Controlling electron transfer in donor-bridge-acceptor molecules using cross-conjugated bridges

Annie Butler Ricks, Gemma C. Solomon, Michael T. Colvin, Amy M Scott, Kun Chen, Mark A. Ratner, Michael R. Wasielewski

Research output: Contribution to journalArticle

115 Citations (Scopus)

Abstract

Photoinitiated charge separation (CS) and recombination (CR) in a series of donor-bridge-acceptor (D-B-A) molecules with cross-conjugated, linearly conjugated, and saturated bridges have been compared and contrasted using time-resolved spectroscopy. The photoexcited charge transfer state of 3,5-dimethyl-4-(9-anthracenyl)julolidine (DMJ-An) is the donor, and naphthalene-1,8:4,5-bis(dicarboximide) (NI) is the acceptor in all cases, along with 1,1-diphenylethene, trans-stilbene, diphenylmethane, and xanthone bridges. Photoinitiated CS through the cross-conjugated 1,1-diphenylethene bridge is about 30 times slower than through its linearly conjugated trans-stilbene counterpart and is comparable to that observed through the diphenylmethane bridge. This result implies that cross-conjugation strongly decreases the π orbital contribution to the donor-acceptor electronic coupling so that electron transfer most likely uses the bridge σ system as its primary CS pathway. In contrast, the CS rate through the cross-conjugated xanthone bridge is comparable to that observed through the linearly conjugated trans-stilbene bridge. Molecular conductance calculations on these bridges show that cross-conjugation results in quantum interference effects that greatly alter the through-bridge donor-acceptor electronic coupling as a function of charge injection energy. These calculations display trends that agree well with the observed trends in the electron transfer rates.

Original languageEnglish (US)
Pages (from-to)15427-15434
Number of pages8
JournalJournal of the American Chemical Society
Volume132
Issue number43
DOIs
StatePublished - Nov 3 2010
Externally publishedYes

Fingerprint

Stilbenes
Electrons
Molecules
Genetic Recombination
Spectrum Analysis
Injections
Charge injection
Naphthalene
xanthone
1,1-diphenylethene
diphenylmethane
3,5-dimethyl-4-(9-anthracenyl)julolidine
Charge transfer
Spectroscopy

ASJC Scopus subject areas

  • Chemistry(all)
  • Catalysis
  • Biochemistry
  • Colloid and Surface Chemistry

Cite this

Ricks, A. B., Solomon, G. C., Colvin, M. T., Scott, A. M., Chen, K., Ratner, M. A., & Wasielewski, M. R. (2010). Controlling electron transfer in donor-bridge-acceptor molecules using cross-conjugated bridges. Journal of the American Chemical Society, 132(43), 15427-15434. https://doi.org/10.1021/ja107420a

Controlling electron transfer in donor-bridge-acceptor molecules using cross-conjugated bridges. / Ricks, Annie Butler; Solomon, Gemma C.; Colvin, Michael T.; Scott, Amy M; Chen, Kun; Ratner, Mark A.; Wasielewski, Michael R.

In: Journal of the American Chemical Society, Vol. 132, No. 43, 03.11.2010, p. 15427-15434.

Research output: Contribution to journalArticle

Ricks, AB, Solomon, GC, Colvin, MT, Scott, AM, Chen, K, Ratner, MA & Wasielewski, MR 2010, 'Controlling electron transfer in donor-bridge-acceptor molecules using cross-conjugated bridges', Journal of the American Chemical Society, vol. 132, no. 43, pp. 15427-15434. https://doi.org/10.1021/ja107420a
Ricks, Annie Butler ; Solomon, Gemma C. ; Colvin, Michael T. ; Scott, Amy M ; Chen, Kun ; Ratner, Mark A. ; Wasielewski, Michael R. / Controlling electron transfer in donor-bridge-acceptor molecules using cross-conjugated bridges. In: Journal of the American Chemical Society. 2010 ; Vol. 132, No. 43. pp. 15427-15434.
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