Ad. Burrows et al., Ether functionalised aminophosphines: synthesis and co-ordination chemistry of palladium(II) and platinum(II) complexes, J CHEM S DA, 10, 2000, pp. 1669-1677
Citations number
36
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS
Ether-functionalised aminophosphines Ph2PNHR [R=CH2CH2OCH3 L-1, CH2CH(OCH3)
(2) L-2, CH2CH2CH2OCH3 L-3 or C6H4OCH3-2 L-4] were prepared from the reacti
on of Ph2PCl and the amine RNH2 in the presence of triethylamine. Reaction
of L1-4 with [MCl2(cod)] (M=Pd or Pt) or [PtBr2(cod)] gave the complexes [M
Cl2L2] (1, M=Pd, L=L-1; 2, M=Pd, L=L-2; 3, M=Pd, L=L-3; 4, M=Pd, L=L-4; 5,
M=Pt, L=L-1; 6, M=Pt, L=L-2; 7, M=Pt, L=L-4) and [PtBr2(L-1)(2)] 8. X-Ray c
rystallographic analyses of complexes 1 and 2 indicated the presence of bif
urcated hydrogen bonds between the NH protons and both the chloride ligands
and the ether oxygen atoms. Reaction of 1, 5 and 7 with two equivalents of
AgBF4 led to formation of trans-[Pd(L-1)(2)][BF4](2) 9 and cis-[PtL2][BF4]
(2) (L=L-1; 10 or L-4 11) containing bidentate P,O-co-ordinated ligands whe
reas reaction of 1 with one equivalent of AgBF4 gave exclusively [{Pd(mu-Cl
)(L-1)(2)}(2)][BF4](2) 12, containing only unidentate aminophosphine ligand
s. Reaction of 5 and 8 with NaNO2 led to formation of cis-[PtX(NO2)(L-1)(2)
] (X=Cl 13 or Br 14). Shielding of one of the NH protons with respect to 5
and 8 suggested loss of N-H ... X hydrogen bonding and this was confirmed b
y an X-ray crystallographic analysis of 14. Reaction of L1-4 with [{M(dmba)
(mu-Cl)}(2)] (M=Pd or Pt; Hdmba=N,N-dimethylbenzylamine) gave [M(dmba)ClL]
(16, M=Pd, L=L-1; 17, M=Pd, L=L-2; 18, M=Pd, L=L-3; 19, M=Pd, L=L-4; 20, M=
Pt, L=L-1; 21, M=Pt, L=L-2; 22, M=Pt, L=L-4). The crystal structure of 16 r
eveals a similar bifurcated hydrogen bond to those observed in 1 and 2, whe
reas the structure of 18 shows the N-H ... Cl interaction to be present but
the N-H ... O interaction absent. Reaction of 16, 20 and 22 with AgBF4 gav
e the bidentate P,O-co-ordinated complexes [M(dmba)L]BF4 (23, M=Pd, L=L-1;
24, M=Pt, L=L-1; 25, M=Pt, L=L-4). Displacement of the co-ordinated ether o
xygen was achieved by reaction of 24 and 25 with CO and of 25 with xylyl is
ocyanide and acetonitrile. Attempts to recrystallise 24 led instead to isol
ation of the dinuclear species [{Pt(dmba)(mu-PPh2O)}(2)] 30 which was chara
cterised by X-ray crystallography.