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961.
The novel N,P,C‐cage complexes 5 a – f and 6 a – f have been obtained by the reaction of the P‐pentamethylcyclopentadienylphosphinidene complex 2 , generated thermally from 2H‐azaphosphirene complex 1 , with N‐methyl‐C‐arylcarbaldimines 3 a – f . Li/Cl phosphinidenoid complex 8 reacted with 3 a , b to give N,P,C‐cage complexes 6 a , b , whereas with 3 c – f , complexes 6 c – f were obtained in negligible amounts only. Both types of ligand N,P,C‐cage structures 5 and 6 were found to be in an unprecedented equilibrium, with 5 a , f as the predominant species. Transient electrophilic terminal phosphinidene complexes 10 a – f serve as intermediates in both ligand interconversions ( 5 a , f ? 6 a , f ), as evidenced through trapping reactions with phenylacetylene and N‐methyl‐C‐phenylcarbaldimine, thus leading to the novel N,P,C‐cage complexes 13 b and 15 . DFT calculations predicted a small difference in the relative energies of the two types of N,P,C‐cage ligands, and a remarkable stabilisation of the aminophosphinidene complex 10 as the common precursor, thereby providing an insight into this surprising 5‐ring–3‐ring interconversion. In depth analysis of intermediate 10 revealed the occurrence of both through‐bond (conventional inductive/mesomeric effects) and through‐space (non‐covalent interactions) mechanisms, which amount to 67.8 and 14.4 kcal mol?1, respectively, and account for the remarkable stabilisation of this intermediate.  相似文献   
962.
For the first time, the Petasis (borono‐Mannich) reaction is employed for the multicomponent labeling and stapling of peptides. The report includes the solid‐phase derivatization of peptides at the N‐terminus, Lys, and N?‐MeLys side‐chains by an on‐resin Petasis reaction with variation of the carbonyl and boronic acid components. Peptides were simultaneously functionalized with aryl/vinyl substituents bearing fluorescent/affinity tags and oxo components such as dihydroxyacetone, glyceraldehyde, glyoxylic acid, and aldoses, thus encompassing a powerful complexity‐generating approach without changing the charge of the peptides. The multicomponent stapling was conducted in solution by linking N?‐MeLys or Orn side‐chains, positioned at i, i+7 and i, i+4, with aryl tethers, while hydroxy carbonyl moieties were introduced as exocyclic fragments. The good efficiency and diversity oriented character of these methods show prospects for peptide drug discovery and chemical biology.  相似文献   
963.
964.
The objective of this work was to synthesize nanocomposites based on cationic polyelectrolytes and silver nanoparticles using poly(N-vinylbenzyl-N-triethylammonium chloride) as polymer phase. For that, a nanostructured crosslinker was synthesized from silver nanoparticles (AgNPs) and acrylic acid. Molybdate retention properties of nanocomposites were studied in function of pH and ionic strength. In addition, their antimicrobial properties were evaluated against E. coli and S. aureus. It was evidenced that AgNPs can be stabilized using acrylic acid and that this material can be incorporated to the polymer phase during polymerization by free radical of cationic monomers. The effect of pH on retention of molybdate, by the nanostructured polymer, was significant only to low ionic strength (the order seen was pH 5.0 > pH 7.0 > pH 9.0 for 0.0% NaCl). Results suggest that the main interaction influencing the molybdate retention is electrostatic in nature. Finally, antimicrobial activity was enhanced by incorporation of polymerizable nanostructured crosslinker based on AgNPs.  相似文献   
965.
Nonlinear Dynamics - In this paper, the dynamics response of a finite extensibility nonlinear elastic (FENE) absorber attached to a nonlinear primary system is investigated by writing the modal...  相似文献   
966.
967.
Reflection electron energy loss spectra (REELS) were measured for five insulating organic compounds: Kapton, polyethylene (PE), poly(methyl methacrylate) (PMMA), polystyrene (PS) and polytetrafluoroethylene (PTFE), as well as for Ni and Si, in the energy range between 200 and 1600 eV. The average number of surface excitations for a single surface crossing were determined from the experimental data and were found to be considerably smaller than for earlier studied materials, which mainly consisted of elemental metals [Surf. Sci. 486(2001)L461]. The surface excitation parameter, a material parameter used to quantify the relative intensity of surface losses in (photo)electron spectroscopy, was extracted from the data and compared with values found in the literature. The results indicate that surface excitations only have a minor influence on quantification of XPS spectra of polymers. On the other hand, a correction for surface excitations turns out to be essential for measurements of the electron inelastic mean free path of polymers when a metal is used as reference material.  相似文献   
968.
Fuzzy Optimization and Decision Making - Cost-allocation problems in a fixed network are concerned with distributing the costs for use by a group of clients who cooperate in order to reduce such...  相似文献   
969.
970.
The components exponential scator function, succinctly labeled “cexp,” is a function of scator variable in 1+n dimensional elliptic scator algebra. This function is introduced here, and its elementary properties are studied. In 1+1 dimensions, the cexp function becomes the usual complex exponential function of complex variable. The cexp function is shown to be scator holomorphic in the entire scator set according to the differential quotient criterion. The scator derivative of the cexp function is the cexp function itself. The relationship between the Cartesian and polar forms of the cexp function can be seen as a higher-dimensional extension of Euler formula. The mappings of grids in 1+2 dimensional space exhibit ellipses and Lissajous-like figures in addition to circles and radial lines. A cusphere surface is generated for the isometric condition in the function's image. An interesting application of the cexp function as propagators regarding the quantum measurement problem is outlined.  相似文献   
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