2017
DOI: 10.3762/bjnano.8.213
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Ester formation at the liquid–solid interface

Abstract: A chemical reaction (esterification) within a molecular monolayer at the liquid–solid interface without any catalyst was studied using ambient scanning tunneling microscopy. The monolayer consisted of a regular array of two species, an organic acid (trimesic acid) and an alcohol (undecan-1-ol or decan-1-ol), coadsorbed out of a solution of the acid within the alcohol at the interface of highly oriented pyrolytic graphite (HOPG) (0001) substrate. The monoester was observed promptly after reaching a threshold ei… Show more

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Cited by 6 publications
(4 citation statements)
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“…273 The esterification of carboxylic acid and alcohol on HOPG could be activated by increasing the precursor concentration either by ultrasonication or by extended stirring. 274…”
Section: Control Of Growth Parametersmentioning
confidence: 99%
“…273 The esterification of carboxylic acid and alcohol on HOPG could be activated by increasing the precursor concentration either by ultrasonication or by extended stirring. 274…”
Section: Control Of Growth Parametersmentioning
confidence: 99%
“…Esters, meanwhile, can be formed through reactions between carboxylic acids and alcohols. These esterification reactions also increase with temperature (61). The presence of oxygen facilitates the oxidation of alcohols to aldehydes, which can further react with carboxylic acids to form esters.…”
Section: Volatile Aroma Compoundsmentioning
confidence: 99%
“…33 A recent example, reported to be catalysed by graphite, is the ester formation between trimesic acid (TMA) (24) and 1-undecanol (25) (Scheme 5). 34 In this experiment, a TMA solution in undecanol is dropcasted on a HOPG substrate heated at 60-80 °C, and the sample is annealed at this temperature for 10 additional minutes. Subsequent STM analysis of the HOPG substrate reveals the formation of a monolayer of monoester 26.…”
Section: Ester Formationmentioning
confidence: 99%