REACTIONS OF SODIUM BIS(N-ARYLIMINOPHOSPHORANYL)ALKANIDES WITH HALIDE-BRIDGED PLATINUM(II) AND PALLADIUM(II) PHOSPHINE DIMERS AFFORDING 4-MEMBERED M-N-P-C METALLACYCLES AND ORTHOMETALATED PLATINUM(II) AND PALLADIUM(II) COMPLEXES

Citation
Mw. Avis et al., REACTIONS OF SODIUM BIS(N-ARYLIMINOPHOSPHORANYL)ALKANIDES WITH HALIDE-BRIDGED PLATINUM(II) AND PALLADIUM(II) PHOSPHINE DIMERS AFFORDING 4-MEMBERED M-N-P-C METALLACYCLES AND ORTHOMETALATED PLATINUM(II) AND PALLADIUM(II) COMPLEXES, Organometallics, 15(9), 1996, pp. 2376-2392
Citations number
102
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
Journal title
ISSN journal
02767333
Volume
15
Issue
9
Year of publication
1996
Pages
2376 - 2392
Database
ISI
SICI code
0276-7333(1996)15:9<2376:ROSBWH>2.0.ZU;2-9
Abstract
Reaction of the sodium bis(iminophosphoranyl)alkanide compounds Na[CR ''(PPh(2)=NC(6)H(4)R'-4)(2)] (1a, R '' = H, R' = CH3; 1b, R '' = H, R' = OCH3; 1c, R '' = CH3, R' = CH3) with M(2)X(4)-(PR(3))(2) (M = Pt, P d; X = Cl, Br; PR(3) = PEt(3), PMe(2)Ph) yields the four-membered meta llacycles MX(PR(3)){CR ''(PPh(2)=NC(6)H(4)R'-4)(2)} (2a-f, M = Pt; 3a- c, M = Pd), containing the bis-(iminophosphoranyl)alkanide ligand coor dinated in a sigma-C,sigma-N chelating fashion. The molecular structur e of 2e (X = Cl, PR(3) = PMe(2)Ph, R '' = CH3, R' = CH3) has been dete rmined by X-ray crystallography. The 1,1-bis(iminophosphoranyl)ethanid e ligand (1c) in 2e is sigma-C,sigma-N-chelated toward the square-plan ar-surrounded Pt, with N coordinated trans to PMe(2)Ph (Pt-N = 2.132(4 ) Angstrom) and C trans to Cl (Pt-C = 2.116(4) Angstrom), resulting in a puckered M-N-P-C metallacycle and one noncoordinated phosphinimine moiety. In solution the complexes 2 and 3 undergo a dynamic process, i nvolving an intermediate (for 2) or fast (for 3) N,N' exchange of coor dinated and noncoordinated P=N groups. Heating (to 60-80 degrees C) or prolonged stirring of solutions of the kinetically obtained four-memb ered metallacycles 2 and 3 gives the orthometalated complexes C(6)H(4) PPh(NHC(6)H(4)R'-4)CHPPh(2)=NC(6)H(4)R'-4} (4a-d,f) and C(6)H(4)PPh(=N C(6)H(4)Me-4)CHPPh(2)NHC(6)H(4)Me-4} (5a,c). The X-ray crystal structu re of 4a (X = Cl, PR(3) = PEt(3), R' = CH3) has been determined. The n ew mononuclear orthometalated Pt complexes 4 contain a sigma-C,sigma-C ' coordinated [2-C6H4-PPh(NHC(6)H(4)R-4')CR '' PPh(2)=NC(6)H(4)R'-4](- ) ligand, in which the ortho-H (Ph) has shifted to a bridge position b etween the two noncoordinating nitrogen atoms. The four-membered plati nacycles 2a,b and the orthometalated platinacycles 4a,b react with 1 e quiv of HER or CF3COOH to give 6a,b and 7a,b, respectively, by protona tion of the noncoordinated P=NC(6)H(4)R'-4 groups only. Addition of CO 2 to 2a,d and 4c,f results in an aza-Wittig reaction, giving PtCl(PR(3 )){CH(PPh(2)=NC(6)H(4)R'-4)(PPh(2)=O)} (8a,d) and X(PR(3)){2-C(6)H(4)P Ph(=O)-CHPPh(2)NHC(6)H(4)R'-4} (9c,f), respectively, together with ary l isocyanate and bis(aryl)carbodiimide.