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1.
V. G. Osmolovskii 《Journal of Mathematical Sciences》2006,135(6):3437-3456
All the equilibrium states of a one-dimensional variational phase-transition problem are explicitly found. The temperature-dependence
of the stability of one-phase equilibrium states is studied. Bibliography: 5 titles.
__________
Translated from Problemy Matematicheskogo Analiza, No. 32, 2006, pp. 3–19. 相似文献
2.
3.
The allure of metal–organic frameworks (MOFs) in heterogeneous electrocatalysis is that catalytically active sites may be designed a priori with an unparalleled degree of control. An emerging strategy to generate coordinatively-unsaturated active sites is through the use of organic linkers that lack a functional group that would usually bind with the metal nodes. To execute this strategy, we synthesize a model MOF, Ni-MOF-74 and incorporate a fraction of 2-hydroxyterephthalic acid in place of 2,5-dihydroxyterephthalic acid. The defective MOF, Ni-MOF-74D, is evaluated vs. the nominally defect-free Ni-MOF-74 with a host of ex situ and in situ spectroscopic and electroanalytical techniques, using the oxidation of hydroxymethylfurtural (HMF) as a model reaction. The data indicates that Ni-MOF-74D features a set of 4-coordinate Ni–O4 sites that exhibit unique vibrational signatures, redox potentials, binding motifs to HMF, and consequently superior electrocatalytic activity relative to the original Ni-MOF-74 MOF, being able to convert HMF to the desired 2,5-furandicarboxylic acid at 95% yield and 80% faradaic efficiency. Furthermore, having such rationally well-defined catalytic sites coupled with in situ Raman and infrared spectroelectrochemical measurements enabled the deduction of the reaction mechanism in which co-adsorbed *OH functions as a proton acceptor in the alcohol oxidation step and carries implications for catalyst design for heterogeneous electrosynthetic reactions en route to the electrification of the chemical industry.The allure of metal–organic frameworks (MOFs) in heterogeneous electrocatalysis is that catalytically active sites may be designed a priori with an unparalleled degree of control. 相似文献
4.
Novella F. Kazanskaya Margarita A. Manenkova Nikolay L. Eremeev 《Applied biochemistry and biotechnology》1996,61(1-2):57-65
The coupling of photosensitive reagents has been carried out with the goal of obtaining the predetermined distribution of binding sites either for “surface” or “spacial” immobilization of biomacromolecules. The correlation holds between light intensity and the number of readant groups emerged in a matrix. 相似文献
5.
Petre BA Youhnovski N Lukkari J Weber R Przybylski M 《European journal of mass spectrometry (Chichester, England)》2005,11(5):513-518
Nitration of tyrosine residues in proteins may occur in cells upon oxidative stress and inflammation processes mediated through generation of reactive nitroxyl from peroxynitrite. Tyrosine nitration from oxidative pathways may generate cytotoxic species that cause protein dysfunction and pathogenesis. A number of protein nitrations in vivo have been reported and some specific Tyrosine nitration sites have been recently identified using mass spectrometric methods. High-resolution Fourier transform ion cyclotron resonance mass spectrometry (MALDI) FT-ICR-MS) is shown here to be a highly efficient method in the determination of protein nitrations. Following the identification of nitration of the catalytic site Tyr-430 residue of bovine prostacyclin synthase, we synthesised several model peptides containing both unmodified tyrosine and 3-nitro-tyrosine residues, using solid-phase peptide synthesis (SPPS). The structures of the nitrotyrosine peptides were characterised both by ESI- and by matrix-assisted laser desorption/ionisation (MALDI)-FT-ICR-MS, using a standard ultraviolet (UV) nitrogen nitrogen laser and a 2.97 microm Nd-YAG infrared laser. Using UV-MALDI-MS, 3-nitrotyrosyl-peptides were found to undergo extensive photochemical fragmentation at the nitrophenyl group, which may hamper or prevent the unequivocal identification of Tyr-nitrations in cellular proteins. In contrast, infrared-MALDI-FT-ICR-MS did not produce fragmentation of molecular ions of Tyr-nitrated peptides. 相似文献
6.
Nikolay Manov 《Tetrahedron》2004,60(10):2387-2391
A solid-phase route for synthesis of 15N-labeled acylpolyamines is described. Utilizing alkylation at benzylic N-atom as a key step, 15N-atoms are incorporated by stepwise construction of the polyamine framework on the solid support. The derivatives were used as reference compounds for the investigation of the MS/MS behavior of spider toxins. 相似文献
7.
V. G. Osmolovskii 《Journal of Mathematical Sciences》1995,73(6):701-710
We prove the following theorem: Suppose the function f(x) belongs toL q (ω, ? n ), ω ? ? m , q∈(1, ∞), and satisfies the inequality $$|\int\limits_\omega {(f(x),{\mathbf{ }}v(x)){\mathbf{ }}dx| \leqslant \mu ||} v||'_q ,{\mathbf{ }}\tfrac{1}{q} + \tfrac{1}{{q'}} = 1,$$ for all n-dimensional vector-valued functions in the kernel of a scalar-valued first-order differential operator £ for which the second-order operatorLL * is elliptic. Then there exists a function p(x)∈W q 1 (ω) such that $$||f(x) - \mathfrak{L}^* p(x)||q \leqslant C_q \mu .$$ Bibliography: 6 titles. 相似文献
8.
Translated from Optimal'nost Upravlyaemykh Dinamicheskikh Sistem, Sbornik Trudov VNIISI, No. 14, pp. 76–86, 1990. 相似文献
9.
Nikolay TzvetkovMarc Schmidtmann Achim MüllerJochen Mattay 《Tetrahedron letters》2003,44(32):5979-5982
Bicyclo[3.3.0]octanone and bicyclo[4.3.0]nonanone derivatives with a cyclopropane unit in the α-position and an unsaturated side chain in the γ-position of the carbonyl group undergo fragmentation-cyclization processes leading to quasi-triquinane systems upon reductive photoinduced electron transfer (PET). For example, the new angular triquinane derivative 6 and the new propellane derivative 12 were synthesized in one step from these starting materials in moderate to good yields. 相似文献
10.
Sergei D. Kirik Julia N. Zaitseva Igor S. Yakimov Nikolay N. Golovnev 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(11):i159-i160
Lithium sodium aluminium fluoride was obtained as a white powder by melting a stoichiometric mixture of AlF3, NaF and LiF at 1223 K, and then cooling to 923 K and sintering at this temperature for 4 h. The ab initio crystal structure determination was carried out using X‐ray powder diffraction techniques. The monoclinic structure of LiNa2AlF6 can be related to cubic elpasolite. The Li and Al atoms lie on inversion centres. The main octahedral AlF6 structural elements are not deformed, but are rotated slightly with respect to the unit‐cell axes. The Li atoms have octahedral coordinations, whereas the Na atoms have cubo‐octahedral coordinations. The Na coordination polyhedron is distorted in comparison with that of elpasolite. 相似文献