Reversible redox modulation of a lanthanide emissive molecular film

2015 ◽  
Vol 51 (30) ◽  
pp. 6515-6517 ◽  
Author(s):  
Joshua Lehr ◽  
Manuel Tropiano ◽  
Paul D. Beer ◽  
Stephen Faulkner ◽  
Jason J. Davis
Keyword(s):  
Redox Modulation ◽  
Molecular Film ◽  
Reversible Redox ◽  
Sensitized Phosphorescence ◽  
Surface Construction

Reactive nitrene insertion is utilized in the surface construction of ferrocene-incorporating europium d–f dyads exhibiting a reversible redox switched sensitized phosphorescence.

An Analysis of Dissociation of Molecules in a High Resolution Electron Microscope

1973 ◽  
Vol 31 ◽  
pp. 486-487
Author(s):  
Mihir Parikh
Keyword(s):  
Electron Microscope ◽  
High Resolution ◽  
Cross Sections ◽  
Resolving Power ◽  
Peak Intensity ◽  
Molecular Film ◽  
Resolution Electron ◽  
Dissociation Cross Section ◽  
High Resolution Electron Microscope ◽  
The Stability

It is well known that the resolution of bio-molecules in a high resolution electron microscope depends not just on the physical resolving power of the instrument, but also on the stability of these molecules under the electron beam. Experimentally, the damage to the bio-molecules is commo ly monitored by the decrease in the intensity of the diffraction pattern, or more quantitatively by the decrease in the peaks of an energy loss spectrum. In the latter case the exposure, EC, to decrease the peak intensity from IO to I’O can be related to the molecular dissociation cross-section, σD, by EC = ℓn(IO /I’O) /ℓD. Qu ntitative data on damage cross-sections are just being reported, However, the microscopist needs to know the explicit dependence of damage on: (1) the molecular properties, (2) the density and characteristics of the molecular film and that of the support film, if any, (3) the temperature of the molecular film and (4) certain characteristics of the electron microscope used

Development of the UHV-STM

1990 ◽  
Vol 48 (1) ◽  
pp. 322-323
Author(s):  
M. Iwatsuki ◽  
S. Kitamura ◽  
A. Mogami
Keyword(s):  
Surface Science ◽  
Real Space ◽  
Atomic Scale ◽  
Scanning Tunneling ◽  
Great Promise ◽  
Force Microscopy ◽  
Atomic Force ◽  
Stm Image ◽  
Surface Construction ◽  
Very High

Since Binnig, Rohrer and associates observed real-space topographic images of Si(111)-7×7 and invented the scanning tunneling microscope (STM),1) the STM has been accepted as a powerful surface science instrument.Recently, many application areas for the STM have been opened up, such as atomic force microscopy (AFM), magnetic force microscopy (MFM) and others. So, the STM technology holds a great promise for the future.The great advantages of the STM are its high spatial resolution in the lateral and vertical directions on the atomic scale. However, the STM has difficulty in identifying atomic images in a desired area because it uses piezoelectric (PZT) elements as a scanner.On the other hand, the demand to observe specimens under UHV condition has grown, along with the advent of the STM technology. The requirment of UHV-STM is especially very high in to study of surface construction of semiconductors and superconducting materials on the atomic scale. In order to improve the STM image quality by keeping the specimen and tip surfaces clean, we have built a new UHV-STM (JSTM-4000XV) system which is provided with other surface analysis capability.

Strongly Coupled Redox-Linked Conformational Switching at the Active Site of the Non-Heme Iron-Dependent Dioxygenase, TauD

2019 ◽  
Author(s):  
Christopher John ◽  
Greg M. Swain ◽  
Robert P. Hausinger ◽  
Denis A. Proshlyakov
Keyword(s):  
Active Site ◽  
Structural Model ◽  
Heme Iron ◽  
Chemical Transformations ◽  
Experimental Conditions ◽  
Strongly Coupled ◽  
Non Heme Iron ◽  
Reversible Redox ◽  
Wide Range ◽  
Complex Structural

2-Oxoglutarate (2OG)-dependent dioxygenases catalyze C-H activation while performing a wide range of chemical transformations. In contrast to their heme analogues, non-heme iron centers afford greater structural flexibility with important implications for their diverse catalytic mechanisms. We characterize an <i>in situ</i> structural model of the putative transient ferric intermediate of 2OG:taurine dioxygenase (TauD) by using a combination of spectroelectrochemical and semi-empirical computational methods, demonstrating that the Fe (III/II) transition involves a substantial, fully reversible, redox-linked conformational change at the active site. This rearrangement alters the apparent redox potential of the active site between -127 mV for reduction of the ferric state and 171 mV for oxidation of the ferrous state of the 2OG-Fe-TauD complex. Structural perturbations exhibit limited sensitivity to mediator concentrations and potential pulse duration. Similar changes were observed in the Fe-TauD and taurine-2OG-Fe-TauD complexes, thus attributing the reorganization to the protein moiety rather than the cosubstrates. Redox difference infrared spectra indicate a reorganization of the protein backbone in addition to the involvement of carboxylate and histidine ligands. Quantitative modeling of the transient redox response using two alternative reaction schemes across a variety of experimental conditions strongly supports the proposal for intrinsic protein reorganization as the origin of the experimental observations.

Discovery of THICZs as Chemical Sensors: Synthesis, Spectrophotometric,Voltammetric and DFT Studies

2019 ◽  
Vol 09 ◽  
Author(s):  
Mardia T. El Sayed ◽  
Ibrahim H.I. Habib ◽  
Nermien M. Sabry ◽  
Sergey A. Pisarev ◽  
Mohamed El-Naggar ◽  
...  
Keyword(s):  
Electrochemical Behaviour ◽  
Molecular Size ◽  
Active Species ◽  
Carbon Paste ◽  
Reversible Redox ◽  
Energy Relationships ◽  
Linear Solvation Energy ◽  
Solute Interactions ◽  
Homo Lumo ◽  
Paste Electrode

Absorption spectra of tetrahydro[3,2-b]indolo-carbazoles (THICZs) with various molecular size and alkyl tails have been recorded in various solvents in the range between 200 to 600 nm. The photo physical behaviour of dissolved THICZs depends on the nature of its environment. The solvatochromic behaviours of THICZs and solvent solute interactions can be analysed by means of linear solvation energy relationships concept proposed by Kamlet and Taft. Compound 4 show excellent properties for sensing small molecules. The electrochemical behaviour of some THICZs was investigated at carbon paste electrode where two electrode reactions were involved, irreversible oxidation-one electron transfer and quasi-reversible redox reactions forming phenolic followed by quinolone moiety electro active species. The DFT-calculated molecular orbital energies (B3LYP/6-31G) and HOMO-LUMO gaps for some presented indolocarbazoles have been performed.

NMDA and GABAA receptors, NO and redox modulation

1996 ◽  
Vol 17 (5) ◽  
pp. 187-189 ◽  
Author(s):  
Henri Gozlan ◽  
Yohezkel Ben-Ari
Keyword(s):  
Gabaa Receptors ◽  
Redox Modulation

scholarly journals Enhanced Production of the Mical Redox Domain for Enzymology and F-actin Disassembly Assays

2021 ◽  
Vol 22 (4) ◽  
pp. 1991
Author(s):  
Jimok Yoon ◽  
Heng Wu ◽  
Ruei-Jiun Hung ◽  
Jonathan R. Terman
Keyword(s):  
Nicotinamide Adenine Dinucleotide Phosphate ◽  
Actin Dynamics ◽  
Specific Substrate ◽  
Actin Assembly ◽  
Redox Enzymes ◽  
Enhanced Production ◽  
Reversible Redox ◽  
Future Work ◽  
Signaling Process

To change their behaviors, cells require actin proteins to assemble together into long polymers/filaments—and so a critical goal is to understand the factors that control this actin filament (F-actin) assembly and stability. We have identified a family of unusual actin regulators, the MICALs, which are flavoprotein monooxygenase/hydroxylase enzymes that associate with flavin adenine dinucleotide (FAD) and use the co-enzyme nicotinamide adenine dinucleotide phosphate (NADPH) in Redox reactions. F-actin is a specific substrate for these MICAL Redox enzymes, which oxidize specific amino acids within actin to destabilize actin filaments. Furthermore, this MICAL-catalyzed reaction is reversed by another family of Redox enzymes (SelR/MsrB enzymes)—thereby revealing a reversible Redox signaling process and biochemical mechanism regulating actin dynamics. Interestingly, in addition to the MICALs’ Redox enzymatic portion through which MICALs covalently modify and affect actin, MICALs have multiple other domains. Less is known about the roles of these other MICAL domains. Here we provide approaches for obtaining high levels of recombinant protein for the Redox only portion of Mical and demonstrate its catalytic and F-actin disassembly activity. These results provide a ground state for future work aimed at defining the role of the other domains of Mical — including characterizing their effects on Mical’s Redox enzymatic and F-actin disassembly activity.

Multilayer surface construction for enhancing barrier properties of cellulose-based packaging

2021 ◽  
Vol 255 ◽  
pp. 117431
Author(s):  
Wangxia Wang ◽  
Feng Gu ◽  
Zhifei Deng ◽  
Yang Zhu ◽  
Jing Zhu ◽  
...  
Keyword(s):  
Barrier Properties ◽  
Surface Construction

scholarly journals A four-electron Zn-I2 aqueous battery enabled by reversible I−/I2/I+ conversion

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yiping Zou ◽  
Tingting Liu ◽  
Qijun Du ◽  
Yingying Li ◽  
Haibo Yi ◽  
...  
Keyword(s):  
Aqueous Electrolyte ◽  
Chloride Ions ◽  
Experimental Characterization ◽  
Redox Couples ◽  
Free Chloride ◽  
Reversible Redox ◽  
Aqueous Battery ◽  
Storage Batteries ◽  
Aqueous Batteries ◽  
Superior Level

AbstractElectrochemically reversible redox couples that embrace more electron transfer at a higher potential are the eternal target for energy storage batteries. Here, we report a four-electron aqueous zinc-iodine battery by activating the highly reversible I2/I+ couple (1.83 V vs. Zn/Zn2+) in addition to the typical I−/I2 couple (1.29 V). This is achieved by intensive solvation of the aqueous electrolyte to yield ICl inter-halogens and to suspend its hydrolysis. Experimental characterization and modelling reveal that limited water activity and sufficient free chloride ions in the electrolyte are crucial for the four-electron process. The merits of the electrolyte also afford to stabilize Zn anode, leading to a reliable Zn-I2 aqueous battery of 6000 cycles. Owing to high operational voltage and capacity, energy density up to 750 Wh kg−1 based on iodine mass was achieved (15–20 wt% iodine in electrode). It pushes the Zn-I2 battery to a superior level among these available aqueous batteries.

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