Localization of Double Bonds in Wax Esters by High-Performance Liquid Chromatography/Atmospheric Pressure Chemical Ionization Mass Spectrometry Utilizing Fragmentation of Acetonitrile-Related Adducts

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F11%3A00359271" target="_blank" >RIV/61388963:_____/11:00359271 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1021/ac1030682" target="_blank" >http://dx.doi.org/10.1021/ac1030682</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1021/ac1030682" target="_blank" >10.1021/ac1030682</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Localization of Double Bonds in Wax Esters by High-Performance Liquid Chromatography/Atmospheric Pressure Chemical Ionization Mass Spectrometry Utilizing Fragmentation of Acetonitrile-Related Adducts

Popis výsledku v původním jazyce

Unsaturated wax esters (WEs) provided molecular adducts with C3H5N ([M+55]+.) in APCI sources in the presence of acetonitrile. CID of [M+55]+. gave fragments allowing localization of double bond(s) in hydrocarbon chains of WEs. These fragments were formed by cleavage of C-C bonds next to the double bond from its both sides. In methylene-interrupted polyunsaturated WEs, the diagnostic fragments related to each double bond were detected; the most abundant were those corresponding to cleavage of C-C bond next to the first and the last double bond. A simple nomenclature based on .alpha. and .omega. ions has been introduced. A data-dependent HPLC/APCI-MS2 method for comprehensive characterizing WEs in their complex mixtures has been developed and applied tonatural mixtures of WEs isolated form jojoba oil and beeswax. More than 50 WE molecular species were completely identified, including information on acid and alcohol chain length and position of double bonds.

Název v anglickém jazyce

Localization of Double Bonds in Wax Esters by High-Performance Liquid Chromatography/Atmospheric Pressure Chemical Ionization Mass Spectrometry Utilizing Fragmentation of Acetonitrile-Related Adducts

Popis výsledku anglicky

Unsaturated wax esters (WEs) provided molecular adducts with C3H5N ([M+55]+.) in APCI sources in the presence of acetonitrile. CID of [M+55]+. gave fragments allowing localization of double bond(s) in hydrocarbon chains of WEs. These fragments were formed by cleavage of C-C bonds next to the double bond from its both sides. In methylene-interrupted polyunsaturated WEs, the diagnostic fragments related to each double bond were detected; the most abundant were those corresponding to cleavage of C-C bond next to the first and the last double bond. A simple nomenclature based on .alpha. and .omega. ions has been introduced. A data-dependent HPLC/APCI-MS2 method for comprehensive characterizing WEs in their complex mixtures has been developed and applied tonatural mixtures of WEs isolated form jojoba oil and beeswax. More than 50 WE molecular species were completely identified, including information on acid and alcohol chain length and position of double bonds.

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

CF - Fyzikální chemie a teoretická chemie

OECD FORD obor

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Projekt

<a href="/cs/project/GA203%2F09%2F0139" target="_blank" >GA203/09/0139: Komplexní lipidomická charakterizace rostlinných a živočišných tkání</a><br>

Návaznosti

Z - Vyzkumny zamer (s odkazem do CEZ)

Rok uplatnění

2011

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Analytical Chemistry

ISSN

0003-2700

e-ISSN

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Svazek periodika

83

Číslo periodika v rámci svazku

8

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

9

Strana od-do

2978-2986

Kód UT WoS článku

000289223700021

EID výsledku v databázi Scopus

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