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11.
Wetting and dewetting transitions play a central role in controlling the hydrophobicity of the lining of biological channels in order to regulate aqueous solution permeation. Understanding of the operational characteristics of biological nanochannels led to experimental efforts to mimic their behavior and to achieve potential-induced, repeatedly-switchable wettability transitions in synthetic nanochannels in the early 2010s. Since then, research has identified conditions needed to produce reversible wettability transitions using a number of different environmental stimuli—such as light, pH, and electrostatic charge—in addition to potential. Furthermore, nascent understanding of the underlying phenomena in synthetic nanochannels was rapidly followed by practical applications, including oil–water separations, drug release, and electroactive flow control based on switchable wettability. More practical applications are being developed continuously, as the physical and chemical principles that govern hydrophobic gating at the nanoscale are further elucidated, making it possible to exploit wettability as a design element in nanofluidic systems. 相似文献
12.
Irradiation (lambda = 670 or >613 nm) of 4,5-benzodiazocycloheptatriene (15), matrix isolated in argon at 10 K, produces primarily 2,3-benzobicyclo[4.1.0]hepta-2,4,6-triene (9) accompanied by small amounts of triplet 4,5-benzocycloheptatrienylidene (2) and 2-naphthylcarbene (10). A reversible photoequilibrium is established in which 9 is converted to 10 at lambda = 290 nm and then regenerated at lambda = 360 nm. Similarly, matrix-isolated 2,3-benzodiazocycloheptatriene (16) produces 4,5-benzobicyclo[4.1.0]hepta-2,4,6-triene (11) at lambda = 670 or >613 nm, but without detection of 2,3-benzocycloheptatrienylidene (4). Irradiation of 11 at lambda = 290 nm induces ring opening to triplet 1-naphthylcarbene (12), which, in turn, cyclizes back to 11 at lambda = 342 or >497 nm. The diazo compounds and photoproducts are characterized by IR, UV/visible, and ESR spectroscopy, where appropriate, and by comparison of the experimental and B3LYP/6-31G calculated IR spectra for each species. Alternate rearrangement products such as allenes 6, 7, and 8 are not detected in the photolysis of either diazo compound. 相似文献
13.
We synthesized a series of n‐alkylthiomethyl‐substituted polystyrenes (#T‐PS, # = 4, 8, 12, and 16) and n‐alkylsulfonylmethyl‐substituted polystyrenes (#S‐PS, # = 4, 8, 12, and 16), where # is the number of carbon atoms in the n‐alkyl side group of the polymers, using polymer analogous reactions to investigate their liquid crystal (LC) alignment properties. In general, the LC cell fabricated using the polymer film having a longer n‐alkyl side group, a thioether linkage group, and a higher molar content of n‐alkyl side group showed homeotropic LC alignment behavior with a pretilt angle of about 90°. The homeotropic alignment behavior was well correlated with the surface energy of the polymer films; when the positive dielectric anisotropic LC (ZLI‐5900‐000 from Merck) and negative dielectric anisotropic LC (MLC‐7026‐000 from Merck) were used to fabricate the LC cells, homeotropic alignment was observed when the surface energy values of the polymer were smaller than about 25 and 32 mJ/m2, respectively. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
14.
We present a simple phenomenological model of the nanografting process with an emphasis on the formation of binary self-assembled monolayers. This model includes dynamical processes that are involved in natural growth experiments, including molecular deposition, surface diffusion, and the phase transition from physisorption to chemisorption, and we show that it predicts domain formation in ungrafted deposition that matches experiment. The one-order-of-magnitude faster kinetics that is found in the nanografting experiments compared to natural self-assembly (or unconstrained self-assembly) is described with a key assumption that the deposition rate is greatly enhanced in the small region confined between the back side of the AFM tip and the edge of the previously deposited self-assembled monolayer. Monte Carlo simulations based on this model reproduce experimental observations concerning the variation of SAM heterogeneity with AFM tip speed. Our simulations demonstrate that the faster the AFM tip displaces adsorbed molecules in a monolayer, the more heterogeneous are the monolayers formed behind the tip, as this allows space and time for the formation of phase-segregated domains. 相似文献
15.
Swallen SF Mapes MK Kim YS McMahon RJ Ediger MD Satija S 《The Journal of chemical physics》2006,124(18):184501
The translational dynamics of the low molecular weight glass-former tris(naphthylbenzene) have been studied on the length scale of a few nanometers at the glass transition temperature Tg. Neutron reflectivity was used to measure isotopic interdiffusion of multilayer samples created by physical vapor deposition. Deposition with the substrate held at Tg-6 K allows observation of dynamics characterizing the equilibrium supercooled liquid. The diffusion coefficient measured at q = 0.03 A(-1) was determined to be 1x10(-17) cm2/s at 342 K (Tg). The self-part of the intermediate scattering function I(s)(q,t) decays exponentially. Samples deposited well below Tg show a substantial thermal history effect during subsequent translational motion at Tg. 相似文献
16.
Gold nanoparticles appear to be superior handles in optical trapping assays. We demonstrate that relatively large gold particles (R(b)=50 nm) indeed yield a sixfold enhancement in trapping efficiency and detection sensitivity as compared to similar-sized polystyrene particles. However, optical absorption by gold at the most common trapping wavelength (1064 nm) induces dramatic heating (266 degrees C/W). We determined this heating by comparing trap stiffness from three different methods in conjunction with detailed modeling. Due to this heating, gold nanoparticles are not useful for temperature-sensitive optical-trapping experiments, but may serve as local molecular heaters. Also, such particles, with their increased detection sensitivity, make excellent probes for certain zero-force biophysical assays. 相似文献
17.
We have experimentally explored and clarified the concept of noise suppression in intrinsically noisy systems by adding noise at the input using a microscopic bead held in a moving and intensity-modulated optical trap. By coupling the stiffness of the optical trap to its position, we have explicitly constructed an experimental model system in which added fluctuations in the trap position result in reduced variance of the observed bead position as compared to a stationary trap. This reduction in variance and the spectral properties of the observed output noise agree with theoretical predictions. Our experiment demonstrates that the essential aspect of noise reduction in such a system is that the added fluctuations drive the system into states with a reduced intensity of intrinsic noise sufficiently often. 相似文献
18.
A one-dimensional heat conduction equation with time- and temperature-dependent heat sources was employed to study the steady-state
and transient response of a composite superconductor subjected to a thermal disturbance. An integral formulation was used
to solve the steady-state problem of current redistribution and heat generation. The results of the integral formulation are
compared with those of an analytical solution. The two solutions agree with each other except when the analytical solution
fails as the temperature in the superconductor begins to exceed the critical temperature. Transient solutions were obtained
by the finite-difference technique and the results are compared with a known analytical solution. Results of numerical calculations
of the transient response of a composite superconductor subjected to an initial pulsed disturbance are presented. It is demonstrated
that the superconductor can switch between the superconducting and the current-sharing state. The transient response and the
stability of the composite conductor depend on the magnitude and duration of the disturbance, the dimensionless temperature
θ*, and the dimensionless parameter φ.
Received on 18 November 1996 相似文献
19.
Mi-Young Son Mi-Ok Lee Hyejin Jeon Binna Seol Jung Hwa Kim Jae-Suk Chang Yee Sook Cho 《Experimental & molecular medicine》2016,48(5):e232
Autoimmune diseases (AIDs), a heterogeneous group of immune-mediated disorders, are a major and growing health problem. Although AIDs are currently treated primarily with anti-inflammatory and immunosuppressive drugs, the use of stem cell transplantation in patients with AIDs is becoming increasingly common. However, stem cell transplantation therapy has limitations, including a shortage of available stem cells and immune rejection of cells from nonautologous sources. Induced pluripotent stem cell (iPSC) technology, which allows the generation of patient-specific pluripotent stem cells, could offer an alternative source for clinical applications of stem cell therapies in AID patients. We used nonintegrating oriP/EBNA-1-based episomal vectors to reprogram dermal fibroblasts from patients with AIDs such as ankylosing spondylitis (AS), Sjögren''s syndrome (SS) and systemic lupus erythematosus (SLE). The pluripotency and multilineage differentiation capacity of each patient-specific iPSC line was validated. The safety of these iPSCs for use in stem cell transplantation is indicated by the fact that all AID-specific iPSCs are integrated transgene free. Finally, all AID-specific iPSCs derived in this study could be differentiated into cells of hematopoietic and mesenchymal lineages in vitro as shown by flow cytometric analysis and induction of terminal differentiation potential. Our results demonstrate the successful generation of integration-free iPSCs from patients with AS, SS and SLE. These findings support the possibility of using iPSC technology in autologous and allogeneic cell replacement therapy for various AIDs, including AS, SS and SLE. 相似文献
20.
We have found strong supporting evidence for the helical structures of single-stranded nucleic acids by stretching individual molecules of polyadenylic acid [poly(A)] and polycytidylic acid [poly(C)]. Analyzing the force versus extension data using a two-state elastic model in which random-coil domains alternate with rigid helical domains allows one to extract the thermodynamic and structural properties. In addition, it also yields moderate to low cooperativity of the helix-coil transition for poly(A) and poly(C), respectively. 相似文献