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Research output: Contribution to Journal/Magazine › Journal article › peer-review
Research output: Contribution to Journal/Magazine › Journal article › peer-review
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TY - JOUR
T1 - In situ formation of H-bonding imidazole chains in break-junction experiments
AU - Wu, C.
AU - Alqahtani, A.
AU - Sangtarash, S.
AU - Vezzoli, A.
AU - Sadeghi, H.
AU - Robertson, Craig M.
AU - Cai, C.
AU - Lambert, C.J.
AU - Higgins, S.J.
AU - Nichols, R.J.
PY - 2020/4/14
Y1 - 2020/4/14
N2 - As a small molecule possessing both strong H-bond donor and acceptor functions, 1H-imidazole can participate in extensive homo- or heteromolecular H-bonding networks. These properties are important in Nature, as imidazole moieties are incorporated in many biologically-relevant compounds. Imidazole also finds applications ranging from corrosion inhibition to fire retardants and photography. We have found a peculiar behaviour of imidazole during scanning tunnelling microscopy-break junction (STM-BJ) experiments, in which oligomeric chains connect the two electrodes and allow efficient charge transport. We attributed this behaviour to the formation of hydrogen-bonding networks, as no evidence of such behaviour was found in 1-methylimidazole (incapable of participating in intramolecular hydrogen bonding). The results are supported by DFT calculations, which confirmed our hypothesis. These findings pave the road to the use of hydrogen-bonding networks for the fabrication of dynamic junctions based on supramolecular interactions. © The Royal Society of Chemistry .
AB - As a small molecule possessing both strong H-bond donor and acceptor functions, 1H-imidazole can participate in extensive homo- or heteromolecular H-bonding networks. These properties are important in Nature, as imidazole moieties are incorporated in many biologically-relevant compounds. Imidazole also finds applications ranging from corrosion inhibition to fire retardants and photography. We have found a peculiar behaviour of imidazole during scanning tunnelling microscopy-break junction (STM-BJ) experiments, in which oligomeric chains connect the two electrodes and allow efficient charge transport. We attributed this behaviour to the formation of hydrogen-bonding networks, as no evidence of such behaviour was found in 1-methylimidazole (incapable of participating in intramolecular hydrogen bonding). The results are supported by DFT calculations, which confirmed our hypothesis. These findings pave the road to the use of hydrogen-bonding networks for the fabrication of dynamic junctions based on supramolecular interactions. © The Royal Society of Chemistry .
KW - Corrosion
KW - Hydrogen
KW - Scanning tunneling microscopy
KW - Supramolecular chemistry
KW - 1-methylimidazole
KW - Corrosion inhibition
KW - Donor and acceptor
KW - H-bonding networks
KW - Hydrogen bonding network
KW - In-situ formations
KW - Intramolecular hydrogen bonding
KW - Supramolecular interactions
KW - Hydrogen bonds
U2 - 10.1039/d0nr00630k
DO - 10.1039/d0nr00630k
M3 - Journal article
VL - 12
SP - 7914
EP - 7920
JO - Nanoscale
JF - Nanoscale
SN - 2040-3364
IS - 14
ER -