Jm. Vila et al., REACTIVITY OF TETRANUCLEAR CYCLOMETALATED PALLADIUM(II) HALIDE-BRIDGED COMPLEXES OF BIS(N-BENZYLIDENE)-1,4-PHENYLENEDIAMINES, Journal of organometallic chemistry, 479(1-2), 1994, pp. 37-46
Treatment of the cyclometallated halide-bridged complexes [{1,4-(Pd[2,
3,4-(MeO)3C6HC(H)=N](X)}2C6H4}2] (Ia, IIa) and [{1,4-{Pd[2,4-(MeO)2C6H
2C(H)=N(X)}2C6H4}2] (Ib, IIb) (X = Cl or Br) with ditertiary diphosphi
nes in a complex/ diphosphine 1:2 molar ratio gave the 26- and 28-memb
ered ring tetranuclear cyclometallated complexes -(MeO)3C6-HC(H)=N](X)
}2C6H4}2{mu-Ph2P(CH2)nPPh2}2] (1a: X = Cl, n = 3; 2a: X = Br, n = 3; 3
a: X = Cl, n = 4; 4a: X = Br, n = 4) and -(MeO)2C6H2C(H)=N](X)}2C6H4}2
{mu-Ph2P(CH2)nPPh2}2] (1b: X = Cl, n = 3; 2b: X = Br, n = 3; 3b: X = C
l, n = 4; 4b: X = Br, n = 4) and in a complex/ diphosphine 1:4 molar r
atio gave the dinuclear cyclometallated complexes (MeO)3C6HC(H)=N]}2C6
H4{Ph2P(CH2)nPPh2-P,P}2][PF6]2 (5a: n = 3; 6a: n = 4) and eO)2C6-HC(H)
=N]}2C6H4}{Ph2P(CH2)nPPh2-P,P)2][PF6]2 (5b: n = 3; 6b: n = 4). Treatme
nt of the cyclometallated halide-bridged complexes [{1,4-{Pd[2,3,4-(Me
O)3C6HC(H)=N](X)}2C6H4}2] (Ia, IIa) and [{1,4-{Pd[4,5-(OCH2O)C6H2C(H)=
N](X)}2C6H4}2] (Ic, IIc) (X = Cl, Br) with tertiary monophosphines in
a complex/phosphine 1:4 or 1:8 molar ratio gave the new dinuclear cycl
ometallated complexes [1,4-{Pd[2,3,4-(MeO)3C6HC(H)=N](X)(L)}2C6H4] [L
= PPh3: 7a (X = Cl), Sa (X = Br); L = PPhEt 2: 9a (X = Cl), 10a (X = B
r); L = PPh(C=CPh)2: 11a (X = Cl), 12a (X = Br)] and [1,4-{Pd[4,5-(OCH
2O)C6H2C(H)=N](X)(L)}2C6H4] [L = PPh3: 7C (X = Cl), 2c (X = Br); L = P
PhEt2: 3c (X = Cl), 4c (X = Br); L = PPh(CPh)2: 5c (X = Cl), 6c (X = B
r)] and non-cyclometallated complexes [1,4-{Pd[2,3,4-(MeO)3C6HC(H)=N(X
)(L)2)2C6H4] [L = PPh3: 13a (X = Cl), 14a (X = Br); L = PPhEt2: 15a (X
= Cl), 16a (X = Br); L = PPh(C=CPh)2: 17a (X = Cl), 18a (X = Br)] and
[1,4-(Pd[4,5-(OCH2O)C6H2C(H)=N](X)(L)2}2C6H4] [L = PPh3: 7c (X = Cl),
8c (X = Br); L = PPhEt2: 9c (X = CI), 10c (X = Br); L = PPh(C=Ph)2: 1
1C (X = Cl), 12c (X = Br)], respectively. Reaction of the halide-bridg
ed complexes with thallium acetylacetonate gave the dinuclear cyclomet
allated complexes 1,4-{Pd[2,3,4-(MeO)3C6HC(H)=N]H3CCOCHCOCH3)}2C6H4] (
19a) and 1,4-(Pd[4,5-(OCH2O)C6H2C(H)=N]H3CCOCHCOCH3)}2C6H4] (13c). The
compounds were characterized by microanalysis (C, H, N), IR and P-31(
H-1) and H-1 spectroscopy.