Chloro(4-cyanophenyl){(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl (diphenylphosphine)}nickel(II) - Names and Identifiers
Chloro(4-cyanophenyl){(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl (diphenylphosphine)}nickel(II) - Physico-chemical Properties
Chloro(4-cyanophenyl){(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl (diphenylphosphine)}nickel(II) - Introduction
Chloro(4-cyanophenyl){(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl (diphenylphosphine)}nickel(II) is a coordination compound commonly used as a catalyst in organic synthesis reactions.
The compound has the following properties:
-Chemical formula: C34H35ClFeNP2Ni
-Molecular weight: 666.28g/mol
-Appearance: Yellow solid
The main purpose of this compound is to participate in organic synthesis reactions as a catalyst, especially reduction, coupling, cross-coupling and cyclization reactions. It has good catalytic activity in catalyzing the cross-coupling reaction of olefins with organic halides.
The method for preparing Chloro(4-cyanophenyl){(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl (diphenylphosphine)}nickel(II) is usually synthesized by ligand substitution reaction. Specific steps include reacting the appropriate ligand with ferrocenyl lead bromide to form the corresponding ligand bromide, which is then reacted with nickel chloride to form the desired compound.
Regarding safety, the toxicity of this compound is low, but the following points still need to be noted:
-Avoid direct contact and inhalation.
-Wear appropriate personal protective equipment, such as gloves and goggles, when using.
-Avoid contact with oxidants, strong acids and strong bases to prevent dangerous reactions.
-Disposal of waste after use, in accordance with local regulations.
Last Update:2024-04-10 22:29:15