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Polarizability reflects the response of the molecular charge distribution to an applied external electric field and thus closely relates to the molecular electron density. For the calculation of polarizability within density functional theory (DFT), it is well known that conventional density functional approximations (DFAs) greatly overestimate the results for polymers with long chains and the π-conjugated system. This is a manifestation of the delocalization error of the commonly used DFAs-they normally produce too delocalized electron de