Chiral titanium and zirconium complexes with the 1-(8-quinolyl)-2,3-dimethylcyclopentadienyl-ligand

被引：24

作者：

Enders, M ^{[1
]}

Rudolph, R ^{[1
]}

Pritzkow, H ^{[1
]}

机构：

[1] Univ Heidelberg, Inst Anorgan Chem, D-69120 Heidelberg, Germany

来源：

JOURNAL OF ORGANOMETALLIC CHEMISTRY | 1997年 / 549卷 / 1-2期

关键词：

N-functionalized cyclopentadienyl; donor ligands; titanium; zirconium;

D O I：

10.1016/S0022-328X(97)00503-2

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Reaction of 8-lithioquinoline with 2,3-dimethylcyclopent-2-en-1-one leads to 1-(8-quinolyl)-2,3-dimethyl-cyclopentadiene (1) after hydrolysis and H2O elimination in acidic solution. With strong bases 1 is deprotonated to the intensively red coloured anion 2. 2 was converted to the trimethylsilyl derivative 3, which could be characterized by crystal structure analysis. 3 reacts with group 4 transition metal chlorides to the chiral trichlorotitanium and trichlorozirconium complexes I and 5. 3 was examined by crystal structure analysis and shows the expected interaction between the quinolyl nitrogen atom and the metal centre.

引用

页码：251 / 256

页数：6

共 33 条

[21] SYNTHESIS, SPECTROSCOPY, AND CRYSTAL-STRUCTURE OF A NEW STABLE BISCYCLOPENTADIENYL URANIUM(IV) DICHLORIDE CONTAINING 2 C5H4-RINGS INTERLINKED BY A METAL-COORDINATED 2,6-BIS(METHYLENE)PYRIDYL UNIT [J].