(C₅H₅)4Zr₂((C₆H₅)2CO)H₂*0.5C₆H₆

Base Information

Chemical Name:(C₅H₅)4Zr₂((C₆H₅)2CO)H₂*0.5C₆H₆
CAS No.:100485-42-5
Molecular Formula:0C₆H₆*C₃₃H₃₂OZr₂
Molecular Weight:666.121
Hs Code.:

(C<sub>5</sub>H<sub>5</sub>)4Zr<sub>2</sub>((C<sub>6</sub>H<sub>5</sub>)2CO)H<sub>2</sub>*0.5C<sub>6</sub>H<sub>6</sub>

Synonyms:(C₅H₅)4Zr₂((C₆H₅)2CO)H₂*0.5C₆H₆

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Chemical Property of (C₅H₅)4Zr₂((C₆H₅)2CO)H₂*0.5C₆H₆

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Technology Process of (C₅H₅)4Zr₂((C₆H₅)2CO)H₂*0.5C₆H₆

There total 4 articles about (C₅H₅)4Zr₂((C₆H₅)2CO)H₂*0.5C₆H₆ which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.0%

: 37342-98-6
bis(cyclopentadienyl)dihydrozirconium

: 76374-50-0
(η2-benzophenone)zirconocene dimer

: 100485-42-5
(C₅H₅)4Zr₂((C₆H₅)2CO)H₂*0.5C₆H₆

Guidance literature:: With benzene; In benzene; a mixt. of Zr-complexes (a slight excess of Cp2ZrH2) was stirred in benzene under Ar for 48 h at room temp.; suspn. was filtered, ppt. dried in vacuo, recrystd. from refluxing benzene; elem. anal.;

Reference yield: 30.0%

: 100485-43-6
(C₅H₅)4ZrHf((C₆H₅)2CO)H₂*0.5C₆H₆

: 100485-42-5
(C₅H₅)4Zr₂((C₆H₅)2CO)H₂*0.5C₆H₆

: 100485-46-9
(C₅H₅)4ZrHf((C₆H₅)2CO)H₂

Guidance literature:: In tetrahydrofuran-d8; a THF-d8 soln. of ZrHf-complex was heated in a sealed NMR tube in an oil bath at 60°C for 2 h; (1)H NMR anal. of the reaction mixt.;

Reference yield:

: Schwartz's reagent

: 76374-50-0
(η2-benzophenone)zirconocene dimer

: 1291-32-3
zirconocene dichloride

: 100485-42-5
(C₅H₅)4Zr₂((C₆H₅)2CO)H₂*0.5C₆H₆

Guidance literature:: In benzene-d6; a benzene-d6 suspn. of Zr-complexes was reacted at room temp. under Ar by shaking in a sealed NMR tube for 15 min; products were identified using (1)H NMR spectroscopy;