Published January 1, 2010 | Version v1
Journal article Open

Ring-Opening Mechanism of Lithium Bromosilacyclopropylidenoids to Silaallenes

  • 1. Univ Balikesir, Dept Chem, TR-10145 Balikesir, Turkey
  • 2. Aksaray Univ, Dept Chem, TR-68100 Aksaray, Turkey

Description

Density functional theory and ab initio quantum mechanical calculations elucidated the ring opening reactions of 1 bromo 1 lithiosilirane (3) and 2 bromo 2 lithiosilirane (4) to 2 silallene (6) and 1 silaallene (7) respectively The ring opening of 3 to 6 can proceed in a stepwise fashion with the intermediacy of a free silacyclopropylidene (9) Here a high energy barrier needs to be overcome in order to open the silacyclopropylidene ring and to generate 6 On the contrary the ring opening of 4 to 7 can occur in a concerted fashion

Files

bib-bcfed2be-dd57-4fff-9b7b-101747ae9312.txt

Files (148 Bytes)

Name Size Download all
md5:842e7a9a9f0a50aee0b962298934451a
148 Bytes Preview Download