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Michael V Mirkin

Publications and source records attributed to Michael V Mirkin.

15 recordsLinked to original sources
PubMed2006

SECM study of solute partitioning and electron transfer at the ionic liquid/water interface.

Molecular partitioning and electron-transfer kinetics have been studied at the ionic liquid/water (IL/water) interface by scanning electrochemical microscopy (SECM). The ionic liquid C8mimC1C1N is immiscible with water and forms a nonpolarizable interface when in contact with it. Partitioning of ferrocene (Fc) across the IL/water interface was studied by SECM and found to be kinetically fast with a partition coefficient CIL/CW of 2400:1. The partition coefficient value was measured by SECM under quasi-steady-state conditions without waiting for complete solute equilibration. To investigate the kinetics of the electron transfer (ET) between aqueous ferricyanide and Fc dissolved in IL, a new approach to the analysis of the SECM current-distance curves was developed to separate the contributions of Fc partitioning and the ET reaction to the tip current. Several combinations of different aqueous and nonaqueous redox species were investigated; however, only the Fc/Fe(CN)63- system behaved according to the Butler-Volmer formalism over the entire accessible potential range.

Journal Article↗
PubMed2006

Shuttling mechanism of ion transfer at the interface between two immiscible liquids.

The transfers of hydrophilic ions between aqueous and organic phases are ubiquitous in biological and technological systems. These energetically unfavorable processes can be facilitated either by small molecules (ionophores) or by ion-transport proteins. In absence of a facilitating agent, ion-transfer reactions are assumed to be "simple", one-step processes. Our experiments at the nanometer-sized interfaces between water and neat organic solvents showed that the generally accepted one-step mechanism cannot explain important features of transfer processes for a wide class of ions including metal cations, protons, and hydrophilic anions. The proposed new mechanism of ion transfer involves transient interfacial ion paring and shuttling of a hydrophilic ion across the mixed-solvent layer.

Journal Article↗
PubMed2006

Kinetics of electron-transfer reactions at nanoelectrodes.

The kinetics of several fast heterogeneous electron-transfer reactions were investigated by steady-state voltammetry at nanoelectrodes and scanning electrochemical microscopy (SECM). The disk-type, polished Pt nanoelectrodes (3.7-400-nm radius) were characterized by a combination of voltammetry, scanning electron microscopy, and SECM. A number of experimental curves were obtained at the same nanoelectrode to attain the accuracy and reproducibility similar to those reported previously for micrometer-sized probes. A new analytical approximation was developed and used for analysis of steady-state tip voltammograms. The self-consistent kinetic parameter values with the uncertainty margin of approximately 10% were obtained for electrodes of different radii and for a wide range of the SECM tip/substrate separation distances. The determined standard rate constants are compared to those previously measured at the electrodes of different dimensions, and the correlation between the heterogeneous and self-exchange rate constants is discussed.

Journal Article↗
PubMed2006

Electrochemical studies of the lateral diffusion of TEMPO in the aqueous liquid/vapor interfacial region.

Surface partitioning and lateral mobility of TEMPO (2,2,6,6-tetramethyl-1-piperidynyloxy free radical) in the aqueous liquid/gas interfacial region were investigated electrochemically with 100 nm wide, 1.0 cm long microband electrodes positioned at the air/water interface. For redox active amphiphiles such as TEMPO, the electrochemical current is the sum of the surface and solution components representing the diffusive transport of TEMPO in both domains as well as the dynamics of equilibration at the air/water interface. Interpretation of the recorded current-voltage curves was aided by a FEMLAB simulation code developed to analyze transport processes in this class of systems. TEMPO and TEMPO(+) partition constants (K(T), K(T)+) and solution diffusivities (D(sol), equal for the two species) were obtained experimentally yielding K(T) = 5.0 +/- 0.7 x 10(2) M(-1), K(T+) = 41 +/- 3 M(-1), and D(sol) = 7.7 +/- 0.35 x 10(-6) cm(2)/s. In view of the low value of K(T)+, TEMPO(+) was assumed not to partition to the air/water interface. We further assumed that the desorption rate constants (k(des)) of both TEMPO and TEMPO(+) were the same. Good fits between the recorded and simulated cyclic voltammograms were obtained using two correlated, adjustable parameters, k(des) and the TEMPO lateral, surface diffusion constant (D(surf)). Detailed analysis of the behavior of this class of systems was obtained for a broad range of D(surf) and k(des) values. In addition, a calibration curve of k(des) versus D(surf) was obtained. Assuming that TEMPO k(des) is in a likely range of 10-100 s(-1), its lateral diffusion constant is in the range of 7.9-3.6 x 10(-5) cm(2)/s. In view of our earlier work (Wu, D. G.; Malec, A. D.; Head-Gordon, M.; Majda, M. J. Am. Chem. Soc. 2005, 127, 4490-4496) showing that at the air/water interface TEMPO is unimmersed, and that its interactions with water are limited to hydrogen bonding with one or two water molecules, D(surf) can be related to the viscosity of the aqueous interfacial region.

Journal Article↗
PubMed2006

Electron transfer kinetics at polarized nanoscopic liquid/liquid interfaces.

Rapid kinetics of electron transfer (ET) reactions across the interface between water and 1,2-dichloroethane were measured by steady-state voltammetry at nanopipet electrodes (50- to 400-nm orifice radius). The origins of previously reported imperfect voltammetric responses of ET reactions at micropipets were investigated. Several new experimental systems were explored, and two of them yielded high-quality voltammograms suitable for kinetic experiments. The determined standard rate constants were compared to those measured previously at polarized and nonpolarized liquid/liquid interfaces. The effect of the interfacial dimensions on the magnitude of the apparent ET rate constant is discussed. A new approach to ET kinetic measurements based on the use of the scanning electrochemical microscope with a nanopipet tip and a metallic substrate has been developed and employed to check the validity of determined kinetic parameters.

Journal Article↗
PubMed2005

An electrochiroptical molecular switch: mechanistic and kinetic studies.

Previously, we reported the synthesis and preliminary characterization of Cu(I/II) complexes of N,N-bis(2-quinilylmethyl)-(l)-methionine (Zahn, S.; Canary, J. W. Science 2000, 288, 1404-7). The chemically oxidized and reduced forms of the complexes gave nearly mirror image circular dichroism (CD) spectra as a result of reorganization of the inner coordination sphere of the copper atom. The reorganization involved exchange of oxygen for sulfur in proceeding from the Cu(II) to Cu(I) oxidation state and corresponding ligand conformational changes required to accommodate this exchange. In this paper, we demonstrate that the complex can be triggered by electrochemical means. The electrochemical and stereochemical details of the redox-induced ligand reorganization were probed by independent synthesis of alternative chemical intermediates, CD spectroelectrochemistry, curve fitting of cyclic voltammograms, CD titration, and scanning electrochemical microscopy (SECM). A square-type mechanism was most consistent with the data: the Cu(II) complex is reduced followed by a ligand reorganization step to give the stable reduced form of the complex. The Cu(I) complex is then oxidized in a fast step followed by another ligand reorganization. A millisecond time scale rate was found by SECM for one of the key conformational conversion steps.

Journal Article↗
PubMed2005

Ion transfer at nanointerfaces between water and neat organic solvents.

Nanopipet voltammetry was used for the first study of ion transfer (IT) reactions between aqueous solutions and neat organic solvents. An extremely wide ( approximately 10 V) polarization window obtained with no electrolyte added to the organic phase allows one to probe charge transfer reactions, which are not normally accessible by electrochemical techniques, for example, the transfer of l-alaninamide cation from water to 1,2-dichloroethane (DCE). While anions (e.g., chloride) and relatively hydrophobic cations (e.g., tetraalkylammonium ions) can be transferred from water to less polar neat solvents such as DCE, the transfers of strongly hydrated metal cations occur only in the presence of organic supporting electrolyte.

Journal Article↗
PubMed2004

Comparative study of electron transfer reactions at the ionic liquid/water and organic/water interfaces.

The rates of electron transfer (ET) reactions at the water/ionic liquid (IL) interface have been measured for the first time using scanning electrochemical microscopy. The standard bimolecular rate constant of the interfacial ET between ferrocene dissolved in 1-octyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide and aqueous ferricyanide (0.4 M-1 cm s-1) was found to be approximately 30 times higher than the corresponding rate constant measured at the water/1,2-dichloroethane interface. The driving force dependence of the ET rate was investigated over a wide range of the interfacial potential drop values (>200 mV). The observed Butler-Volmer-type dependence is discussed in terms of the interfacial model. The ET was also probed at the interface between aqueous solution and the mixture of the IL and 1,2-dichloroethane. The mole fractions in this mixture were varied systematically to investigate the transition from the water/organic to the water/IL interface. The observed decrease in the rate constant with increasing mole fraction of 1,2-dichloroethane is in contrast with the previously reported direct correlation between the electrochemical rate constant and the diffusion coefficient of redox species in solution.

Journal Article↗
PubMed2004

Electron transfer at self-assembled monolayers measured by scanning electrochemical microscopy.

New approaches have been developed for measuring the rates of electron transfer (ET) across self-assembled molecular monolayers by scanning electrochemical microscopy (SECM). The developed models can be used to independently measure the rates of ET mediated by monolayer-attached redox moieties and direct ET through the film as well as the rate of a bimolecular ET reaction between the attached and dissolved redox species. By using a high concentration of redox mediator in solution, very fast heterogeneous (10(8) s(-1)) and bimolecular (10(11) mol(-1) cm(3) s(-1)) ET rate constants can be measured. The ET rate constants measured for ferrocene/alkanethiol on gold were in agreement with previously published data. The rates of bimolecular heterogeneous electron transfer between the monolayer-bound ferrocene and water-soluble redox species were measured. SECM was also used to measure the rate of ET through nonelectroactive alkanethiol molecules between substrate gold electrodes and a redox probe (Ru(NH(3))(6)(3+)) freely diffusing in the solution, yielding a tunneling decay constant, beta, of 1.0 per methylene group.

Alkanes↗
PubMed2004

Scanning electrochemical microscopy: detection of human breast cancer cells by redox environment.

Scanning electrochemical microscopy (SECM) can be used to measure the redox activity of individual human breast cells. A chemical mediator (e.g. quinone) that rapidly crosses the membrane participates in intracellular redox reactions that are recorded on a microsecond timescale by an ultramicroelectrode positioned close to the membrane. Measurements of redox reactivity yield rate constants that are different for cancerous and non-transformed human breast cells. With non-transformed or metastatic cells, rate constants are modulated by altered expression or activity of protein kinase Calpha, an enzyme involved in the mechanism of cell metastasis. When used in two-dimensional scanning, SECM produces a spatially resolved redox map of an individual cell or field of cells and can detect individual breast cancer cells in a field of non-transformed cells. These studies identify a new technology for cancer detection and establish a framework for future analysis of malignant cells in human breast tissues and biopsies.

Animals↗
PubMed2003

Scanning electrochemical microscopy of living cells. 5. Imaging of fields of normal and metastatic human breast cells.

Scanning electrochemical microscopy (SECM) was used to image fields of different types of human breast cells in monolayer culture. The goal of these experiments was to demonstrate the possibility of distinguishing between nontransformed human breast epithelial cells (MCF-10A) and metastatic breast cells (MDA-MB-231) by their redox activities. Imaging of densely packed cells by SECM requires approaches that differ from previously reported experiments with well-separated single cells. The combination of SECM with optical and fluorescence microscopies was used to locate individual cells in a homogeneous or heterogeneous field of cells. To establish that metastatic breast cells can be detected against a field of normal cells, the former were preloaded with fluorescent nanospheres and plated together with unlabeled MCF-10A cells. By matching SECM and fluorescence images of a selected group of metastatic cells, the level of discrimination and fidelity of the SECM signal could be shown. Several factors (distance between the electrode and the cells, cell density, choice of mediator, and its concentration) were identified that can be used to maximize the contrast between images of metastatic and nontransformed cells. These studies provide a framework for future analysis of malignant cells in human breast tissue samples.

Breast↗
PubMed2002

Scanning electrochemical microscopy of living cells. 4. Mechanistic study of charge transfer reactions in human breast cells.

Scanning electrochemical microscopy (SECM) has recently been employed for probing the redox properties of individual mammalian cells. It was shown that intracellular redox activity can be probed noninvasively by measuring the rate of mediator regeneration by the cell. Depending on the properties of the mediator species (e.g., formal potential, ionic charge, and hydrophobicity), different steps can limit the rate of the mediator regeneration reaction. This paper describes the evaluation of several factors that determine the rates of different steps of the process. These include intracellular concentration of redox centers, mixed redox potential inside the cell, and the rate of membrane permeation by mediator species. The kinetic analysis has been carried out to clarify the origins of different rates of the overall charge-transfer reaction in different cell types and with different redox mediators. The results can be used to facilitate differentiation between different types of cells, for example, normal and metastatic breast cells, on the basis of differences in redox responses.

Breast↗
PubMed2002

Steady-state limiting currents at finite conical microelectrodes.

The investigation of steady-state diffusion-limiting currents at finite conical microelectrodes is reported. Such electrodes are of particular interest as probes in studies of kinetic reactions, measurements in microenvironments, and high-resolution electrochemical imaging. The diffusion-limiting currents were calculated using numerical (finite element) analysis and compared to those obtained at inlaid disk and hemispheroidal microelectrodes. Time-dependent simulations demonstrating the approach of the diffusion current to a steady-state value are also reported. The steady-state diffusion-limiting currents obtained were found to be a strong function of the electrode geometry, including the aspect ratio of the cone and the thickness of the insulating sheath. Thus, simple, approximate analytical expressions which account for these geometrical dependencies in the simulated steady-state diffusion-limited currents are also reported. As a limiting case, an analytical approximation was obtained for the steady-state current to a microdisk as a function of the insulator thickness. The use of these approximate equations in calculating electrode radii from steady-state diffusion-limiting currents is demonstrated, and good agreement was found with previously reported experimental studies. Use of the frequently implemented hemispherical theory to analyze steady-state diffusion-limiting currents obtained with finite conical microelectrodes is shown to result in an experimentally acceptable underestimation of the electrode radius.

Journal Article↗
PubMed2002

Scanning electrochemical microscopy of living cells. 3. Rhodobacter sphaeroides.

The scanning electrochemical microscope (SECM) was used to probe the redox activity of individual purple bacteria (Rhodobacter sphaeroides). The approaches developed in our previous studies of mammalian cells were expanded to measure the rates and investigate the pathway of transmembrane charge transfer in bacteria. The two groups of redox mediators (i.e., hydrophilic and hydrophobic redox species) were used to shuttle the electrons between the SECM tip electrode in solution and the redox centers inside the cell. The analysis of the dependencies of the measured rate constant on formal potential and concentration of mediator species in solution yielded information about the permeability of the outer cell membrane to different ionic species and intracellular redox properties. The maps of redox reactivity of the cell surface were obtained with a micrometer or submicrometer spatial resolution.

Cell Membrane↗