1 / 6

Experimental conditions for MS Analysis

Experimental conditions for MS Analysis.

selah
Download Presentation

Experimental conditions for MS Analysis

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Experimental conditions for MS Analysis For direct APPI, each of the solutions was injected into the APPI source at a flow rate of 40 µL/min using a Harvard (Holliston, MA, USA) Model 11 syringe pump. The APPI source temperature was held at 400°C. Other operating mass spectrometric parameters were as follows: 10, 5, and 0 arbitrary units for the sheath, auxiliary, and sweep gas flow rates, respectively; 300°C for the capillary temperature; 15 V for the capillary voltage; and 70 V for the tube lens. Boil-off from liquid nitrogen was used as both the sheath and auxiliary gases for the ionization source.

  2. Figure 1S. The proposed electron transfer coupled hydrogen transfer reaction mechanism for to generate protonated PAH ions with toluene solvent in the previous study.1 (S: solvent, M: PAH analyte)

  3. Figure 2S. Pictorial description of simulated configuration of transition states described in Figure 3a. TS (Ortho H) TS (Methyl H) TS (Meta H) TS (Para H)

  4. Figure 2S. Pictorial description of simulated configuration of transition states described in Figure 3b. TS (Methyl H) TS (Ortho H) TS (Meta H) TS (Para H)

  5. Figure 3S. Relative energy diagram calculated by quantum mechanical calculation for the reactions between acridine and solvent molecular ions. C13H9N + S•+ C13H9N •++ S H+(C13H9N) + (S-H)• S= Solvent

  6. Table 1S. Thermochemical data from NIST webbook.

More Related