Slice imaging of methyl bromide photofragmentation at 193 nm
Literature Information
M. Laura Lipciuc, Peter C. Samartzis, Xueming Yang
The photodissociation of methyl bromide at 193 nm is studied using slice imaging. From the measured photofragment translational energy and angular distributions we were able to extract methyl-state-specific dissociation channel yields and crossing probabilities between 3Q0 and 1Q1 surfaces. The angular distributions for the Bromine photofragments show a strong dependence on the total translational energy release. Nonadiabatic transition probabilities from the 3Q0 to 1Q1 surface dominate the dynamics in this excitation energy region and for most of the methyl vibrational states probed.
Related Literature
Single atom catalyst-mediated generation of reactive species in water treatment
Virender K. Sharma, Xingmao Ma
DOI: 10.1039/D3CS00627A
Towards multimodal cellular imaging: optical and X-ray fluorescence
Marcus E. Graziotto, Clinton J. Kidman, Simon A. James, Hugh H. Harris
DOI: 10.1039/D3CS00509G
Recent advances in the design of afterglow materials: mechanisms, structural regulation strategies and applications
Geoffrey I. N. Waterhouse, Siyu Lu
DOI: 10.1039/D2CS00993E
Strategies to engineer various nanocarrier-based hybrid catalysts for enhanced chemodynamic cancer therapy
Ji-Na Hao, Kaiming Ge, Guoli Chen, Bin Dai
DOI: 10.1039/D3CS00356F
Nuclear localization signal-tagged systems: relevant nuclear import principles in the context of current therapeutic design
Ritabrita Goswami, Aarohi Gupta, Olga Bednova, Gaël Coulombe, Dipika Patel, Vincent M. Rotello
DOI: 10.1039/D1CS00269D
The synthesis and application of crystalline–amorphous hybrid materials
Hao Lan, Jiawei Wang, Liwei Cheng, Dandan Yu, Hua Wang, Lin Guo
DOI: 10.1039/D3CS00860F
Boryl-substituted low-valent heavy group 14 compounds
Chenxi Duan, Chunming Cui
DOI: 10.1039/D3CS00791J
Photocatalysis with atomically thin sheets
Yingying Fan, Jinguang Hu, Hyeon Suk Shin, Damien Voiry, Qingye Lu, Jimmy C. Yu
DOI: 10.1039/D2CS00205A
Visible light-mediated halogenation of organic compounds
Alexey A. Festa, Olga A. Storozhenko, Leonid G. Voskressensky
DOI: 10.1039/D3CS00366C
You might also like
How should waste containing 6-Chloro-5-(2'-hydroxy-3'-methoxy-4-biphenylyl)-3-(3-methoxyphenyl)-1H-pyrrolo[3,2-d]pyrimidine-2,4(3H,5H)-dione (CAS: 1346607-05-3) be handled?
Waste containing 6-Chloro-5-(2'-hydroxy-3'-methoxy-4-biphenylyl)-3-(3-methoxyphe...
What are the main uses of (3alpha,5alpha)-3-Hydroxypregnane-11,20-dione (CAS: 23930-19-0)?
(3alpha,5alpha)-3-Hydroxypregnane-11,20-dione is primarily used in the pharmaceu...
What is the market or research trend for 4-Amino-6-chloro-2-pyridinecarboxylic acid (CAS: 546141-56-4)?
The market for 4-Amino-6-chloro-2-pyridinecarboxylic acid (CAS: 546141-56-4) is ...
Are there alternatives to (2-Benzoylethyl)trimethylammonium chloride (CAS: 24472-88-6) in synthesis?
Alternatives to (2-Benzoylethyl)trimethylammonium chloride (CAS: 24472-88-6) in ...
Is N-[4-Nitro-3-(trifluoromethyl)phenyl]acetamide (CAS: 393-12-4) safe?
N-[4-Nitro-3-(trifluoromethyl)phenyl]acetamide (CAS: 393-12-4) is generally safe...
Are there alternatives to [(4R,5R,6S)-5-hydroxy-10-imino-3,7-dioxa-1,9-diazatricyclo[6.4.0.02,6]dodeca-8,11-dien-4-yl]methyl dihydrogen phosphate (CAS: 39679-56-6) in synthesis?
Alternative reagents such as other phosphates or similar functional groups can b...
Are there alternatives to N,N'-Bis(3-aminopropyl)-1,3-propanediamine (CAS: 4605-14-5) in synthesis?
There are alternatives to N,N'-Bis(3-aminopropyl)-1,3-propanediamine (CAS: 4605-...
What precautions should be taken when handling Aluminium trihexadecanoate (CAS: 555-35-1)?
When handling Aluminium trihexadecanoate, it is important to use appropriate per...
What is (1,1-Dioxido-3-oxo-1,2-benzothiazol-2(3H)-yl)acetic acid (CAS: 52188-11-1)?
(1,1-Dioxido-3-oxo-1,2-benzothiazol-2(3H)-yl)acetic acid is a chemical compound ...
Are there alternatives to 5,5-dimethyloxolan-2-one (CAS: 3123-97-5) in synthesis?
Several alternatives to 5,5-dimethyloxolan-2-one (CAS: 3123-97-5) can be used in...
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.











![(3-{[4-(Aminomethyl)-6-(trifluoromethyl)-2-pyridinyl]oxy}phenyl)[(3R,4R)-3-fluoro-4-hydroxy-1-pyrrolidinyl]methanone structure (3-{[4-(Aminomethyl)-6-(trifluoromethyl)-2-pyridinyl]oxy}phenyl)[(3R,4R)-3-fluoro-4-hydroxy-1-pyrrolidinyl]methanone structure](https://static.chemtradehub.com/structs/200/2007885-39-2-affc.webp)
![Benzo[b]naphtho[2,1-d]thiophene structure Benzo[b]naphtho[2,1-d]thiophene structure](https://static.chemtradehub.com/structs/239/239-35-0-ff90.webp)

