REACTIVITY OF TETRANUCLEAR CYCLOMETALATED PALLADIUM(II) HALIDE-BRIDGED COMPLEXES OF BIS(N-BENZYLIDENE)-1,4-PHENYLENEDIAMINES

Citation
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
Citations number
31
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
ISSN journal
0022328X
Volume
479
Issue
1-2
Year of publication
1994
Pages
37 - 46
Database
ISI
SICI code
0022-328X(1994)479:1-2<37:ROTCPH>2.0.ZU;2-X
Abstract
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.