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71.
Roman L. Antipin Elena K. Beloglazkina Nikolay V. Zyk Nikolay S. Zefirov 《Tetrahedron letters》2007,48(4):729-731
Arylselenenation of conjugated and non-conjugated dienes by arylselenenamides in the presence of phosphorus(V) oxyhalides has been studied. Reactions with conjugated dienes lead to 1,4-adducts whilst only addition to double bonds takes place in reactions with non-conjugated dienes. 相似文献
72.
M.Antonietta Loreto Lucio Pellacani Paolo A Tardella Elena Toniato 《Tetrahedron letters》1984,25(38):4271-4274
Ethoxycarbonylnitrene (EtOCON) generated by α-elimination adds cleanly to allylic ethers giving substituted aziridines. Similar addition via nitrenium ion (EtOCONH+) gives derivatives of β-amino alcohols. 相似文献
73.
Justicia J Rosales A Buñuel E Oller-López JL Valdivia M Haïdour A Oltra JE Barrero AF Cárdenas DJ Cuerva JM 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(7):1778-1788
The titanocene-catalyzed cascade cyclization of epoxypolyenes, which are easily prepared from commercially available polyprenoids, has proven to be a useful procedure for the synthesis of C(10), C(15), C(20), and C(30) terpenoids, including monocyclic, bicyclic, and tricyclic natural products. Both theoretical and experimental evidence suggests that this cyclization takes place in a nonconcerted fashion via discrete carbon-centered radicals. Nevertheless, the termination step of the process seems to be subjected to a kind of water-dependent control, which is unusual in free-radical chemistry. The catalytic cycle is based on the use of the novel combination Me(3)SiCl/2,4,6-collidine to regenerate the titanocene catalyst. In practice this procedure has several advantages: it takes place at room temperature under mild conditions compatible with different functional groups, uses inexpensive reagents, and its end step can easily be controlled to give exocyclic double bonds by simply excluding water from the medium. 相似文献
74.
Abstract— In order to investigate the intramolecular "quenching" of the photoexcitation of some 5-alkenyloxypsoralen derivatives, we have prepared model compounds in which a psoralen moiety was linked at position 5 to a terminal double bond via a polymethylenic chain of various length (n = 2-9). The isolation and characterization of photocycloadducts obtained for each compound after irradiation at 365 nm in a polar solvent was performed. The results on the photoreactivity of this series of compounds show that the 3,4-pyrone double bond of 5-alkoxypsoralens is the most reactive. Four kinds of intramolecular photocycloadducts between the 3,4-pyrone double bond and the chain unsaturation were obtained according to the length of the linking chain: cis-syn, trans-syn, cis-anti and trans-anti. Their structures were established by a combination of 1 H and 13 C NMR and fully assigned by l H NOE (nuclear Overhauser effect) and 1 H-13 C HMQC (heteronuclear multiquantum correlation) spectroscopies. No traces of 4',5' adducts were detected. 相似文献
75.
Core-shell nanostructures from single poly(N-vinylcaprolactam) macromolecules: stabilization and visualization 总被引:1,自引:0,他引:1
Bronstein LM Kostylev M Tsvetkova I Tomaszewski J Stein B Makhaeva EE Okhapkin I Khokhlov AR 《Langmuir : the ACS journal of surfaces and colloids》2005,21(7):2652-2655
Formation of core-shell poly(N-vinylcaprolactam) (PVCL) single-molecule nanostructures due to interaction of PVCL with metal ions was studied using transmission electron microscopy, 13C NMR, and light scattering. This study demonstrates that addition of CoCl2 to PVCL in its globular conformation yields unimolecular core-shell polymer particles with the core decorated with Co(II) ions. The crucial condition for formation of well-defined unimolecular nanostructures is the presence of stable globular aggregates in aqueous solution. Moreover, the metal ions should have a sufficiently high coordination number (higher than 2) to provide a cross-linking and stabilization of the core. 相似文献
76.
Reductive amination of 4′-formyl[benzo-15-crown-5] with sodium cyanoborohydride in the NH4Ac/MeOH medium followed by acid addition and extraction with CHCl3 unexpectedly lead to the isolation of the salt (B15C5-CH2-NH3)+-(H3BCNBH2CN)− with an unusual dicyanodiborohydride anion. The self-complementary 4′-ammoniomethyl[benzo-15-crown-5] cation was found to exist as a supramolecular dimer in the solid state, acetonitrile solution, and gas phase as revealed by X-ray crystallography, NMR and mass spectrometry, respectively. 相似文献
77.
García G Rodríguez JL Lacconi GI Pastor E 《Langmuir : the ACS journal of surfaces and colloids》2004,20(20):8773-8780
In the present paper, a systematic electrochemical investigation on thiourea (TU) electrooxidation was developed on polycrystalline and (111) single-crystal gold electrodes in 0.1 M perchloric acid. The combination of cyclic voltammetry with in situ Fourier transform infrared spectroscopy (FTIRS) and differential electrochemical mass spectrometry techniques have allowed the nature of the species formed during the electroadsorption and electrooxidation of TU to be established. FTIRS experiments were performed in D2O to clean up the region of the H2O bending around 1600 cm(-1). It was concluded that TU adsorbs tilted on the surface in the 0.05-0.40 VRHE potential range. A dual-path reaction mechanism was evidenced in the oxidation process. The first pathway takes place from adsorbed TU at E > 0.40 VRHE and implies the formation of [Au(I)-(TU)2]+, which is oxidized to NH2CN and S0 at E > 0.80 VRHE. In a following oxidation step at E > 1.20 V, N2, CO2, and HSO4-/SO4(2-) were produced. The second parallel reaction occurs from TU in solution at E > 0.50 VRHE to form (TU)2(2+). All these species were characterized from the spectroscopic experiments. Similar results were obtained for both surfaces. 相似文献
78.
Various combinations of Cu(0), CuCl, 2,2′-bipyridine (bpy) and 1,10-phenanthroline (phen) were used as catalysts for the grafting polymerizations of styrene from polysiloxane macroinitiators functionalized with benzyl chloride. While Cu(0)/bpy alone promotes the grafting, narrower polydispersities were obtained in the presence of CuCl. Analysis of the Cu(0) surface before and after polymerization by a combination of AFM, TGA and FTIR investigations reveals the formation of bpy or phen films on Cu(0). In the presence of CuCl, the ligand film appears decorated with CuCl particles which increase in size with increasing the CuCl concentration. The initial layer occurs most likely as a result of complexation between the ligands and the Cu(0) surface and acts as a support for the rest of the film. These observations are consistent with the film formation on Cu(0) from related nitrogen donors and indicate that the reactivity of the Cu surface may depend not only on its prior treatment but also on the deposition of ligands from the reaction mixture. 相似文献
79.
Elena Supponeva Surat Hotchandani Robert Carpentier 《Photochemistry and photobiology》1996,63(6):831-836
In this report, the effect of platinization on the photosynthetic activity of the chloroplast membranes is studied. Oxygen evolution, fluorescence emission and thermal de-activation processes are modified after platinization. It is shown that photosystem II activity is affected by the hydrogen purging involved in the platinization procedure as seen by the reduced rates of oxygen evolution and a decrease in variable fluorescence. Depletion of bicarbonate from photosystem II during purging is suggested to be responsible partly for the decreased electron transfer rates and for a lower half-saturation light intensity required for energy storage as measured by photoacoustic spectroscopy. On the other hand, the electron sink created by the reduction of hydrogen at the acceptor side of photosystem I is shown to reoxidize efficiently the plas-toquinone pool of photosystem II. 相似文献
80.
Kraineva J Narayanan RA Kondrashkina E Thiyagarajan P Winter R 《Langmuir : the ACS journal of surfaces and colloids》2005,21(8):3559-3571
We investigated the effect of incorporation of a small aqueous peripheral membrane protein (cyt c) into the three-dimensional periodic nanochannel structures formed by the lipid monoolein (MO) on its rich phase behavior as a function of temperature, pressure, and protein concentration using synchrotron X-ray small-angle diffraction. By simultaneous use of the pressure-jump relaxation technique and time-resolved synchrotron X-ray diffraction, we also studied the kinetics of various lipid mesophase transformations of the system for understanding the mechanistic pathways of their formation influenced by the protein-lipid interactions. Cyt c incorporated into the bicontinuous cubic phase Ia3d of MO has a significant effect on the lipid structure and the pressure stability of the system already at low protein concentrations. Concentrations higher than 0.2 wt % of cyt c led to an increase in interfacial curvature due to interaction of the protein with the lipid headgroups. This promotes the formation of a new, probably partially micellar cubic phase of crystallographic space group P4(3)32. Upon pressurization, the P4(3)32 phase undergoes a phase transition to a cubic Pn3m phase with smaller partial specific volume. Increase in protein concentration increases the pressure stability of the P4(3)32 phase. The formation of this phase from the cubic phase Pn3m is a slow process taking many seconds and having a time lag in the beginning. It seems to occur as a two-state process without ordered intermediate states. At temperatures above 60 degrees C, the P4(3)32 phase is unable to accommodate the unfolded protein and transforms to a bicontinuous cubic Ia3d phase. Time-resolved small-angle X-ray scattering studies show that the L(alpha) --> Ia3d transition in pure MO dispersions under limited hydration conditions occurs within a time interval of 1 s at 35 degrees C preceded by a lag phase of 1.5 s. The Ia3d cubic phase initially forms with a much larger lattice constant due to hydration and experiences an initially lower curvature that relaxes within about 1 s. Interestingly, no other cubic phases are involved as intermediates in the transition, i.e., the gyroid cubic phase is able to form directly from the L(alpha) phase. The mechanism behind the L(alpha) --> Ia3d transition in pure MO dispersions has been discussed within the framework of recent stalk models for membrane fusion. In the presence of cyt c, the L(alpha) --> Ia3d transition is much slower. The rather long relaxation times of the order of seconds are probably due to a kinetic trapping of the system and limitation by the transport and redistribution of water and lipid in the evolving new lipid phases. We also studied the transition from the pure lamellar L(alpha) phase to the Ia3d-P4(3)32 two phase region and observed a rather complex transition behavior with transient lamellar and cubic intermediate states. 相似文献