Details
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | 6217-6226 |
| Seitenumfang | 10 |
| Fachzeitschrift | Journal of Organometallic Chemistry |
| Jahrgang | 690 |
| Ausgabenummer | 24-25 |
| Publikationsstatus | Veröffentlicht - 2 Nov. 2005 |
Abstract
Some new half sandwich cyclopentadienyl aminocarbene complexes were prepared by treatment of the corresponding alkoxycarbene complexes with primary and secondary amines, including enantiopure chiral aminoalcohols and amines with acetyl, phosphine, alkene, and alkyne functionalities, all of which proved to be compatible with the substrates. In two cases the complexes were crystallographically characterized indicating that the metal-carbon double bond is - in contrast to some alkoxycarbene analogues - not in conjugation with the cyclopentadienyl π-system in the solid state. Some of the complexes were characterized by cyclic voltammetry showing similar behavior as the corresponding alkoxycarbene complexes. The complexes are the first examples of half sandwich complexes with a cyclopentadienyl-aminocarbene ligand system.
ASJC Scopus Sachgebiete
- Biochemie, Genetik und Molekularbiologie (insg.)
- Biochemie
- Chemie (insg.)
- Physikalische und Theoretische Chemie
- Chemie (insg.)
- Organische Chemie
- Chemie (insg.)
- Anorganische Chemie
- Werkstoffwissenschaften (insg.)
- Werkstoffchemie
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in: Journal of Organometallic Chemistry, Jahrgang 690, Nr. 24-25, 02.11.2005, S. 6217-6226.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - New metal aminocarbene-substituted cyclopentadienyliron half sandwich complexes
AU - Schwarz, Markus
AU - Wartchow, Rudolf
AU - Butenschön, Holger
PY - 2005/11/2
Y1 - 2005/11/2
N2 - Some new half sandwich cyclopentadienyl aminocarbene complexes were prepared by treatment of the corresponding alkoxycarbene complexes with primary and secondary amines, including enantiopure chiral aminoalcohols and amines with acetyl, phosphine, alkene, and alkyne functionalities, all of which proved to be compatible with the substrates. In two cases the complexes were crystallographically characterized indicating that the metal-carbon double bond is - in contrast to some alkoxycarbene analogues - not in conjugation with the cyclopentadienyl π-system in the solid state. Some of the complexes were characterized by cyclic voltammetry showing similar behavior as the corresponding alkoxycarbene complexes. The complexes are the first examples of half sandwich complexes with a cyclopentadienyl-aminocarbene ligand system.
AB - Some new half sandwich cyclopentadienyl aminocarbene complexes were prepared by treatment of the corresponding alkoxycarbene complexes with primary and secondary amines, including enantiopure chiral aminoalcohols and amines with acetyl, phosphine, alkene, and alkyne functionalities, all of which proved to be compatible with the substrates. In two cases the complexes were crystallographically characterized indicating that the metal-carbon double bond is - in contrast to some alkoxycarbene analogues - not in conjugation with the cyclopentadienyl π-system in the solid state. Some of the complexes were characterized by cyclic voltammetry showing similar behavior as the corresponding alkoxycarbene complexes. The complexes are the first examples of half sandwich complexes with a cyclopentadienyl-aminocarbene ligand system.
KW - Aminocarbene complexes
KW - Bimetallic complexes
KW - Carbene complexes
KW - Chromium complexes
KW - Iron complexes
UR - http://www.scopus.com/inward/record.url?scp=27744503943&partnerID=8YFLogxK
U2 - 10.1016/j.jorganchem.2005.09.039
DO - 10.1016/j.jorganchem.2005.09.039
M3 - Article
AN - SCOPUS:27744503943
VL - 690
SP - 6217
EP - 6226
JO - Journal of Organometallic Chemistry
JF - Journal of Organometallic Chemistry
SN - 0022-328X
IS - 24-25
ER -