The first carbonyl iron complexes with dihydroacepentalene ligands

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  • Universität Hamburg
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Details

OriginalspracheEnglisch
Seiten (von - bis)1721-1729
Seitenumfang9
FachzeitschriftTETRAHEDRON
Jahrgang42
Ausgabenummer6
PublikationsstatusVeröffentlicht - 1986
Extern publiziertJa

Abstract

1,4-Dibromo- (8) as well as 1,4,7-trichloro- (11a) and 1,4,7-tribromotriquinacene (11b) react with Fe2(CO)9 in THF to yield (dihydroacepentalene)hexacarbonyldiiron complexes 9 and 10, the first representatives with a 7,10-dihydroacepentalene ligand. By reaction with Fe2(CO)9, the readily accessible 4,7-bis (dialkylamino)tricyclo[5.2.1.04.10]deca-1(10),2,5,8-tetraenes 14, derivatives of the unknown 4,7-dihydroacepentalene, were transfomed into their tricarbonyliron complexes 15. Upon reduction with sodium in THF, the η4-(diene)tricarbonyliron 15 selectively gave the novel 1,10η2-(olefin)tricarbonylferrates(-2)17 as a result of a twofold electron transfer. The intermediate green radical anion 16, which is persistent in the absence of excess sodium, was characterized by its ESR signal. Complexes 17 are the first of their class with complete structural characterization by 1H- and 13C-NMR spectroscopy.

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The first carbonyl iron complexes with dihydroacepentalene ligands. / Butenschön, Holger; de Meijere, Armin.
in: TETRAHEDRON, Jahrgang 42, Nr. 6, 1986, S. 1721-1729.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Butenschön H, de Meijere A. The first carbonyl iron complexes with dihydroacepentalene ligands. TETRAHEDRON. 1986;42(6):1721-1729. doi: 10.1016/S0040-4020(01)87589-X
Butenschön, Holger ; de Meijere, Armin. / The first carbonyl iron complexes with dihydroacepentalene ligands. in: TETRAHEDRON. 1986 ; Jahrgang 42, Nr. 6. S. 1721-1729.
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abstract = "1,4-Dibromo- (8) as well as 1,4,7-trichloro- (11a) and 1,4,7-tribromotriquinacene (11b) react with Fe2(CO)9 in THF to yield (dihydroacepentalene)hexacarbonyldiiron complexes 9 and 10, the first representatives with a 7,10-dihydroacepentalene ligand. By reaction with Fe2(CO)9, the readily accessible 4,7-bis (dialkylamino)tricyclo[5.2.1.04.10]deca-1(10),2,5,8-tetraenes 14, derivatives of the unknown 4,7-dihydroacepentalene, were transfomed into their tricarbonyliron complexes 15. Upon reduction with sodium in THF, the η4-(diene)tricarbonyliron 15 selectively gave the novel 1,10η2-(olefin)tricarbonylferrates(-2)17 as a result of a twofold electron transfer. The intermediate green radical anion 16, which is persistent in the absence of excess sodium, was characterized by its ESR signal. Complexes 17 are the first of their class with complete structural characterization by 1H- and 13C-NMR spectroscopy.",
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T1 - The first carbonyl iron complexes with dihydroacepentalene ligands

AU - Butenschön, Holger

AU - de Meijere, Armin

N1 - Funding information: Acknowledgement-This work was supported by the Stiftung Volkswagenwerk, the Fonds der Chemischen Industrie, BASF AG, Ludwigshafen am Rhein, Bayer AG, Leverkusen, Chemische Werke Hiils AG, Marl, and Hoechst AG, Frankfurt am Main. H.B. is much obliged to the Studientiftung des Deutschen Volkes for a graduate fellowship.

PY - 1986

Y1 - 1986

N2 - 1,4-Dibromo- (8) as well as 1,4,7-trichloro- (11a) and 1,4,7-tribromotriquinacene (11b) react with Fe2(CO)9 in THF to yield (dihydroacepentalene)hexacarbonyldiiron complexes 9 and 10, the first representatives with a 7,10-dihydroacepentalene ligand. By reaction with Fe2(CO)9, the readily accessible 4,7-bis (dialkylamino)tricyclo[5.2.1.04.10]deca-1(10),2,5,8-tetraenes 14, derivatives of the unknown 4,7-dihydroacepentalene, were transfomed into their tricarbonyliron complexes 15. Upon reduction with sodium in THF, the η4-(diene)tricarbonyliron 15 selectively gave the novel 1,10η2-(olefin)tricarbonylferrates(-2)17 as a result of a twofold electron transfer. The intermediate green radical anion 16, which is persistent in the absence of excess sodium, was characterized by its ESR signal. Complexes 17 are the first of their class with complete structural characterization by 1H- and 13C-NMR spectroscopy.

AB - 1,4-Dibromo- (8) as well as 1,4,7-trichloro- (11a) and 1,4,7-tribromotriquinacene (11b) react with Fe2(CO)9 in THF to yield (dihydroacepentalene)hexacarbonyldiiron complexes 9 and 10, the first representatives with a 7,10-dihydroacepentalene ligand. By reaction with Fe2(CO)9, the readily accessible 4,7-bis (dialkylamino)tricyclo[5.2.1.04.10]deca-1(10),2,5,8-tetraenes 14, derivatives of the unknown 4,7-dihydroacepentalene, were transfomed into their tricarbonyliron complexes 15. Upon reduction with sodium in THF, the η4-(diene)tricarbonyliron 15 selectively gave the novel 1,10η2-(olefin)tricarbonylferrates(-2)17 as a result of a twofold electron transfer. The intermediate green radical anion 16, which is persistent in the absence of excess sodium, was characterized by its ESR signal. Complexes 17 are the first of their class with complete structural characterization by 1H- and 13C-NMR spectroscopy.

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