Results 131 to 140 of about 925 (184)
Some of the next articles are maybe not open access.
(Pentamethylcyclopentadienyl)molybdenum Bromides and Iodides
Inorganic Chemistry, 1994Contrary to the (pentamethylcyclopentadienyl)trichloromolybdenum(IV) system, for which the molecular [Cp{sup *}MoCl{sub 2{minus}}({mu}-Cl)]{sub 2} complex is the only form observed, the corresponding chemistry of the heavier halide systems is much more complex.
Jahanvi U. Desai +7 more
openaire +1 more source
Pentamethylcyclopentadienyl imido compounds of chromium
Journal of the Chemical Society, Dalton Transactions, 1996The interaction of the pentamethylcyclopentadienylchromium(III) complex [CrBr(µ-Br)(η-C5Me5)]2 with alkyl- and aryl-lithium amido compounds, LiNHR, gave products whose nature depends on the reactants and on reaction conditions. For the aryl (R) 2,6-Pri2C6H3 both [(η-C5Me5)Cr(µ-NR)(µ-NHR)(µ-Br)Cr(η-C5Me5)]1 and [Cr(η-C5Me5)(µ-NR)]22 were obtained ...
Andreas A. Danopoulos +3 more
openaire +1 more source
Amidobis(pentamethylcyclopentadienyl)titanium(III)
Acta Crystallographica Section C Crystal Structure Communications, 1995The title compound, [Ti(NH 2 )(Me 5 C 5 ) 2 ] (I), is a bent metallocene with the NH 2 group oriented so as to maximize the π interaction between the N and Ti atoms.
E. Brady +3 more
openaire +1 more source
Pentamethylcyclopentadienyl-rhodium and -iridium complexes
Journal of Organometallic Chemistry, 1975Abstract The synthesis of the novel di-μ-hydridoiridium complexes [H 2 (IrC 5 Me 5 ) 2 X 2 ] (X = Br, Cl) is described. These complexes react with butadiene, but only in very polar solvents, to give η-1-methylallyl complexes, with phosphines to give [HIrC 5 Me 5 (X)(R 3 P)], and with AgOCOR to give [H 2 (IrC 5 Me 5 ) 2 OCOR] + .
D.S. Gill, P.M. Maitlis
openaire +1 more source
Journal of Organometallic Chemistry, 1994
Abstract Reaction of [Pt2(η5-C5Me5)2(η-Br)3]3+(Br−)3 with C5R5H (R = H,Me) in the presence of AgBF4 gives the first platinocenium dications, [Pt(η5-C5Me5)(η5-C5R5)]2+(BF4− )2. On electrochemical reduction, [pt(η5-C5Me5)2]2+ yields [Pt(η4-C5Me5H)(η2-C5Me5)]+ BF4−.
Oleg V. Gusev +6 more
openaire +1 more source
Abstract Reaction of [Pt2(η5-C5Me5)2(η-Br)3]3+(Br−)3 with C5R5H (R = H,Me) in the presence of AgBF4 gives the first platinocenium dications, [Pt(η5-C5Me5)(η5-C5R5)]2+(BF4− )2. On electrochemical reduction, [pt(η5-C5Me5)2]2+ yields [Pt(η4-C5Me5H)(η2-C5Me5)]+ BF4−.
Oleg V. Gusev +6 more
openaire +1 more source
Tetramethylphospholyluranium complexes and their pentamethylcyclopentadienyl analogues
Journal of Organometallic Chemistry, 1994Abstract The mono- and bis-(tetramethylphospholyl)uranium complexes [U(tmp)(Cl) 3 (L) 2 ] (tmp = C 4 Me 4 P, L = tetrahydrofuran or L 2 ...
Philippe Gradoz +5 more
openaire +1 more source
Ammonolysis of Mono(pentamethylcyclopentadienyl) Titanium(IV) Derivatives
Inorganic Chemistry, 2000Ammonolyses of mono(pentamethylcyclopentadienyl) titanium(IV) derivatives [Ti(eta5-C5Me5)X3] (X = NMe2, Me, Cl) have been carried out in solution to give polynuclear nitrido complexes. Reaction of the tris(dimethylamido) derivative [Ti(eta5-C5Me5)(NMe2)3] with excess of ammonia at 80-100 degrees C gives the cubane complex [[Ti(eta5-C5Me5)]4(mu3-N)4] (1)
A, Abarca +5 more
openaire +2 more sources
Pentamethylcyclopentadienyl Aminoborole Complexes of Hafnium
1997The tricyclophosphate ligand, (P₃O₉)³⁻, was investigated as an oxidation resistant ligand for ruthenium chemistry. The silver salt of tricyclophosphate, Ag₃(P₃O₉).H₂O, was found to be a useful synthon in the preparation of organic soluble tricyclophosphate salts. The complex [(P₃O₉)Ru(C₆H₆)]⁻ was prepared and characterized.
openaire +1 more source
Preparation of pentamethylcyclopentadienyl-dialkylnitrosyliron complexes
Journal of Organometallic Chemistry, 1985Abstract The dimer [(CH 3 ) 5 C 5 Fe(NO)] 2 has been prepared by octane reflux of [(CH 3 ) 5 C 5 Fe(CO) 2 ] 2 under a NO atmosphere. Oxidative cleavage of the dimer with iodine yields (CH 3 ) 5 C 5 Fe(NO)I 2 . Alkylation with two equivalents of RLi or RMgX (R = CH 3 , CH 2 C 6 H 5 , or CH 2 SC 6 H 5 ) leads to the dialkyl derivatives in good ...
openaire +1 more source
Journal of the American Chemical Society, 1979
Die Titelverbindung (II), in der U(III) durch Pentamethylcyclopentadienyl-Liganden komplexiert ist, ist eine ausgezeichnete Ausgangsverbindung fur weitere U(III)-Verbindungen.
Juan M. Manriquez +5 more
openaire +1 more source
Die Titelverbindung (II), in der U(III) durch Pentamethylcyclopentadienyl-Liganden komplexiert ist, ist eine ausgezeichnete Ausgangsverbindung fur weitere U(III)-Verbindungen.
Juan M. Manriquez +5 more
openaire +1 more source

