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1.
Microwave energy has been employed for cleavage of sulfur bonds in the S8ring. Cleavage of S–S bonds was carried out in extraction of elemental sulfur in simple amide solvents. Due to the use of microwave energy and the polarity of amides, up to, 100 times lower concentration of a nucleophilic reducer, such as azide or nitrite, may be used to cleave the sulfur bonds. The time needed for cleavage of sulfur bonds at sulfur concentration higher than 0.1 mg S/100 mg solvent was reduced from hours to minutes. This cleavage was quantitative when carried out in a Teflon container in a microwave oven with continuous or pulsed heating. UV spectra show from which value of absorption there will be a sulfur sol at different sulfur concentrations. This allows us to adjust the microwave exposure power and time to avoid sulfur sol formation and not destroy the sample. 相似文献
2.
Wieslaw Wojnowski Barbara Becker Karl Peters Eva-Maria Peters Hans Georg von Schnering 《无机化学与普通化学杂志》1987,553(10):287-292
Structure of Pentaphenyldisilane For the first time Pentaphenyldisilane was prepared by Gilman and Goodman. It is produced by the reaction of Ph3SiLi with Ph2ClSiH. The crystal structure presents an ideally staggered conformation. The distance d(Si? Si) = 235.7 pm corresponds to a normal single bond length. This emphasizes the complete relief of the central Si? Si bond by the insertion of only one hydrogen atom. 相似文献
3.
Wieslaw Jamroz 《Optical and Quantum Electronics》1980,12(6):443-447
The dispersion of the third-order electric susceptibilities(; , , –) and(; , 0, 0) of NaCl and KCl monocrystals has been calculated by means of experimental data on the electro-optic Kerr effect. The result has been obtained by using semi-classical models of anharmonic oscillators. An ionic contribution to the electro-optic coefficients has been presented. From the result obtained it follows that the third-order electric susceptibilities are of the order of 10–22 m2 V–2. 相似文献
4.
Contributions to the Chemistry of Silicon-Sulphur Compounds. 46. 29Si-N.M.R. Chemical Shifts of Trialkoxysilylthio Derivatives of Permethylpolysilanes 29Si-N.M.R. chemical shifts of trialkoxysilythio derivatives of permethylpolysilanes of the two series: α, ω-(RO)3SiS(SiMe2)nSSi(OR)3, n = 2, 3, 4, 6 and 1-(RO)3SiS(SiMe2)nMe, n = 2, 4; R = i-Pr, t-Bu and also 31C-NMR shifts are given. The relationship of 29Si-NMR chemical shift from the netto charge at the silicon atom q(Si) which value has been corrected according to the Sandorfy C quantum-chemical model is discussed. The greater reduction of the electron density at silicon in compounds with Si? X bond (X = S, P, Cl) has been explained by a conjugation of the lone of sulphur with the Si? X bonding pair. 相似文献
5.
RESOLUTION OF TWO EMISSION SPECTRA FOR TRYPTOPHAN USING FREQUENCY-DOMAIN PHASE-MODULATION SPECTRA 总被引:1,自引:0,他引:1
Joseph R. Lakowicz Ranjith Jayaweera Henryk Szmacinski Wieslaw Wiczk 《Photochemistry and photobiology》1989,50(4):541-546
We describe a novel application of frequency-domain fluorometry which allows resolution of the decay times and emission spectra of samples which display multi-exponential decay kinetics. This method does not require any previous knowledge about the decay times or any assumptions about the shape of the emission spectra. We record the wavelength-dependent phase angles and modulations (phase angle and modulation spectra) using a number of light modulation frequencies. The data is analyzed by non-linear least-squares to recover the emission spectra and their associated decay times. Phase and modulation spectra (PM Spec) were used to recover the emission spectra associated with the two decay times of tryptophan at pH = 7 (0.54 and 3.44 ns). The emission spectra of these components are centered at 340 and 355 nm, respectively, with the amplitude of the 0.54 ns component contributing 6% to the total emission. These results are in agreement with previous time-resolved studies by Szabo and Rayner [J. Am. Chem. Soc. 102, 554-563 (1980)]. Control experiments were performed on mixtures of N-acetyl-L-tryptophanamide (NATA) and PPD, which demonstrate our ability to recover the spectra and decay times from two component mixtures. NATA itself displayed a single decay time and only one emission spectrum. 相似文献
6.
Wieslaw Pusz 《Letters in Mathematical Physics》1991,21(1):59-67
The natural S U(2) action on the creation and annihilation operators satisfying twisted canonical commutation relations (TCCR) is investigated. It is shown that the Fock representation is the only covariant irreducible representation of TCCR.Partially supported by the program RP.1.10. 相似文献
7.
8.
Michal Nowak Wieslaw Tryniszewski Agata Sarniak Anna Wlodarczyk Piotr J. Nowak Dariusz Nowak 《Molecules (Basel, Switzerland)》2022,27(11)
Hydroxyl radical (•OH) scavenging and the regeneration of Fe2+ may inhibit or enhance peroxidative damage induced by a Fenton system, respectively. Plant polyphenols reveal the afore-mentioned activities, and their cumulative net effect may determine anti- or pro-oxidant actions. We investigated the influence of 17 phenolics on ultra-weak photon emission (UPE) from a modified Fenton system (92.6 µmol/L Fe2+, 185.2 µmol/L EGTA (ethylene glycol-bis(β-aminoethyl-ether)-N,N,N′,N,-tetraacetic acid) and 2.6 mmol/L H2O2 pH = 7.4). A total of 8 compounds inhibited (antioxidant effect), and 5 enhanced (pro-oxidant effect) UPE at all studied concentrations (5 to 50 µmol/L). A total of 4 compounds altered their activity from pro- to antioxidant (or vice versa) along with increasing concentrations. A total of 3 the most active of those (ferulic acid, chlorogenic acid and cyanidin 3-O-glucoside; mean UPE enhancement by 63%, 5% and 445% at 5 µmol/L; mean UPE inhibition by 28%, 94% and 24% at 50 µmol/L, respectively) contained catechol or methoxyphenol structures that are associated with effective •OH scavenging and Fe2+ regeneration. Most likely, these structures can determine the bidirectional, concentration-dependent activity of some phenolics under stable in vitro conditions. This is because the concentrations of the studied compounds are close to those occurring in human fluids, and this phenomenon should be considered in the case of dietary supplementation with isolated phenolics. 相似文献
9.
Physically unacceptable chaotic numerical solutions of nonlinear circuits and systems are discussed in this paper. First, as an introduction, a simple example of a wrong choice of a numerical solver to deal with a second-order linear ordinary differential equation is presented. Then, the main result follows with the analysis of an ill-designed numerical approach to solve and analyze a particular nonlinear memristive circuit. The obtained trajectory of the numerical solution is unphysical (not acceptable), as it violates the presence of an invariant plane in the continuous systems. Such a poor outcome is then turned around, as we look at the unphysical numerical solution as a source of strong chaotic sequences. The 0–1 test for chaos and bifurcation diagrams are applied to prove that the unacceptable (from the continuous system point of view) numerical solutions are, in fact, useful chaotic sequences with possible applications in cryptography and the secure transmission of data. 相似文献
10.
We give an abstract characterization of algebras of partial functions from A n to A endowed with the operations of the Menger superposition and the set-theoretic difference of functions as subsets of A n+1. 相似文献