Abstract

The dimetallic [M(2)(bpy)(2)(NO(3))(2)](NO(3))(2) moieties (M = Pd(II) or Pt(II)) react preferentially at the pyrazolyl end of the pyridyl-pyrazole ligand, giving rise to dimetallic corners. Subsequently, the dimetallic corner building blocks featuring two pyridine donors are coordinated by monometallic [M(bpy)(NO(3))(2)] moieties (M = Pd(II) or Pt(II)) to form homo- or hetero-metallomacrocycles.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call