Dihapto coordination of aromatic molecules by the asymmetric pi-bases {TpRe(CO)(L)} (Tp = hydridotris(pyrazolyl)borate; L = (BuNC)-Bu-t, PMe3, pyridine, 1-methylimidazole, or NH3)

Citation
Sh. Meiere et al., Dihapto coordination of aromatic molecules by the asymmetric pi-bases {TpRe(CO)(L)} (Tp = hydridotris(pyrazolyl)borate; L = (BuNC)-Bu-t, PMe3, pyridine, 1-methylimidazole, or NH3), ORGANOMETAL, 20(17), 2001, pp. 3661-3671
Citations number
39
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANOMETALLICS
ISSN journal
02767333 → ACNP
Volume
20
Issue
17
Year of publication
2001
Pages
3661 - 3671
Database
ISI
SICI code
0276-7333(20010820)20:17<3661:DCOAMB>2.0.ZU;2-4
Abstract
A variety of rhenium asymmetric T-basic dearomatization agents of the gener al formula TpRe(CO)(L)(L-pi) (Tp = hydridotris(pyrazolyl)borate; L = (BuNC) -Bu-t, pyridine, PMe3, 1-methylimidazole, or NH3; L-pi = dihapto-coordinate d ligand) have been synthesized via three different routes. By varying the ligand, L, the steric and electronic properties of these complexes can be t uned, and thus the stability and selectivity of the eta (2)-aromatic system s can be adjusted. Comparisons among the various rhenium complexes are pres ented as well as comparisons to the established pentaammineosmium(II) syste m.