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11.
Uwe Klingebiel Dieter Bentmann Anton Meller 《Monatshefte für Chemie / Chemical Monthly》1978,109(5):1067-1073
Aminofluorosilanes react with lithiated amines undergoing LiF-elimination and substitution (1). The acyclic silicon-nitrogen-compound2 is isolated in the reaction with a difluorosilane after renewed lithiation.2 is cyclisated in the reaction with butyllithium by butane- and LiF-elimination (3). Aminofluorosilanes with bulky (4) or mesomeric stabilized (5) ligands form stable lithioaminofluorosilanes, which react with fluorosilanes giving substitution products (6, 7).6 and7 react with the lithium salt oftert-butylamin in a molar ratio of 12 to give8 and9 by intramolecular cyclisation.—The mass,1H and19F nmr spectra of the compounds are reported. 相似文献
12.
Uwe Klingebiel Peter Werner Anton Meller 《Monatshefte für Chemie / Chemical Monthly》1976,30(6):939-943
The reaction of RSiCl3 (R=CH3, C2H5, C6H5) and R2SiCl2 (R=CH3) with one mole of the phosphenimidous amides R2N–P=NR [R=R=Si(CH3)3; R=Si(CH3)3, R=C(CH3)3] yieds a four membered PN2Si-ring system under elimination of (CH3)3SiCl. 相似文献
13.
Eugen Jóna Marian Koman Anton Sirota 《Journal of inclusion phenomena and macrocyclic chemistry》1998,30(1):1-12
The stoichiometry and spectral properties of [Ni(4-Etpy)4(NCS)2]nG clathrates have been studied where n = 2 for G = 1-BrN (N = naphthalene), n = 1 or 2 for G = 1-MeN, and n = 0.5 for 2-MeN and 2-BrN. The complexes under study show electronic absorption spectra typical of an octahedral environment of the Ni(II) central atom. The differences found in IR spectra for the (CN) and (Ni–-NNCS) vibrations are discussed. The crystal structure of [Ni(4-Etpy)4(NCS)2]1-MeN was determined by X-ray diffraction and refined to R = 0.0586. Discrete non-centrosymmetric [Ni(4-Etpy)4(NCS)2] molecules form layers of a host structure and the space between the layers is occupied by 1-MeN. The relationship between interatomic distances in the host complex of similar clathrates are discussed. 相似文献
14.
Uwe Klingebiel Dieter Bentmann Anton Meller 《Journal of organometallic chemistry》1978,144(3):381-388
Aminofluorsilanes are obtained by the reaction of fluorosilanes with the lithium salts of the corresponding amines. The reaction of aminofluorosilanes with butyllithium in a (2 + 2)cyclo addition reaction leads to the formation of fourmembered silicon-nitrogen ring compounds. The mechanism of the reaction is discussed, the mass, 1H and 19F NMR spectra of the compounds are reported. 相似文献
15.
We establish a previously conjectured connection betweenp-adics and quantum groups. We find in Sklyanin's two parameter elliptic quantum algebra and its generalizations, the conceptual basis for the Macdonald polynomials, which interpolate between the zonal spherical functions of related real andp-adic symmetric spaces. The elliptic quantum algebras underlie theZ
n
-Baxter models. We show that in then limit, the Jost function for the scattering offirst level excitations in the 1+1 dimensional field theory model associated to theZ
n
-Baxter model coincides with the Harish-Chandra-likec-function constructed from the Macdonald polynomials associated to the root systemA
1. The partition function of theZ
2-Baxter model itself is also expressed in terms of this Macdonald-Harish-Chandrac-function, albeit in a less simple way. We relate the two parametersq andt of the Macdonald polynomials to the anisotropy and modular parameters of the Baxter model. In particular thep-adic regimes in the Macdonald polynomials correspond to a discrete sequence of XXZ models. We also discuss the possibility of q-deforming Euler products.Work supported in part by the NSF: PHY-9000386 相似文献
16.
We study a neural network model consisting ofN neurons where a dendritic connection between each pair of neurons exists with probabilityp and is absent with probability 1-p. For the Hopfield Hamiltonian on such a network, we prove that ifp c[(lnN)/N]1/2, the model can store at leastm=
cpN patterns, where
c 0.027 ifc 3 and decreases proportional to 1/(–lnc) forc small. This generalizes the results of Newman for the standard Hopfield model. 相似文献
17.
Abstract— Three covalently-linked porphyrin hybrid dimers were synthesized, each containing a metallotetraarylporphyrin [Zn(II), Cu(II), or Ni(II)], and a free base tetraarylporphyrin. Transfer of singlet excitation energy from the metalloporphyrin center to the free base porphyrin center was determined by measuring fluorescence properties. The Zn hybrid dimer displayed excellent intramolecular transfer of energy ( 85%) from the excited singlet state of the Zn(II) chromophore to the free base chromophore. No evidence for such transfer of the excited singlet state energy was found in the Ni(II) or Cu(II) analogues. From our experimental data, the fluorescence quantum yield of the Zn hybrid dimer was the same as for the free base monomer porphyrin (0.11; Seybold and Gouterman, 1969). Thus, the covalent attachment of another fluorescent porphyrin center effectively doubled the antenna size without decreasing the quantum yield even though the fluorescence quantum yield of the Zn(II) containing monomer was substantially less (0.03, according to Seybold and Gouterman, 1969) than that of the free base porphyrin. The donor-acceptor distance and the rate constant for energy transfer were calculated using the Forster equation. Assuming random orientation, a donor-acceptor distance of 15 Å was calculated with an associated rate constant (kci) for energy transfer of 1.9 ± 109 s–1. 相似文献
18.
Olga Bakulina Anton Bannykh Ekaterina Levashova Mikhail Krasavin 《Molecules (Basel, Switzerland)》2022,27(12)
Screening of a library of novel N-hydroxylactams amenable by the Castagnoli-Cushman reaction identified four lead compounds that facilitated 55Fe transport into P. aeruginosa cells (one of these synthetic siderophores was found to be as efficient at promoting iron uptake as the natural siderophores pyoverdine, pyochelin or enterobactin). Conjugates of the four lead siderophores with ciprofloxacin were tested for antibacterial activity against P. aeruginosa POA1 (wild type) and the ∆pvdF∆pchA mutant strain. The antibacterial activity was found to be pronounced against the ∆pvdF∆pchA mutant strain grown in CAA medium but not for the POA1 strain. This may be indicative of these compounds being ‘Trojan horse’ antibiotics. Further scrutiny of the mechanism of the antibacterial action of the newly developed conjugates is warranted. 相似文献
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