Four approaches have been explored for the preparation of maleimido-functionalized self-assembled monolayers (SAMs) on silicon. SAMs prepared by self-assembly of maleimido-functionalized alkyltrichlorosilanes (11-maleimido-undecyl-trichlorosilane) on oxide-covered silicon yield higher signals from maleimido functionalities in ATR-IR (attenuated total reflection IR) spectroscopy and XPS (X-ray photoelectron spectroscopy) than the other three methods. The surface composition of maleimido groups was tailored further by the formation of mixed monolayers with nonfunctionalized alkyltrichlorosilanes (decyltrichlorosilane). The order of the alkyl chains within the monolayers only slightly depends on the composition of the mixed monolayers. We utilized the maleimido-terminated SAMs to bind various nucleophilic compounds, alkylamines, alkylthiols, and thiol-tagged DNA oligonucleotides by means of conjugate addition.
Kirakosian, A.; Rauscher, H.; Himpsel, F.J.; and Dowben, Peter A., "Self-assembled Fe nanowires using organometallic chemical vapor deposition and CaF 2 masks on stepped Si(111)" (2001). Peter Dowben Publications. 96.
Recent advances in the control of thin films and surfaces have brought an intriguing question within reach: Is it possible to tailor the electronic properties of solids by controlling them layer by layer or row by row? Customized molecules are commonplace in biochemistry. Can the same idea be brought to bear on solids and electronic materials? Electronic properties of semiconductor devices have been controlled by hetero-structures, quantum wells, and super-lattices. Magnetism as a cooperative phenomenon lends itself to manipulation in small structures, where neighbor atoms can be replaced systematically by species with stronger or weaker magnetism. In fact, a class of magnetic/nonmagnetic multilayers termed spin valves has recently been introduced into commercial read heads for magnetically stored data. The optimum thickness of their active region lies in the single-digit-nanometer regime.The smallest nanostructures may be viewed as objects consisting only of interfaces with no bulk behind them. More typically, single-digit-nanometer dimensions are sufficient for realizing the benefits of structuring (e.g., operating a quantum-well device at room temperature). This regime is difficult to reach with lithography methods, particularly when macroscopic amounts are to be fabricated. Self-assembly becomes the method of choice.
Metallocene adsorption on clean Si͑111͒ and CaF 2 /CaF 1 /Si͑111͒ substrates has been investigated with scanning tunneling microscopy. The surface chemical composition is found to strongly change the adsorption site selectivity, leading to an enhanced edge selectivity on modified substrates. Templates with well-defined local chemical reactivity have been created via self-assembly. The selective adsorption of metallocenes on such tailored substrates facilitates patterning ordered arrays of magnetic nanowires and stripes on the single digit nanometer scale.
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