Dibromobis(triphenylphosphine)nickel(II)
[CAS# 14126-37-5]

Identification

• Classification: Organic raw materials >> Organometallic compound >> Organic nickel
• Name: Dibromobis(triphenylphosphine)nickel(II)
• Synonyms: Nickel(II) bromide bis(triphenylphosphine)
• Molecular Formula: C₃₆H₃₀Br₂NiP₂
• Molecular Weight: 743.07
• CAS Registry Number: 14126-37-5
• EC Number: 628-538-7
• SMILES: C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.[Ni](Br)Br

Properties

• Melting point: 219-223 ºC

Safety Data

• Hazard Symbols: GHS07 Warning
• Hazard Statements: H302-H312-H332
• Precautionary Statements: P261-P264-P270-P271-P280-P301+P317-P302+P352-P304+P340-P317-P321-P330-P362+P364-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Acute toxicity	Acute Tox.	4	H302
Acute toxicity	Acute Tox.	4	H332
Acute toxicity	Acute Tox.	4	H312

Discovory and Applicatios

Dibromobis(triphenylphosphine)nickel(II) is a notable organonickel compound with significant utility in coordination chemistry and catalysis. This compound, featuring a nickel center coordinated by two bromine atoms and two triphenylphosphine ligands, represents a valuable member of the class of nickel(II) complexes that are extensively used in various chemical processes.

The discovery of Dibromobis(triphenylphosphine)nickel(II) emerged from efforts to explore the coordination chemistry of nickel(II) with phosphorus-based ligands. The triphenylphosphine ligands are known for their ability to stabilize metal centers and influence the reactivity of metal complexes. When coordinated to nickel(II), these ligands impart stability to the metal center, which is crucial for various applications.

One of the primary applications of Dibromobis(triphenylphosphine)nickel(II) is in catalysis. The compound is employed as a catalyst in several important organic reactions, including cross-coupling reactions and polymerization processes. Its catalytic activity is largely attributed to the ability of the nickel center to participate in oxidative addition and reductive elimination processes. This makes the compound valuable for facilitating the formation of carbon-carbon bonds, which is a key step in the synthesis of complex organic molecules.

Dibromobis(triphenylphosphine)nickel(II) is also used in the field of organometallic chemistry to study the behavior of nickel(II) complexes with different ligands. The compound serves as a model system for understanding the interactions between nickel centers and various ligands, which is essential for designing new catalysts and materials. The bromine atoms in the complex play a crucial role in the reactivity of the nickel center, influencing its ability to participate in chemical reactions.

Additionally, Dibromobis(triphenylphosphine)nickel(II) finds applications in materials science. The compound is used as a precursor in the synthesis of nickel-based materials with specific properties. For instance, it can be utilized to prepare nickel-containing polymers and materials with tailored electronic and optical characteristics. The ability to control the properties of these materials through the choice of ligands and metal centers is valuable for developing advanced materials for various technological applications.

In summary, Dibromobis(triphenylphosphine)nickel(II) is a significant compound in the realm of organonickel chemistry. Its stability and reactivity make it a valuable tool in catalysis, materials science, and the study of nickel coordination chemistry. The compound’s ability to facilitate important organic reactions and its role in the development of new materials highlight its importance in both research and practical applications.

References

2009. Use of the NiBr2(PPh3)2/Zn catalytic system for homo- and copolymerization of styrene and methyl methacrylate. Polymer Science, Series B. D. F. Grishin, I. S. Il�ichev, N. B. Valetova.
DOI: 10.1134/s1560090409030038

2010. Transition-Metal-Mediated Oligomerization Reactions. Science of Synthesis.
DOI: SD-045-00507

2008. Polymerization of methyl methacrylate using the NiX2(PPh3)2/Zn catalytic system. Kinetics and Catalysis. I. S. Il�ichev, N. B. Valetova, M. V. Moskalev, D. F. Grishin.
DOI: 10.1134/s0023158408040125