36309-88-3

Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride Chemical Structure
36309-88-3

Chemical Structure

Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride

Synonym(s): [Ru(DPP)3]Cl2

  • CAS No.: 36309-88-3
  • Formula:C72H48Cl2N6Ru
  • Molecular Weight:1169.17

InChIKey: SKZWFYFFTOHWQP-UHFFFAOYSA-L

SMILES: C1(C2=C(C=CC3=C4[N]([Ru+2]567([N]8=C9C%10=C(C(C%11=CC=CC=C%11)=CC=[N]7%10)C=CC9=C(C%12=CC=CC=C%12)C=C8)[N]%13=C%14C%15=C(C(C%16=CC=CC=C%16)=CC=[N]6%15)C=CC%14=C(C%17=CC=CC=C%17)C=C%13)=CC=C3C%18=CC=CC=C%18)C4=[N]5C=C2)=CC=CC=C1.[Cl-].[Cl-]

Biological Activity: Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride ([Ru(dpp)3]2+) is an electrochemiluminescent (ECL) probe and oxygen-sensitive sensor. Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride can be used to modify electrode surfaces for the detection of sulfates (S2O82-) and oxalates, based on electrochemical reactions that generate excited-state species, releasing photons through irreversible redox reactions. Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride utilizes the oxygen quenching of fluorescence mechanism, where fluorescence intensity reflects the metabolic rate of living microorganisms or oxygen levels within cells/tumors, allowing for real-time detection. Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride's main applications include microbial detection, antibacterial activity studies, and tumor microenvironment research[1][2].

Cat. No. Product Name Purity Description Pricing
HY-W074143
Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride 99.78% Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride ([Ru(dpp)3]2+) is an electrochemiluminescent (ECL) probe and oxygen-sensitive sensor. Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride can be used to modify electrode surfaces for the detection of sulfates (S2O82-) and oxalates, based on electrochemical reactions that generate excited-state species, releasing photons through irreversible redox reactions. Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride utilizes the oxygen quenching of fluorescence mechanism, where fluorescence intensity reflects the metabolic rate of living microorganisms or oxygen levels within cells/tumors, allowing for real-time detection. Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride's main applications include microbial detection, antibacterial activity studies, and tumor microenvironment research.
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