2019
DOI: 10.1039/c9ta04364k
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Charge transport enhancement in supramolecular oligothiophene assemblies using Pt(ii) centers as a guide

Abstract: The self-assembly properties of a series of square planar Pt(ii) complexes have been related to their charge transport properties, finding higher mobility values in the complexes placing the Pt centers in closer proximity.

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Cited by 8 publications
(13 citation statements)
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“…Trithiophenes containing two 3,4-ethylenedioxythiophene (EDOT) and one thiophene block (BisEDOT-Th) and with different alkyl side chains denoted as BisEDOT-ThR (R = methyl, hexyl, and octyl) as precursor in Scheme were synthesized, and the procedures were recorded in the Supporting Information. The thiophene-based monomers composed of three organic molecules were designed and synthesized because their polymers usually exhibit good electron transport properties in organic electrons. , Many efforts have been focused on high-performance polymer film based on the large planar skeleton and smooth morphology of oligomer to improve the electrical properties of polymer films. , Moreover, it has been accepted that the conjugated system is prone to form self-rigidification and planarization owing to the noncovalent interaction of intramolecular between sulfur and oxygen atoms in oligothiophene containing EDOT units . Additionally, the oligomer usually shows a lower oxidation potential compared with its single thiophene-based unit during polymerization, which allows a much easier polymerization and better polymer film with the more superior physical or chemical properties. One can find the trithiophenes (BisEDOT-Th and BisEDOT-ThR) as precursor having an oxidation potential less than 0.6 V vs Ag/AgCl during electrodeposition in Figure S1, which is significantly lower than thiophene (Th) and EDOT.…”
Section: Resultsmentioning
confidence: 99%
“…Trithiophenes containing two 3,4-ethylenedioxythiophene (EDOT) and one thiophene block (BisEDOT-Th) and with different alkyl side chains denoted as BisEDOT-ThR (R = methyl, hexyl, and octyl) as precursor in Scheme were synthesized, and the procedures were recorded in the Supporting Information. The thiophene-based monomers composed of three organic molecules were designed and synthesized because their polymers usually exhibit good electron transport properties in organic electrons. , Many efforts have been focused on high-performance polymer film based on the large planar skeleton and smooth morphology of oligomer to improve the electrical properties of polymer films. , Moreover, it has been accepted that the conjugated system is prone to form self-rigidification and planarization owing to the noncovalent interaction of intramolecular between sulfur and oxygen atoms in oligothiophene containing EDOT units . Additionally, the oligomer usually shows a lower oxidation potential compared with its single thiophene-based unit during polymerization, which allows a much easier polymerization and better polymer film with the more superior physical or chemical properties. One can find the trithiophenes (BisEDOT-Th and BisEDOT-ThR) as precursor having an oxidation potential less than 0.6 V vs Ag/AgCl during electrodeposition in Figure S1, which is significantly lower than thiophene (Th) and EDOT.…”
Section: Resultsmentioning
confidence: 99%
“…Furthermore, the charge carrier transport behaviours of Pt(II) complexes have been probed using the SCLC method. 80–82 For instance, De Cola, Ruiz-Carretero and coworkers in 2019 reported thiophene oligomer-based neutral Pt( ii ) complexes 21a – 21c and integrated them into the SCLC devices. 80 The average μ h values were determined to be ca.…”
Section: Mom-based Ofetsmentioning
confidence: 99%
“…80–82 For instance, De Cola, Ruiz-Carretero and coworkers in 2019 reported thiophene oligomer-based neutral Pt( ii ) complexes 21a – 21c and integrated them into the SCLC devices. 80 The average μ h values were determined to be ca. 3.5 × 10 −3 , 6.0 × 10 −4 and 1.1 × 10 −3 cm 2 V −1 s −1 for 21a , 21b and 21c , respectively.…”
Section: Mom-based Ofetsmentioning
confidence: 99%
“…23 , 24 The presence of π-conjugated bridging segments such as OTs between two metal chelating sites introduces potential for enhanced metal–metal coupling allowing for potential application as switchable devices in molecular electronics. 25 , 26 The majority of devices developed so far are based on ruthenium polypyridyl derivatives 27 , 28 ; however, copper complexes of 2,9-arylated phens showed favorable photophysical properties. 29 , 30 Replacement of less abundant ruthenium by copper was considered to be a less expensive alternative.…”
Section: Introductionmentioning
confidence: 99%