Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Oisin J. Shiels"'
Autor:
Dmitri Babikov, Michael P. Burke, Piergiorgio Casavecchia, William H. Green, Alon Grinberg Dana, Hua Guo, Dwayne E. Heard, David Heathcote, Majdi Hochlaf, Ahren W. Jasper, Stephen J. Klippenstein, Marsha I. Lester, Carles Martí, Alexander M. Mebel, Amy S. Mullin, Thanh Lam Nguyen, Matthias Olzmann, Andrew J. Orr-Ewing, David L. Osborn, Patrick A. Robertson, Matthew S. Robinson, Robin J. Shannon, Oisin J. Shiels, Arthur G. Suits, Craig A. Taatjes, Jürgen Troe, Xuefei Xu, Xiaoqing You, Feng Zhang, Rui Ming Zhang, Judit Zádor
Publikováno v:
Faraday Discussions. 238:121-143
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::648e11609433cde218ecaabd5f9b4258
https://doi.org/10.1039/d2fd90048c
https://doi.org/10.1039/d2fd90048c
Autor:
Jeroen Aerssens, Michael P. Burke, Carlo Cavallotti, Nicholas J. B. Green, William H. Green, Hua Guo, Dwayne Heard, Majdi Hochlaf, Ahren W. Jasper, Stephen J. Klippenstein, Keith T. Kuwata, Joseph E. Lawrence, Alexander M. Mebel, Amy S. Mullin, Thanh Lam Nguyen, Matthias Olzmann, David L. Osborn, Mark Pfeifle, John M. C. Plane, Patrick A. Robertson, Struan H. Robertson, Magdalena Salzburger, Paul W. Seakins, Robin J. Shannon, Oisin J. Shiels, Adam J. Trevitt, Claire Vallance, Oliver Welz, Xuefei Xu, Judit Zádor, Rui Ming Zhang
Publikováno v:
Faraday discussions. 238
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7adc34fb195f62415b343d384b2bd9dc
https://pubmed.ncbi.nlm.nih.gov/36222351
https://pubmed.ncbi.nlm.nih.gov/36222351
Autor:
Cameron C. Bright, Oisin J. Shiels, Stephen J. Blanksby, Berwyck L. J. Poad, Gabriel da Silva, Adam J. Trevitt, Patrick D Kelly
Publikováno v:
Journal of the American Society for Mass Spectrometry. 32:537-547
A key step in gas-phase polycyclic aromatic hydrocarbon (PAH) formation involves the addition of acetylene (or other alkyne) to σ-type aromatic radicals, with successive additions yielding more complex PAHs. A similar process can happen for N-contai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d78991c171ba97974943ecb238015e4
https://doi.org/10.1021/jasms.0c00386
https://doi.org/10.1021/jasms.0c00386
Five vs. six membered-ring PAH products from reaction of o-methylphenyl radical and two C3H4 isomers
Autor:
David L. Osborn, Craig A. Taatjes, Oisin J. Shiels, John D. Savee, Adam J. Trevitt, Stephen J. Blanksby, Matthew B. Prendergast, Gabriel da Silva
Publikováno v:
Physical Chemistry Chemical Physics. 23:14913-14924
Gas-phase reactions of the o-methylphenyl (o-CH3C6H4) radical with the C3H4 isomers allene (H2C[double bond, length as m-dash]C[double bond, length as m-dash]CH2) and propyne (HC[triple bond, length as m-dash]C-CH3) are studied at 600 K and 4 Torr (5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e209c2d11eb046d2be53543f31416fa
https://doi.org/10.1039/d1cp01764k
https://doi.org/10.1039/d1cp01764k
Autor:
Oisin J, Shiels, Matthew B, Prendergast, John D, Savee, David L, Osborn, Craig A, Taatjes, Stephen J, Blanksby, Gabriel, da Silva, Adam J, Trevitt
Publikováno v:
Physical chemistry chemical physics : PCCP. 23(27)
Gas-phase reactions of the o-methylphenyl (o-CH3C6H4) radical with the C3H4 isomers allene (H2C[double bond, length as m-dash]C[double bond, length as m-dash]CH2) and propyne (HC[triple bond, length as m-dash]C-CH3) are studied at 600 K and 4 Torr (5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::94ce5a85f084e5984d7e2168a968461b
https://pubmed.ncbi.nlm.nih.gov/34223848
https://pubmed.ncbi.nlm.nih.gov/34223848
Autor:
Stephen J. Blanksby, Patrick D Kelly, Gabriel da Silva, Oisin J. Shiels, Adam J. Trevitt, Samuel J. P. Marlton
Publikováno v:
Proceedings of the 2021 International Symposium on Molecular Spectroscopy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f572126d66e5f01fa82e9dc471146e11
https://doi.org/10.15278/isms.2021.wb10
https://doi.org/10.15278/isms.2021.wb10
Five vs Six Membered-Ring PAH Products from Reaction of o- Methylphenyl Radical and two C3H4 Isomers
Autor:
Adam J. Trevitt, David L. Osborn, John D. Savee, Stephen J. Blanksby, Gabriel da Silva, Oisin J. Shiels, Matthew B. Prendergast, Craig A. Taatjes
Using VUV synchrotron photoionization mass spectrometry, quantum chemistry and RRKM kinetic modeling, our paper identifies the products formed when a substituted aromatic free radical (ortho- methylphenyl) reacts with two C3H4 isomers found in flames
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::952f413089b0440ad14ce3da04d2e832
https://doi.org/10.26434/chemrxiv.14538516.v1
https://doi.org/10.26434/chemrxiv.14538516.v1
Autor:
Oisin J, Shiels, P D, Kelly, Cameron C, Bright, Berwyck L J, Poad, Stephen J, Blanksby, Gabriel, da Silva, Adam J, Trevitt
Publikováno v:
Journal of the American Society for Mass Spectrometry. 32(2)
A key step in gas-phase polycyclic aromatic hydrocarbon (PAH) formation involves the addition of acetylene (or other alkyne) to σ-type aromatic radicals, with successive additions yielding more complex PAHs. A similar process can happen for N-contai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::04ab460d96681c8801a139cb049d903c
https://pubmed.ncbi.nlm.nih.gov/33444019
https://pubmed.ncbi.nlm.nih.gov/33444019
Autor:
Cameron C. Bright, Adam J. Trevitt, Patrick D Kelly, Oisin J. Shiels, Berwyck L. J. Poad, Stephen J. Blanksby, Gabriel da Silva
A key step in gas-phase polycyclic aromatic hydrocarbon (PAH) formation involves the addition of acetylene (or other alkyne) to σ-type aromatic radicals, with successive additions yielding more complex PAHs. A similar process can happen for N- conta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7129a7dcfcf49a1a9f069842b518274
https://doi.org/10.26434/chemrxiv.13078334.v1
https://doi.org/10.26434/chemrxiv.13078334.v1
Autor:
Samuel J. P. Marlton, Boris Ucur, Adam J. Trevitt, Oisin J. Shiels, Phillip Greißel, Benjamin I. McKinnon
Publikováno v:
The Journal of Chemical Physics. 155:184302
Certain chemical groups give rise to characteristic excited-state deactivation mechanisms. Here, we target the role of a protonated N-N chemical group in the excited-state deactivation of protonated indazole by comparison to its isomer that lacks thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::944719dd6f7a06d9787b3820aa1d7959
https://doi.org/10.1063/5.0071847
https://doi.org/10.1063/5.0071847