GAS-PHASE REACTIVITY OF THE ORGANOMETALLIC COMPLEX [FE(C10H8)](+) - AN ION-TRAP STUDY

被引:15
作者
BOISSEL, P
MARTY, P
KLOTZ, A
DEPARSEVAL, P
CHAUDRET, B
SERRA, G
机构
[1] UNIV TOULOUSE 3,CTR ETUD SPATIALE RAYONNEMENTS,CNRS,UPR 8002,F-31029 TOULOUSE,FRANCE
[2] UNIV TOULOUSE 3,CHIM ORGANOMINERAUX LAB,CNRS,UP 8241,F-31077 TOULOUSE,FRANCE
[3] UNIV TOULOUSE 3,PHYS QUANT LAB,URA 505,F-31077 TOULOUSE,FRANCE
关键词
D O I
10.1016/0009-2614(95)00703-7
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Using an ion trap, we investigated the reactions of [Fe(C10H8)](+) with a variety of small molecules L known to be present or close to existing molecules in the interstellar medium. These reactions generally yield stable adducts [Fe(C10H8)L](+). Under visible irradiation, the ligand L is eliminated and the initial complex is restored. The reactions performed with O-2 are of special interest. A spontaneous oxidation is observed, leading to the ejection of an H2O fragment and the formation of a new cationic complex [Fe(C10H6O)](+). This complex releases a CO molecule under visible irradiation, indicating that a carbon ring has been attacked. A further oxidation of [Fe(C10H6O)](+) leads to the formation of anew species [FeC9H5O2](+). Reasonable assumptions concerning the structure of the different products are proposed.
引用
收藏
页码:157 / 162
页数:6
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