Ultrafast Dynamics of Manganese(III), Manganese(II), and Free-Base Bacteriochlorin: Is There Time for Photochemistry?

Inorg Chem. 2017 Mar 6;56(5):2677-2689. doi: 10.1021/acs.inorgchem.6b02871. Epub 2017 Feb 16.

Abstract

Manganese(III) and manganese(II) complexes of halogenated sulfonamide tetraphenylbacteriochlorins were prepared for the first time via a transmetalation reaction and shown to be stable at room temperature. The behavior of the electronic states of the paramagnetic complexes is remarkably different from those of the metal-free bacteriochlorins or diamagnetic metallobacteriochlorins. The Mn3+ complex exhibits eight electronic transitions between different states from 300 to 1100 nm, with a very prominent band (molar absorption coefficient of ca. 50000 M-1 cm-1) at 829 nm. Ultrafast transient absorption showed the formation of an excited singquintet state that decays to a tripquintet state with a femtosecond lifetime. The tripquintet state decays in 5 ps, yielding a tripseptet state with a 570 ps lifetime. The electronic absorption of the Mn2+ complex more closely resembles those of diamagnetic metallobacteriochlorins, but the longest decay lifetime is only ca. 8 ps. The intense photoacoustic waves generated with near-infrared excitation suggest the use of these complexes in photoacoustic tomography.

MeSH terms

  • Calorimetry
  • Coordination Complexes / chemical synthesis
  • Coordination Complexes / chemistry*
  • Manganese / chemistry*
  • Molecular Structure
  • Photochemical Processes
  • Porphyrins / chemistry*
  • Quantum Theory*
  • Time Factors

Substances

  • Coordination Complexes
  • Porphyrins
  • bacteriochlorin
  • Manganese