A novel probe for determination of electrical surface potential of surfactant micelles: N,N'‐di‐n‐octadecylrhodamine

The peculiarities of the structure of the fluorescent dye N,N'‐di‐n‐octadecylrhodamine advantage its using as an interfacial acid–base probe in aqueous micellar solution of colloidal surfactants. Two long hydrocarbon tails of the dye provide similar orientation of both cation and zwitterion on the micelle/water interface, with the ionizing group COOH exposed to the Stern region in all the systems studied. Further, the charge type of the acid–base couple, A⁺B^±, ensures similar values of the ‘intrinsic’ contribution, pK, to the ‘apparent’ pK value in micelles of different surfactants. This makes the indicator suitable for determination of electrical surface potentials, Ψ. The pKs have been obtained in cationic, anionic, zwitterionic, and nonionic surfactant systems, at various salt background. In total 17 systems were studied. At bulk counterion concentration of ca. 0.05 M, the pK values vary from 2.14 ± 0.07 in n–C₁₈H₃₇N(CH₃)Cl^– micelles to 5.48 ± 0.06 in n–C₁₆H₃₃OSONa⁺ micelles. The Ψ values, corresponding to the Stern region of micelles, have been evaluated as Ψ = 59.16 pK–pK for T = 298.15 K. The pK parameter was equated to the average value of 4.23 in nonionic surfactants (4.12–4.32, depending on the surfactant type). For cetyltrimethylammonium bromide and sodium n‐dodecylsulfate micelles, the Ψ values (±(7–11) mV) appeared to be +118 mV and at bulk Br^? concentration 0.019 M and ?76 mV at bulk Na⁺ concentration 0.020 M, respectively. This satisfactorily agrees with the theoretical values +111 and ?84 mV, estimated using the Oshima, Healy, and White equation for these well‐defined colloidal systems. Finally, not only absorption, but also fluorescence spectra display the same response to changes in bulk pH. Copyright © 2007 John Wiley & Sons, Ltd.     

The quadratic Graver cone, quadratic integer minimization, and extensions

It has been shown in a number of recent papers that Graver bases methods enable to solve linear and nonlinear integer programming problems in variable dimension in polynomial time, resulting in a variety of applications in operations research and statistics. In this article we continue this line of investigation and show that Graver bases also enable to minimize quadratic and higher degree polynomial functions which lie in suitable cones. These cones always include all separable convex polynomials and typically more.     

Simultaneous immobilization of glucose oxidase and peroxidase to urea derivative of regenerated acetylcellulose granules

A method for simultaneous covalent immobilization of glucose oxidase and peroxidase with previously oxidized carbohydrate residues to urea derivative of regenerated acetylcellulose granules is described. The effect of immobilization on the catalytic properties of the separately immobilized enzymes are studied. The immobilized enzymes manifested no change in their pH and temperature optima and slight increase ofK _m x compared to data for the soluble enzymes. A column packed with simultaneously immobilized enzymes is used for manual glucose determination in blood sera. The results are in high correlation with those obtained by the Beckman Glucose Analyzer method (r = 0.976). The method is economic (the enzyme-carrier conjugate may be used more than 300 times), easy to perform, and less time consuming than the manual methods utilizing soluble enzymes. The established manual method can be proposed for emergency clinical analysis and smaller clinical laboratories.     

Isomeric composition of ditolyls formed upon the thermal decomposition of an anionic Pt(IV) σ-tolyl chloride complex

Conclusion Heating a solution of PtCl₆ ^2– ions and toluene in CF₃CO₂H-H₂O leads to the formation of a platinum(IV) -tolyl complex which decomposes in the presence of free toluene to give 3,3-, 4,4-, 3,4-, 2,3- and 2,4-ditolyls.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 10, pp. 2377–2380, October, 1986.This study was carried out in the framework of the Cooperation Program of Catalysis Scientists at the academies of sciences of the Socialist countries.     

Transition metal-free cross-coupling of furan ring with haloacetylenes

On the example of menthofuran, a naturally abundant compound, it has been shown for the first time that the furan ring can be readily cross-coupled with acylhaloacetylenes in the solid Al₂O₃ powder at room temperature to afford the corresponding 2-ethynyl derivatives in up to 88% yield. The reaction represents a ring closing/ring opening process that includes reversible formation of the intermediate cycloadducts further producing acetylene derivatives with elimination of HHal.     

High-efficiency deflection of high-energy protons through axial channeling in a bent crystal

Beam deflection due to axial channeling in a silicon crystal bent along the 111 axis was observed with 400 GeV/c protons at the CERN Super Proton Synchrotron. The condition for doughnut scattering of protons by the atomic strings of the crystal was attained. Such a condition allowed one to observe a beam deflection of 50 murad with about 30% efficiency. The contribution of hyperchanneled states of protons to the observed beam deflection was less than 2% according to simulation results.     

1,2,5-Oxadiazolo[3,4-g]indoles via annelation of 6,7-dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one oxime with acetylene

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Synthesis,structure, and magnetic properties of a Yb<Superscript>III</Superscript> complex with the iminopyridine radical-anionic ligand

The reaction of equimolar amounts of ytterbocene (C₅Me₄H)₂Yb(THF)₂ and iminopyridine 2,6-Prⁱ₂C₆H₃N=CH(C₅H₄N) accompanied by the one-electron oxidation of the ytterbium ion produced the unique lanthanide complex (C₅Me₄H)₂Yb^III[2,6-Prⁱ₂-C₆H₃NCH(C₅H₄N)]–? with the iminopyridine radical-anionic ligand. The structure of the complex in the crystalline state was established by X-ray diffraction and its magnetic properties were studied in the temperature range of 1.8—300 K.     

Light‐Harvesting Three‐Chromophore Systems Based on Biphenyl‐Bridged Periodic Mesoporous Organosilica

Three‐chromophore systems with light‐harvesting behavior were prepared, which are based on periodic mesoporous organosilica (PMO) with crystal‐like ordered structure. The organic bridges of biphenyl‐PMO in the pore walls act as donors and two types of dye are incorporated in the one‐dimensional channels. Consecutive two‐step‐Förster resonance energy transfer is observed from the biphenyl moieties to mediators (diethyl‐aminocoumarin or aminoacridone), followed by energy transfer from mediators to acceptors (dibenzothiacarbocyanine, indodicarbocyanine, sulforhodamine G). High energy‐transfer efficiencies ranging from 70 to 80 % are obtained for two‐step‐FRET, indicating that the mesochannel structure with one‐dimensional ordering provides spatial arrangement of chromophore pairs for an efficient direct energy transfer. The emission wavelength can be tuned by a choice of acceptor dye: 477 nm (diethylaminocoumarin), 519 nm (aminoacridone), 567 nm (sulforhodamine G), 630 nm (dibenzothiacarbocyanine), and 692 nm (indodicarbocyanine).