Ether functionalised aminophosphines: synthesis and co-ordination chemistry of palladium(II) and platinum(II) complexes

Citation
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
ISSN journal
03009246 → ACNP
Volume
10
Year of publication
2000
Pages
1669 - 1677
Database
ISI
SICI code
0300-9246(2000)10:<1669:EFASAC>2.0.ZU;2-Q
Abstract
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.