Abstract
Arching a bay area of triphenyleno[1,12-bcd]thiophene with group 14 functionalities gave the first triphenylene derivatives whose two pairs of bay carbons are connected by two different heteroatom functionalities. Triphenyleno[1,12-bcd:4,5-b′c′d′]dithiophene, which had been only accessible through the very severe reaction conditions, was synthesized under the mild reaction conditions. Photophysical properties of newly-obtained heterolotriphenylene derivatives are discussed with theoretical calculations.
Original language | English |
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Pages (from-to) | 1035-1041 |
Number of pages | 7 |
Journal | Journal of Organometallic Chemistry |
Volume | 695 |
Issue number | 7 |
DOIs | |
Publication status | Published - Apr 1 2010 |
Externally published | Yes |
Keywords
- Electronic absorption
- Fluorescence
- Silolotriphenyleno[1,12-bcd]thiophene
- Stannolotriphenyleno[1,12-bcd]thiophene
- Triphenyleno[1,12-bcd:4,5-b′c′d′]dithiophene
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry
- Materials Chemistry