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Spin-selective Energy Transfer from Quantum Dots to Molecules: An Application in Stereoselective Organic Synthesis

Emily Weiss

Tetrasubstituted cyclobutyl structures are precursors to, or core components of, many important bioactive molecules, including prospective drugs. Light-driven [2+2] cycloaddition is the most direct strategy for construction of these structures. [2+2] photocycloadditions that proceed through the triplet excited state can be triggered with visible light through excitation of a triplet sensitizer followed by triplet-triplet energy transfer (TT EnT). Achieving selectivities for a particular regioisomer or diastereomer of the cyclobutane product and for homo- vs. hetero-coupling within a mixture of reactive olefins still remains a challenge. Here, we discuss the use of colloidal CdSe quantum dots (QDs) as visible light absorbers, triplet exciton donors, and scaffolds to drive homo- (photodimerization) and hetero- (cross coupling) intermolecular [2+2] photocycloadditions of 4-vinylbenzoic acid derivatives, with perfect and switchable regioselectivity and 97-98% diastereoselectivity for the previously minor syn-head-to-head (HH) or syn-head-to-tail (HT) configurations of the adducts. The diasteromeric ratios (d.r.) we achieve are a factor of 5 - 10 higher than those reported with all other triplet sensitizers. Furthermore, the size-tunable triplet energy of the QD enables regioselective hetero-intermolecular couplings through selective sensitization of only one of the reagent olefins.

Speaker: Emily Weiss, Northwestern University

Tuesday, 01/28/20


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Latimer Hall

UC Berkeley
Room 120
Berkeley, CA 94720