It is shown that the ligand 2,ll-bis(diphenylphosphinomethyl)benzo[c]phenanthrene (1) reacts with nickel(II), palladium(I1) and platinum(l1) substrates giving either exclusively, or predominantly, mononuclear complexes of the type trans-[MXz (l)] in which the organic ligand spans trans-positions. It
Transition metal complexes with bidentate ligands spanning trans-positions. XII. The preparation and properties of complexes trans-[MX2 (1)] and trans-[PtHCl (1)] (M = Ni, Pd and Pt; X = Cl and NCS; 1 = ditertiary phosphine)
✍ Scribed by Pramesh N. Kapoor; Paul S. Pregosin; Luigi M. Venanzi
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- German
- Weight
- 394 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
Complexes [MX~2~(1)] (M = Ni, Pd and Pt; X=Cl and NCS; 1 = 2,11‐bis(dialkyl‐[or diaryl]phosphinomethyl)benzo[c]phenanthrene; alkyl = cyclohexyl t‐butyl; aryl = m‐tolyl, p‐anisyl and m‐CF~3~ C~6~H~4~) have been synthesized.
An NMR. study of the t‐butyl complexes provides evidence for a “fan‐like” motion of the benzo[c]phenanthrene moiety over the plane of the complex.
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The structures of [RhCl(CO)(l)] and [PdC1,(1)], where 1 is the bidentate ligand (C6H5)2P . CH2 . ClsHlo . CH2 . P (C6H5),, have been determined from threedimensional X-ray counter data collected on single crystals of the C6H5. CN solvates. The two compounds are isomorphous and crystallize in the tri
## Abstract The five‐coordinate mononuclear complexes [M(CO)~3~(**1**)] (M = Fe, Ru; (**1**) = 2,11‐bis(diphenylphosphinomethyl)benzo[c]phenanthrene) have been prepared and assigned trigonal bipyramidal structures with apical phosphorus atoms from IR. and NMR. data.