Effects of Connectivity Isomerization on Electron Transport Through Thiophene Heterocyclic Molecular Junction.

Connectivity isomerization of the same aromatic molecular core with different substitution positions profoundly affects electron transport pathways and single-molecule conductance. Herein, we designed and synthesized all connectivity isomers of a thiophene ( TP ) aromatic ring substituted by two dihydrobenzo[b]thiophene ( BT ) groups with ethynyl spacers ( m , n -TP-BT, ( m , n = 2,3; 2,4; 2,5; 3,4)), to systematically probe how connectivity contributes to single-molecule conductance. Single-molecule conductance measurements using a scanning tunneling microscopy break junction (STM-BJ) technique show ∼12-fold change in conductance values, which follow an order of 10 -4.83 G 0 ( 2,4-TP-BT ) < 10 -4.78 G 0 ( 3,4-TP-BT ) < 10 -4.06 G 0 ( 2,3-TP-BT ) < 10 -3.75 G 0 ( 2,5-TP-BT ). Electronic structure analysis and theoretical simulations show that the connectivity isomerization significantly changes electron delocalization and HOMO-LUMO energy gaps. Moreover, the connectivity-dependent molecular structures lead to different quantum interference (QI) effects in electron transport, e.g., a strong destructive QI near E = E F leads the smallest conductance value for 2,4-TP-BT . This work proves a clear relationship between the connectivity isomerization and single-molecule conductance of thiophene heterocyclic molecular junctions for the future design of molecular devices.