Singlet fission (SF), in which two triplet excitons are generated from a single absorbed photon, is a key third generation solar cell concept. Conservation of angular momentum requires that SF populates correlated multiexciton states, which can subsequently dissociate to generate free triplets. However, little is known about electronic and spin correlations in these systems since, due to its typically short lifetime, the multiexciton state is challenging to isolate and study. Here, we use bridged pentacene dimers, which undergo intramolecular SF while isolated in solution and in solid matrices, as a unimolecular model system that can trap long-lived multiexciton states. We combine transient absorption and time-resolved electron spin resonance (ESR) spectroscopy to show that spin correlations in the multiexciton state persist for 100s of nanoseconds. Furthermore, we confirm longstanding predictions that SF produces triplet pair states (TT) of quintet character -the first direct observation of quintet states in closed shell organic molecules. We compare two different pentacene-bridge-pentacene chromophores, systematically tuning the coupling between the pentacenes to understand how differences in molecular structure affect the population and dissociation of multiexciton quintet states.