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
Transition Metal Complexes with Bidentate Ligands Spanning trans-Positions. VIII. The reactions of the nucleophile trans-[RuCl(NO)(1)] (1 = 2,11-bis(diphenylphosphinomethyl)benzo[c]-phenanthrene) with carbon monoxide and the phosphite ligand (2) (2 = 1-ethyl-3,5,8-trioxa-4-phosphabicyclo (2.2.2)octane)
✍ Scribed by Rolf Holderegger; Luigi M. Venanzi; Fiorella Bachechi; Pasquale Mura; Luigi Zambonelli
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- German
- Weight
- 540 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0018-019X
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## 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.
## Abstract The bidentate ligand 2,11‐bis(diphenylphosphinomethyl)benzo[__c__]phenanthrene (**1**) was synthesized from 2,11‐dimethyl‐benzo[__c__]phenanthrene (**3**) __via__ the corresponding bromomethyl derivative **9. 3** was obtained from the cyclization with boron trifluoride etherate of 1,1‐d
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
Sunznzary. The preparation of monomcric complexes [MX(l)] is reported where 1LI. = Cu, Ag, Au; X = I, C1, 7 3 0 3 , BF4 and 1 = 2,ll-bis(diphenylphosphinomethyl)benzo[c]phenanthrene. The solution structure of the complexes is discussed on the basis of molecular weight, conductivity and NMR. measure
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