Synthesis and Structure of η4-Enone Complexes of Ruthenium(0)
✍ Scribed by Alessandro Marcuzzi; Anthony Linden; Wolfgang von Philipsborn
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- German
- Weight
- 648 KB
- Volume
- 76
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
A variety of [Ru(CO)~2~L(η^4^enone)] complexes (L = phosphines, phosphites, and arsines, enone = (E)‐4‐phenylbut‐3‐en‐2‐one) have been synthesized. ^1^H‐, ^13^C‐, and ^31^P‐NMR spectra are reported and the X‐ray structures of two Ru complexes with L Ph~3~P(7), Et~3~P (10) and one Fe complex with L Ph~3~P (14) are presented. All three compounds crystallize in the same monoclinic space group __P__2~1~/n with a = 10.575(2) Å, b =9.213(2) Å, and c = 27.608(5) Å, β = 100.04(2)°, Z = 4 for 7, a = 10.276(3) Å, b = 12.935(3) Å, and c = 14.854(2) Å, β = 96.96(2)°, Z = 4 for 10, and a = 10.492(2) Å, b = 9.232(3) Å, and c = 27.129(3) Å, β = 98.67(2)°, Z = 4 for 14. The structures of the Ru complexes are compared with the Fe analogues. In the case of M Ru and L (EtO)~3~P, (MeO)~3~P, and (i‐PrO)~3~P (9, 11, and 13, respectively) stereoisomers could be detected by ^31^P‐NMR at room temperature, wich arise from rotation at the coordinated metal centre.
📜 SIMILAR VOLUMES
The complex chemical behaviour of 2-phosphaindolizines 1 strong upfield signal (δ 31 P = 6.1) was observed with a coordination shift of ∆δ = -161.7, which is typical for π-(1,3-azaphospholo[1,5-a]pyridines) towards metal carbonyl compounds was studied. (η 1 -2-Phosphaindolizine)M(CO) 5 coordination.