Lin W.-YWang H.-WLiu Z.-CXu JChen C.-WYang Y.-CHuang S.-LYang H.-CTIEN-YAU LUH2022-12-142022-12-14200718614728https://www.scopus.com/inward/record.uri?eid=2-s2.0-34250683317&doi=10.1002%2fasia.200700011&partnerID=40&md5=8eb79b2085193343a1bd46397d7414fdhttps://scholars.lib.ntu.edu.tw/handle/123456789/626320Two dimers and a series of polymers with 5,6-endo pendant aryl groups that contain different substituents at the para positions were synthesized. The conformation and stereochemistry of the dimers and polymers were determined by nonlinear optical analysis (EFISH) as well as UV/Vis and 13C NMR spectroscopy. The chemical shifts of C7 for the polymers appeared as two peaks in the 13C NMR spectra when the substituents are electron-withdrawing groups. The percentage decrease in the relative extinction coefficient of the polymers. εd, was linearly related to the Hammett constant σ. Polynorbornenes with electron-with-drawing substituents may adopt isotactic stereochemistry with all pendant groups aligned in one direction. The nature of the interactions between neighboring chromophores may be one of the most important factors in directing the stereoregularity and conformation of these polymers. The corresponding polymers derived from the exo isomers appeared to be less stereoregular. © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.Chromophores; Pendant groups; Polynorbornenes; Ring-opening polymerization; Tacticity[SDGs]SDG14aromatic hydrocarbon; norbornane derivative; polymer; chemistry; dimerization; nuclear magnetic resonance spectroscopy; review; spectroscopy; stereoisomerism; Dimerization; Hydrocarbons, Aromatic; Magnetic Resonance Spectroscopy; Norbornanes; Polymers; Spectrum Analysis; Stereoisomerismreview10.1002/asia.200700011174589172-s2.0-34250683317