Thursday, July 1, 2010, 11:00 am — CFN, Bldg 735, Conference Room B
One of the key challenges in molecular machines and devices is the reproducible assembly of functional units in an addressable arrangement. By combining concepts of supra-molecular chemistry [1] and surface science, increasingly complex functional layers have been manufactured and explored. Site specific molecular interaction is the generic origin of molecular self assembly [2] and distinctively different mechanisms have been identified: Selective chemical bonding [3], conformational bi-stability [4], and 2D phase behaviour [5] produce distinctly different functional layers. Binary molecular systems which involve longer range dipole forces and entropic mobility provide the basis for an increased periodicity [5]. In conjunction with a conformational mechanism the spacing between individual supramolecular units has very recently been increased to 7.2 nm [6]. Beyond supra-molecular assembly, extended networks have been created by a thermally activated chemical reaction [7] and have been used as a template for supra-molecular organisation of ad molecules [8], and for the confinement of coupled quantum dots from delocalised substrate electronic states [9]. A single chain covalent polymer has also been formed [10]. Ultimately, adressable supra-molecular rotor-stator systems [11,12], in particular a supra-molecular rotational switch [12] have been described. Molecular layers on insulator thin films [13] and on ferromagnetic substrates [14] have been characterised for their electronic and magnetic coupling. Notably also tunable porous networks [15] and supramolecular macroscycles [16] have been described, as well as self assembling arrays of C60 / Phthalocyanine systems [17].
Hosted by: Peter Sutter
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