Related Experiment Video
Updated: Nov 24, 2025

Synthesis of 1,2-Azaborines and the Preparation of Their Protein Complexes with T4 Lysozyme Mutants
Published on: March 25, 2017
Single-Molecule Conductance of 1,4-Azaborine Derivatives as Models of BN-doped PAHs
Lucía Palomino-Ruiz1,2, Sandra Rodríguez-González3,4, Joel G Fallaque2
1Departamento de Química Orgánica, Facultad de Ciencias, Unidad de Excelencia de Química Aplicada a Biomedicina y Medioambiente (UEQ), Universidad de Granada, 18071, Granada, Spain.
Abstract:
The single-molecule conductance of a series of BN-acene-like derivatives has been measured by using scanning tunneling break-junction techniques. A strategic design of the target molecules has allowed us to include azaborine units in positions that unambiguously ensure electron transport through both heteroatoms, which is relevant for the development of customized BN-doped nanographenes. We show that the conductance of the anthracene azaborine derivative is comparable to that of the pristine all-carbon anthracene compound. Notably, this heteroatom substitution has also allowed us to perform similar measurements on the corresponding pentacene-like compound, which is found to have a similar conductance, thus evidencing that B-N doping could also be used to stabilize and characterize larger acenes for molecular electronics applications. Our conclusions are supported by state-of-the-art transport calculations.
Related Concept Videos
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds
Basicity of Heterocyclic Aromatic Amines
Aromatic Hydrocarbon Anions: Structural Overview
Due to the absence of continuous...
NMR Spectroscopy of Benzene Derivatives
Structure of Benzene: Molecular Orbital Model
Basicity of Aromatic Amines

