A novel mechanophore with acid-releasing capability is designed to produce a simple catalyst for chemical change in materials under mechanical stress. The mechanophore, based on a gem-dichlorocyclopropanated indene, is synthesized and used as a cross-linker in poly(methyl acrylate). Force-dependent rearrangement is demonstrated for cross-linked mechanophore samples loaded in compression, while the control shows no significant response. The availability of the released acid is confirmed by exposing a piece of insoluble compressed polymer to a pH indicator solution. The development of this new mechanophore is the first step toward force-induced remodeling of stressed polymeric materials utilizing acid-catalyzed cross-linking reactions.

An alkyne-azide addition, i.e., click, reaction in conjunction with an electrostatic self-assembly and covalent fixation (ESA-CF) process has been demonstrated to effectively construct a variety of unprecedented multicyclic polymer topologies. A series of single cyclic poly(tetrahydrofuran), poly(THF), precursors having an alkyne group (Ia), an azide group (Ib), two alkyne groups at the opposite positions (Ic), and an alkyne group and an azide group at the opposite positions (Id) have been prepared by the ESA-CF process. Moreover, a bicyclic 8-shaped precursor having two alkyne groups at the opposite positions (Ie) was synthesized. The subsequent click reaction of Ia with linear (IIa) and three-armed star (IIb) telechelic precursors having azide groups has been performed to construct bridged-type two-way (IIIa) and three-way (IIIb) paddle-shaped polymer topologies, respectively. Likewise, spiro-type tandem tricyclic (IVa) and tetracyclic (IVb) topologies resulted from Ib/Ic and Ib/Ie, respectively. Furthermore, three types of multicyclic topologies that are composed of repeating ring (Va), alternating ring/linear (Vb), and alternating ring/star (Vc) units have been synthesized from Id, Ic/IIa, and Ic/IIb, respectively.

A tandem alkyne-azide addition, i.e., click, and an olefin metathesis condensation, i.e., clip, reactions in conjunction with an electrostatic self-assembly and covalent fixation (ESA-CF) process, have been demonstrated as effective means to produce constructions of programmed folding of polymers having doubly fused tricyclic and triply fused tetracyclic topologies. Thus, a series of cyclic poly(tetrahydrofuran), poly(THF), precursors having an allyloxy group and an alkyne group (Ia), an allyloxy group and an azide group (Ib), and two alkyne groups (Ic) at the opposite positions was prepared by means of the ESA-CF method. The subsequent click reactions of Ia with a linear telechelic poly(THF) precursor having azide end groups (Id) and of Ib with Ic afforded a bridged dicyclic polymer (IIa) and a tandem spiro tricyclic precursor (IIb), respectively, both having two allyloxy groups at the opposite positions of the ring units. Finally, the intramolecular metathesis condensation reaction of IIa and of IIb in the presence of a Grubbs catalyst was performed to construct effectively a doubly fused tricyclic and a triply fused tetracyclic polymer topologies (III and IV), respectively.

A pair of orientationally isomeric cyclic stereoblock polylactides (PLAs) possessing head-to-head (HH) and head-to-tail (HT) linkages between the poly(L-lactide) (PLLA) and poly(Dlactide) (PDLA) segments was synthesized through click chemistry and ring-closing metathesis (RCM) of three asymmetrically functionalized telechelic precursors. Thus, α-ethenyl-ω-azido-PLLA (2a) was reacted with α-ethenyl-ω-ethynyl-PDLA (2b) and α-ethynyl-ω-ethenyl-PDLA (2c) via click chemistry to form ethenyl telechelic stereoblock PLAs with HH and HT orientations (3a and 3b), respectively. The subsequent RCM produced cyclic stereoblock PLAs with the corresponding linking manners (4a and 4b).The effect of the topology on the melting temperature of the series of isomeric linear and cyclic PLAs having the contrastive linking orientations was systematically investigated.

A new methodology for a stimuli-responsive polymer was proposed on the basis of cyclization and photocleavage. This requires only a single reaction per polymer molecule.