PubMed Health⌕ Search

PubMed · 11412080

Switching devices based on interlocked molecules.

Abstract

An architectural rationale and an experimental program aimed at the development of molecular electronics switching devices for memory and computing applications are discussed. Two-terminal molecular switch tunnel junctions are identified as the critical device components of molecular electronics-based circuitry. They can be tiled in two dimensions and are tolerant of manufacturing defects. Singly and multiply configurable solid-state switching devices that are based upon electrochemically switchable molecular and supramolecular systems are discussed in terms of both the synthesis of the molecular components and the fabrication and performance of the devices.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

A R Pease, J O Jeppesen, J F Stoddart, Y Luo, C P Collier, J R Heath. 2001. Switching devices based on interlocked molecules.. https://doi.org/10.1021/ar000178q

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Electrochromic modulation of excited-state intramolecular proton transfer: the new principle in design of fluorescence sensors.

Internal Stark effect (or internal electrochromy) consists of the shift of light absorption and emission bands under the influence of electric field produced by proximal charges. In the studies of 3-hydroxyflavone (3HF) derivatives exhibiting the excited-state intramolecular proton transfer (ESIPT), we describe a new phenomenon - a very strong internal electrochromic modulation of this reaction. Fluorescence spectra of 3HF derivatives with charged groups attached to the chromophore from the opposite sides without pi-electronic conjugation, N-[(4'-diethylamino)-3-hydroxy-6-flavonyl]methyl-N,N-dimethyloctylammonium bromide and 4-[4-[4'-(3-hydroxyflavonyl)]piperazino]-1-(3-sulfopropyl)pyridinium, were compared with those of their neutral analogues in a series of representative solvents. The introduction of the proximal charge results in shifts of absorption spectrum and of both normal (N) and tautomer (T) emission bands, which correspond to initial and phototautomer states of the ESIPT reaction. The observed shifts are in accordance with the Stark effect theory. The direction of the shift depends on the position of the proximal charge with respect to the chromophore. The magnitude of the shift depends strongly on the solvent dielectric constant and on screening or unscreening produced by addition of the hydrophobic salts. In all of these cases, the spectral shifts are accompanied by extremely strong variations of relative intensities of N and T emission bands. This signifies a strong influence of internal electric field on the ESIPT reaction, which produces a dramatic change of emission color. Thus, the coupling of the initial electrochromic sensory signal with the ESIPT reaction allows for the breaking of the limit in magnitude of response inherent to common electrochromic dyes. This suggests a new principle of designing the ultrasensitive electrochromic two-wavelength fluorescence sensors and probes for analytical chemistry, macromolecular science, and cellular biology.

Electrochemistry↗

Control of electroosmotic flow in zirconia-coated capillaries.

The inner surface of a silica capillary has been modified using an anhydrous sol-gel method: zirconium propoxide reacted with silanol groups to give, after hydrolysis, a "zirconia-like" surface. The electroosmotic properties of zirconia-modified capillaries have been studied under various conditions: working parameters were nature and concentration of the electrolyte, ionic strength, pH and solvent composition. Using different ions such as sodium, potassium, chloride, nitrate or methanoate, a positive electroosmotic flow (cathodic flow) was observed in the pH range 5-11. But below pH 5, a negative electroosmotic flow (anodic flow) occurred, corresponding to a permanent positive surface charge of the capillary walls. The value of the electroosmotic flow (including the sign) can be easily controlled by adding multivalent ions in the electrolyte. Some of these modifications of surface charge can be made irreversible. The observed electroosmotic flow has been related to surface characteristics using the triple layer model. With the large set of working parameters, the optimisation of separations can be facilitated. An example of flow control is given for the separation of four antihistaminic compounds.

Electrochemistry↗

Determination of total phenols in environmental wastewater by flow-injection analysis with a biamperometric detector.

A flow injection (FI) method with a biamperometric detector, based on the biamperometry for an irreversible redox couple, is described for the determination of phenols in environmental wastewater. The method relies on coupling of the oxidation of phenols at one platinum-wire electrode with the reduction of MnO4- at another platinum wire electrode to enable biamperometric detection with an applied potential difference of 0 V. The linear dynamic range for the dependence of current on phenol concentration was from 1.0 x 10(-6) to 1.0 x 10(-4) mol L(-1), with a detection limit of 4.0 x 10(-7) mol L(-1) (signal-to-noise ratio, S/N=3). In comparison with the 4-aminoantipyrine (4-AAP) standard method and the 3-methyl-2-benzothiazoline hydrazone (MBTH) method the proposed method can be used to detect many para-substituted phenols that do not react with 4-AAP and MBTH, and response factors are higher for most of the phenols tested. The method, which is simple, economic, and rapid (180 samples h(-1)), has been applied to the analysis of four wastewater samples. The results obtained were compared with those from 4-AAP method. The recoveries obtained by adding phenol standards to samples ranged from 94.3 to 105.2% with a standard deviation of 3.6%.

Electrochemistry↗