Journal
ORGANIC LETTERS
Volume 14, Issue 12, Pages 3052-3055Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol300985h
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Funding
- Natural Science Foundation of China [21073112, 21173136]
- Natural Science Foundation of Shandong Province [ZR2010EZ007]
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A series of perylenetetracarboxylic diimide (PDI) compounds linked with spirobifluorene have been prepared. The orthogonal configuration of the PDI subunits efficiently hindered their molecular aggregation in solution. Energy transfer from a 1,7-diphenoxyl group substituted PDI (PO-PDI) to a 1,7-dipyrrolidinyl group substituted PDI (PY-PDI) occurred with a large efficiency when PO-PDI was selectively excited, despite the orthogonal orientation of the two units. This observation was in direct conflict with predictions derived from the Forster theory. More interestingly, this efficient energy transfer also occurred in the solid state.
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