Dissociation dynamics of positive-ion and negative-ion fragments of gaseous and condensed Si(CH3)2Cl2 via Si 2p, Cl 2p, and Cl 1s core-level excitations

2006 ◽  
Vol 125 (21) ◽  
pp. 214303 ◽  
Author(s):  
J. M. Chen ◽  
K. T. Lu ◽  
J. M. Lee ◽  
C. K. Chen ◽  
S. C. Haw
2011 ◽  
Vol 135 (4) ◽  
pp. 044303 ◽  
Author(s):  
K. T. Lu ◽  
J. M. Chen ◽  
J. M. Lee ◽  
S. C. Haw ◽  
Y. C. Liang ◽  
...  

1936 ◽  
Vol 32 (3) ◽  
pp. 482-485 ◽  
Author(s):  
R. A. Smith

When an electron makes a transition from a continuous state to a bound state, for example in the case of neutralization of a positive ion or formation of a negative ion, its excess energy must be disposed of in some way. It is usually given off as radiation. In the case of neutralization of positive ions the radiation forms the well-known continuous spectrum. No such spectrum due to the direct formation of negative ions has, however, been observed. This process has been fully discussed in a recent paper by Massey and Smith. It is shown that in this case the spectrum would be difficult to observe.


2020 ◽  
Author(s):  
Lin Yang ◽  
Liang Wang ◽  
Yangyang Deng ◽  
Lizhe Sun ◽  
Bowen Low ◽  
...  

Abstract Background: Ischemic heart disease (IHD) is a common cardiovascular disorder associated with inadequate blood supply to the myocardium. Chronic coronary ischemia leads to ischemic cardiomyopathy (ICM). Despite their rising prevalence and morbidity, few studies have discussed the lipids alterations in these patients. Methods: In this cross-sectional study, we analyzed serum lipids profile in IHD and ICM patients using a lipidomics approach. Consecutive consenting patients admitted to the hospital for IHD and ICM were enrolled. Serum samples were obtained after overnight fasting. Non-targeted metabolomics was applied to demonstrate lipids metabolic profile in control, IHD and ICM patients. Results: A total of 63 and 62 lipids were detected in negative and positive ion mode respectively. Among them, 16:0 Lyso PI, 18:1 Lyso PI in negative ion mode, and 19:0 Lyso PC, 12:0 SM d18:1/12:0, 15:0 Lyso PC, 17:0 PC, 18:1-18:0 PC in positive ion mode were significantly altered both in IHD and ICM as compared to control. 13:0 Lyso PI, 18:0 Lyso PI, 16:0 PE, 14:0 PC DMPC, 16:0 ceramide, 18:0 ceramide in negative ion mode, and 17:0 PE, 19:0 PC, 14:0 Lyso PC, 20:0 Lyso PC, 18:0 PC DSPC, 18:0-22:6 PC in positive ion mode were significantly altered only in ICM as compared to IHD and control. Conclusion: Using non-targeted lipidomics profiling, we have successfully identified a group of circulating lipids that were significantly altered in IHD and ICM. The lipids metabolic signatures shed light on potential new biomarkers and therapeutics for preventing and treating ICM.


1960 ◽  
Vol 38 (4) ◽  
pp. 503-507 ◽  
Author(s):  
C. A. McDowell ◽  
J. R. Rowlands

The electron spin resonance spectra of the positive and negative ions of diphenylene have been measured. It has been found that these spectra consist of five lines showing that the observed hyperfine interaction is caused by four equivalent protons. The over-all extent of the positive ion spectrum is 18 gauss compared with that of 12.9 gauss for the negative ion. The hyperfine splittings observed are 4.0 gauss and 2.75 gauss respectively.


2016 ◽  
Vol 120 (32) ◽  
pp. 6389-6393 ◽  
Author(s):  
Christian Stråhlman ◽  
Antti Kivimäki ◽  
Robert Richter ◽  
Rami Sankari
Keyword(s):  

2019 ◽  
Vol 26 (2) ◽  
pp. 131-143 ◽  
Author(s):  
Monika Stróżyńska ◽  
Jürgen H. Gross ◽  
Katrin Schuhen

A structural investigation of perfluorocarboxylic acid derivatives formed in the reaction with N,N-dimethylformamide dialkylacetals employing several techniques of mass spectrometry (MS) is described. Two derivatizing reagents, dimethylformamide dimethyl acetal (DMF-DMA) and dimethylformamide diethylacetal (DMF-DEA) were used. In contrast to carboxylic acids, perfluorocarboxylic acids are not able to form alkyl esters as the main product in this reaction. We found that perfluorooctanoic acid (PFOA) forms a salt with N,N-dimethylformamide dialkylacetals. This salt undergoes a further reaction inside the injection block of a gas chromatograph (GC) by loss of CO2 and then forms 1,1-perfluorooctane-(N,N,N,N-tetramethyl)-diamine. The GC-MS experiments using both electron ionization (EI) and positive-ion chemical ionization (PCI) revealed that the same reaction products are formed with either derivatizing reagent. Subjecting the perfluorocarboxylic acid derivative to electrospray ionization (ESI) and direct analysis in real time (DART), both positive- and negative-ion modes indicated that cluster ions are formed. In the positive-ion mode, this cluster ion consists of two iminium cations and one PFOA anion, while in the negative-ion mode, it comprises two PFOA anions and one cation. The salt structure was further confirmed by liquid injection field desorption/ionization (LIFDI) as well as infrared (IR) spectroscopy. We propose a simple mechanism of N,N,N′,N′-tetramethylformamidinium cation formation. The structure elucidation is supported by specific fragment ions as obtained by GC-EI-MS and GC-PCI-MS analyses.


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