Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 136, Issue 36, Pages 12580-12583Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja506980p
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Funding
- CREST, JST
- Ministry of Education, Culture, Sports, Science, and Technology (MEXT) of Japan [24109007]
- JSPS
- Grants-in-Aid for Scientific Research [13J04117, 24750038, 24109007] Funding Source: KAKEN
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The synthesis of a planarized trinaphthylborane with partially fused structure is presented. This compound shows not only high chemical and thermal stability but also sufficient Lewis acidity to form Lewis adducts with pyridine derivatives in solution. The BN Lewis adducts exhibit unprecedented photodissociation behavior in the excited state, reminiscent of the photogeneration of carbenium ions from triarylmethane leuco dyes. Consequently, these BN Lewis adducts exhibit dual fluorescence emission arising from the initial tetracoordinate BN adducts and the photodissociated tricoordinate boranes.
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