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Synthesis, Molecular Structure, Fluxional Behavior, and Tricarbonyliron Transfer Reactions of (η4-1-Azabuta-1,3-diene)tricarbonyliron Complexes

✍ Scribed by Hans-Joachim Knölker; Gerhard Baum; Norbert Foitzik; Helmut Goesmann; Peter Gonser; Peter G. Jones; Herbert Röttele


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
549 KB
Volume
1998
Category
Article
ISSN
1434-1948

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✦ Synopsis


The (η 4 -1-azabuta-1,3-diene)tricarbonyliron complexes 10 spectroscopy, as well as X-ray crystallography of 10b, 10c, and 10l. Using variable temperature 13 C-NMR spectroscopy are easily prepared in high yield by condensation of the corresponding arylamines 7 with the cinnamaldehydes 8 and the fluxionality of the complexes 10a, 10b, 10c, 10e, and 2 is investigated and the activation barrier for the turnstile subsequent ultrasound-promoted complexation of the resulting 1-azabuta-1,3-dienes 9 with nonacarbonyldiiron. rotation of the tricarbonyliron fragment is determined. The transfer reaction and the structural factors influencing the The complexes 10 are shown to represent excellent reagents for the transfer of the tricarbonyliron fragment onto transfer of the tricarbonyliron fragment are extensively investigated. cyclohexa-1,3-diene (1a). The structural characterization for the complexes 10 is achieved by IR, 1 H-NMR, and 13 C-NMR


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## Abstract 4,4‐Dichloro‐1,1‐diphenyl‐2‐azabuta‐1,3‐diene (1) oxidatively adds to [Pd(PPh~3~)~4~] and [Pt(C~2~H~4~)(PPh~3~)~2~] giving rise to the σ‐alkenyl complexes __trans__‐[MCl{[C(Cl)=C(H)−N=CPh~2~]}(PPh~3~)~2~] (2a: M = Pd; 2b: M = Pt). When 1 is treated with [Pd(PPh~3~)~4~] in a 1:2 ratio in