2018
DOI: 10.1039/c8sc00294k
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Spatially resolved acyl transfer on surface by organo-catalytic scanning probe nanolithography (o-cSPL)

Abstract: Local and catalytic acyl transfer for multipatterning of surfaces.

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Cited by 2 publications
(3 citation statements)
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“…Part of the reactants was provided on a surface in the form of a self-assembled monolayer (SAM) bearing reactive end groups, and the remaining reactants were solvated in the surrounding liquid. A chemical coupling reaction was initiated locally by mechanical application of the catalytic tip, and various chemical compounds could be grafted selectively, with a spatial resolution in the order of a few tens of nanometers. The technique could be extended to the use of a homogeneous catalyst immobilized onto the tip upon modification with an appropriate ligand (see Figure b). , The use of a homogeneous catalyst in principle opens the way to a large variety of chemical reactions. It was shown that the catalytic activity of the tip-supported catalyst was barely affected during the reaction process, and large areas could be covalently modified without significant loss of the reactivity.…”
Section: Alternative Activation Methodsmentioning
confidence: 99%
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“…Part of the reactants was provided on a surface in the form of a self-assembled monolayer (SAM) bearing reactive end groups, and the remaining reactants were solvated in the surrounding liquid. A chemical coupling reaction was initiated locally by mechanical application of the catalytic tip, and various chemical compounds could be grafted selectively, with a spatial resolution in the order of a few tens of nanometers. The technique could be extended to the use of a homogeneous catalyst immobilized onto the tip upon modification with an appropriate ligand (see Figure b). , The use of a homogeneous catalyst in principle opens the way to a large variety of chemical reactions. It was shown that the catalytic activity of the tip-supported catalyst was barely affected during the reaction process, and large areas could be covalently modified without significant loss of the reactivity.…”
Section: Alternative Activation Methodsmentioning
confidence: 99%
“…Various chemical compounds could be grafted selectively, with a spatial resolution on the order of a few tens of nanometers. 294,297306…”
Section: Toward Functional Materialsmentioning
confidence: 99%
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