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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196113Generated: October 26, 2026

Chloride → N~9~,N~10~-Bis(trimethylsilyl)phenanthrene-9,10-diimine

https://huagongshe.com/reaction/1196113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
Reactant9,10-PhenanthrenedioneHCID 6763—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant1,2-PhenanthrenedioneHCID 3080566—
ReactantPhenanthrenequinone diimineHCID 86745785—
ProductN~9~,N~10~-Bis(trimethylsilyl)phenanthrene-9,10-diimineHCID 7134975837%

Reaction Steps

Ligand Synthesis. 9,10-Phenanthrenequinone bis((trimethylsilyl)-imine) (silylphi) was synthesized from 9,10-phenanthrenequinone (Aldrich) and sodium bis(trimethylsilyl)amide (Fluka) as described by Tuchtenhagan and Ruhlmann. (11) Important modifications to this synthesis include a reaction temperature of no greater than 65° C. and a final phenanthrenequinone concentration of 0.08 M. Under these conditions, orange crystalline silylphi was obtained in 37% yield and stored under nitrogen. The phenanthrenequinone diimine ligand (phi) was generated and chelated in situ by combining the silylated imine ligand with an ethanolic solution of metal chloride by using a modificaiton of Schlosser's method. (12)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112974
Source datasetuspto-grants-1992_05
ORD IDord-0f445a9289244094b55915f4cb38ef55
Source noteuspto-grants-1992_05