Triptycene core

However, preorganization by reversible interactions via hydrogen bonds does not necessarily need a further template such as an anion. Direct intermolecular hydrogen bonds between derivatives of isophthalic acid and 2,6-pyridine diacid were used to synthesize a series of new catenanes [17,18], rotaxanes [18c,19], and trefoil knots [20]. The interaction of dibenzylammonium cations and dibenzo[24]crown[8] [21] led to the preparation of rotaxanes by the attachment of stoppers to the thread ends (Scheme 5.5) [22], or similarly by clipping of the crown ether chain wrapped around the ammonium dumbbell [23]. Recently, several novel catenanes were synthesized via the macrocydic connection of three ammonium cations threaded through three crown ether rings attached to a triptycene core [24]. 

Hart et al P7,78 also reported the preparation of symmetric iptycenes possessing benzene cores, for example, nonadecaiptycene (50) via bicyclic vinyl halide trimerization of triptycene dimer 51, as well as the synthesis of the related asymmetric iptycenes178 (Scheme 4.16). 

A unique class of structures referred to as iptycenes has recently been reported by Hart et al. [129-131]. These architectures represent the first examples of all-hydrocarbon dendrimer prototypes. Starting with either benzene or triptycene as the initiator core, branch junctures were constructed in situ by Diels-Alder adduct formation to give the heptaiptycene (A) and the nonaiptycene (tri-... 

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