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21.
The photoreaction of biacetyl and tetramethylethylene yields four products (1–4). A substantial variation in product yield and quenching kinetics with temperature and isotopic substitution is found for this photoreaction. 相似文献
22.
In this paper are presented quantum mechanical t-initial and t-average cross sections and rate constants for the reactions D + H2(ν1 = 0, 1) → HD(νf = 0, 1) + H. The calculations were done employing the infinite order sudden approximation. It was found that the t-average total cross sections overlap very nicely with the available classical cross sections. As for rate constants a reasonably good fit was found with available experimental results. 相似文献
23.
Function of the Reaction Center of Green Sulfur Bacteria 总被引:1,自引:0,他引:1
The reaction center (RC) of green sulfur bacteria belongs to the Fe-S type RC, as do the photosystem I of oxygenic photosynthetic organisms and the RC of heliobacteria. The core parts of the green sulfur bacterial and the heliobacterial RC are assumed to be homodimeric, in contrast to those of purple bacteria, photosystem I and photosystem II. This paper describes recent advances in the study of the function of the green sulfur bacterial RC. 相似文献
24.
Funasaki N Ishikawa S Hirota S Neya S Nishimoto T 《Chemical & pharmaceutical bulletin》2004,52(6):708-713
The structure and ethanol complexation of a cyclic tetrasaccharide (CTS) in aqueous solution were investigated by proton NMR spectroscopy and molecular mechanics calculations. Two glucose units, A and B, of CTS are alternatively bonded by alpha-1,3 and alpha-1,6 linkages. The overlapped signals of protons A5, A6S, A6R, B3, B6S and B6R were resolved by spectral simulations to determine their chemical shifts and vicinal coupling constants. All vicinal coupling constants except for the A5-A6 spin system are consistent with the dihedral angles in the X-ray crystal structure. Each of protons A5, A6S, and A6R in the two units of A is equivalent with respect to the chemical shift. The vicinal coupling constants of (3)J(5-6S) and (3)J(5-6R) for unit A are close to the average of two rotamers that are present in crystals. The intensities of cross-peaks in the rotating frame nuclear Overhauser effect spectroscopy (ROESY) spectrum were rather well correlated with the effective distances calculated for the X-ray structure and molecular mechanics structures calculated in vacuo and water, although they are slightly better correlated with molecular mechanics structure in vacuo than with the other structures. From the changes of the chemical shifts of several CTS protons with increasing ethanol concentration, it was suggested that adsorption sites of ethanol on the plate structure of CTS are protons B2 and B4 (site B) in the concave face side and protons A1 and A2 (site A) in the convex back side. The binding constants for sites A and B are 0.0061 and 0.0176 M(-1), respectively. These binding constants are much smaller than a value of 4.1 M(-1) for the ethanol-alpha-cyclodextrin complex. 相似文献
25.
26.
Hidetsura Cho Yoshiko Ohnaka Mariko Hayashimatsu Masaru Ueda Keiyuu Shima 《Tetrahedron letters》1986,27(52):6377-6380
Chlorination of 5,6-dihydropyrimidine-4-(3H)-one derivatives (1) with POCl3 gave 1,4(3,4)-dihydropyrimidines (3), whose alkoxycarbonylation (ClCOOREt3N or NaH) afforded regioselectively novel compounds (4). A new Pummerer
rearrangement of compound (1, X=
---S(O)CH3) with
3, gave compound (5h). 相似文献
27.
28.
Ditzler WR Hill D Hoftiezer J Johnson KF Lopiano D Shima T Shimizu H Spinka H Stanek R Underwood D Wagner RG Yokosawa A Burleson GR Faucett JA Fontenla CA Garnett RW Luchini C Rawool-Sullivan MW Bhatia TS Glass G Hiebert JC Kenefick RA Nath S Northcliffe LC Damjanovich R Jarmer JJ Vaninetti J Jeppesen RH Tripard GE 《Physical review D: Particles and fields》1992,46(7):2792-2830
29.
Okimoto N Nakamura T Suenaga A Futatsugi N Hirano Y Yamaguchi I Ebisuzaki T 《Journal of the American Chemical Society》2004,126(40):13132-13139
Two molecular dynamics (MD) simulations totaling 25 ns of simulation time of monomeric scytalone dehydratase (SD) were performed. The enzyme has a ligand-binding pocket containing a cone-shaped alpha+beta barrel, and the C-terminal region covers the binding pocket. Our simulations clarified the difference in protein dynamics and conformation between the liganded protein and the unliganded protein. The liganded protein held the ligand molecule tightly and the initial structure was maintained during the simulation. The unliganded protein, on the other hand, fluctuated dynamically and its structure changed largely from the initial structure. In the equilibrium state, the binding pocket was fully solvated by opening of the C-terminal region, and the protein dynamics was connected with hydration water molecules entry into and release from the binding pocket. In addition, the cooperative motions of the unliganded protein and the hydration water molecules produced the path through the protein interior for ligand binding. 相似文献
30.
Molecular Diversity - This research describes a simple and efficient one-pot synthetic approach for the preparation of tetrahydrodiazepine and dihydropyrazine (or dihydroquinoxaline) derivatives in... 相似文献