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2,7-Di-4-pyridinylbenzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetrone

  • CAS No. 34151-49-0

  • Cat. No. CS-0098915
  • Purity≥95%
  • MDL No.MFCD00326861

*For research and further manufacturing use only, not for direct human use.

2,7-Di-4-pyridinylbenzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetrone|CS-0098915

Structure of 34151-49-0

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General Information

  • CAS No. 34151-49-0
  • Cat. No. CS-0098915
  • Purity ≥95%
  • MDL No. MFCD00326861
  • Storage 4°C, protect from light, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₄H₁₂N₄O₄
  • Molecular Weight 420.38
  • Synonym(s) 2,7-Di(4-pyridinyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetrone
  • SMILES O=C1C2=CC=C3C(=O)N(C(=O)C4=CC=C(C(=O)N1C=5C=CN=CC5)C2=C34)C=6C=CN=CC6

Description

This tetrone-based ligand features two pyridyl groups at the 2,7-positions, enabling strong chelation in transition metal complexes. Its extended aromatic system enhances electron delocalization, supporting applications in luminescent materials and catalytic systems requiring rigid, planar coordination geometry.

Application

2,7-Di-4-pyridinylbenzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetrone serves as a robust, multi-dentate ligand scaffold for transition metal coordination, enabling the assembly of well-defined polynuclear complexes. Its extended π-conjugated core and orthogonal pyridyl donors facilitate strong chelation with late-transition metals, while the tetrone functionalization enhances solubility and stability in organic media. The molecule exhibits excellent bench stability and compatibility with standard synthetic protocols, making it suitable for applications in catalysis, materials science, and coordination-driven self-assembly.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   100.54
  • LogP   3.231
  • H_Acceptors   6
  • H_Donors   0
  • Rotatable_Bonds   2

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