HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloride → N~9~,N~10~-Bis(trimethylsilyl)phenanthrene-9,10-diimine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | 9,10-Phenanthrenedione | HCID 6763 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 1,2-Phenanthrenedione | HCID 3080566 | — |
| Reactant | Phenanthrenequinone diimine | HCID 86745785 | — |
| Product | N~9~,N~10~-Bis(trimethylsilyl)phenanthrene-9,10-diimine | HCID 71349758 | 37% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05112974 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-0f445a9289244094b55915f4cb38ef55 |
| Source note | uspto-grants-1992_05 |