Amphiphilic diblock dendrimers: Synthesis and incorporation in Langmuir and Langmuir-Blodgett films

Citation
Jf. Nierengarten et al., Amphiphilic diblock dendrimers: Synthesis and incorporation in Langmuir and Langmuir-Blodgett films, J AM CHEM S, 123(40), 2001, pp. 9743-9748
Citations number
52
Categorie Soggetti
Chemistry & Analysis",Chemistry
Journal title
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
ISSN journal
00027863 → ACNP
Volume
123
Issue
40
Year of publication
2001
Pages
9743 - 9748
Database
ISI
SICI code
0002-7863(20011010)123:40<9743:ADDSAI>2.0.ZU;2-R
Abstract
A new dendron with peripheral long alkyl chains and containing five C-60 un its in the branching shell has been prepared and attached to a Frechet-type dendron functionalized with ethylene glycol chains. The peripheral substit ution of the resulting globular dendrimer with hydrophobic chains on one he misphere and hydrophilic groups on the other provides the perfect hydrophob ic/hydrophilic balance allowing the formation of stable Langmuir films. Fur thermore, a perfect reversibility has been observed in successive compressi on/decompression cycles. The diblock structure of the dendrimer has been al so crucial for the efficient transfer of the Langmuir films in order to obt ain well-ordered multilayered Langmuir-Blodgett films. This approach appear s particularly interesting since functional groups not well adapted for the preparation of Langmuir and Langmuir-Blodgett films such as fullerenes can be attached into the branching shell of the dendritic structure and, thus, efficiently incorporated in thin ordered films.