Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Alan R. Cutler"'
Autor:
Stephen M. Tetrick, Alan R. Cutler
Publikováno v:
Organometallics. 18:1741-1746
The rhenium η1-C carboxylate Cp(PPh3)(NO)ReCO2- (1Li+ or 1K+) undergoes an unusual reductive disproportionation sequence in the presence of excess CO2 that generates a new Re2(μ2-η3-CO2) complex Cp(PPh3)(NO)ReCO2Re(CO)(NO)(PPh3)(η1-Cp) (2) plus C
Publikováno v:
Journal of Organometallic Chemistry. 566:1-7
Treatment of the carbon disulfide adducts FpCS 2 K and Fp′CS 2 K [Fp′=( η 5 -C 5 H 4 CH 3 )Fe(CO) 2 ] with Cp 2 ZrCl 2 affords the μ -( η 1 -C: η 2 -S,S′) dithiocarboxylate complexes FpCS 2 ZrClCp 2 ( 1 ) and Fp′CS 2 ZrClCp 2 ( 2 ). Both
Publikováno v:
Organometallics. 17:1993-2002
The manganese carbonyl acyl complexes L(CO)4MnC(O)R (L = CO, R = CH3 (2a); L = CO, R = Ph (2b); L = PPh3, R = CH3 (2c)) are precatalysts for the PhSiH3 hydrosilation−deoxygenation of Cp(CO)2FeC(O)CH3 (1a) to Cp(CO)2FeCH2CH3 (6a). Thus, 2a (4%) and
Publikováno v:
Organometallics. 17:1861-1867
The M2Rh2 bis(μ3-CO2) complexes [Cp*(CO)(NO)Re(CO2)Rh(η4-cod)]2 (1) and [Cp*(CO)2MCO2Rh(η4-cod)]2, M = Fe (2) and Ru (3), were synthesized in moderate to high yields from treating [Rh(OH)(η4-cod)]2 (cod = 1,5-cyclooctadiene) with the carbonyl sal
Publikováno v:
Journal of Organometallic Chemistry. 547:173-182
The reactivity of selected organotransition metal methoxycarbonyl complexes towards hydrosilanes differs significantly from their acetyl analogs in that hydrosilation does not occur across the methoxycarbonyl ligand. Only hydrosilane/manganese carbon
Publikováno v:
Journal of Organometallic Chemistry. 538:41-48
Three synthetic approaches to the rhenium silyl esters Cp * (CO)(NO)ReC(O)OSiEt 3 ( 3 ) and Cp * (COXNO)ReC(O)OSiMe 2 Ph ( 4 ) were evaluated. (a) Treatment of a CH 2 Cl 2 solution of Cp * (CO) 2 (NO)Re + BF 4 − with a silanolate NaOSiEt 3 ( 5 ) or
Publikováno v:
Inorganic Chemistry. 36:70-79
The metallocarboxylates FpCO2- (1-Mg2+, -Li+, -Na+, -K+), Cp*(CO)2FeCO2-K+ (3-K+), and Cp(CO)2RuCO2- (4-Na+, -K+) were generated in THF at −78 °C by treating the CpM(CO)2--Li+, -Na+, -K+, or -Mg2+ metalate with 1.0−1.2 equiv of CO2 (or 13CO2). T
Publikováno v:
Organometallics. 15:2764-2769
Manganese carbonyl complexes catalyze the hydrosilation of ketones with PhMe2SiH and Ph2SiH2 in C6D6 solutions. Efficacy of the manganese carbonyl precatalysts (2.4 mol %) toward acetone hydrosilation with 1.1 equiv of PhMe2SiH to give (CH3)2CH(OSiMe
Autor:
Alan R. Cutler, Brian T. Gregg and
Publikováno v:
Journal of the American Chemical Society. 118:10069-10084
Treatment of the manganese acetyl (CO)5MnC(O)CH3 (1) with 1−2 equiv of a monohydrosilane furnished mixtures of α-siloxyethyl (CO)5MnCH(OSiR3)CH3 (2) and α-siloxyvinyl (CO)5MnC(OSiR3)CH2 (3) complexes. Relative yields of 2 and 3 varied from 80% an
Autor:
Alan R. Cutler, Brian T. Gregg
Publikováno v:
Organometallics. 13:1039-1043
The dimeric manganese carbonyl bromide [Mn(CO)[sub 4]Br][sub 2] is an effective catalyst for the alcoholysis of dimethylphenylsilane in benzene at room temperature. Preparative scale procedures using a 1200:1200:1 mixture of alcohol, HSiMe[sub 2]Ph,