Section 3: Compound 4 [4] (80 mg, 0.075 mmol) and KC 8 (22 mg, 0.163 mmol) were placed in a reaction tube with a magnetic stirrer. Oxygen-free, dry THF (2 mL) was introduced into the reaction tube by vacuum transfer, and the reaction mixture was stirred at room temperature to produce a yellow soluti
The Proton Catalyzed Transformation of a Cobaltacyclopentadiene into a η4-Cyclobutadiene Complex
✍ Scribed by Lutz Brandt; Prof. Michael Green; Dr. Adrian W. Parkins
- Book ID
- 101557859
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 380 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Experimental Section 3: Compound 4 [4] (80 mg, 0.075 mmol) and KC 8 (22 mg, 0.163 mmol) were placed in a reaction tube with a magnetic stirrer. Oxygen-free, dry THF (2 mL) was introduced into the reaction tube by vacuum transfer, and the reaction mixture was stirred at room temperature to produ
Platinum complexes / Carbene platinum complexes / Carbene zirconium complexes / Carbene complex synthesis, non-nucleophilic / Zirconium complexes While (q4-butadiene)zirconocene and -hafnocene do not react with Pt(PPh,),(CO), (2) in toluene solution at room temperature, cp2Zr(q4-C4HG) (1 a: cp = q5-