Features of the First and Second Order Electrospray Ionization Mass Spectra for Salt-Like Products Derived from Monools and Diols Using Combined Reagents Based on ω-Bromoacyl Chlorides and Nitrogen Bases
- Авторлар: Ilyushenkova V.1, Kulikova L.2, Borisov R.1,2, Zaikin V.1
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Мекемелер:
- Topchiev Institute of Petrochemical Synthesis
- People’s Friendship University of Russia (RUDN University)
- Шығарылым: Том 72, № 14 (2017)
- Беттер: 1383-1389
- Бөлім: Articles
- URL: https://journals.rcsi.science/1061-9348/article/view/182743
- DOI: https://doi.org/10.1134/S1061934817140052
- ID: 182743
Дәйексөз келтіру
Аннотация
Derivatization by composite reagents based on ω-bromoacyl chlorides [ClCO(C2)nBr (n = 1–4)] and pyridine was applied to study aliphatic and alicyclic alcohols and diols by ordinary and tandem electrospray ionization (ESI) mass spectrometry. The applied derivatization involves the simultaneous acylation of hydroxyl groups with an acyl chloride moiety and the quaternization of pyridine with a terminal bromoalkyl group. Under the ESI conditions, quaternary salts produce corresponding mono and diammonium cations, which are detected in the first-order mass spectra. Collision-induced dissociation (CID) of primary cations generated from monool derivatives gives rise to ammonium cations of the corresponding acids HOOC(CH2)n–N+(C5H5). The CID of primary dications affords the same cations which are also eliminated from dications to form mono-charged fragments.
Авторлар туралы
V. Ilyushenkova
Topchiev Institute of Petrochemical Synthesis
Email: borisov@ips.ac.ru
Ресей, Moscow, 119991
L. Kulikova
People’s Friendship University of Russia (RUDN University)
Email: borisov@ips.ac.ru
Ресей, Moscow, 117198
R. Borisov
Topchiev Institute of Petrochemical Synthesis; People’s Friendship University of Russia (RUDN University)
Хат алмасуға жауапты Автор.
Email: borisov@ips.ac.ru
Ресей, Moscow, 119991; Moscow, 117198
V. Zaikin
Topchiev Institute of Petrochemical Synthesis
Email: borisov@ips.ac.ru
Ресей, Moscow, 119991