E. Lindner et al., Palladium(II) complexes with hemilabile etherdiphos ligands in the alternating copolymerization of carbon monoxide with olefins, INORG CHIM, 296(1), 1999, pp. 103-113
The potentially hexadentate diphos ligands (ROCH2CH2)(2)P(CH2)(3)P(CH2CH2OR
)(2) (1a-d) (R = Et (a), n-Bu (b), t-Bu (c), Cy (d)) are accessible by phot
ochemically induced hydrophosphination of the vinyl ethers CH2=CH-OR with t
he diprimary phosphine H2P(CH2)(3)PH2. Treatment of 1a-d with (PhCN)(2)PdCl
2 in CH2Cl2 leads to the dichlorodiphospalladium(II) complexes 2a-d, from w
hich the dicationic palladium(II) complexes 3a-d were obtained by abstracti
on of the chlorides with AgBF4 in CH2Cl2. In 3a-d the etherdiphos ligands a
re coordinated in a eta(4)(O,P;O',P') fashion. A rapid chemical exchange be
tween the eta(2)-(PO)-O-boolean AND chelated and the eta(1)-P coordinated p
art of the ligands in 3a-d was demonstrated by means of temperature-depende
nt C-13{H-1} NMR spectroscopy. Both Pd-O bonds in 3a-d are easily cleaved b
y polar solvents such as acetonitrile and water resulting in the formation
of the adducts 3b . 2CH(3)CN, 3c . H2O, and 3c . 2H(2)O. The molecular stru
ctures of 2a and 3c . H2O were determined by single crystal X-ray diffracti
on methods. Under a total pressure of 60 bar ethene/CO and propene/CO, resp
ectively, 3a-d are highly active catalysts in the copolymerization of olefi
ns with carbon monoxide. GPC measurements revealed high molecular weights o
f these polyketones. (C) 1999 Elsevier Science S.A. All rights reserved.