Butterfly-Shaped Thiophene-Pyridine Hybrids: Green Electroluminescence and Large Third-Order Optical Nonlinearities.

A set of four symmetric, butterfly-shaped 4-(4-(decyloxy)phenyl)-2,6-di(thiophen-2-yl)pyridine (TPY) derivatives 2TPA-TPY (TPY center and triphenylamine end groups), 2CBZ-TPY (TPY center and N-ethyl carbazole end groups), 2TPY-TPA (triphenylamine center and TPY at the periphery) and 2TPY-CBZ (N-ethyl carbazole center and TPY at the periphery) was synthesized. The molecules show reverse saturable absorption (RSA) which is consistent with two-photon absorption (2PA) associated with excited-state absorption (ESA) when excited using a 532 nm laser beam. The molecules 2TPA-TPY and 2TPY-TPA possess extremely low limiting thresholds of 1.

Facile synthesis and exploration of excited state assisted two-photon absorption properties of D-A-D type thiophene-pyridine derivatives.

A series of trigonal-shaped molecules (TPyT and TPyP) and a polymer (P2TPy) with donor-acceptor-donor (D-A-D) structural arrangement were designed with thiophene and 2,4,6-trisubstituted pyridine as the backbone i.e., a 4-(4-(decyloxy)phenyl)-2,6-di(thiophen-2-yl)pyridine core structure, for the first time and synthesized via a microwave assisted one pot reaction.