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1',4'-C5H4[(C5H5-5-exo-η4)Fe(CO)2(PPh3)]2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

333316-29-3

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333316-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 333316-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,3,3,1 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 333316-29:
(8*3)+(7*3)+(6*3)+(5*3)+(4*1)+(3*6)+(2*2)+(1*9)=113
113 % 10 = 3
So 333316-29-3 is a valid CAS Registry Number.

333316-29-3Downstream Products

333316-29-3Relevant academic research and scientific papers

(η5-C5H5)-Ring alkylation reaction with the C5H5 anion: towards the construction of tri-Fe complex Fe{[μ,η5:η4-5-exo-(1'-C5H4)C5H5]Fe(CO)2(PPh3)}2

Luh, Lung-Shiang,Liu, Ling-Kang

, p. 549 - 557 (2007/10/03)

The reaction of (η5-C5H5)Fe(CO)2I with C5H5M (M=Na, Li) in the presence of PPh3 gives the Cp-ring alkylation η4-Fe products 10a,b. The compounds 10a,b could be deprotonated with n-BuLi to generate 12. When 12 reacts with FeCl3, the r

Ferrocenediyl-bridged triiron complexes

Luh, Lung-Shiang,Wen, Yuh-Sheng,Vanko, Gyorgy,Liu, Ling-Kang

, p. 2198 - 2206 (2008/10/08)

The reaction of 2 equiv of CpFe(CO)2I and 1,1′-dilithioferrocene in the presence of 2 equiv of PPh3 is an intermolecular version of the reaction of CpFe(CO)2I and (η5-C5H4Li)Fe (C5H4PPh2). In the three-component procedure, the PPh3 substitution for iodide on CpFe(CO)2I is much faster than the nucleophilic Fc-addition at the Fe-center or at a CO ligand of CpFe(CO)2I. This one-pot reaction proceeds through [CpFe(CO)2PPh3+] and yields CpFe(CO)(PPh3)- [μ,C:η5-C(O)C5H4 ]Fe[μ,η5:η4-5-exo- (1′-C5H4)C5H5]Fe (CO)2(PPh3) (4) in 50% yield, with the 1,1′-dilithioferrocene participating twice in the nucleophilic Fc-additions: at the Cp-ring and at a CO ligand of [CpFe(CO)2PPh3+]. Complex 4 is a ferrocenediyl-bridged tri-Fe complex with three different Fe-centers: a metallocene Fe(II), a square-pyramidal pentacoordinate Fe(O), and a half-sandwich acyl-Fe(II). It has been found that, in the second Fc-additions, the pathway from (η5-C5H4Li)Fe[μ,η5: C-C5H4C(O)]FeCp(CO)(PPh3) (9) to 4 proceeds normally, but the pathway from 9 to Fe[(μ,η5: C-C5H4)C(O)FeCp(CO)(PPh3)]2 (5) has been turned off. The preference of Fc-addition of 9 onto the Cp-ring of [CpFe(CO)2PPh3+] could be reasoned by a localization of the Li+ cation in 9.

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