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A study of the nontilted diagonal Bianchi type-V perfect fluid models is undertaken in the nonlocally rotationally symmetric case. It is shown that in such a model, the singularity is necessarily velocity dominated and the upper bound for the ratio of the shear to the expansion is 1/3. A class of such exact models is also presented; the structure of the singularity and the effect of the anisotropy on the scale are discussed. Lastly, an attempt is made to solve exactly the equations of motion for the coordinates of the null geodesics. 相似文献
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The apparent and limiting apparent molar volumes of dilute aqueous solutions of KBF4, and the complexes [Fe(DMSO)6](BF4)3, [Fe(Py)4(H2O)2](BF4)3, [Fe(4-Mepy)2(H2O)2](BF4)3, and [Fe(4-Etpy)2(H2O)2](BF4)3 were determined from density data measured at 5, 15, and 25°C. The apparent and limiting apparent molar adiabatic compressibilities of these complexes were determined from ultrasonic sound velocities measured at the same temperatures in dilute aqueous solutions. The volume change associated with complex formation is discussed in terms of the nature of the coordinate bond and also the role of the central metal atom and ligands in the solvation behavior of these complexes. 相似文献
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Synthesis of some analogues of indole based marine alkaloid (±)gelliusine F, (±)gelliusine E, and total synthesis of 2,2-di(6′-bromo-3′-indolyl)ethylamine are reported. 相似文献
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Some dihydrofuro-fused coumarin derivatives were synthesized from 3-aminoalkyl-4-hydroxycoumarin via in situ generation of N-ylide. The 3-aminoalkylated 4-hydroxycoumarin derivatives were synthesized from one-pot, three-component reaction of 4-hydroxycoumarin, aryl aldehydes, and secondary amines in ethanol at room temperature. Again, when salicylaldehyde was employed instead of benzaldehyde, interestingly pyranocoumarins were obtained. The reaction protocol can be further explored toward the synthesis of many other heterocyclic fused dihydrofurans. 相似文献
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Pyrimido[4,5-d]pyrimidine derivatives 4 have been prepared in an efficient and regioselective manner in water via multi-component reaction of isothiocyanate 1, aromatic aldehyde 2, N,N-dimethyl-6-amino uracil 3 in the presence of p-toluenesulfonic acid (p-TSA) as a Lewis acid catalyst. 相似文献
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Adachi I Aihara H Arinstein K Asner DM Aushev T Aziz T Bakich AM Barberio E Belous K Bhardwaj V Bhuyan B Bondar A Bračko M Brodzicka J Browder TE Chang P Chen A Chen P Cheon BG Chilikin K Chistov R Cho IS Cho K Choi Y Dalseno J Danilov M Drásal Z Drutskoy A Eidelman S Epifanov D Esen S Fast JE Feindt M Gaur V Gabyshev N Garmash A Goh YM Golob B Hara T Hayasaka K Hayashii H Hoshi Y Hou WS Hsiung YB Hyun HJ Iijima T Ishikawa A Iwabuchi M Iwasaki Y Jaegle I Julius T Kang JH Katayama N Kawasaki T 《Physical review letters》2012,108(3):032001
We report the first observations of the spin-singlet bottomonium states h(b)(1P) and h(b)(2P). The states are produced in the reaction e(+)e(-)→h(b)(nP)π(+)π(-) using a 121.4 fb(-1) data sample collected at energies near the Υ(5S) resonance with the Belle detector at the KEKB asymmetric-energy e(+)e(-) collider. We determine M[h(b)(1P)]=(9898.2(-1.0-1.1)(+1.1+1.0)) MeV/c(2) and M[h(b)(2P)]=(10,259.8±0.6(-1.0)(+1.4)) MeV/c(2), which correspond to P-wave hyperfine splittings ΔM(HF)=(+1.7±1.5) and (+0.5(-1.2)(+1.6)) MeV/c(2), respectively. The significances of the h(b)(1P) and h(b)(2P) are 5.5σ and 11.2σ, respectively. We find that the production of the h(b)(1P) and h(b)(2P) is not suppressed relative to the production of the Υ(1S), Υ(2S), and Υ(3S). 相似文献
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We explain the recently observed interesting structure in the dynamic structure factor S(k, ω) of various metallic systems by considering processes that involve single-particle and multi-particle excitations. 相似文献
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Some novel functionalized indeno[1,2-b]furans were synthesized from the reaction of indandione/indanone and aldehydes at room temperature followed by the reaction of the Knoevenagel condendensed intermediate with 4-hydroxycoumarins in the presence of iodine as catalyst in dimethyl sulfoxide (DMSO) under thermal conditions. The reaction involved in a condensation and Michael addition followed by lactone ring opening and intramolecular cyclization process to afford the product in high yield in easy work-up procedure. 相似文献