Solvated electrons at the water–air interface: surface versus bulk signal in low kinetic energy photoelectron spectroscopy
Literature Information
Franziska Buchner, Thomas Schultz, Andrea Lübcke
Time-resolved photoelectron spectroscopy at low kinetic energies (≲5 eV) is applied to dilute iodide solutions with different surface and bulk contributions. The results indicate a pronounced surface sensitivity. Signals assigned to solvated electrons near the liquid surface decay rapidly on a sub-ps timescale. In contrast to the literature, a long-lived surface solvated electron at 1.6 eV binding energy is not observed.
Related Literature
Accelerating chemical replication steps of RNA involving activated ribonucleotides and downstream-binding elements
Stephanie R. Vogel, Christopher Deck, Clemens Richert
DOI: 10.1039/B510775J
The synthesis of isostructural Mo2+porphyrin and N-confused porphyrin complexes
John D. Harvey, Janet L. Shaw, Richard S. Herrick, Christopher J. Ziegler
DOI: 10.1039/B508913A
Concomitant crystallization of two polymorphs—a ring and a helix: concentration effect on supramolecular isomerism
Katharina M. Fromm, Jorge L. Sagué Doimeadios, Adeline Y. Robin
DOI: 10.1039/B506389B
The first synthesis of organic–inorganic hybrid materials with chiral bis(oxazoline) ligands
José M. Fraile, José I. García, Clara I. Herrerías, José A. Mayoral
DOI: 10.1039/B507739G
A ligand-free solid-supported system for Sonogashira couplings: applications in nucleoside chemistry
Neil K. Garg, Carolyn C. Woodroofe, Christopher J. Lacenere, Stephen R. Quake, Brian M. Stoltz
DOI: 10.1039/B505737J
Rhodium-catalyzed tandem cyclization–cycloaddition reactions of enynebenzaldehydes: construction of polycyclic ring systems
Seunghoon Shin, Arun Kumar Gupta, Chul Yun Rhim, Chang Ho Oh
DOI: 10.1039/B506003F
Strongly luminescent binuclear aluminium chelate with polymer-like molecular packing and solution-processibility
Juan Qiao, Li. D. Wang, Jun. F. Xie, Gang. T. Lei, Guo. S. Wu, Yong Qiu
DOI: 10.1039/B506907F
Preparation of helical nanostructures using chiral cationic surfactants
Yonggang Yang, Masahiro Suzuki, Sanae Owa, Hirofusa Shirai, Kenji Hanabusa
DOI: 10.1039/B508106H
You might also like
Is 6-(3-Fluorophenyl)picolinic acid (CAS: 887982-40-3) safe?
6-(3-Fluorophenyl)picolinic acid is generally considered safe for laboratory use...
What industries use (3R)-3-Pyrrolidinol (CAS: 2799-21-5)?
(3R)-3-Pyrrolidinol is used in the pharmaceutical industry as a precursor for dr...
What precautions should be taken when handling (4R,5R)-4,5-Diethoxycarbonyl-2,2-dimethyldioxolane (CAS: 59779-75-8)?
When handling (4R,5R)-4,5-Diethoxycarbonyl-2,2-dimethyldioxolane (CAS: 59779-75-...
How is 1-(6-Chloroimidazo[1,2-b]pyridazin-3-yl)ethanone (CAS: 90734-71-7) typically synthesized?
1-(6-Chloroimidazo[1,2-b]pyridazin-3-yl)ethanone is often synthesized via a mult...
What is the market or research trend for N-Ethyl-3,4-dimethylbenzylamine (CAS: 39180-83-1)?
The market for N-Ethyl-3,4-dimethylbenzylamine (CAS: 39180-83-1) remains steady,...
What is Tert-butyl 3-(pyrrolidin-1-yl)azetidine-1-carboxylate (CAS: 1019008-21-9)?
Tert-butyl 3-(pyrrolidin-1-yl)azetidine-1-carboxylate is a chemical compound wit...
What regulatory guidelines apply to 1-Bromo-3-chloro-2,4-dimethoxybenzene (CAS: 1228956-93-1)?
1-Bromo-3-chloro-2,4-dimethoxybenzene (CAS: 1228956-93-1) falls under the classi...
Is 8-Bromo-2-methyl-3,4-dihydroisoquinolin-1(2H)-one (CAS: 1368622-07-4) safe?
The safety of 8-Bromo-2-methyl-3,4-dihydroisoquinolin-1(2H)-one (CAS: 1368622-07...
Is Benzyl [(3S)-2,6-dioxo-3-piperidinyl]carbamate (CAS: 22785-43-9) safe?
Benzyl [(3S)-2,6-dioxo-3-piperidinyl]carbamate is generally safe when handled wi...
How should 1-{[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]sulfonyl}pyrrolidine (CAS: 928657-21-0) be stored?
1-{[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]sulfonyl}pyrrolidine s...
Source Journal
Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.











![2-[({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)methyl]isonicotinic acid structure 2-[({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)methyl]isonicotinic acid structure](https://static.chemtradehub.com/structs/473/473924-63-9-973b.webp)


