Experimental studies of light-induced charge transfer and charge redistribution in (X2-Bipyridine)Re1(CO)3Cl complexes

Keith A. Walters, Young Jin Kim, Joseph T Hupp

Research output: Contribution to journalArticle

54 Citations (Scopus)

Abstract

Stark emission spectroscopy, transient DC photoconductivity (TDCP), and ground-state dipole moment measurements have been used to evaluate charge transfer (CT) within various (X2-bipyridine)Re1(CO)3Cl complexes following 3MLCT excited-state formation. The Stark technique reports on vector differences between ground-state (μg) and excited-state (μu) dipole moments, while TDCP, when combined with independently obtained μg information, reports on scalar differences. For systems featuring collinear, same-signed ground- and excited-state dipole moments, the scalar and vector differences are equivalent. However, for the low symmetry systems studied here, they are distinctly different. The vector difference yields the effective adiabatic one-electron-transfer distance (R12), while the combined vector and scalar data yield information about dipole rotation upon ground-state/excited-state interconversion. For the systems examined, charge transfer distances are substantially smaller than geometric electron-donor/electron-acceptor site separation distances. The measured distances are significantly affected by changes in acceptor ligand substituent composition. Electron-donating substituents decrease CT distances, while electron-withdrawing substituents increase CT distances, as do aromatic substituents that are capable of expanding the bipyridyl ligand (acceptor ligand) π system. The Stark measurements additionally indicate that the CT vector and the transition dipole moment are significantly orthogonal, a consequence of strong polarization of the Re-Cl bond (orthogonal to the metal/ acceptor-ligand plane) in the ground electronic state and relaxation of the polarization in the upper state. The ground-state Re-Cl bond polarization is sufficiently large that the overall ground-state scalar dipole moment exceeds the overall excited-state scalar dipole moment, despite transfer of an electron from the metal center to the diimine ligand. This finding provides an explanation for the otherwise puzzling negative solvatochromism exhibited in this family of compounds. Combining TDCP and Stark results, we find that the dipole moment can be rotated in some instances by more than 90° upon 3MLCT excited-state formation. The degree of rotation or reorientation can be modulated by changing the identity of the acceptor ligand substituents. Reorientational effects are smallest when the compounds feature aromatic substituents capable of spatially extending the π system of the acceptor ligand.

Original languageEnglish
Pages (from-to)2909-2919
Number of pages11
JournalInorganic Chemistry
Volume41
Issue number11
DOIs
Publication statusPublished - Jun 3 2002

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Dipole moment
Carbon Monoxide
Charge transfer
Excited states
dipole moments
Ground state
charge transfer
Ligands
ligands
ground state
Electrons
scalars
Photoconductivity
photoconductivity
excitation
direct current
Polarization
electrons
polarization
Metals

ASJC Scopus subject areas

  • Inorganic Chemistry

Cite this

Experimental studies of light-induced charge transfer and charge redistribution in (X2-Bipyridine)Re1(CO)3Cl complexes. / Walters, Keith A.; Kim, Young Jin; Hupp, Joseph T.

In: Inorganic Chemistry, Vol. 41, No. 11, 03.06.2002, p. 2909-2919.

Research output: Contribution to journalArticle

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