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10.1021/acs.analchem.5b00601

http://scihub22266oqcxt.onion/10.1021/acs.analchem.5b00601
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C4455108!4455108!25946522
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suck abstract from ncbi


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pmid25946522      Anal+Chem 2015 ; 87 (11): 5614-9
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  • Laser-Induced Acoustic Desorption of Natural and Functionalized Biochromophores #MMPMID25946522
  • Sezer U; Wörner L; Horak J; Felix L; Tüxen J; Götz C; Vaziri A; Mayor M; Arndt M
  • Anal Chem 2015[Jun]; 87 (11): 5614-9 PMID25946522show ga
  • Laser-induced acoustic desorption (LIAD) has recently been established as a tool for analytical chemistry. It is capable of launching intact, neutral, or low charged molecules into a high vacuum environment. This makes it ideally suited to mass spectrometry. LIAD can be used with fragile biomolecules and very massive compounds alike. Here, we apply LIAD time-of-flight mass spectrometry (TOF-MS) to the natural biochromophores chlorophyll, hemin, bilirubin, and biliverdin and to high mass fluoroalkyl-functionalized porphyrins. We characterize the variation in the molecular fragmentation patterns as a function of the desorption and the VUV postionization laser intensity. We find that LIAD can produce molecular beams an order of magnitude slower than matrix-assisted laser desorption (MALD), although this depends on the substrate material. Using titanium foils we observe a most probable velocity of 20 m/s for functionalized molecules with a mass m = 10?000 Da.
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