21361-04-6 Usage
Description
[(2,9-dimethyl-1,10-phenanthroline)dichloro nickel(II)] is a coordination complex consisting of a nickel(II) ion coordinated with two molecules of 2,9-dimethyl-1,10-phenanthroline and two chloride ions. This complex is characterized by its unique structure and properties, making it a versatile compound in the fields of coordination chemistry and materials science.
Uses
Used in Catalytic Applications:
[(2,9-dimethyl-1,10-phenanthroline)dichloro nickel(II)] is used as a catalyst in various chemical reactions due to its unique properties. The complex acts as a catalyst by facilitating the reaction process, thereby increasing the reaction rate and improving the overall efficiency of the process.
Used in Electrochemical Applications:
[(2,9-dimethyl-1,10-phenanthroline)dichloro nickel(II)] is also utilized in electrochemical applications, where it plays a crucial role in the transfer of electrons between the electrode and the electrolyte. Its unique properties make it suitable for use in electrochemical cells, sensors, and other related devices.
Used as a Precursor in Synthesis:
[(2,9-dimethyl-1,10-phenanthroline)dichloro nickel(II)] serves as a precursor for the synthesis of other nickel-containing compounds, such as coordination polymers and molecular magnets. These synthesized compounds have potential applications in various fields, including magnetic storage, drug delivery, and advanced materials.
Used in Coordination Chemistry Research:
The specific structure and properties of [(2,9-dimethyl-1,10-phenanthroline)dichloro nickel(II)] make it an important compound for research in coordination chemistry. It provides valuable insights into the behavior of metal ions and their interactions with ligands, contributing to the development of new coordination complexes with tailored properties and applications.
Used in Materials Science:
In the field of materials science, [(2,9-dimethyl-1,10-phenanthroline)dichloro nickel(II)] is employed for the development of new materials with specific properties. Its unique structure and properties can be exploited to create materials with enhanced performance in areas such as catalysis, energy storage, and sensing.
Check Digit Verification of cas no
The CAS Registry Mumber 21361-04-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,6 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 21361-04:
(7*2)+(6*1)+(5*3)+(4*6)+(3*1)+(2*0)+(1*4)=66
66 % 10 = 6
So 21361-04-6 is a valid CAS Registry Number.
21361-04-6Relevant articles and documents
Synthesis and Reactivity of Paramagnetic Nickel Polypyridyl Complexes Relevant to C(sp2)–C(sp3)Coupling Reactions
Mohadjer Beromi, Megan,Brudvig, Gary W.,Hazari, Nilay,Lant, Hannah M. C.,Mercado, Brandon Q.
, p. 6094 - 6098 (2019)
A number of new transition metal catalyzed methods for the formation of C(sp2)–C(sp3) bonds have recently been described. These reactions often utilize bidentate polypyridyl-ligated Ni catalysts, and paramagnetic NiI halide or aryl species are proposed in the catalytic cycles. However, there is little knowledge about complexes of this type. Here, we report the synthesis of paramagnetic bidentate polypyridyl-ligated Ni halide and aryl complexes through elementary reactions proposed in catalytic cycles for C(sp2)–C(sp3) bond formation. We investigate the ability of these complexes to undergo organometallic reactions that are relevant to C(sp2)–C(sp3) coupling through stoichiometric studies and also explore their catalytic activity.
