L. Resconi et al., rac-[methylene(3-tert-butyl-1-indenyl)(2)]ZrCl2: A simple, high-performance zirconocene catalyst for isotactic polypropene, ORGANOMETAL, 19(4), 2000, pp. 420-429
The synthesis and propene polymerization performance of the novel rac-[CH2(
3-tert-butyl-1-indenyl)(2)]ZrCl2 (2) and rac-[CH2(3-tert-butyl-1-indenyl)(2
)]ZrMe2(2-Me-2) are described. The ligand precursor, bis(1-tert-butyl-3-ind
enyl)methane (L2), is obtained in ca. 80% conversion from the condensation
of 3-tert-butylindene and formaldehyde in DMF at room temperature and is is
olated as a yellow powder by washing with pentane. Red 2 is obtained in 50-
60% yield and free from its meso stereoisomer by reacting an Et2O solution
of the ligand dianion, (L2)Li-2(Et2O)(x), with a slurry of ZrCl4 in either
pentane or toluene. Yellow 2-Me-2 is prepared in 90% yield by reaction of 2
with excess MeMgCl in toluene. Alternatively, 2-Me-2 (contaminated with ab
out 5% of its meso isomer) can be obtained directly from the ligand L2, by
reacting L2 in Et2O with 4 equiv of MeLi and then 1 equiv of ZrCl4 in tolue
ne. Both 2 and 2-Me-2 are remarkably soluble in pentane (2, ca. 1.7 g/L; 2-
Me-2, ca. 13 g/L) and toluene (2, ca. 50 g/L). 2/MAO and 2-Me-2/MAO polymer
ize liquid propene with good activities to highly isotactic (mmmm = 95-98%)
, fully regioregular polypropene with medium-high molecular weights ((M) ov
er bar(w) = 70 000-780 000) and high melting points (T-m = 154-163 degrees
C) in the T-p range 30-70 degrees C. The behavior of 2 is compared to that
of the prototypical Montell zirconocene rac-[Me2C(3-t-Bu-Ind)(2)]ZrCl2 (1).
2 is the first example of a highly efficient and at the same time simple a
nd inexpensive zirconocene catalyst for isotactic polypropene. The molecula
r structures of 2 and its Hf analogue (Hf-2) have been determined and compa
red to that of 1.