M. Westerhausen et al., 2,3,4,5-tetraethylpentela-cyclo-pentadienides (2,3,4,5-tetraethylpentolides) of the alkaline earth metals magnesium, calcium, strontium, and barium, Z ANORG A C, 627(8), 2001, pp. 1741-1750
Citations number
74
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE
The reaction of bis(cyclopentadienyl)-1-zircona-2,3,4,5-tetraethyl-cyclo-pe
nta-2,4-diene with ECl3 (E = P, As, Sb) yields 1-chloro-tetraethylphosphole
(1), -arsole (2) und -stibole (3). The reduction of these pentoles gives i
n a first step the corresponding octaethyldiphospholyle (4), -diarsolyle (5
) and -distibolyle (6). Further reduction of these dipentolyles with magnes
ium and calcium leads in the presence of the corresponding dihalides to the
formation of magnesium chlorid (2,3,4,5-tetraethylphospholide) (7), -arsol
ide) (8) and -stibolide) (9) and calcium chlorid (2,3,4,5-tetraethylphospho
lide) (10), -arsolide) (11) and -stibolide) (12), respectively. In the abse
nce of alkaline earth metal dihalides no reaction is observed. For the larg
er metals strontium and barium the reduction of the dipentolyles succeeds i
n THF also without the addition of halides and the 1,1 ' -dipentelaoctaethy
lstrontocene [E = P (13), As (14), Sb (15)] as well as -barocene [E = P (16
), As (17), Sb (18)] are isolated halogen-free. The strontocene crystallize
s as a THF adduct whereas the barocene precipitates coligand-free but with
a chain structure. The molecular structures of 7, 10, and 16 are discussed.