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Location, Location, Location ‐ Strategic Positioning of 2,1,3‐Benzothiadiazole Units within Trigonal Quaterfluorene‐Truxene Star‐Shaped Structures
Author(s) -
Belton Colin R.,
Kanibolotsky Alexander L.,
Kirkpatrick James,
Orofino Clara,
Elmasly Saadeldin E. T.,
Stavrinou Paul N.,
Skabara Peter J.,
Bradley Donal D. C.
Publication year - 2013
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.201202644
Subject(s) - photoluminescence , materials science , molecule , acceptor , conjugated system , star (game theory) , core (optical fiber) , luminescence , crystallography , chemical physics , polymer , optoelectronics , condensed matter physics , chemistry , physics , organic chemistry , astrophysics , composite material
The fused, bicyclic molecule, 2,1,3‐Benzothiadiazole (BT), has become a key ingredient in the design of new organic semiconductors for light emission and energy harvesting applications. Here, the synthesis is reported of a series of trigonal, star‐shaped compounds comprising a truxene core and three quater‐dialkylfluorene arms into each of which a BT unit is inserted sequentially at each possible position (T4BT‐A to T4BT‐E). Analysis of the resulting electronic properties shows that as a consequence of conjugative coupling to the core and the resulting symmetry there are three distinct locations for the BT unit and the influence that these locations have on light emission and other spectroscopic characteristics is discussed. The systematic variation in photophysical properties for the different structural isomers helps to clarify the influence of BT unit addition to 9,9‐dialkylfluorene chains. It also helps to establish a design template for the construction of donor‐acceptor conjugated materials with targeted properties. For T4BT‐E with a BT unit at the terminal position of each arm, the photoluminescence quantum efficiency is significantly reduced and no amplified spontaneous emission is observed under typical pumping conditions. Theoretical calculations assist in understanding the variation in behaviors among the T4BT‐X family of compounds, especially in relation to their photoluminescence decay times and the Raman scattering intensities of their dominant BT‐unit‐centred molecular vibrations.