排序方式: 共有57条查询结果,搜索用时 9 毫秒
31.
Mahshid Chekini Elisabeth Prince Lily Zhao Haridas Mundoor Ivan I. Smalyukh Eugenia Kumacheva 《Advanced Optical Materials》2020,8(4)
Hybrid nanoparticles composed of cellulose nanocrystals (CNCs) and carbon‐dots (C‐dots) have promising applications in chemistry, biology, and nanomedicine, owing to the photoluminescence, sensory properties, and cytocompatibility of C‐dots, and chirality, cytobiocompatibility, and high cellular uptake of CNCs. The possibility of circularly polarized luminescence in such nanoparticles is particularly attractive. Herein, scalable and straightforward hydrothermal synthesis of nitrogen‐doped fluorescent C‐dots under reflux condition by using CNCs as a carbon source and chiral substrate is reported. Under ultraviolet irradiation, hybrid C‐dot/CNC nanoparticles exhibit stronger emission of left‐handed, than right‐handed, circularly polarized light, with high dissymmetry factor up to 0.2. The nanoparticles are biocompatible: the normalized proliferation index above 100% is determined for MCF 7 cells cultured in the suspension of C‐dot/CNC nanoparticles. These hybrid nanoparticles can find applications as biotags for labeling, sensing, and therapeutics and as building blocks of photoluminescent cholesteric CNC films with photonic applications. 相似文献
32.
Subhajit Pal Mahshid Alizadeh Phally Kong Andreas F. M. Kilbinger 《Chemical science》2021,12(19):6705
Higher ring-opening metathesis propagation rates of exo-norbornene derivatives over endo derivatives are well established in the literature. Here, we report for the first time that endo-isomers of oxanorbornene derivatives show higher reactivity towards ring-opening metathesis with Grubbs'' 3rd generation catalyst (G3) than the corresponding exo-isomers. A very high selectivity for the reaction of G3 with endo over the exo-isomers could be shown. Furthermore, single molecular addition of the endo-isomers with G3 was observed. On the other hand, pure exo-monomers could successfully be homopolymerized. Mixtures of exo- and endo- monomers, however, prevented the homopolymerization of the exo-monomer. Such mixtures could successfully be copolymerized with cycloalkenes, resulting in alternating copolymers. An oxanorbornadiene derivative could be shown to undergo single addition reactions, exploited in the preparation of mono-end functional ROMP polymers. These could be selectively derivatized via endgroup selective thiol-ene click reactions. A thiol and alcohol end functional ROMP polymer was synthesized, and the efficient end functionalization was confirmed by 1H NMR spectroscopy and MALDI-ToF spectrometry.Bridgehead revisited: endo-7-oxa norborneneimide derivatives (green) initiate faster but propagate more slowly than the analogous exo-derivatives (red) in ring-opening metathesis allowing the synthesis of alternating and end functional polymers. 相似文献
33.
The level lines of the Gaussian free field are known to be related to SLE4. It is shown how this relation allows to define chordal SLE4 processes on doubly connected domains, describing traces that are anchored on one of the two boundary components. The precise
nature of the processes depends on the conformally invariant boundary conditions imposed on the second boundary component.
Extensions of Schramm’s formula to doubly connected domains are given for the standard Dirichlet and Neumann conditions and
a relation to first-exit problems for Brownian bridges is established. For the free field compactified at the self-dual radius,
the extended symmetry leads to a class of conformally invariant boundary conditions parametrised by elements of SU(2). It
is shown how to extend SLE4 to this setting. This allows for a derivation of new passage probabilities à la Schramm that interpolate continuously from
Dirichlet to Neumann conditions. 相似文献
34.
Amarnath Bheemaraju Mahshid Pourmand Boqian Yang Sravan K. Surampudi Travis L. Benanti Marc Achermann 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(12):986-993
We have probed the effect of side chains on the charge transfer dynamics in dyads containing quaterthiophene (QT) donor and naphthalene diimide (NDI) acceptor. The donor and the acceptor are covalently linked using a flexible linker. Four dyads (1–4) were synthesized with the quaterthiophene bearing hexyl side chain and the naphthalene diimide bearing hydrocarbon, fluorocarbon, branched or polar side chains. The UV-Vis spectra for these dyads showed the existence of a donor-acceptor complex. The time-resolved fluorescence (TRF) decay studies show a rapid quenching of fluorescence in all the dyads upon excitation of the donor. We found that the side chains on the NDI did not alter the quenching rates in solution. 相似文献
35.
Let ${\mathcal{G}}$ be a group of invertible linear transformations on a finite-dimensional vector space over an algebraically closed field. We show that if ${\mathcal{G}=\mathcal{H}\vee\mathcal{K}}$ , where ${\mathcal{H}}$ is a normal subgroup consisting of singleton spectrum operators and ${\mathcal{K}}$ is a triangularizable subgroup, then ${\mathcal{G}}$ is triangularizable. 相似文献
36.
Kamal AlimohammadiYaghoub Sarrafi Mahmood TajbakhshSaeed Yeganegi Mahshid Hamzehloueian 《Tetrahedron》2011,67(8):1589-1597
The regio- and stereochemical polar [3+2] cycloaddition of the azomethine ylides, which were generated in situ by the reaction of isatin derivatives and proline, with trans-β-nitrostyrene and (E)-1-phenyl-2-nitropropene were studied using experimental and theoretical methods. In comparison with trans-β-nitrostyrene, when the reactions were performed with (E)-1-phenyl-2-nitropropene, a remarkable inversion in the regioselectively was observed. The regioselectivity of the reactions was investigated using global and local reactivity indices and frontier molecular orbital (FMO) analysis at the B3LYP/6-31G(d,p) level of theory. The effects of the electronic and steric factors on the regioselectivity of the reactions were discussed. The inspection of geometries and energetics of transition states revealed the importance of weak interactions in regioselectivity of the cycloaddition reactions. 相似文献
37.
Reduction of a variety of imine compounds with triethylsilane in the presence of catalytic amounts of palladium(II) acetate in ethanol resulted in the formation of the corresponding amines in excellent yields after short reaction times. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
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39.
In the present paper, we study Casimir effect for a conformally coupled scalar field propagating on background of \(4+1\)-dimensional de Sitter (dS) space-time. The field is supposed to obey Dirichlet boundary condition on two 4-dimensional curved boundaries. Technically, we accomplish our calculations using an indefinite field quantization scheme, which already has been successfully applied to the dS minimally coupled massless scalar field and the dS linear gravity to obtain a causal and fully covariant quantum field on dS space-time. 相似文献
40.
Maryam Mirza‐Aghayan Mahboubeh Khoshkameh Langrodi Mahshid Rahimifard Rabah Boukherroub 《应用有机金属化学》2009,23(7):267-271
An efficient synthesis of 1,4‐dihydropyridine derivatives has been achieved by the one‐pot cyclocondensation reaction of methyl 3‐aminocrotonate and a range of aldehydes in the presence of chlorotrimethylsilane as a promoter under solvent‐free conditions. The cyclocondenstion reaction requires a very short time and takes place in good to excellent yields. Furthermore iodotriethylsilane, generated in situ by the reaction of triethylsilane and methyl iodide in the presence of palladium chloride, has been investigated for the synthesis of 1,4‐dihydropyridine derivatives. This facile and efficient method affords high yields for the preparation of 1,4‐dihydropyridines at room temperature and short reaction times. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献