| pubmed-article:16573125 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16573125 | lifeskim:mentions | umls-concept:C0025663 | lld:lifeskim |
| pubmed-article:16573125 | lifeskim:mentions | umls-concept:C0018026 | lld:lifeskim |
| pubmed-article:16573125 | lifeskim:mentions | umls-concept:C0205332 | lld:lifeskim |
| pubmed-article:16573125 | lifeskim:mentions | umls-concept:C1521827 | lld:lifeskim |
| pubmed-article:16573125 | lifeskim:mentions | umls-concept:C1450054 | lld:lifeskim |
| pubmed-article:16573125 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:16573125 | pubmed:dateCreated | 2006-3-31 | lld:pubmed |
| pubmed-article:16573125 | pubmed:abstractText | The preparation and properties of tert-dodecanethiol protected gold nanoparticles amenable to very rapid surface functionalization by associative mechanism is described. The new material can be easily prepared by controlling the reaction time, because only a limited but enough number of tert-dodecanethiol to stabilize the gold clusters is bond to the surface until about an hour. Accordingly, it can be isolated as a solid and handled much like the highly stabilized Brust-Schiffrin analogues, but reacted very rapidly with any molecular species containing one or multiple functional groups such as thiol, disulfide, pyridine, etc. These characteristics are ideal for the preparation of a variety of new organic-inorganic hybrid nanomaterials by coordinative self-assembly. This possibility was illustrated using meso-tetra(4-pyridyl)porphyrin, which promptly bonded to the reactive protected gold nanoparticles generating a solid that can be grown as thin films with layer-by-layer control on a suitably modified surface. | lld:pubmed |
| pubmed-article:16573125 | pubmed:language | eng | lld:pubmed |
| pubmed-article:16573125 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16573125 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:16573125 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16573125 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16573125 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16573125 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16573125 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:16573125 | pubmed:issn | 1533-4880 | lld:pubmed |
| pubmed-article:16573125 | pubmed:author | pubmed-author:TanakaHirofum... | lld:pubmed |
| pubmed-article:16573125 | pubmed:author | pubmed-author:ArakiKoitiK | lld:pubmed |
| pubmed-article:16573125 | pubmed:author | pubmed-author:OgawaTakujiT | lld:pubmed |
| pubmed-article:16573125 | pubmed:author | pubmed-author:MizuguchiEisu... | lld:pubmed |
| pubmed-article:16573125 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:16573125 | pubmed:volume | 6 | lld:pubmed |
| pubmed-article:16573125 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16573125 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16573125 | pubmed:pagination | 708-12 | lld:pubmed |
| pubmed-article:16573125 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:16573125 | pubmed:meshHeading | pubmed-meshheading:16573125... | lld:pubmed |
| pubmed-article:16573125 | pubmed:meshHeading | pubmed-meshheading:16573125... | lld:pubmed |
| pubmed-article:16573125 | pubmed:meshHeading | pubmed-meshheading:16573125... | lld:pubmed |
| pubmed-article:16573125 | pubmed:meshHeading | pubmed-meshheading:16573125... | lld:pubmed |
| pubmed-article:16573125 | pubmed:meshHeading | pubmed-meshheading:16573125... | lld:pubmed |
| pubmed-article:16573125 | pubmed:meshHeading | pubmed-meshheading:16573125... | lld:pubmed |
| pubmed-article:16573125 | pubmed:meshHeading | pubmed-meshheading:16573125... | lld:pubmed |
| pubmed-article:16573125 | pubmed:meshHeading | pubmed-meshheading:16573125... | lld:pubmed |
| pubmed-article:16573125 | pubmed:meshHeading | pubmed-meshheading:16573125... | lld:pubmed |
| pubmed-article:16573125 | pubmed:year | 2006 | lld:pubmed |
| pubmed-article:16573125 | pubmed:articleTitle | Preparation of very reactive thiol-protected gold nanoparticles: revisiting the Brust-Schiffrin method. | lld:pubmed |
| pubmed-article:16573125 | pubmed:affiliation | Research Center for Molecular-Scale Nanoscience, Institute for Molecular Science, National Institutes of Natural Science, 5-1 Higashiyama, Myodaiji-cho, Okazaki, Aichi 444-8787, Japan. | lld:pubmed |
| pubmed-article:16573125 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16573125 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
