Six nearly monodisperse substituted poly(styrene) homopolymers, poly(styrene) (PS), poly(2-methylstyrene) (P2MS), poly(3-methylstyrene) (P3MS), poly(4-methylstyrene) (P4MS), poly(tertiary-butylstyrene) (PtBS), and poly(alpha-methylstyrene) (P alpha MS) were anionically polymerized and subsequently saturated using heterogeneous hydrogenation techniques to poly(vinylcyclohexane) (PVCH), poly(2-methylvinylcyclohexane) (P2MVCH), poly(3-methylvinylcyclohexane) (P3MVCH), poly (4-methylvinylcyclohexane) (P4MVCH), and poly(tertiary-butylvinylcyclohexane) (PtBVCH), respectively. In each case, except P alpha MS, the materials were saturated to > 99% conversion with no chain degradation. PS hydrogenations required the addition of small amounts of tetrahydrofuran to the reaction solvent cyclohexane to enhance miscibility and eliminate large-scale chain degradation. Density gradient and differential scanning calorimetry (DSC) measurements were used to characterize the density and glass transition temperature, T-g, of the unsaturated and saturated polymers. Saturation reduces the density by 3% to 11% and changes T-g substantially. The greatest variation in T-g is obtained with the 3-methyl substituted species where a 63 degrees C increase is observed, while the highest measured T-g is 186 degrees C for P2MVCH. Small-angle neutron scattering (SANS) experiments on binary mixtures of hydrogenous and deuterium labeled PVCH derivatives provided a determination of bulk chain statistics. The statistical segment length is relatively insensitive to vinylcyclohexane ring substitution, except with P3MVCH where a 20% greater value is obtained.