I have to check out that reference sometime when I can access the full text, but I don't think that real high-molecular-weight polyacetylene is soluble in anything.
I also don't think that Diels-Alder crosslinking reaction is going to happen very efficiently. What you'll probably wind up with is a mass of crosslinked carbon.
Most importantly, polyacetylene is (CH)n, meaning that you have a mole of hydrogen to get rid of. You would need some kind of oxidizing agent in your scheme.
I've made polyacetylene before; it's a black, intractable, insoluble crud. Difficult to work with.