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111.
Summary Arylbiguanides2 a–e react with benzoin (1) at thepH of the base to two different products.1 undergoes in presence of the base2 a–e oxidation to benzil and benzoic acid, which reacts fast with the arylbiguanides2 a–e to yield N-[4-(arylamino)-6-phenyl-1,3,5-triazine-2-yl]benzamides3 a–d. After lowering thepH of the reaction mixture, the bases2 b–e react with benzil to yield 2-[1-aryl-5-oxo-4,4-diphenyl-2-imidazoline-2-yl]guanidine4 b–e. The mechanism of the formation is discussed. The structure of4b was established from a single crystal x-ray structure analysis. The analysis was carried out at 100K: C23H21N5O,M
r=383.5, monoclinic, C 2/c,a=15.842(6),b=8.419(3),c=30.223(10) Å, =98.44(3)°,V=3 987.3(9) Å3,Z=8,d
x=1.277 g/cm3, =0.81 cm–1,R=5.89%R
w=4.97% (1 537 observations, 233 parameters). 相似文献
112.
Fattakhova Rohlfing D Rathouský J Rohlfing Y Bartels O Wark M 《Langmuir : the ACS journal of surfaces and colloids》2005,21(24):11320-11329
Mesoporous silica thin films were shown to be an appropriate matrix for immobilization of discrete electroactive moieties, yielding uniform transparent thin film electrodes with defined texture and enhanced electrochemical activity. The mesoporous silica films prepared on conducting FTO-coated glass substrate were postsynthetically functionalized. Alkoxysilanes were used as precursors for subsequent grafting via ionic or covalent bonds of representative electroactive species, such as polyoxometalate PMo12O(40)3-, hexacyanoferrate(III), and ferrocene. The electrochemically active concentration within the silica-based composite electrodes achieves 90, 260, and 60 micromol cm(-3) for polyoxometalate, hexacyanoferrate(III), and ferrocene, respectively. The amount of molecules involved in the charge-transfer sequence is proportional to the film thickness and comparable to the total amount of embedded guests. Thus, eventually the whole bulk volume of the modified silica films is electrochemically accessible. Immobilization in the chemically modified silica matrix alters the redox potential of the electroactive molecules. Electron exchange between the adjacent redox centers (electron hopping) is proposed as a possible charge propagation pathway through the insulating silica matrix, which is supported by the fact that the high charge uptake is observed also for the hybrid electrodes with the covalently anchored redox guests. 相似文献
113.
The compounds Ce(10)Cl(4)Ga(5) and Ln(3)ClGa(4) (Ln = La, Ce) were synthesized from stoichiometric mixtures of Ln, LnCl(3), and Ga under Ar atmosphere in sealed Ta ampules at 910-1020 degrees C for 25-26 days. Ce(10)Cl(4)Ga(5) is isostructural to La(10)Cl(4)Ga(5) (space group I4/mcm, No. 140) with lattice constants a = 7.9546(11) A, c = 31.793(6) A. Ln(3)ClGa(4) represents a new structural type, also in the space group I4/mcm, with a = 8.1955(8) and 8.1123(11) A, c = 11.363(2) and 11.229(2) A, respectively, for Ln = La and Ce. Ce(10)Cl(4)Ga(5) features building blocks of Ga-centered Ce(6) trigonal prisms and distinctive two-dimensional intermetallic CuAl(2) and U(3)Si(2) type nets. Its electronic structure falls within the realm of reduced rare-earth halides. Ln(3)ClGa(4) also contains the intermetallic CuAl(2) type nets, but the interstitials are inverted: The building blocks are Cl-centered Ln(6) octahedra. Its electronic structure is characterized by strong peripheral Ln-Ga bonding stabilizing the Ln(6)Cl octahedron which normally would have its Ln-Ln antibonding orbitals filled with electrons from interstitials beyond chalcogen. Magnetic susceptibility and conductivity measurements confirm the metallic nature of all three compounds. 相似文献
114.
115.
Oded Schramm 《Inventiones Mathematicae》1992,107(1):543-560
Summary This paper proves that given a convex polyhedronP 3 and a smooth strictly convex bodyK 3, there is some convex polyhedronQ combinatorically equivalent toP whichmidscribes K; that is, all the edges ofQ are tangent toK. Furthermore, with some stronger smoothness conditions on K, the space of all suchQ is a six dimensional differentiable manifold.Oblatum 18-V-1991 相似文献
116.
117.
Winfried Wendelin Ilse Zmölnig Hans-Wolfgang Schramm 《Monatshefte für Chemie / Chemical Monthly》1980,111(5):1189-1202
Guanidine reacts with cyclohexanone, cycloheptanone, acetone and 3-pentanone, resp., in a molar ratio 2∶1 to give the 1,3,5-triazaspiro[5.5]undeca-and [5.6]dodeca-1,3-dien-2,4-diamines3 a and3 b resp. and the 6,6-dimethylresp. diethyl-1,6-dihydro-1,3,5-triazin-2,4-diamines3 d and3 e resp. On the contrary, action of guanidine on cyclopentanone yields not3 c, but the 1′,5′,7′-tetrahydrospiro[cyclopentane-1,4′-cyclopentapyrimidine]-2′(3′H)-imines2 c, 5 c and6 c resp., which are 1∶2- and 1∶3-condensates. Phenylacetone is transformed by guanidine (1∶2) to give 6-phenyl-2,4-pyrimidindiamine (8 f). The structure of the compounds cited is proved by NMR-, IR-, and (partially) mass spectra. The different courses of the formation of3 a, b, d, e, 2 c, 5 c and6 c resp. and8 f are also discussed. The structural formulae of some additional bases, which were synthesized from guanidine and cyclopentanone, 3-pentanone and phenylacetone resp. could not be established. 相似文献
118.
We have provided a model to interpret the non-quadratic-intensity dependence behavior commonly observed in the two-photon fluorescence (TPF) experiment excited with high laser intensity. The model also provides one with a different technique to measure the two-photon absorption cross section of an organic chromophore in solution. In contrast to the commonly used low intensity technique that depends on the quadratic-intensity law, the present technique is based on the non-quadratic-intensity dependence of two-photon fluorescence. Auxiliary data such as two-photon quantum efficiency and fluorescence collection efficiency, essential in the low intensity method, are not required in the present technique. TPF measurements of Rhodamine B in methanol are carried out to demonstrate the validity of the present method. The method is used to determine the two-photon absorption cross section of a new chromophore attached with tricyano-derivatized furan as the electron acceptor. The two-photon absorption cross section measured using this method is also compared with that using a conventional transmission technique. 相似文献
119.
The underlying metal was observed to corrode when a ruthenium dioxide-coated titanium electrode was anodized in an aqueous methanol solution. With a similarly coated platinum electrode peaks were observed on the voltammogram below 1.0 V which were attributed to methanol oxidation on the underlying metal. This effect was more pronounced when the electrode was subjected during cycling to potentials close to 0 V. Rapid oxidation of methanol on RuO2 was observed at potentials above 1.0 V, the rate at a given potential increasing in an approximately linear manner with increasing alcohol concentration. The rate of reaction also increased with increasing temperature and increasing surface roughness. Tafel slope values were rather high (>100 mV decade?1) and a mechanism involving anodically generated species such as OHads was proposed to account for these results. The variation of activity with pH was similar to that reported earlier for oxygen evolution at these anodes and this was again explained in terms of partial deactivation of the surface due to a combination of proton loss and phosphate ion adsorption at intermediate pH values. The release of carbon dioxide from aqueous solutions of higher alcohols at 25°C confirmed the high oxidizing power of RuO2 anodes. 相似文献
120.
We present experimental data of second interaction virial coefficients of ArH2 at temperatures of 77.3, 87.1 and 90.1 K. The results are in excellent agreement with calculations based on the Le Roy-Carley potential energy surface. 相似文献