CO-Induced ethane formation from ethylene and hydrogen on Fe(100): effects of ligands in surface reactions

1991 ◽  
Vol 113 (5) ◽  
pp. 1475-1484 ◽  
Author(s):  
M. L. Burke ◽  
R. J. Madix
Keyword(s):  
Surface Reactions ◽  
Ethane Formation

Superoxide-and Ethane-Formation in Subchloroplast Particles: Catalysis by Pyridinium Derivatives

1980 ◽  
Vol 35 (9-10) ◽  
pp. 770-775 ◽  
Author(s):  
E. F. Elstner ◽  
H. P. Fischer ◽  
W. Osswald ◽  
G. Kwiatkowski
Keyword(s):  
Electron Transport ◽  
Photosystem I ◽  
Photosynthetic Electron Transport ◽  
Redox Potentials ◽  
Light Reaction ◽  
Pyridinium Bromide ◽  
Superoxide Formation ◽  
Fatty Acid Peroxidation ◽  
Chlorophyll Bleaching ◽  
Ethane Formation

Abstract Oxygen reduction by chloroplast lamellae is catalyzed by low potential redox dyes with E′0 values between -0 .3 8 V and -0 .6 V. Compounds of E′0 values of -0 .6 7 V and lower are inactive. In subchloroplast particles with an active photosystem I but devoid of photosynthetic electron transport between the two photosystems, the active redox compounds enhance chlorophyll bleaching, superoxide formation and ethane production independent on exogenous substrates or electron donors. The activities of these compounds decrease with decreasing redox potential, with one exception: 1-methyl-4,4′-bipyridini urn bromide with an E′0 value of lower -1 V (and thus no electron acceptor of photosystem I in chloroplast lamellae with intact electron transport) stimulates light dependent superoxide formation and unsaturated fatty acid peroxidation in sub­ chloroplast particles, maximal rates appearing after almost complete chlorophyll bleaching. Since this activity is not visible with compounds with redox potentials below -0 .6 V lacking the nitrogen atom at the 1-position of the pyridinium substituent, we assume that 1 -methyl-4,4′-bi-pyridinium bromide is “activated” by a yet unknown light reaction.

Low Energy Electron- and Ion-Induced Surface Reactions of Fe(CO)5 Thin Films

2021 ◽  
Author(s):  
Elif Bilgilisoy ◽  
Rachel M. Thorman ◽  
Michael S. Barclay ◽  
Hubertus Marbach ◽  
D. Howard Fairbrother
Keyword(s):  
Thin Films ◽  
Surface Reactions ◽  
Low Energy ◽  
Energy Electron ◽  
Low Energy Electron

Surface Reactions and Electronic Structure of Carboxylic Acid Porphyrins Adsorbed on TiO2(110)

2021 ◽  
Author(s):  
Daniel Wechsler ◽  
Priscila Vensaus ◽  
Nataliya Tsud ◽  
Hans-Peter Steinrück ◽  
Ole Lytken ◽  
...  
Keyword(s):  
Electronic Structure ◽  
Carboxylic Acid ◽  
Surface Reactions

Transport of Ions and Molecules in Nanofluidic Devices

2008 ◽  
Author(s):  
Rohit Karnik ◽  
Chuanhua Duan ◽  
Kenneth Castelino ◽  
Rong Fan ◽  
Peidong Yang ◽  
...  
Keyword(s):  
Surface Charge ◽  
Surface Area ◽  
Field Effect ◽  
Electrostatic Interactions ◽  
Surface Reactions ◽  
Molecular Transport ◽  
Large Surface Area ◽  
Ionic Concentrations ◽  
Nanofluidic Devices ◽  
Transport Of Ions

Interesting transport phenomena arise when fluids are confined to nanoscale dimensions in the range of 1–100 nm. We examine three distinct effects that influence ionic and molecular transport as the size of fluidic channels is decreased to the nanoscale. First, the length scale of electrostatic interactions in aqueous solutions becomes comparable to nanochannel size and the number of surface charges becomes comparable to the number of ions in the channel. Second, the size of the channel becomes comparable to the size of biomolecules such as proteins and DNA. Third, large surface area-to-volume ratios result in rapid rates of surface reactions and can dramatically affect transport of molecules through the channel. These phenomena enable us to control transport of ions and molecules in unique ways that are not possible in larger channels. Electrostatic interactions enable local control of ionic concentrations and transport inside nanochannels through field effect in a nanofluidic transistor, which is analogous to the metal-oxide-semiconductor field effect transistor. Furthermore, by controlling surface charge in nanochannels, it is possible to create a nanofluidic diode that rectifies ionic transport through the channel. Biological binding events result in partial blockage of the channel, and can thus be sensed by a decrease in nanochannel conductance. At low ionic concentrations, the effect of biomolecular charge is dominant and it can lead to an increase in conductance. Surface reactions can also be used to control transport of molecules though the channel due to the large surface area-to-volume ratios. Rapid surface reactions enable a new technique of diffusion-limited patterning (DLP), which is useful for patterning of biomolecules and surface charge in nanochannels. These examples illustrate how electrostatic interactions, biomolecular size, and surface reactions can be used for controlling ionic and molecular transport through nanochannels. These phenomena may be useful for operations such as analyte focusing, pH and ionic concentration control, and biosensing in micro- and nanofluidic devices.

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