1998
DOI: 10.1002/(sici)1521-3773(19981002)37:18<2466::aid-anie2466>3.3.co;2-v
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Colloid-Bound Catalysts for Ring-Opening Metathesis Polymerization: A Combination of Homogenous and Heterogeneous Properties

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Cited by 42 publications
(56 citation statements)
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“…Applications of thiol-stabilized AuNPs in catalysis include the asymmetric dihydroxylation reactions, [94] carboxylic ester cleavage, [95] electrocatalytic reductions by anthraquinone functionalized AuNPs, [96] and particle-bound ring opening metathesis polymerization. [97] These catalytic applications have in common the exploitation of the carefully designed chemical functionality of the ligand shell, rather than the potential catalytic activity of a nanostructured clean metal surface. One of the most prominent potential long-term applications for AuNPs and clusters is the development of new, ultimately small electronic devices.…”
Section: Applicationsmentioning
confidence: 99%
“…Applications of thiol-stabilized AuNPs in catalysis include the asymmetric dihydroxylation reactions, [94] carboxylic ester cleavage, [95] electrocatalytic reductions by anthraquinone functionalized AuNPs, [96] and particle-bound ring opening metathesis polymerization. [97] These catalytic applications have in common the exploitation of the carefully designed chemical functionality of the ligand shell, rather than the potential catalytic activity of a nanostructured clean metal surface. One of the most prominent potential long-term applications for AuNPs and clusters is the development of new, ultimately small electronic devices.…”
Section: Applicationsmentioning
confidence: 99%
“…They found much higher turnover frequencies for the surfacebound Ru catalyst compared to the same catalyst in bulk solution. [132] This phenomenon is tentatively attributed to the favorable orientation of the Ru species, which facilitates their interactions with the growing polymer chain. Most mechanistic studies in SAMs, however, report diminished reactivity (vide infra), due to partially blocked access of an external reagent to the monolayer-embedded reaction center.…”
Section: ªStericº Effects In Monolayersmentioning
confidence: 99%
“…[8] In previous studies we employed SAMs of various thiols for a number of applications such as direct crystallization or polymerization catalysis. [9] The use of thiol monolayer surfaces on gold has been extended by us to the use of thiol coated gold colloids. This has opened new dimensions in the chemistry of protected surfaces as colloids show a similar behavior as molecules, that is they can be precipitated or redissolved.…”
Section: Introductionmentioning
confidence: 99%