| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10572660 | Inorganica Chimica Acta | 2005 | 9 Pages |
Abstract
1,3,2-Diazabora-[3]ferrocenophanes bearing various functionalities at the boron atom are readily accessible by the reaction of the dilithiated 1,1â²-bis(trimethylsilylamino)ferrocene with boron halides. Strong endocyclic BN(pp)Ï interactions are indicated by an essentially planar arrangement of the atoms Fe, C1, N1, B, N2 and C1â², as shown by X-ray analysis and NMR spectroscopy.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Bernd Wrackmeyer, Elena V. Klimkina, Wolfgang Milius, Oleg L. Tok, Max Herberhold,
![First Page Preview: Novel 1,3,2-diazabora-[3]ferrocenophanes and a 1,4,2,3-diazadibora-[4]ferrocenophane Novel 1,3,2-diazabora-[3]ferrocenophanes and a 1,4,2,3-diazadibora-[4]ferrocenophane](/preview/png/10572660.png)