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21.
Treatment of [Cp*Rh(H(2)O)(3)](OTf)(2) (1) with Me(3)SiNH-t-Bu in acetone gave a hydroxyl-capped half-cubane [Cp*(3)Rh(3)(mu-OH)(3)(mu(3)-OH)](OTf)(3)(t-BuNH(3)) (2). Slow diffusion of Me(3)SiN(3) in diethyl ether into compound in acetone produced an azido-capped half-cubane [Cp*(3)Rh(3)(mu-N(3))(3)(mu(3)-N(3))](OTf)(2) (3). On the other hand, treating 1 with Me(3)SiN(3) in acetone gave an azido-bridged, dinuclear rhodium(III) complex [Cp*Rh(mu-N(3))(OH(2))](2)(OTf)(2) (4). Complexes 2 and 3 represent the first azido- or hydroxyl-capped, incomplete cubane-type Rh clusters. Under appropriate conditions, complexes 2 and 3 could be converted to complex 4. The structures of all products were determined by X-ray diffraction. 相似文献
22.
d-wave superconductor as a model of high-Tc superconductors 总被引:1,自引:0,他引:1
23.
Silver ions dissolved in a polymer matrix are additionally coordinated by carbonyl oxygens of asparagines and their counter anions interact with cationic sites, resulting in the enhanced activity of the silver ion as an olefin carrier for facilitated olefin transport. 相似文献
24.
25.
Won Sick Woo Sam Sik Kang Otto Seligmann V. Mohan Chari Hildebert Wagner 《Tetrahedron letters》1980,21(44):4255-4258
From the seeds of Phytolacca americana two new lignans, Americanin B and D, have been isolated and their structures elucidated mainly by spectroscopic methods 相似文献
26.
Won Ok Choi Mitsuo Sawamoto Toshinobu Higashimura 《Journal of polymer science. Part A, Polymer chemistry》1990,28(11):2923-2935
In the living cationic polymerization of isobutyl vinyl ether (IBVE) initiated by the hydrogen iodide/zinc halide (HI/ZnX2; X = I, Br, Cl) systems, the concentration ([P*]) of the living propagating species was determined by quenching with sodiomalonic ester ( 1 ). The quenching reaction was shown to be clean, instantaneous, and quantitative to give poly (IBVE) with a terminal malonate group from which [P*] was obtained by 1H-NMR spectroscopy. In the polymerizations in toluene below +25°C, [P*] was constant and equal to the initial concentration ([HI]0) of hydrogen iodide, independent of the type and concentrations of ZnX2 as well as monomer conversion. At 0 and +25°C, however, the living species started decaying immediately after the complete consumption of monomer. In contrast, such a decay process was absent at ?15°C even in the absence of monomer until about an hour (depending on the conditions) after the end of polymerization. The deactivation reaction was first order in [P*], and the lifetime (half-life) of the living species was longer at lower temperature and at lower ZnX2 concentration. On the basis of these [P*] and lifetime measurements, the HI/ZnX2 systems were also compared with the HI/I2 counterpart. 相似文献
27.
Kang MS Kim JH Kim YJ Won J Park NG Kang YS 《Chemical communications (Cambridge, England)》2005,(7):889-891
The ionic conductivity of polymer electrolytes and their interfacial contact with dye-attached TiO2 particles were enhanced markedly by the addition of amorphous oligomer into polymer electrolytes, resulting in very high overall energy conversion efficiency. 相似文献
28.
Pyun DK Kim BJ Jung HJ Kim JH Lee JS Lee WK Lee CH 《Chemical & pharmaceutical bulletin》2002,50(3):415-418
A new series of 1beta-methylcarbapenems 1a-d bearing 5-methyl-4-mercaptopyrrolidinone rings has been prepared and evaluated for in vitro antibacterial activity and pharmacokinetic parameters. Most compounds showed excellent antibacterial activity and high stability to dehydropeptidase-1. We have synthesized optically active 5-methyl-4-hydroxypyrrolidinones from enantiomerically pure aziridine esters. 相似文献
29.
Regio- and stereoselective iodinative cleavage of 2′,3′-anhydropurine nucleosides was achieved with samarium diiodide and ethyl bromoacetate to produce the corresponding 3′-iodopurine nucleosides, which were then converted to 3′-deoxypurine nucleosides including the natural product cordycepin. 相似文献
30.
Dong Won Kim Young Shin Jeon Young Kyu Jeong Moo Yul Suh Kih Soo Joe 《Journal of Radioanalytical and Nuclear Chemistry》1995,189(2):219-227
The chromatographic separation of lithium isotopes was investigated by chemical exchange with the recently synthesized polymer-bound dibenzo pyridino diamide azacrown (DBPDA) and reduced dibenzo pyridino diamide azacrown (RDBPDA). Column chromatography was employed for the determination of the effect of solvents and ligand conformation on the separation coefficients. The maximum separation coefficients, , for the DBPDA and RDBPDA at 20.0±0.02°C with acetonitrile as eluent, were found to be 0.034±0.002 and 0.035±0.002, respectively. The isotope separation coefficient and adsorption capability of the lithium ion on the DBPDA and RDBPDA were only slightly dependent on ligand structure, but strongly dependent on the solvent. DBPDA and RDBPDA appeared to have almost the same value for the isotope separation coefficient of lithium. 相似文献