NICKEL(II), PALLADIUM(II), AND PLATINUM(II) COMPLEXES CONTAINING CIS-1,2-BIS(DIPHENYLPHOSPHINO)ETHENE OR TRANS-1,2-BIS(DIPHENYLPHOSPHINO)ETHENE - ISOMORPHOUS CRYSTAL-STRUCTURES IN THE CYANIDE CASE
W. Oberhauser et al., NICKEL(II), PALLADIUM(II), AND PLATINUM(II) COMPLEXES CONTAINING CIS-1,2-BIS(DIPHENYLPHOSPHINO)ETHENE OR TRANS-1,2-BIS(DIPHENYLPHOSPHINO)ETHENE - ISOMORPHOUS CRYSTAL-STRUCTURES IN THE CYANIDE CASE, Polyhedron, 17(18), 1998, pp. 3211-3220
Mono- and binuclear Ni-II, Pd-II, and Pt-II complexes of cis- or trans
- 1,2-bis(diphenylphosphino)ethene (cis- or trans-dppen) have been pre
pared and characterized by X-ray diffraction methods, Pt-195 H-1 and P
-31 H-1 NMR spectroscopy, FAB mass spectrometry, IR spectroscopy, elem
ental analyses and melting points. The Xray structures of some rare ex
amples of cis-dicyanide complexes of the type [M(CN)(2)(cis-dppen)] (M
=Ni (I), M=Pd (2), M=Pt (3)) are given for the first time. All three c
rystal lattices are isomorphous and allow comparison of the radii of N
i, Pd, and Pt atoms. In 1-3 the coordination is square planar. In all
cases the ethene bridges are nearly coplanar with the coordination pla
nes, which can be explained by pi-bonding interactions. Due to the iso
morphous crystal lattices, 1-3 show analogous shortest intermolecular
repulsive C-H ... M contact approaches leading to small deviations fro
m coplanarity. The removal of one coordinated chloride in [NiCl2(cis-d
ppen)] by AgBF4 followed by subsequent treatment with bis(diphenylphos
phino)amine, NH(PPh2)(2) (dppam), leads to the novel complex [NiCl(cis
-dppen) (dppam)](BF4) (4). However, the analogous abstraction of both
chlorides in [MCl2(cis-dppen)] (M=Pd, Pt) and reaction with dppam prod
uces [M(cis-dppen)(dppam)](BF4)(2) (M-pd (5), M=Pt (6)). In the case o
f trans dppen, the reaction with Pd(CN)(2) leads to another novel cis-
dicyanide complex of the type [Pd-2(CN)(4)(mu-trans-dppen)(2)] (7). Su
bstitution of chloride in [Pt2Cl4(mu-trans-dppen)(2)] by cyanide leads
to the analogous Pt-II compound [Pt-2(CN)(4)(mu-trans-dppen)(2)] (8).
It is believed, that the unsaturated nature of cis- or trans-dppen le
ading to pi-bonding interactions with the metal ligand bonds, is respo
nsible for the unusual stability of cis-dicyanide complexes. For dppam
the presence of electronic delocalization is well-known. These effect
s are discussed in view of the X-ray structures of 1-3 and related com
pounds. (C) 1998 Elsevier Science Ltd. All rights reserved.