scholarly journals Non-sequential and sequential fragmentation dynamics of OCS3+in collision with 500 eV electron

2015 ◽  
Vol 635 (7) ◽  
pp. 072044
Author(s):  
ZhenJie Shen ◽  
MaoMao Gong ◽  
EnLiang Wang ◽  
Xu Shan ◽  
XiangJun Chen
2020 ◽  
Vol 45 (s1) ◽  
pp. 864-892
Author(s):  
Cristiano Bee ◽  
Stavroula Chrona

AbstractThis article investigates media representations of the European financial crisis in Greece and Italy. We study the Euro crisis as an ‘emergency situation’ with domino effects, where media played a central role in shaping communication practices at the national level as well as between the two countries. Drawing upon vertical and horizontal dynamics of Europeanization, we map the convergences and divergences in media discourses that surround the period 2011–2015. In doing so, we elaborate a qualitative analysis of newspaper articles focusing, in particular, on the themes of austerity and the fragmentation of Europe. Our argument suggests that national public spheres in times of transnational crisis become increasingly nationalized; yet under certain circumstances such as when the supranational infrastructure is the target of blame, they converge, opening the path toward a transnational discursive dialogue.


2015 ◽  
Vol 17 (26) ◽  
pp. 16767-16778 ◽  
Author(s):  
Dariusz Grzegorz Piekarski ◽  
Rudy Delaunay ◽  
Sylvain Maclot ◽  
Lamri Adoui ◽  
Fernando Martín ◽  
...  

Experimental and theoretical investigations show that hydroxyl migration leads to unexpected fragmentation dynamics of β-alanine dication in the gas phase.


2021 ◽  
Vol 103 (3) ◽  
Author(s):  
Sumit Srivastav ◽  
Arnab Sen ◽  
Deepak Sharma ◽  
Bhas Bapat

2021 ◽  
Vol 17 (9) ◽  
pp. e1008964
Author(s):  
Magali Tournus ◽  
Miguel Escobedo ◽  
Wei-Feng Xue ◽  
Marie Doumic

The dynamics by which polymeric protein filaments divide in the presence of negligible growth, for example due to the depletion of free monomeric precursors, can be described by the universal mathematical equations of ‘pure fragmentation’. The rates of fragmentation reactions reflect the stability of the protein filaments towards breakage, which is of importance in biology and biomedicine for instance in governing the creation of amyloid seeds and the propagation of prions. Here, we devised from mathematical theory inversion formulae to recover the division rates and division kernel information from time dependent experimental measurements of filament size distribution. The numerical approach to systematically analyze the behaviour of pure fragmentation trajectories was also developed. We illustrate how these formulae can be used, provide some insights on their robustness, and show how they inform the design of experiments to measure fibril fragmentation dynamics. These advances are made possible by our central theoretical result on how the length distribution profile of the solution to the pure fragmentation equation aligns with a steady distribution profile for large times.


2018 ◽  
Vol 67 (4) ◽  
pp. 043401
Author(s):  
Shen Li-Li ◽  
Yan Shun-Cheng ◽  
Ma Xin-Wen ◽  
Zhu Xiao-Long ◽  
Zhang Shao-Feng ◽  
...  

2001 ◽  
Vol 64 (3) ◽  
Author(s):  
F. A. Rajgara ◽  
M. Krishnamurthy ◽  
D. Mathur ◽  
T. Nishide ◽  
T. Kitamura ◽  
...  

1994 ◽  
Vol 73 (14) ◽  
pp. 1919-1922 ◽  
Author(s):  
H. Hohmann ◽  
C. Callegari ◽  
S. Furrer ◽  
D. Grosenick ◽  
E. E. B. Campbell ◽  
...  

2018 ◽  
Vol 616 ◽  
pp. A166 ◽  
Author(s):  
P. Castellanos ◽  
A. Candian ◽  
J. Zhen ◽  
H. Linnartz ◽  
A. G. G. M. Tielens

Polycyclic aromatic hydrocarbons (PAHs) constitute a major component of the interstellar medium carbon budget, locking up to 10–20% of the elemental carbon. Sequential fragmentation induced by energetic photons leads to the formation of new species, including fullerenes. However, the exact chemical routes involved in this process remain largely unexplored. In this work, we focus on the first photofragmentation steps, which involve the dehydrogenation of these molecules. For this, we consider a multidisciplinary approach, taking into account the results from experiments, density functional theory (DFT) calculations, and modeling using dedicated Monte-Carlo simulations. By considering the simplest isomerization pathways — i.e., hydrogen roaming along the edges of the molecule — we are able to characterize the most likely photodissociation pathways for the molecules studied here. These comprise nine PAHs with clearly different structural properties. The formation of aliphatic-like side groups is found to be critical in the first fragmentation step and, furthermore, sets the balance of the competition between H- and H2-loss. We show that the presence of trio hydrogens, especially in combination with bay regions in small PAHs plays an important part in the experimentally established variations in the odd-to-even H-atom loss ratios. In addition, we find that, as PAH size increases, H2 formation becomes dominant, and sequential hydrogen loss only plays a marginal role. We also find disagreements between experiments and calculations for large, solo containing PAHs, which need to be accounted for. In order to match theoretical and experimental results, we have modified the energy barriers and restricted the H-hopping to tertiary atoms. The formation of H2 in large PAHs upon irradiation appears to be the dominant fragmentation channel, suggesting an efficient formation path for molecular hydrogen in photodissociation regions (PDRs).


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