Gradual decomposition occurs above the temperature stated. b, Recorded in CHCI, solution. ') Recorded in a nujol mull; shoulders at 2190 and 2100 are also observed. d, Recorded in a nulol mull.
Transition Metal Complexes with Bidentate Ligands Spanning trans-Positions. Part XIII. Preparation, properties and crystal and molecular structures of chlorocarbonyl-2,11-bis(diphenylphosphinophenyl) benzo[c]phenanthreneiridium (I) and trichlorocarbonyl-2,11-bis(diphenylphosphinomethyl) benzo[c]phenanthreneiridium(III)
✍ Scribed by E. Baumgartner; F. J. S. Reed; L. M. Venanzi; Fiorella Bachechi; Pasquale Mura; Luigi Zambonelli
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- German
- Weight
- 502 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The complex [IrCl~3~(CO)(1)](4,1=2,11‐bis (diphenylphosphinomethyl)benzo[c]phenanthrene) has been prepared by CuCl~2~‐oxidation of IrCl(CO)(1). It is shown that the chlorine oxidation of 2a gives a mixture of products whose composition depends on the reaction conditions. The X‐ray crystal structures of 2a and 4 have been determined. The small conformational differences observed for the trans‐spanning ligand 1 in the two complexes are likely to be caused by the difference in Ir‐P bond lengths in square planar 2a and octahedral 4 (2.310(4) and 2.411(3) Å, respectively).
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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
The ligand 2,1 l-bis(diphenylphosphinomethyl)benzo[c]phenanthrene (1) has been used to prepare complexes of the type [PtL(l)] (L = C,H,, CH,=CH-CO,Me, PhC-CPh, MeC-CMe, MeO,CC=CCO,Me, (i-Pr)O,CC-CCO,(i-Pr), Ph,P and CO). It is shown that these complexes are less labile than the corresponding species
## 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
## Abstract The preparation of the ditertiary phosphines 2,11‐bis (di‐__m__‐tolylphosphinomethyl)benzo [__c__]phenanthrene (**1b**), 2,11‐bis (di‐__p__‐anisylphosphinomethyl)benzo‐[__c__]phenanthrene (**1c**), 2,11‐bis (di‐__m__‐trifluoromethylphenylphosphinomethyl) benzo‐[__c__]phenanthrene (**1d*