A norbornene-based cross-linker was synthesized and mixed at different loadings with two separate monomers for self-healing polymer applications: 5-ethylidene-2-norbornene (ENB) and endo-dicyclopentadiene (endo-DCPD). The monomer/cross-linker systems were polymerized by ring-opening metathesis polymerization (ROMP) with Grubbs' catalyst. The thermal-mechanical properties of the polymerized networks were evaluated by dynamic mechanical analysis (DMA) and differential scanning calorimetry (DSC) and the curing process was monitored by parallel plate oscillatory rheometry. The viscosities of the pre-polymer blends are shown to be adequately low for self-healing, and exhibit a high ROMP reactivity to form cross-linked networks with enhanced thermal-mechanical properties. The addition of cross-linker increases the glass transition temperature (T-g) and the storage modulus both above and below Tg. The storage modulus increase above Tg is used to estimate the molecular weight (M-c) between entanglements or cross-link sites for both ENB and endo-DCPD-based networks. The crosslinker also greatly accelerates network formation as defined by the gelation time. (c) 2009 Elsevier Ltd. All rights reserved.