Two‐photon‐ionization mass spectroscopy of ammonia clusters in a pulsed supersonic nozzle beam

1983 ◽  
Vol 79 (4) ◽  
pp. 1732-1740 ◽  
Author(s):  
Hisanori Shinohara

1986 ◽  
Vol 130 (3) ◽  
pp. 231-235 ◽  
Author(s):  
Hisanori Shinohara ◽  
Kenji Sato ◽  
Yohji Achiba ◽  
Nobuyuki Nishi ◽  
Katsumi Kimura






2015 ◽  
Vol 8 (5) ◽  
pp. 2225-2231 ◽  
Author(s):  
P. R. Veres ◽  
J. M. Roberts

Abstract. A dynamic system for the calibration of acyl peroxynitrate compounds (APNs) has been developed in the laboratory to reduce the difficulty, required time, and instability of laboratory-produced standards for difficult-to-synthesize APN species. In this work we present a photochemical source for the generation of APN standards: acetyl peroxynitrate (PAN), propionyl peroxynitrate (PPN), acryloyl peroxynitrate (APAN), methacryloyl peroxynitrate (MPAN), and crotonyl peroxynitrate (CPAN). APNs are generated via photolysis of a mixture of acyl chloride (RC(O)Cl) and ketone (RC(=O)R) precursor compounds in the presence of O2 and NO2. Subsequent separation by a prep-scale gas chromatograph and detection with a total NOy instrument serve to quantify the output of the APN source. Validation of the APN products was performed using iodide ion chemical ionization mass spectroscopy (I- CIMS). This method of standard production is an efficient and accurate technique for the calibration of instrumentation used to measure PAN, PPN, APAN, MPAN, and CPAN.



2010 ◽  
Vol 9 (3) ◽  
pp. 474-478
Author(s):  
Khairan Khairan ◽  
Umar A. Jenie ◽  
Retno S. Sudibyo

Semisynthesis of D6,7-Anhydroerythromycin-A was done by biomodification technique by addition of 0.2% INH into a culture fermentation of Saccharopolyspora erythraea ATCC 11635 in medium Hutchinson. The aim of this research is to studies of fragmentation pattern from new matabolite of D6,7-Anhydroerythromycin-A by Liquid Chromatography-Mass Spectroscopy (LC-MS) and the ionization of mass spectroscopy is use by ESI (Electrospray Ionization) pattern. The FT-IR spectrometric analyzes showed a stretching vibration of C=C conjugated group at wave number 1602.7 cm-1. This C=C conjugated vibration indicated the existence of double bond between C6 and C7 (D6,7), this confirmed that isolate contained D6,7-Anhydroerythromycin-A (the possibility of D6,7 was positive). For complementation, a LC-MS (Liquid Chromatography-Mass Spectroscopy) analyzes using ESI-MS (Electrospray Ionization-Mass Spectroscopy) ionization pattern was conducted to the isolate which resulted Quassimolecular ions [M+H]+ of D7,8- and D6,7-Anhydroerythromycin-A. LC-MS spectrogram of the isolate, which gave two peaks of m/z 732.2460 and m/z 716.2522, confirmed that the m/z 732.2460 possibly was D7,8-Anhydroerythromycin-A, while the m/z 716.2502 and m/z 715.2522 possibly were D6,7-Anhydroerythromycin-A.   Keywords: isoniazid, enoyl reduction, D6,7-Anhidroeritromisin-A, fragmentation, LC-MS.





2000 ◽  
Vol 37 (5) ◽  
pp. 697-700 ◽  
Author(s):  
Hyunmin Park ◽  
Miran Lee ◽  
E. C. Jung ◽  
Jonghoon Yi ◽  
Yongjoo Rhee ◽  
...  






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