Crankshafts: Using Simple, FlatC_2h-Symmetric Molecules to Direct the Assembly of Chiral 2D Nanopatterns

Abstract

Linear D2h-symmetric bisisophthalic acids 1 and 2 and related substances have well-defined flattened structures, high affinities for graphite, and strong abilities to engage in specific intermolecular interactions. Their adsorption produces characteristic nanopatterns that reveal how 2D molecular organization can be controlled by reliable interadsorbate interactions such as hydrogen bonds when properly oriented by molecular geometry. In addition, the behavior of these compounds shows how large-scale organization can be obstructed by programming molecules to associate strongly according to competing motifs that have similar stability and can coexist smoothly without creating significant defects. Analogous new bisisophthalic acids 3a and 4a have similar associative properties, and their unique C2h-symmetric crankshaft geometry gives them the added ability to probe the poorly understood effect of chirality on molecular organization. Their adsorption shows how nanopatterns composed predictably of a single enantiomer can be obtained by depositing molecules that can respect established rules of association only by accepting neighbors of the same configuration. In addition, an analysis of the adsorption of crankshaft compounds 3a and 4a and their derivatives by STM reveals directly on the molecular level how kinetics and thermodynamics compete to control the crystallization of chiral compounds. In such ways, detailed studies of the adsorption of properly designed compounds on surfaces are proving to be a powerful way to discover and test rules that broadly govern molecular organization in both 2D and 3D.

Molecular trapping in two-dimensional chiral organic Kagomé nanoarchitectures composed of Baravelle spiral triangle enantiomers

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Synthesis of dilactone bridged terphenyls with crankshaft architectures

“…1) by first exploring C 2h symmetric ('crankshaft'-architecture) 8 terphenyl analogs (A and B) of our previously studied DeA biphenyl lactones. 7 It is known that increasing the number of conjugated arene units in unsubstituted poligophenylenes causes a bathochromic shift in both absorbance and emission spectra and also causes a dramatic increase in fluorescence quantum yield.…”

Coronene and Phthalocyanine Trapping Efficiency of a Two-Dimensional Kagomé Host-Nanoarchitecture

“…Carboxylic groups have been grafted onto the triphenylamine group to promote intermolecular double hydrogen-bonds (O–H···O). This interaction has been successfully used to stabilize the formation of porous as well as compact nanoarchitectures on surfaces [ 41 , 42 , 43 , 44 , 45 , 46 , 47 ]. The compound-1 was synthesized according to the procedure described in ref.…”