Sassin Nicholas A, Everhart Stephanie C, Dangi Beni B, Ervin Kent M, Cline Joseph I
Department of Chemistry and Chemical Physics Program, University of Nevada, Reno, Reno, Nevada, USA.
J Am Soc Mass Spectrom. 2009 Jan;20(1):96-104. doi: 10.1016/j.jasms.2008.09.009. Epub 2008 Sep 18.
The fluorescence and photodissociation of rhodamine 575 cations confined to a quadrupole ion trap are observed during laser irradiation at 488 nm. The kinetics of photodissociation is measured by time-dependent mass spectra and time-dependent fluorescence. The rhodamine ion signal and fluorescence decay are studied as functions of buffer gas pressure, laser fluence, and irradiation time. The decay rates of the ions in the mass spectra agree with decay rates of the fluorescence. Some of the fragment ions also fluoresce and further dissociate. The photodissociation rate is found to depend on the incident laser fluence and buffer gas pressure. The implications of rapid absorption/fluorescence cycling for photodissociation of dye-labeled biomolecular ions under continuous irradiation are discussed.
在488nm激光照射下,观察了限制在四极离子阱中的若丹明575阳离子的荧光和光解离。通过时间相关质谱和时间相关荧光测量光解离动力学。研究了若丹明离子信号和荧光衰减与缓冲气体压力、激光能量密度和照射时间的关系。质谱中离子的衰减率与荧光衰减率一致。一些碎片离子也会发出荧光并进一步解离。发现光解离速率取决于入射激光能量密度和缓冲气体压力。讨论了在连续照射下染料标记生物分子离子快速吸收/荧光循环对光解离的影响。