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There are several binding groups used within molecular electronics for anchoring molecules to metal electrodes (e.g., R-SMe, R-NH, R-CS , R-S). However, some anchoring groups that bind strongly to electrodes have poor/unknown stability, some have weak electrode coupling, while for some their binding motifs are not well defined. Further binding groups are required to aid molecular design and to achieve a suitable balance in performance across a range of properties. We present an in-depth investigation into the use of carbodithioate esters as contact groups for single-molecule conductance measurements, using scanning tunnelling microscopy break junction measurements (STM-BJ) and detailed surface spectroscopic analysis. We demonstrate that the methyl carbodithioate ester acts as an effective contact for gold electrodes in STM-BJ measurements. Surface enhanced Raman measurements demonstrate that the C=S functionality remains intact when adsorbed on to gold nanoparticles. A gold(I) complex was also synthesised showing a stable C=S→Au interaction from the ester. Comparison with a benzyl thiomethyl ether demonstrates that the C=S moiety significantly contributes to charge transport in single-molecule junctions. The overall performance of the CSMe group demonstrates it should be used more extensively and has strong potential for the fabrication of larger area devices with long-term stability.
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http://dx.doi.org/10.1002/anie.202403577 | DOI Listing |
ACS Omega
August 2025
Chemical Pathology Department, Cairo University Hospital, Cairo University, Giza 12613, Egypt.
Hydrazono-[1,3,4]-thiadiazoles have a prominent position among the heterocyclic compounds due to their broadening aspects of biological activities. In the current study, a neoteric series of [1,3,4]-thiadiazoles tethered to alkoxyaryl hydrazone has been formulated via the treatment of methyl 2-[3-(pentyloxy)-benzylidene]-hydrazine-1-carbodithioate and hydrazonoyl chlorides in ethanolic solution under thermal conditions. DABCO, as an environmentally nontoxic material, was utilized as a superior basic catalyst for the latter reaction.
View Article and Find Full Text PDFCurr Org Synth
January 2025
School of Polymer Science and Engineering, The University of Southern Mississippi, Hattiesburg, Mississippi, 39406, Unites States.
Background: Thiadiazoles exhibit a variety of biological activities, including antimicrobial, antiviral, antituberculosis, carbonic anhydrase inhibitor, antitrypanosomal agent, and anticonvulsant properties.
Methods: The new polymers are made in two distinct stages. The first stage is to prepare the starting material bis-(methyl-2-arylidenehydrazone-carbodithioates) via a condensation reaction between methyl-hydrazinecarbodithioate and dicarbonyl compounds in suitable solvent as isopropyl alcohol.
Angew Chem Int Ed Engl
July 2024
Department of Chemistry, University of Liverpool, Crown St., Liverpool, L69 7ZD, UK.
There are several binding groups used within molecular electronics for anchoring molecules to metal electrodes (e.g., R-SMe, R-NH, R-CS , R-S).
View Article and Find Full Text PDFAdv Mater
July 2024
School of Physical Science and Technology, ShanghaiTech University, Shanghai, 201210, China.
Accurate structure control in dissipative assemblies (DSAs) is vital for precise biological functions. However, accuracy and functionality of artificial DSAs are far from this objective. Herein, a novel approach is introduced by harnessing complex chemical reaction networks rooted in coordination chemistry to create atomically-precise copper nanoclusters (CuNCs), specifically Cu(µ-Cl)(µ-Cl)LCl (L = 4-methyl-piperazine-1-carbodithioate).
View Article and Find Full Text PDFMolecules
November 2023
Chemistry Department, Faculty of Science, South Valley University, Qena 83523, Egypt.
In this investigation, 4-antipyrinecarboxaldhyde was reacted with methyl hydrazinecarbodithioate to afford the carbodithioate derivative . The as-prepared carbodithioate derivative is considered to be a key molecule for the preparation of new antipyrine-1,3,4-thiadiazole-based molecules (-) through its reaction with the appropriate hydrazonoyl halides. Furthermore, a typical Biginelli three-component cyclocondensation reaction involving ethyl acetoacetate, 4-antipyrinecarboxaldhyde, and thiourea under the standard conditions is carried out in the presence of sulfuric acid to afford the corresponding antipyrine-pyrimidine hybrid molecule ().
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