Dendrimer-encapsulated nanoparticle precursors to supported platinum catalysts.
Journal of the American Chemical Society, ISSN: 0002-7863, Vol: 125, Issue: 48, Page: 14832-6
2003
- 274Citations
- 810Usage
- 139Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations274
- Citation Indexes274
- 274
- CrossRef213
- Usage810
- Downloads778
- Abstract Views32
- Captures139
- Readers139
- 139
Article Description
In this contribution, we report the successful preparation of supported metal catalysts using dendrimer-encapsulated Pt nanoparticles as metal precursors. Polyamidoamine (PAMAM) dendrimers were first used to template and stabilize Pt nanoparticles prepared in solution. These dendrimer-encapsulated nanoparticles were then deposited onto a commercial high surface area silica support and thermally activated to remove the organic dendrimer. The resulting materials are active oxidation and hydrogenation catalysts. The effects of catalyst preparation and activation on activity for toluene hydrogenation and CO oxidation catalysis are discussed.
Bibliographic Details
https://works.bepress.com/bert_d_chandler/10; https://digitalcommons.trinity.edu/chem_faculty/8; http://works.bepress.com/bert_d_chandler/10
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0344430094&origin=inward; http://dx.doi.org/10.1021/ja0364120; http://www.ncbi.nlm.nih.gov/pubmed/14640659; https://pubs.acs.org/doi/10.1021/ja0364120; https://works.bepress.com/bert_d_chandler/10; https://works.bepress.com/cgi/viewcontent.cgi?article=1009&context=bert_d_chandler; https://digitalcommons.trinity.edu/chem_faculty/8; https://digitalcommons.trinity.edu/cgi/viewcontent.cgi?article=1007&context=chem_faculty; http://works.bepress.com/bert_d_chandler/10; http://works.bepress.com/cgi/viewcontent.cgi?article=1009&context=bert_d_chandler; http://pubs.acs.org/doi/abs/10.1021/ja0364120
American Chemical Society (ACS)
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