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(η5-3-P-i-Pr2-indenyl)Fe(η5-C5Me5) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

960058-67-7

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960058-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 960058-67-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,0,5 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 960058-67:
(8*9)+(7*6)+(6*0)+(5*0)+(4*5)+(3*8)+(2*6)+(1*7)=177
177 % 10 = 7
So 960058-67-7 is a valid CAS Registry Number.

960058-67-7Downstream Products

960058-67-7Relevant academic research and scientific papers

New racemic planar-chiral metalloligands derived from donor-substituted indenes: A synthetic, structural, and catalytic investigation

Wechsler, Dominik,Ranking, Matthew A.,McDonald, Robert,Ferguson, Michael J.,Schatte, Gabriele,Stradiotto, Mark

, p. 6418 - 6427 (2008/10/09)

The synthesis and characterization of a new family of (η5- indenyl)MLn complexes (MLn = Mn(CO)3, Cp*Ru, or Cp*Fe; Cp* = η5-C5Me 5) derived from 3-PiPr2-indene, 1-P iPr2-2-NMe2-indene (1a[H]), or 1-P(S) iPr2-2-NMe2-indene (1b[H]) are described. Lithiation of 1b[H] followed by treatment with BrMn-(CO)5, 0.25 equiv of [Cp*RuCl]4, or Cp*Li/FeCl2 provided the corresponding (η5-1b)MLn complexes (MLn = Mn(CO)3, 2a, 96%; Cp*Ru, 2b, 87%; or Cp*Fe, 2c, 55%). Similarly, treatment of 1a[Li] with 0.25 equiv of [Cp*RuCl]4 or Cp*Li/FeCl2 provided the corresponding (η5-1a) MLn complexes (MLn = Cp*Ru, 3b, 74%; or Cp*Fe, 3c, 62%). Whereas combination of 3b and 0.5 equiv of [(COD)RhCl]2 afforded [(COD)Rh(κ2-P,N-3b)]+Cl- ([4b]+Cl-; 49% isolated yield), under similar conditions 3c was observed to undergo a decomposition reaction resulting in the formation of the zwitterionic complex (COD)Rh(κ2-P,N-1a) (5; COD = η4-1,5-cyclooctadiene). Each of 3a-c was observed to react cleanly with [(COD)Rh(THF)2]+BF4- (prepared in situ) to give the corresponding [(COD)Rh(κ2-P,N- 3a-c)]+BF4- complex ([4a-C]+BF 4-; 87%, 96%, and 89% isolated yield, respectively). Whereas lithiation of 3-Pi-Pr2-indene followed by the addition of BrMn(CO)5 generated a complex mixture of products, similar reactions employing 0.25 equiv of [Cp*RuCl]4 or Cp*Li/FeCl2 afforded 6b or 6c in 98% and 43% yield, respectively. Treatment of 6b with 0.5 equiv of [(COD)RhCl]2 allowed for the isolation of (COD)RhCl-(κ1-P-6b) 7 in 96% isolated yield. Each of [4a-C]+BF4- proved to be an active catalyst for addition of pinacolborane to styrene, with the observed regioselectivity being dependent on the nature of the η5- coordinated metal fragment, as well as the solvent employed. Single-crystal X-ray diffraction data for 2a, 2b, 2c, 3b, [4c]+BF4 -, and 7 are provided.

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