Metallorganische Synthesen mit freien Cyclopentadienyl-Radikalen, I. Zweikernige Carbonylnickel-Komplexe mit mehrfach alkylierten Cyclopentadienyl-Liganden Metalorganic Syntheses with Free Cyclopentadienyl Radicals, I. Dinuclear Carbonyl Nickel Complexes with Alkylated Cyclopentadienyl Ligands

نویسندگان

  • Helmut Sitzmann
  • Gotthelf Wolmershäuser
چکیده

Cyclopentadienyl nickel com plexes [(C 5 H 2rBu3 -l,2 ,4)N i(M -C O ) ] 2 (1) and [(C 5 H/Pr4 )N i(//-C O ) ] 2 (2) have been synthesized from nickel tetracarbonyl and the corre­ sponding lithium cyclopentadienide, and [(C 5 /Pr5 )N i(//-C O ) ] 2 (3) has been obtained in high yield from nickel tetracarbonyl and the free pentaisopropylcyclopentadienyl radical. The crystal structure o f 1 shows a com plex on a crystallographic mirror plane with a bent N i C N i C core whereas the crystal structure o f 2 exhibits two independent planar m ole­ cules possessing crystallographic inversion symmetry.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Stereoselective Alkane Oxidation with meta-Chloroperoxybenzoic Acid (MCPBA) Catalyzed by Organometallic Cobalt Complexes.

Cobalt pi-complexes, previously described in the literature and specially synthesized and characterized in this work, were used as catalysts in homogeneous oxidation of organic compounds with peroxides. These complexes contain pi-butadienyl and pi-cyclopentadienyl ligands: [(tetramethylcyclobutadiene)(benzene)cobalt] hexafluorophosphate, [(C₄Me₄)Co(C₆H₆)]PF₆ (1); diiodo(carbonyl)(pentamethylcyc...

متن کامل

Carbonyl(diphenylcyclopentadienyl)- und Carbonyl(tetraphenylcyclopentadienyl)rhodium(I) Komplexe Carbonyl(diphenylcyclopentadienyl)- and Carbonyl(tetraphenylcyclopentadienyl)rhodium(I) Complexes

[Rh(CO)2Cl] 2 reacts with 1,3-diphenylcyclopentadienyl sodium or tetraphenylcyclopentadienyl sodium with formation of (l,3-P h2C5H3)Rh(CO ) 2 (1) or (C5HPh4)Rh(CO )2 (2), respectively. The reaction of 1 or 2 with PPh3 yields the corresponding carbonyl(cyclopentadienyl)(triphenylphosphane)rhodium complexes (l,3 -P h 2C5H3)Rh(CO)(PPh3) (3) or (C5HPh4)Rh(CO)(PPh3) (4). The 'H and ' C reported and ...

متن کامل

Versatile coordination of cyclopentadienyl-arene ligands and its role in titanium-catalyzed ethylene trimerization.

Cationic titanium(IV) complexes with ansa-(eta(5)-cyclopentadienyl,eta(6)-arene) ligands were synthesized and characterized by X-ray crystallography. The strength of the metal-arene interaction in these systems was studied by variable-temperature NMR spectroscopy. Complexes with a C(1) bridge between the cyclopentadienyl and arene moieties feature hemilabile coordination behavior of the ligand ...

متن کامل

SUPPORTED CYCLOPENTADIENYLMETAL CARBONYL COMPLEXES II *. POLYSTYRENE.sUPPORTED CARBONYL AND NITROSYL DERIVATIVES OF GROUP VI TRANSITION METALS

Tricarbonyl hydride derivatives of cyclopentadienyl-chromium, -molybdenum and -tungsten compounds covalently linked to a macroreticular polystyrene support are obtained by treatment of polystyrene-attached cyclopentadienyl anions with the respective metal hexacarbonyl and subsequent acidification. In contrast to the ease with which unsupported cyclopentaruenyl·chromium and -molybdenum tricarbon...

متن کامل

Structure and Reactivity of (η5-Cyclopentadienyl)(triphenylphosphine)- (undecamethylcyclohexasilyl)nickel(II)-Hexane (2/1)

The nickel cyclohexasilyl complex CpNi(PPh3)Si6Me11 was synthesized from nickelocene, triphenylphosphine, and undecamethylcyclohexasilyl potassium and was fully characterized. It shows a relationship between its Si–Si bond lengths and its reactivity towards oxygen. The cleavage of one cyclopentadienyl ligand from nickelocene by silyl anions in the presence of additional ligands opens a promisin...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2013