corrole) conjugate did not show any measurable (C60 or C70) fullerene binding. 相似文献
49.
Thang M. Ngo Nam M. Hoang Tram T. M. Tran 《Journal of Radioanalytical and Nuclear Chemistry》2010,286(1):287-293
The effects of absorbed doses, initial pH and 1-naphthol concentration onto its radiolysis in aqueous sulphuric and hydrochloric
acids by gamma rays from 60Co were investigated. Under the experimental conditions, 1-naphthol degradation yields increased with increasing the absorbed
doses (0.3–3.0 kGy) and with decreasing the initial 1-naphthol concentration (20–1 ppm). It was found out that the hydrated
electrons did not play any significant roles in 1-naphthol radiolysis, as the degradation yields were higher at pH0 ~ 0.46 compared to those at pH0 ~ 2.0–5.0. The corresponding radiolytic yields G(−1-naphthol) were (6.13 ± 1.00)) × 10−2 and (5.11 ± 0.22) × 10−2 μmol/J in sulphuric acids, (15.61 ± 3.85) × 10−2 and (4.76 ± 0.48) × 10−2 μmol/J in hydrochloric acids. 1-Naphthol degradation rates could be described by the kinetic equations of pseudo-first-order
reactions. An empirical relation between the observed reaction constants k
D and the initial 1-naphthol concentrations was established, enabling to predict the absorbed doses required for a given treatment
efficiency. Three products of 1-naphthol degradation were revealed using an HPLC/UV procedure. 相似文献
50.
Long Giang BachMd. Rafiqul Islam Yeon Tae JeongYeong Soon Gal Kwon Taek Lim 《Applied Surface Science》2012,258(7):2816-2822
The synthesis of chemically anchored adenosine with biocompatible poly(2-hydroxylethyl methacrylate) grafted gold nanoparticles (Ado-i-PHEMA-g-AuNPs) was realized by employing a simple strategy. Disulfide-containing poly(2-hydroxylethyl methacrylate) (DT-PHEMA) was initially synthesized by atom transfer radical polymerization (ATRP). The formation of DT-PHEMA was confirmed by 1H-NMR and FT-IR. The molecular weight and molecular weight distribution were found to be 9.6 kg/mol and 1.40 from GPC analysis. DT-PHEMA was subsequently used for the synthesis of PHEMA-g-AuNPs by a grafting to protocol. The grafting of DT-PHEMA on the surface of AuNPs was confirmed by FT-IR, TGA, XPS, and EDX analyses. The particle size of the PHEMA-g-AuNPs was found to be ca. 5.0 nm from HR-TEM analysis. Boronic acid was used for functionalization of PHEMA-g-AuNPs, which was then subjected for covalent immobilization with adenosine via strong interaction between free hydroxyl groups of adenosine and boronic acid. Characterization and properties of the Ado-i-PHEMA-g-AuNPs were investigated by taking advantage from FT-IR, XPS, EDX, and UV-visible spectroscopy. The Ado-i-PHEMA-g-AuNPs nanocomposite exhibits a surface plasmon resonance peak at 586 nm which is red shifted from AuNPs (521 nm), indicating significant changes of surface property upon PHEMA-adenosine immobilization onto the surface of AuNPs. 相似文献