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Fe(C5H5)(CO)(C3H2N2(C6H2(CH3)3)(CH2C5H4N))(1+)*BF4(1-)=[(C5H5)Fe(CO)(C3H2N2(C6H2(CH3)3)(CH2C5H4N))]BF4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

916171-53-4

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916171-53-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 916171-53-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,1,7 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 916171-53:
(8*9)+(7*1)+(6*6)+(5*1)+(4*7)+(3*1)+(2*5)+(1*3)=164
164 % 10 = 4
So 916171-53-4 is a valid CAS Registry Number.

916171-53-4Downstream Products

916171-53-4Relevant academic research and scientific papers

Piano-stool iron(II) complexes as probes for the bonding of N-heterocyclic carbenes: Indications for π-acceptor ability

Mercs, Laszlo,Labat, Gael,Neels, Antonia,Ehlers, Andreas,Albrecht, Martin

, p. 5648 - 5656 (2006)

A series of new piano-stool iron(II) complexes comprising mono- and bidentate chelating N-heterocyclic carbene ligands [Fe(cp)(CO)(NHC)(L)]X have been prepared and analyzed by spectroscopic, electrochemical, crystallographic, and theoretical methods. Selectively substituting the L site with a series of ligands going from carbene to pyridine to CO suggests that CO is the strongest π acceptor, while the behavior of pyridine and carbene is nearly identical. This suggests that in these complexes comprising an electron-rich iron(cp)(carbene) fragment, N-heterocyclic carbenes are not pure σ donors but also moderate π acceptors. Theoretical calculations support this bonding model and indicate charge saturation at the metal as key for π back-bonding to N-heterocyclic carbenes. On the basis of voltammetric measurements, the Lever electrochemical parameter of these carbenes has been determined: EL = +0.29. Systematic substitution of the wingtip groups of the carbene revealed only subtle changes in the electronic properties of the iron center, thus providing a suitable methodology for ligand-induced fine-tuning of the coordinated metal.

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