Impact of the 2,2'-Bithienyl Framework on the Charge-Transfer Emission of Triarylborane-Based o,o'-Substituted Biaryls

2,2'-联噻吩骨架对三芳基硼烷基邻位取代联芳基化合物电荷转移发射的影响

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Abstract

Two new triarylborane-based o,o'-substituted 2,2'-bithienyls, BT-BNMe (2) and BT-BNBn (2) , which contain BMes(2) and NMe(2)/NBn(2) groups at the 3,3'-positions, have been synthesized. Similar to the o,o'-substituted biphenyl analogues, BP-BNMe (2) and BP-BNBn (2) , which contain BMes(2) and NMe(2)/NBn(2) groups at the 2,2'-positions, the steric effect of the amino group has significant influence on the conformation of the 2,2'-bithienyl skeleton. The boryl and amino groups are located at the same side of 2,2'-bithienyls axis with a short B···N distance (3.63 Å) for the NMe(2)-substituted BT-BNMe (2) . On the contrary, the two substituents are arranged on the two different sides of the 2,2'-bithienyls axis for BT-BNBn (2) , which is modified with bulky NBn(2). Despite the remarkable differences in the steric structure, the two 2,2'-bithienyls display fluorescence at close wavelengths, which is in sharp contrast to the much red-shifted fluorescence of BP-BNMe (2) than BP-BNBn (2) . The theoretical calculations demonstrated that the two 2,2'-bithienyls have close highest occupied molecular orbital-lowest unoccupied molecular orbital gaps in the excited state, which firmly support the experimental results. Thus, the parent main chain framework can exhibit great impact on the charge-transfer emission of o,o'-substituted biaryls.

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