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Results: 293
Number of items: 293
  • Wu, R. R., He, C. C., Hamlow, L. A., Nei, Y., Berden, G., Oomens, J., & Rodgers, M. T. (2016). Protonation induces base rotation of purine nucleotides pdGuo and pGuo. Physical Chemistry Chemical Physics, 18(22), 15081-15090. https://doi.org/10.1039/c6cp01354f
  • Wu, R. R., He, C. C., Hamlow, L. A., Nei, Y., Berden, G., Oomens, J., & Rodgers, M. T. (2016). N3 Protonation Induces Base Rotation of 2 '-Deoxyadenosine-5 '-monophosphate and Adenosine-5 '-monophosphate. The journal of Physical Chemistry. B, 120(20), 4616-4624. https://doi.org/10.1021/acs.jpcb.6b04052
  • Kempkes, L. J. M., Martens, J. K., Grzetic, J., Berden, G., & Oomens, J. (2016). Deamidation reactions of protonated asparagine and glutamine investigated by ion spectroscopy. Rapid Communications in Mass Spectrometry, 30(4), 483-490. https://doi.org/10.1002/rcm.7464
  • Gao, J., Berden, G., Rodgers, M. T., & Oomens, J. (2016). Interaction of Cu+ with cytosine and formation of i-motif-like C-M+-C complexes: alkali versus coinage metals. Physical Chemistry Chemical Physics, 18(10), 7269-7277. https://doi.org/10.1039/c6cp00234j
  • Wu, R. R., Yang, B., Frieler, C. E., Berden, G., Oomens, J., & Rodgers, M. T. (2016). 2,4-Dihydroxy and O2 Protonated Tautomers of dThd and Thd Coexist in the Gas Phase: Methylation Alters Protonation Preferences versus dUrd and Urd. Journal of the American Society for Mass Spectrometry, 27(3), 410-421. https://doi.org/10.1007/s13361-015-1303-y
  • Hu, S.-X., Gibson, J. K., Li, W.-L., Van Stipdonk, M. J., Martens, J., Berden, G., Redlich, B., Oomens, J., & Li, J. (2016). Electronic structure and characterization of a uranyl di-15-crown-5 complex with an unprecedented sandwich structure. Chemical Communications, 52(86), 12761-12764. https://doi.org/10.1039/c6cc07205d
  • Open Access
    Maltseva, E., Petrignani, A., Candian, A., Mackie, C. J., Huang, X., Lee, T. J., Tielens, A. G. G. M., Oomens, J., & Buma, W. J. (2016). High-resolution IR absorption spectroscopy of polycyclic aromatic hydrocarbons in the 3 μm region: role of periphery. Astrophysical Journal, 831(1), Article 58. https://doi.org/10.3847/0004-637X/831/1/58
  • Open Access
    Martens, J., Grzetic, J., Berden, G., & Oomens, J. (2016). Structural identification of electron transfer dissociation products in mass spectrometry using infrared ion spectroscopy. Nature Communications, 7, Article 11754. https://doi.org/10.1038/ncomms11754
  • Open Access
    Álvaro Galué, H., Oomens, J., Buma, W. J., & Redlich, B. (2016). Electron-​flux infrared response to varying π-​bond topology in charged aromatic monomers. Nature Communications, 7, Article 12633. https://doi.org/10.1038/ncomms12633
  • Open Access
    Bouwman, J., de Haas, A. J., & Oomens, J. (2016). Spectroscopic evidence for the formation of pentalene(+) in the dissociative ionization of naphthalene. Chemical Communications, 52(12), 2636-2638. https://doi.org/10.1039/c5cc10090a
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