Delocalized Electron System Research Articles

Atomically Dispersed Dual-Site Cathode with a Record High Sulfur Mass Loading for High-Performance Room-Temperature Sodium-Sulfur Batteries.

Room-temperature sodium-sulfur (RT-Na/S) batteries possess high potential for grid-scale stationary energy storage due to their low cost and high energy density. However, the issues arising from the low S mass loading and poor cycling stability caused by the shuttle effect of polysulfides seriously limit their operating capacity and cycling capability. Herein, sulfur-doped graphene frameworks supporting atomically dispersed 2H-MoS2 and Mo1 (S@MoS2 -Mo1 /SGF) with a record high sulfur mass loading of 80.9wt.% are synthesized as an integrated dual active sites cathode for RT-Na/S batteries. Impressively, the as-prepared S@MoS2 -Mo1 /SGF display unprecedented cyclic stability with a high initial capacity of 1017mAhg-1 at 0.1Ag-1 and a low-capacity fading rate of 0.05% per cycle over 1000cycles. Experimental and computational results including X-ray absorption spectroscopy, in situ synchrotron X-ray diffraction and density-functional theory calculations reveal that atomic-level Mo in this integrated dual-active-site forms a delocalized electron system, which could improve the reactivity of sulfur and reaction reversibility of S and Na, greatly alleviating the shuttle effect. The findings not only provide an effective strategy to fabricate high-performance dual-site cathodes, but also deepen the understanding of their enhancement mechanisms at an atomic level.

Fast charge transfer between iodide ions and a delocalized electron system on the graphite surface for boosting hydrogen production

The graphite-based materials with a delocalized π electron system exhibited fast charge transfer with physically adsorbed iodide ions, thus revealing desirable IOR catalytic activity.

Applications of molecular modeling to flavoproteins: Insights and challenges.

The general field of molecular simulation provides a wide spectrum of methods for studying the structure and function of biomolecules. Depending on the scale and question of interest, appropriate approaches may range from ab initio quantum mechanical calculations (when detailed aspects of and changes in electronic structure must be considered) to Brownian dynamics and coarse-grained molecular dynamics (to track large scale conformational motions, diffusion, and inter-molecular interactions). The entire range of molecular simulation methods has been fruitfully applied to a range of flavoenzymes, allowing researchers to address everything from the specific intermediates involved in the photoreactions of flavin chromophore-containing light sensors, to the very long timescale motions induced by covalent modifications to bound flavin. The unique challenge posed by flavoproteins to all types of molecular simulation arises from the chemistry of the flavin isoalloxazine moiety, which presents an unusually large delocalized electron system which must be carefully treated in order to represent its contributions to the overall behavior of the system. Here we outline the particular considerations required for appropriate treatment of flavoproteins in simulations ranging from electronic structure calculations to long-timescale modeling of flavoprotein conformational transitions.

Alternative pathway linked by hydrogen bonds connects heme-Fe of cytochrome c with subunit II-CuA of cytochrome a

The bridging element for electron transfer in proteins is the hydrogen bond according to the new experimental perspective in preference to carbon-carbon σ-bond presently used. The purpose of this study is to identify an alternative pathway linked by hydrogen bonds suitable for electron transfer from heme-Fe of cytochrome c to subunit II-CuA of cytochrome a. A pathway consisting of 15 delocalized electron systems including peptide bonds, 5 polar groups of side chains of amino acid residues and 8 water molecules, linked by 27 hydrogen bonds, exists between the two metal electron centers of heme-Fe of cytochrome c, cytochrome c and of subunit II-CuA of cytochrome a. Pathways built of delocalized π-electron systems, polar groups and water molecules linked by hydrogen bonds may be considered for intramolecular and intermolecular electron transfer in proteins.

Have photosynthetic pigments been formulated for chemical stability? A cursory insight into the reactivity of magnesium porphyrinoids

Magnesium complexes with reduced tetrapyrrolic ligands are active compounds of plant and bacteria photosystems. However, also the porphyrin complex appears as an intermediate on the biosynthetic pathway of the photosynthetic pigments. Its transformations, in particular the reduction of pyrrole rings, lead to the acquisition of the properties that are primary for activity in antenna systems and reaction centers. On the other hand, modifications of the porphyrin system must affect the resistance to destructive processes, such as loss of metal ion and its substitution. In order to compare the stability of three natural Mg complexes, namely Mg protoporphyrin IX, chlorophyll a, and bacteriochlorophyll a, spectroscopic studies in solution were performed. The difference in the electronic structure of the macrocyclic ligand was the basic variable in testing the action against d-electron metal salts and acetic acid. The spectroscopic studies were supplemented with calculations using the Density Functional Theory which provided insight into the stability of M(II)-N bonds depending on the dimension of the delocalized electron system. The results indicate the decreasing stability of Mg(II) complexes on the biosynthetic pathway, thereby providing an additional justification for incorporation of the metal ion into porphyrin prior to the electronic modifications of the tetrapyrrolic system.

Water as the main regulator of intracellular processes

This paper addresses the investigation of water as the main regulator of intracellular processes. The research is based on assessing the impact associated water phase electromagnetic activity has on biological processes as well as determining its relationship to quantum states of delocalized electron system. The study demonstrates that the characteristics of electromagnetic emissions of water in SHF- and low-frequency (Hz–kHz) ranges are determined by dynamic states of superconductivity of associated water phase and are described within the framework of self-organization of hightemperature granulated superconductor with on-off intermittency. The paper describes the importance of obtained quantum laws in order to substantiate a regulatory role of associated water phase related to high organism sensitivity to electromagnetic emissions, and the detection of reasons for human diseases of metabolic etiology.

Dimensionality effects on magnetic properties of [formula omitted] nanoclusters on Pt(1 1 1)

The behavior of local magnetic moments and exchange coupling parameters of FexCo1-x nanostructures (nanowires and compact clusters) on the fcc Pt(111) surface is here investigated using the first-principles real-space RS-LMTO-ASA method, in the framework of the DFT. Different configurations of FexCo1-x trimers and heptamers on Pt(111) are considered, varying the positions and the concentration of Fe or Co atoms. We discuss the influence of dimensionality and stoichiometry changes on the magnetic properties, specially on the orbital moments, which are very important in establishing a nanoscopic understanding of delocalized electron systems. We demonstrate the existence of a strictly decreasing nonlinear trend of the average orbital moments with the Fe concentration for the compact clusters, different from what was found for FexCo1-x nanowires on Pt(111) and also for corresponding higher-dimensional systems (FexCo1-x monolayer on Pt(111) and FexCo1-x bulk). The average spin moments, however, are invariably described by a linear function with respect to stoichiometry. In all studied cases, the nearest neighbors exchange couplings have shown to be strongly ferromagnetic.

Ultrafast third-order nonlinear optical response of pyrene derivatives

Two mono-substituted pyrene derivatives with delocalized electron system 1-(pyren-1-yl)−3-(4-Methyl thiophene-2-yl) acrylic ketone (13#) and 1-(pyren-1-yl)−3-(4-bromo thiophene-2-yl) acrylic ketone (15#) were successfully synthesized. The resultant compounds were characterized by nuclear magnetic resonance (NMR), infrared spectroscopy (IR), high resolution mass spectrum (HR-MS), and UV–vis spectra. The third-order nonlinear optical properties of the compounds were investigated using Z-scan technique with femtosecond laser pulses at 500nm and 700nm, respectively. Both of the compounds showed a decrease in transmittance about the focus, which are typical of two-photon absorption. It was found that the two-photon absorption behavior of the pyrene derivatives were modified by substituents on thiophene ring. These results indicate that both compounds can be promising candidates for future optoelectronic and bio-imaging applications.

High-conductive organometallic molecular wires with delocalized electron systems strongly coupled to metal electrodes.

Besides active, functional molecular building blocks such as diodes or switches, passive components, for example, molecular wires, are required to realize molecular-scale electronics. Incorporating metal centers in the molecular backbone enables the molecular energy levels to be tuned in respect to the Fermi energy of the electrodes. Furthermore, by using more than one metal center and sp-bridging ligands, a strongly delocalized electron system is formed between these metallic "dopants", facilitating transport along the molecular backbone. Here, we study the influence of molecule-metal coupling on charge transport of dinuclear X(PP)2FeC4Fe(PP)2X molecular wires (PP = Et2PCH2CH2PEt2); X = CN (1), NCS (2), NCSe (3), C4SnMe3 (4), and C2SnMe3 (5) under ultrahigh vacuum and variable temperature conditions. In contrast to 1, which showed unstable junctions at very low conductance (8.1 × 10(-7) G0), 4 formed a Au-C4FeC4FeC4-Au junction 4' after SnMe3 extrusion, which revealed a conductance of 8.9 × 10(-3) G0, 3 orders of magnitude higher than for 2 (7.9 × 10(-6) G0) and 2 orders of magnitude higher than for 3 (3.8 × 10(-4) G0). Density functional theory (DFT) confirmed the experimental trend in the conductance for the various anchoring motifs. The strong hybridization of molecular and metal states found in the C-Au coupling case enables the delocalized electronic system of the organometallic Fe2 backbone to be extended over the molecule-metal interfaces to the metal electrodes to establish high-conductive molecular wires.

Ring Current Effects: Factors Affecting the NMR Chemical Shift of Molecules Adsorbed on Porous Carbons

Nuclear magnetic resonance (NMR) spectroscopy is increasingly being used to study the adsorption of molecules in porous carbons, a process which underpins applications ranging from electrochemical energy storage to water purification. Here we present density functional theory (DFT) calculations of the nucleus-independent chemical shift (NICS) near various sp2-hybridized carbon fragments to explore the structural factors that may affect the resonance frequencies observed for adsorbed species. The domain size of the delocalized electron system affects the calculated NICSs, with larger domains giving rise to larger chemical shieldings. In slit pores, overlap of the ring current effects from the pore walls is shown to increase the chemical shielding. Finally, curvature in the carbon sheets is shown to have a significant effect on the NICS. The trends observed are consistent with existing NMR results as well as new spectra presented for an electrolyte adsorbed on carbide-derived carbons prepared at different t...

The Potential of Dyes Removal from Textile Wastewater by Using Different Treatment Technology, a Review

Water pollution due to color dyestuff industries is topics of major concern today. Many industries use dyes extensively in different operation such as textile, paper, plastic leather, tanning etc. Dyes are ioni c aromatic compounds with structures including aryl rings, which have delocal ized electron system. A synthetic dye in wastewater cannot be efficiently decolorized by traditional methods. This is because of the high cost and disposal problems for treatin g dye wastewater at large scale in the textile and paper industries. The tech nologies for colour removal can be divided into thr ee categories: biological, chemical and physical .All of them have advantages and drawbacks. Biological treatment is the most eco nomical methods compared to other physical and chemical processes. Biological treatment is incapable of obtaining sati sfactory color elimination with current conventional biodegradatio n processes. Integrated way dye removal is the best wastewater treatment method if it is applicable.

Fabrication of a Novel and Simple Microcystin-LR Photoelectrochemical Sensor with High Sensitivity and Selectivity

Microcystin-LR (MC-LR), an inert electrochemical species, is difficult to be detected by a simple and direct electrochemical method. In the present work, a novel photoelectrochemical sensor is developed on highly ordered and vertically aligned TiO(2) nanotubes (TiO(2) NTs) with convenient surface modification of molecularly imprinted polymer (MIP) (denoted as MIP@TiO(2) NTs) for highly sensitive and selective determination of MC-LR in solutions. Molecularly imprinted polypyrrole (PPy) of MC-LR is chosen as the recognition element. The designed MIP@TiO(2) NTs photoelectrochemical sensor presents excellent applicability in MC-LR determination, with linear range from 0.5 to 100 μg L(-1) and limit of detection of 0.1 μg L(-1). Moreover, the sensor exhibits outstanding selectivity while used in coexisting systems containing 2,4-dichorophenoxyacetic acid, atrazine, paraquat, or monosultap with high concentration, 100 times that of MC-LR. The sensor presents good photoelectric conversion efficiency and detection sensitivity, as well as broad linear detection range, mainly because of the high specific surface area and photoelectric activity of TiO(2) NTs and the π bond delocalized electron system of PPy that promotes the separation of electron-holes. The prominent selectivity is from the MIP by forming multiple hydrogen bonds between PPy and MC-LR. Mechanisms for photoelectrochemical analysis and selective recognition are also discussed.

The Induced Magnetic Field

Aromaticity is indispensable for explaining a variety of chemical behaviors, including reactivity, structural features, relative energetic stabilities, and spectroscopic properties. When interpreted as the spatial delocalization of π-electrons, it represents the driving force for the stabilization of many planar molecular structures. A delocalized electron system is sensitive to an external magnetic field; it responds with an induced magnetic field having a particularly long range. The shape of the induced magnetic field reflects the size and strength of the system of delocalized electrons and can have a large influence on neighboring molecules. In 2004, we proposed using the induced magnetic field as a means of estimating the degree of electron delocalization and aromaticity in planar as well as in nonplanar molecules. We have since tested the method on aromatic, antiaromatic, and nonaromatic compounds, and a refinement now allows the individual treatment of core-, σ-, and π-electrons. In this Account, we describe the use of the induced magnetic field as an analytical probe for electron delocalization and its application to a large series of uncommon molecules. The compounds include borazine; all-metal aromatic systems Al(4)(n-); molecular stars Si(5)Li(n)(6-n); electronically stabilized planar tetracoordinate carbon; planar hypercoordinate atoms inside boron wheels; and planar boron wheels with fluxional internal boron cluster moieties. In all cases, we have observed that planar structures show a high degree of electron delocalization in the π-electrons and, in some examples, also in the σ-framework. Quantitatively, the induced magnetic field has contributions from the entire electronic system of a molecule, but at long range the contributions arising from the delocalized electronic π-system dominate. The induced magnetic field can only indirectly be confirmed by experiment, for example, through intermolecular contributions to NMR chemical shifts. We show that calculating the induced field is a useful method for understanding any planar organic or inorganic system, as it corresponds to the intuitive Pople model for explaining the anomalous proton chemical shifts in aromatic molecules. Indeed, aromatic, antiaromatic, and nonaromatic molecules show differing responses to an external field; that is, they reduce, augment, or do not affect the external field at long range. The induced field can be dissected into different orbital contributions, in the same way that the nucleus-independent chemical shift or the shielding function can be separated into component contributions. The result is a versatile tool that is particularly useful in the analysis of planar, densely packed systems with strong orbital contributions directly atop individual atoms.

Identification of Organic Colorants in Fibers, Paints, and Glazes by Surface Enhanced Raman Spectroscopy

Organic dyes extracted from plants, insects, and shellfish have been used for millennia in dyeing textiles and manufacturing colorants for painting. The economic push for dyes with high tinting strength, directly related to high extinction coefficients in the visible range, historically led to the selection of substances that could be used at low concentrations. But a desirable property for the colorist is a major problem for the analytical chemist; the identification of dyes in cultural heritage objects is extremely difficult. Techniques routinely used in the identification of inorganic pigments are generally not applicable to dyes: X-ray fluorescence because of the lack of an elemental signature, Raman spectroscopy because of the generally intense luminescence of dyes, and Fourier transform infrared spectroscopy because of the interference of binders and extenders. Traditionally, the identification of dyes has required relatively large samples (0.5-5 mm in diameter) for analysis by high-performance liquid chromatography. In this Account, we describe our efforts to develop practical approaches in identifying dyes in works of art from samples as small as 25 microm in diameter with surface-enhanced Raman scattering (SERS). In SERS, the Raman scattering signal is greatly enhanced when organic molecules with large delocalized electron systems are adsorbed on atomically rough metallic substrates; fluorescence is concomitantly quenched. Recent nanotechnological advances in preparing and manipulating metallic particles have afforded staggering enhancement factors of up to 10(14). SERS is thus an ideal technique for the analysis of dyes. Indeed, rhodamine 6G and crystal violet, two organic compounds used to demonstrate the sensitivity of SERS at the single-molecule level, were first synthesized as textile dyes in the second half of the 19th century. In this Account, we examine the practical application of SERS to cultural heritage studies, including the selection of appropriate substrates, the development of analytical protocols, and the building of SERS spectral databases. We also consider theoretical studies on dyes of artistic interest. Using SERS, we have successfully documented the earliest use of a madder lake pigment and the earliest occurrence of lac dye in European art. We have also found several examples of kermes and cochineal glazes, as well as madder, cochineal, methyl violet, and eosin lakes, from eras ranging from ancient Egypt to the 19th century. The ability to rapidly analyze very small samples with SERS makes it a particularly valuable tool in a museum context.

Novel Fusogenic Liposomes for Fluorescent Cell Labeling and Membrane Modification

Efficient delivery of biomolecules into membranes of living cells as well as cell surface modifications are major biotechnological challenges. Here, novel liposome systems based on neutral and cationic lipids in combination with lipids modified by aromatic groups are introduced for such applications. The fusion efficiency of these liposome systems was tested on single cells in culture like HEK293, myofibroblasts, cortical neurons, human macrophages, smooth muscle cells, and even on tissue. Fusogenic liposomes enabled highly efficient incorporation of molecules into mammalian cell membranes within 1 to 30 min at fully unchanged cell growth conditions and did not affect cell behavior. We hypothesize that membrane fusions were induced in all cases by the interaction of the positively charged lipids and the delocalized electron system of the aromatic group generating local dipoles and membrane instabilities. Selected applications ranging from basic research to biotechnology are envisaged here.

Potential-Induced Conformational Changes in an α-CN-terthiophene Thiolate Film on GaAs(110)

Second harmonic generation (SHG) investigations on alpha-CN-terthiophene-thiolate-covered GaAs(110) electrodes in 1 N H2SO4 solution revealed significant changes in the rotational anisotropy of the SH response. The enhancement of the 1- and the 3-fold contributions around -250 mV suggests changes in the symmetry properties of the delocalized electron system due to an alteration of the adsorption geometry induced by the applied potentials. The analysis of the EIS data showed that in the potential region where the SH signal exhibits the more important changes the Mott-Schottky plot undergoes a pronounced shift to more negative potentials as a result of the charging of the surface states grouped about 1.06 eV below the conduction band edge. Semiempirical MO calculations suggest that the most energetically favorable interaction implies electron transfer from the semiconductor conduction band to the lowest unoccupied molecular orbital of the organic molecule with epsilon(LUMO)=-1.707 eV. Such a chemisorption bond bringing the organic molecule to a quasi-planar position is well supported by the major changes in the XPS spectra of the electrochemically biased samples with respect to the as-prepared ones. Two distinct N 1s species instead of one and a shift of 1.6 eV to higher BE of the terthiophene S 2s core level are strong evidence for a potential-induced change in the adsorption geometry. Taking into account that the acceptor-like surface state group located close to the semiconductor valence edge (EC,S=-1.06 eV) may correspond to the LUMO level (shifted downward by the adsorption process), we assume that the organic molecule, initially adsorbed by the thiolate end, undergoes a conformational change from a tilted to an almost flat position when the applied potential brings the semiconductor Fermi level into its neighborhood. This assumption is in a very good agreement with the potential-induced variation in the thiol thickness estimated from the thiol capacitance.

Nonlinear optical properties of oligothiophene self-assembled monolayers on gold substrate

Liner and nonlinear-optical properties of oligothiophenes self-assembled monolayers (SAM) are studied by optical second harmonic interference technique. Linear polarizability and first hyperpolarizability as functions of the number of thiophene rings are calculated using a self-consistent approach for linear and nonlinear optical properties. Both of these dependencies can be described by a power law; a nonzero first hyperpolarizability points to the asymmetry of delocalized electron system that might be due to an adsorption of thiophene molecules on a metal substrate. The influence of a dipole–dipole interaction of molecules arranged in the SAM is discussed.

Cyclosiloxane sandwich complexes of a lanthanide metal: Na 6{[(C 6H 5SiO 2) 8] 2Nd 4( μ4-O)}

The oligocyclosiloxane cluster (‘sandwich’) complex of Nd 3+, Na 6{[(C 6H 5SiO 2) 8] 2Nd 4( μ 4-O)} has been prepared and characterized by analyses, infrared spectra, single crystal X-ray diffraction, magnetic susceptibility, conductivity and cyclic voltammetry. The μ 4-O 2− anion is in a square planar coordination environment. Electrochemical studies identify the cluster core as a moiety with a delocalized electron system.

The dimerization of ferrihaems: II. Equilibrium and kinetic studies of mesoferrihaem dimerization

Spectrophotometric data have been determined for mesoferrihaem at several pH values and over a range of concentration covering four orders of magnitude. The data reveal a dimerization process according to the equation 2 monomer ⇌ dimer + H +, analogous to earlier findings for deuteroferrihaem and protoferrihaem. The value of K (defined as K = [dimer][H +] [ monomer]) 2 ) was found to be 6.92 · 10 −2. This is close to the value for deuteroferrihaem but much less than that for protoferrihaem. This is interpreted in terms of possible additional bonding between the delocalized electron systems in protoferrihaem dimers relative to those of mesoferrihaem and deuteroferrihaem. Rate constants for dimerization were determined by temperature-jump spectrophotometry. The pH dependence of the rate constants is explained in terms of two distinct pathways for the dimerization process. These involve either direct reaction between two undissociated monomer molecules or alternatively an initial acid dissociation of a monomer molecule followed by reaction between an undissociated and a dissociated molecule.