Adsorption Forms of NO on Iridium-Doped Rhodium Clusters in the Gas Phase Revealed by Infrared Multiple Photon Dissociation Spectroscopy

Author(s):  
Yufei Zhang ◽  
Masato Yamaguchi ◽  
Kimihiro Kawada ◽  
Satoshi Kudoh ◽  
Olga V. Lushchikova ◽  
...  



2011 ◽  
Vol 115 (10) ◽  
pp. 2282-2286 ◽  
Author(s):  
Gianluca Giorgi ◽  
Leopoldo Ceraulo ◽  
Giel Berden ◽  
Jos Oomens ◽  
Vincenzo Turco Liveri


2008 ◽  
Vol 129 (24) ◽  
pp. 244302 ◽  
Author(s):  
Jeffrey D. Steill ◽  
Jos Oomens ◽  
John R. Eyler ◽  
Robert N. Compton


2014 ◽  
Vol 16 (44) ◽  
pp. 24223-24234 ◽  
Author(s):  
Michael Burt ◽  
Kathleen Wilson ◽  
Rick Marta ◽  
Moaraj Hasan ◽  
W. Scott Hopkins ◽  
...  

The gas-phase structures of two halide-bound phenylalanine anions (PheX−, X = Cl− or Br−) and five fluorinated derivatives have been identified using infrared multiple photon dissociation (IRMPD) spectroscopy.



2014 ◽  
Vol 118 (29) ◽  
pp. 5407-5418 ◽  
Author(s):  
Michael J. van Stipdonk ◽  
Partha Basu ◽  
Sara A. Dille ◽  
John K. Gibson ◽  
Giel Berden ◽  
...  




2020 ◽  
Author(s):  
Jacob A. Berenbeim ◽  
Natalie Wong ◽  
Martin C. R. Cockett ◽  
Giel Berden ◽  
Jos Oomens ◽  
...  

Avobenzone (AB) is a widely used UVA filter known to undergo irreversible photodegradation. Here, we investigate the detailed pathways by which AB photodegrades by applying UV laser-interfaced mass spectrometry to protonated AB ions. Gas-phase infrared multiple-photon dissociation (IRMPD) spectra obtained with the free electron laser for infrared experiments, FELIX, (600-1800 cm-1) are also presented to confirm the geometric structures. The UV gas-phase absorption spectrum (2.5-5 eV) of protonated AB contains bands that correspond to selective excitation of either the enol or diketo forms, allowing us to probe the resulting, tautomer-dependent photochemistry. Numerous photofragments (i.e. photodegradants) are directly identified for the first time, with m/z 135 and 161 dominating, and m/z 146 and 177 also appearing prominently. Analysis of the production spectra of these photofragments reveals that that strong enol to keto photoisomerism is occurring, and that protonation significantly disrupts the stability of the enol (UVA active) tautomer. Close comparison of fragment ion yields with the TDDFT-calculated absorption spectra give detailed information on the location and identity of the dissociative excited state surfaces, and thus provide new insight into the photodegradation pathways of avobenzone, and photoisomerisation of the wider class of β-diketone containing molecules.<br>



Molecules ◽  
2021 ◽  
Vol 26 (21) ◽  
pp. 6546
Author(s):  
Ruxia Feng ◽  
Yicheng Xu ◽  
Xianglei Kong

Although metal cations are prevalent in biological media, the species of multi-metal cationized biomolecules have received little attention so far. Studying these complexes in isolated state is important, since it provides intrinsic information about the interaction among them on the molecular level. Our investigation here demonstrates the unexpected structural diversity of such species generated by a matrix-assisted laser desorption ionization (MALDI) source in the gas phase. The photodissociation spectroscopic and theoretical study reflects that the co-existing isomers of [Arg+Rb+K−H]+ can have energies ≥95 kJ/mol higher than that of the most stable one. While the result can be rationalized by the great isomerization energy barrier due to the coordination, it strongly reminds us to pay more attention to their structural diversities for multi-metalized fundamental biological molecules, especially for the ones with the ubiquitous alkali metal ions.



Author(s):  
Christopher P. McNary ◽  
Maria Demireva ◽  
Jonathan Martens ◽  
Giel Berden ◽  
Jos Oomens ◽  
...  

The gas-phase structures of protonated unsymmetrical 1,1-dimethylhydrazine (UDMH) and the proton-bound dimers of UDMH and hydrazine are examined by infrared multiple photon dissociation (IRMPD) action spectroscopy utilizing light generated by...



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