Published September 25, 2014 | Version Supplemental Material + Published
Journal Article Open

Symmetry-Breaking Charge Transfer of Visible Light Absorbing Systems: Zinc Dipyrrins

Abstract

Zinc dipyrrin complexes with two identical dipyrrin ligands absorb strongly at 450–550 nm and exhibit high fluorescence quantum yields in nonpolar solvents (e.g., 0.16–0.66 in cyclohexane) and weak to nonexistent emission in polar solvents (i.e., <10^(–3), in acetonitrile). The low quantum efficiencies in polar solvents are attributed to the formation of a nonemissive symmetry-breaking charge transfer (SBCT) state, which is not formed in nonpolar solvents. Analysis using ultrafast spectroscopy shows that in polar solvents the singlet excited state relaxes to the SBCT state in 1.0–5.5 ps and then decays via recombination to the triplet or ground states in 0.9–3.3 ns. In the weakly polar solvent toluene, the equilibrium between a localized excited state and the charge transfer state is established in 11–22 ps.

Additional Information

© 2014 American Chemical Society. ACS AuthorChoice - This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes. Received: July 9, 2014; Revised: August 27, 2014; Published: August 27, 2014. We thank Dr. Ralf Haiges for the help with crystallographic studies and Dr. Sean Roberts for helpful discussion regarding the TA data. We acknowledge financial support from following organizations: the synthesis and characterization of zinc dipyrrins were supported by the Nanoflex Power Corp.; Xray crystallography was performed on a Bruker APEX II CCD system, acquired with funds provided by the NSF CRIF program (Award 1048807); some of the NMR spectra were recorded on a Varian 400-MR spectrometer, acquired with funds provided by the NSF CRIF program (Award 0840366); ns-to-ms TA experiments were performed at the Beckman Institute Laser Resource Center at Caltech; M.E.E. was supported by NIH Grant RO1-DK019038; ultrafast (fs-to-ns) TA studies were supported by the Center for Energy Nanoscience (CEN) at USC. CEN is an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences (DESC0001013).

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Supplemental Material - jp506855t_si_002.cif

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Additional details

Identifiers

PMCID
PMC4174994
Eprint ID
51051
Resolver ID
CaltechAUTHORS:20141030-092012977

Funding

Nanoflex Power Corp
NSF
CHE-1048807
NSF
CHE-0840366
Caltech Beckman Institute
NIH
RO1-DK019038
USC Center for Energy Nanoscience (CEN)
Department of Energy (DOE)
DE-SC0001013

Dates

Created
2014-10-30
Created from EPrint's datestamp field
Updated
2021-11-10
Created from EPrint's last_modified field