| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-163 |
Sentence |
denotes |
Positional identification of fluorine in methyl per-O-acetyl-x-deoxy-x-fluoro-alpha-D-hexopyranosides by electron impact and chemical ionisation mass spectrometry. |
| TextSentencer_T2 |
164-320 |
Sentence |
denotes |
Fully acetylated methyl x-deoxy-x-fluoro-alpha-D-glucopyranosides have been studied using electron impact and ammonia chemical ionisation mass spectrometry. |
| TextSentencer_T3 |
321-507 |
Sentence |
denotes |
Mass analysed metastable ion kinetic energy spectroscopy (MIKE), collisional activation (CID), and accelerated voltage scanning have been used to evaluate complete fragmentation schemes. |
| TextSentencer_T4 |
508-707 |
Sentence |
denotes |
Characteristic differences in the fragmentation of positional isomers were noted on analysis of the spectra, and these make it possible to determine the location of fluorine in the molecules studied. |
| TextSentencer_T5 |
708-864 |
Sentence |
denotes |
Collisionally activated fragmentation of [M-OCH3]+ ions, produced by electron impact, provides an alternative method for localisation of the fluorine atoms. |
| TextSentencer_T6 |
865-1005 |
Sentence |
denotes |
To the contrary, MIKE and CID spectra of [M + NH4]+ cluster ions produced by chemical ionisation did not afford such structural information. |
| T1 |
0-163 |
Sentence |
denotes |
Positional identification of fluorine in methyl per-O-acetyl-x-deoxy-x-fluoro-alpha-D-hexopyranosides by electron impact and chemical ionisation mass spectrometry. |
| T2 |
164-320 |
Sentence |
denotes |
Fully acetylated methyl x-deoxy-x-fluoro-alpha-D-glucopyranosides have been studied using electron impact and ammonia chemical ionisation mass spectrometry. |
| T3 |
321-507 |
Sentence |
denotes |
Mass analysed metastable ion kinetic energy spectroscopy (MIKE), collisional activation (CID), and accelerated voltage scanning have been used to evaluate complete fragmentation schemes. |
| T4 |
508-707 |
Sentence |
denotes |
Characteristic differences in the fragmentation of positional isomers were noted on analysis of the spectra, and these make it possible to determine the location of fluorine in the molecules studied. |
| T5 |
708-864 |
Sentence |
denotes |
Collisionally activated fragmentation of [M-OCH3]+ ions, produced by electron impact, provides an alternative method for localisation of the fluorine atoms. |
| T6 |
865-1005 |
Sentence |
denotes |
To the contrary, MIKE and CID spectra of [M + NH4]+ cluster ions produced by chemical ionisation did not afford such structural information. |
