1996
DOI: 10.1038/384150a0
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Self-replicating amphiphilic monolayers

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Cited by 126 publications
(120 citation statements)
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“…14,15,[32][33][34] Chlorosilane head groups of the OTS molecules are prone to react with both the terminal amine group of APTMS and the -OH and COO -groups of citrate capping the NPs. [35][36][37] Moreover, OTS can polymerized laterally, though siloxane bonds, forming a capping layer over the surface and NPs. Evidence of the correct grafting of OTS is the observation of an increase of the water contact angle from ∼30-40° for APTMS/NPs surface to ∼90-100° after silanization.…”
Section: Resultsmentioning
confidence: 99%
“…14,15,[32][33][34] Chlorosilane head groups of the OTS molecules are prone to react with both the terminal amine group of APTMS and the -OH and COO -groups of citrate capping the NPs. [35][36][37] Moreover, OTS can polymerized laterally, though siloxane bonds, forming a capping layer over the surface and NPs. Evidence of the correct grafting of OTS is the observation of an increase of the water contact angle from ∼30-40° for APTMS/NPs surface to ∼90-100° after silanization.…”
Section: Resultsmentioning
confidence: 99%
“…Furthermore, Maoz et al developed a unique technique for preparing multilayers. 19 Their process was based on the formation of alkylsilane bilayers from alkyltrichlorosilanes within the polar interlayer region of preorganized organosilane bilayers. The growth of multilayers is performed by the repeated intercalation of the alkylsilane bilayers, enabling control of the number of stacked bilayers.…”
Section: Multilayered Hybrids Derived From Trifunctional Alkylsilanesmentioning
confidence: 99%
“…The combined use of these techniques with others, such as photolithography, allows also the organization of carbon nanotubes on a surface [15]. Furthermore, sequential self-assembly of SAM can be used to create 3D structures [3,29,30,45].…”
Section: Self-assembly: Interestmentioning
confidence: 99%