The mass spectrometric behaviour of some halogen-containing epoxyethers

被引:1
作者
Favretto, D
DAlpaos, M
Traldi, P
Begue, JP
BonnetDelpon, D
Rock, MH
机构
[1] CNR,CTR STUDIO STABIL COMPOSTI COORDINAZ,I-35100 PADUA,ITALY
[2] CNRS,BIOCIS,F-92296 CHATENAY MALABR,FRANCE
来源
EUROPEAN MASS SPECTROMETRY | 1997年 / 3卷 / 01期
关键词
epoxyethers; fluorinated compounds; S(N)2-like ring opening; alkoxy carbenium ion;
D O I
10.1255/ejms.1
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
The mass spectrometric behaviour of 1,2-epoxy-1-phenyl-2-ethoxy-3,3,3-trifluoropropane (1), 1,2-epoxy-1-phenyl-2-ethoxy-3,3-difluoro-3-chloropropane (2) and 2,3-epoxy-1-cyclohexyl-3-ethoxy-4,4,4-trifluorobutane (3) has been studied by means of electron impact and fast atom bombardment experiments, The decomposition pathways of odd electron molecular ions and protonated molecules have been studied by means of metastable ion spectra, Specific fragmentation channels are present for the three compounds; while for all the compounds C2H5O. loss is highly favoured for 2 the ethyl radical loss becomes predominant, This has been justified by formation of a chloronium cation, Compound 3 only exhibits a product ion related to cleavage of the oxirane ring, suggesting that the lack of conjugation leads to labilisation of the oxirane ring, The protonated molecules partially decompose according to the structure of the alkoxycarbenium ion already proposed in the condensed phase, In the case of 1 the hydroxyl localisation on C(2) has also been evidenced.
引用
收藏
页码:37 / 48
页数:12
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