Ultraviolet Photoactivation Using Synchrotron Radiation for Tandem Mass Spectrometry of Polysiloxanes

Gas-phase decompositions of polymer ions play an important role in mass spectrometry to obtain accurate structural information. In this work, UV photoactivation experiments were performed from two poly(dimethylsiloxane)s bearing different end groups (two trimethylsilyl, or α-sec-butyl and ω- trimethylsilyl). Precursor ions, such as [Polysiloxane+Cation]+ produced by an electrospray source, were stored in a linear ion trap and then submitted to synchrotron UV irradiation during different activation times and over a range of wavelengths (52 to 248 nm) from extreme UV (XUV) to deep UV. Upon photoactivation of a precursor ion from poly(dimethylsiloxane) (PDMS; with two trimethylsilyl end groups, [PDMS25+Na]+), important fragmentations were observed, including the loss of a methyl radical followed by various heterolytic cleavages along the polymer backbone, for photon energies typically >9.5-10 eV (ionization threshold of the neutral oligomer). This report focuses on different aspects: (i) the identification of the UV photodissociation (UV-PD) products of PDMS, (ii) the influence of the irradiation time for two photon energies (10 or 20 eV), (iii) the influence of the energy of the photon for two activation times (100 or 5000 ms), (iv) the influence of the nature of the cation, and (v) the influence of the end groups of PDMS. Synchrotron UV irradiation with a tunable wavelength was a great opportunity to study the effect of the photon energy and to probe the original mechanisms of ion decomposition from poly(dimethylsiloxane).