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Synthesis, Structure and Conformation of cis- and trans-(μ-1,6-Dimethylheptalene)bis(tricarbonyliron)

Grimm, Felix W. ; Hafner, Klaus ; Lindner, Hans Jörg (1996)
Synthesis, Structure and Conformation of cis- and trans-(μ-1,6-Dimethylheptalene)bis(tricarbonyliron).
In: Chemische Berichte, 129 (12)
doi: 10.1002/cber.19961291226
Artikel, Bibliographie

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Kurzbeschreibung (Abstract)

The reaction of 1,6-dimethylheptalene (2) with Fe₂(CO)₉ affords two binuclear iron complexes 4a and 4b, each bearing two tricarbonyliron moieties, in trans and cis orientation, respectively. The reaction leads additionally to the formation of the monocomplexed compound 3. NMR studies indicate that the heptalene moiety of the new compounds is a π-bond isomer of 2, and this is clearly attributable to steric factors. Single-crystal X-ray structure analyses of the metal complexes 4a and 4b confirm that the Fe(CO)₃ fragments adopt trans and cis geometries, respectively, with respect to the plane of the carbocycle. The ring systems of the two isomers adopt different conformations in the solid state. In the case of 4a, a hitherto unknown chair-like conformation is determined, whereas in complex 4b the ring system shows a twisted double boat conformation.

Typ des Eintrags: Artikel
Erschienen: 1996
Autor(en): Grimm, Felix W. ; Hafner, Klaus ; Lindner, Hans Jörg
Art des Eintrags: Bibliographie
Titel: Synthesis, Structure and Conformation of cis- and trans-(μ-1,6-Dimethylheptalene)bis(tricarbonyliron)
Sprache: Englisch
Publikationsjahr: 1996
Ort: Darmstadt
Verlag: Wiley
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Chemische Berichte
Jahrgang/Volume einer Zeitschrift: 129
(Heft-)Nummer: 12
DOI: 10.1002/cber.19961291226
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Kurzbeschreibung (Abstract):

The reaction of 1,6-dimethylheptalene (2) with Fe₂(CO)₉ affords two binuclear iron complexes 4a and 4b, each bearing two tricarbonyliron moieties, in trans and cis orientation, respectively. The reaction leads additionally to the formation of the monocomplexed compound 3. NMR studies indicate that the heptalene moiety of the new compounds is a π-bond isomer of 2, and this is clearly attributable to steric factors. Single-crystal X-ray structure analyses of the metal complexes 4a and 4b confirm that the Fe(CO)₃ fragments adopt trans and cis geometries, respectively, with respect to the plane of the carbocycle. The ring systems of the two isomers adopt different conformations in the solid state. In the case of 4a, a hitherto unknown chair-like conformation is determined, whereas in complex 4b the ring system shows a twisted double boat conformation.

Freie Schlagworte: Heptalenes / Carbonyliron complexes / cis and trans complexation
Sachgruppe der Dewey Dezimalklassifikatin (DDC): 500 Naturwissenschaften und Mathematik > 540 Chemie
Fachbereich(e)/-gebiet(e): 07 Fachbereich Chemie
07 Fachbereich Chemie > Clemens-Schöpf-Institut
07 Fachbereich Chemie > Clemens-Schöpf-Institut > Fachgebiet Organische Chemie
Hinterlegungsdatum: 02 Aug 2024 12:45
Letzte Änderung: 02 Aug 2024 12:45
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