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Dichloro(1,10-phenanthroline)platinum(II)
Catalog Number
ACM18432956-2
Product Name
Dichloro(1,10-phenanthroline)platinum(II)
Structure
![{[CurrentData.Name]}](https://resource.alfachemic.com/structure/18432-95-6.gif)
CAS
18432-95-6
Synonyms
Dichloro(1,10-phenanthroline)platinum(II);18432-95-6;dichloroplatinum; 1,10-phenanthroline;AC1MRUZ6;AC1O1L2O;SCHEMBL691376;CTK8F9142;Dichloro(1,10-phenanthroline)platinum(II), >=95.0%;
IUPAC Name
dichloroplatinum;1,10-phenanthroline;
Molecular Weight
446.19
Molecular Formula
C₁₂H₈Cl₂N₂Pt
Canonical SMILES
C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1.Cl[Pt]Cl;
InChI
InChI=1S/C12H8N2.2ClH.Pt/c1-3-9-5-6-10-4-2-8-14-12(10)11(9)13-7-1;;;/h1-8H;2*1H;/q;;;+2/p-2;
InChI Key
VONLGUDYJIAGQI-UHFFFAOYSA-L;
Storage
room temperature
Complexity
185
Covalently-Bonded Unit Count
2
Exact Mass
444.971g/mol
H-Bond Acceptor
2
Heavy Atom Count
17
Monoisotopic Mass
444.971g/mol
Topological Polar Surface Area
25.8A^2
Application
Dichloro(1,10-phenanthroline)platinum(II) serves as a versatile reactant and catalyst in various chemical syntheses. It is used in the formation of mixed-metal complexes combining platinum and lanthanide centers, essential for advancing materials science. Additionally, it plays a role in the synthesis of platinum complexes with a chelating di-fluoro-substituted thiourea ligand, which are significant in developing new coordination compounds. This compound also facilitates adduct formation between ternary Pt(III)-amino acid-aromatic diimine complexes and flavin mononucleotide, highlighting its utility in biochemical applications. Moreover, it acts as a catalyst for the selective synthesis of monoorganotin trihalides, contributing to the efficient production of organotin compounds used in various industrial processes.
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