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dicarbonyl(η2-vinyl-p-chloroaniline)(η5-cyclopentadienyl)iron(II) hexafluorophosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

799261-16-8

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799261-16-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 799261-16-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,9,2,6 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 799261-16:
(8*7)+(7*9)+(6*9)+(5*2)+(4*6)+(3*1)+(2*1)+(1*6)=218
218 % 10 = 8
So 799261-16-8 is a valid CAS Registry Number.

799261-16-8Upstream product

799261-16-8Downstream Products

799261-16-8Relevant academic research and scientific papers

Measurement of olefin bond rotation barriers in a series of vinylaniline complexes of the cyclopentadienyliron(II) dicarbonyl cation and their correlation to metal-olefin bond asymmetry

Matchett, Stephen A.,Zhang, Guirong,Frattarelli, David

, p. 5440 - 5449 (2004)

H NMR techniques (selective inversion, total line shape analysis, and T1measurement) have been used to measure the olefin bond rotation rates in a series of compounds of the general formula CpFe(CO) 2[η2-CH1C(H)NH(p-C8H 4X)], where X = OMe (4), H (6), CN (9), N02 (10), Cl (11), COOMe (12). Complexes 4, 6, 11, and 12 enabled the use of all three methods to yield data sets that spanned a wide temperature range and allowed for reliable determination of the thermodynamic activation parameters for olefin bond rotation. When these three methods were combined with a bootstrap statistical analysis of the Eyring plots, it was possible to resolve the small differences in the ΔH? values between three of the four complexes. A clear trend is established between increasing electron donation from the aniline ligand and the facilitation of olefin bond rotation. These results are placed in the context of previous work, providing additional experimental evidence that electronic control from the para position of the aniline influences the overlap of the nitrogen lone pair with the adjacent olefinic carbon. This overlap controls the asymmetry in the metal-olefin bond by displacing the Fp+ moiety away from the nitrogen-bearing carbon, which is reflected in a drop in the ΔH? value for olefin bond rotation.

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