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Band Gap Control in Conjugated Oligomers via Lewis Acids
Abstract
A simple and effective strategy for optical band gap control is demonstrated through the use of a novel small acceptor/donor/acceptor molecule, 1, and group-13 Lewis acids. Chromophore 1 contains a dithienolesilole donor unit end-capped with benzo-2,1,3-thiadiazole (BT) acceptor units. Addition to 1 of stoichiometeric quantities of Lewis acids of varying strength resulted in the formation of Lewis adducts with progressively red-shifted primary charge-transfer absorption bands. These complexes have absorption spectra that approach those of known conjugated copolymers containing related units. NMR spectroscopy and X-ray diffraction studies revealed that 1 binds 2 equiv of Lewis acid via the nitrogen at the 3-position of BT.
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“Optical properties of an A-D-A chromophore with CT character has been tuned simply by a complexation of Lewis acid to a basic site of the π-delocalized framework.70”
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Cites
Pearson, R. G. (1963) · Journal of the American Chemical Society · doi:10.1021/ja00905a001 · Cited by 10,475
Design Rules for Donors in Bulk‐Heterojunction Solar Cells—Towards 10 % Energy‐Conversion Efficiency
Scharber, M., Mühlbacher, D., Koppe, M., Denk, P., Waldauf, C., Heeger, A. J., & Brabec, C. J. (2006) · Advanced Materials · doi:10.1002/adma.200501717 · Cited by 5,198
Grätzel, M. (2003) · Journal of Photochemistry and Photobiology C: Photochemistry Reviews · doi:10.1016/s1389-5567(03)00026-1 · Cited by 4,405
Efficient Tandem Polymer Solar Cells Fabricated by All-Solution Processing
Kim, J. Y., Lee, K., Coates, N. E., Moses, D. J., Nguyen, T., Dante, M., & Heeger, A. J. (2007) · Science · doi:10.1126/science.1141711 · Cited by 3,270
Efficiency enhancement in low-bandgap polymer solar cells by processing with alkane dithiols
Peet, J., Kim, J. Y., Coates, N. E., L., W., Moses, D. J., Heeger, A. J., & Bazan, G. C. (2007) · Nature Materials · doi:10.1038/nmat1928 · Cited by 3,203
Self-citationPolymer‐Fullerene Bulk‐Heterojunction Solar Cells
Dennler, G., Scharber, M. C., & Brabec, C. J. (2009) · Advanced Materials · doi:10.1002/adma.200801283 · Cited by 3,161
Hou, J., Chen, H.-Y., Zhang, S., Li, G., & Yang, Y. (2008) · Journal of the American Chemical Society · doi:10.1021/ja806687u · Cited by 1,126
Molecular Engineering of the Band Gap of π‐Conjugated Systems: Facing Technological Applications
Roncali, J. (2007) · Macromolecular Rapid Communications · doi:10.1002/marc.200700345 · Cited by 722
Jacobsen, H., Berke, H., Döring, S., Kehr, G., Erker, G., Fröhlich, R., & Meyer, O. G. J. (1999) · Organometallics · doi:10.1021/om981033e · Cited by 359
Kato, S., Matsumoto, T., Shigeiwa, M., Gorohmaru, H., Maeda, S., Ishi‐i, T., & Mataka, S. (2005) · Chemistry - A European Journal · doi:10.1002/chem.200500921 · Cited by 244
Research works printed but not linked: 1
- Piers W. E., 2005, Adv. Organomet. Chem., 52, 1
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Huang, Y., Welch, G. C., Bazan, G. C., Chabinyc, M. L., & Su, W. (2012) · Chemical Communications · doi:10.1039/c2cc32401f · Cited by 20
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Tanaka, D., Ohshita, J., Ooyama, Y., & Morihara, Y. (2013) · Polymer Journal · doi:10.1038/pj.2013.46 · Cited by 17
Metadata
- Authors
- Welch, G. C., Coffin, R., Peet, J., & Bazan, G. C.
- Affiliations
- University of California, Santa Barbara (US)
- Corresponding author
- Bazan, Guillermo C.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2009-07-08
- Volume
- 131
- Issue
- 31
- Pages
- 10802-10803
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W1978926229
- Cited by
- 159
- References
- 24
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 8 · 2023: 11 · 2022: 11 · 2021: 7 · 2020: 10 · 2019: 12 · 2018: 11 · 2017: 6 · 2016: 12 · 2015: 13 · 2014: 9 · 2013: 9 · 2012: 12
- FWCI
- 9.52
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of the American Chemical Society (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Physical Sciences › Engineering › Electrical and Electronic Engineering › Organic Electronics and Photovoltaics
- Physical Sciences › Engineering › Electrical and Electronic Engineering › Organic Light-Emitting Diodes Research
- Physical Sciences › Chemistry › Organic Chemistry › Organoboron and organosilicon chemistry
- Keywords
- conjugated oligomers, Lewis acid adducts, benzo[2,1,3]thiadiazole, charge-transfer absorption, bathochromic shift, conjugated copolymers
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