[2. n](2, 6) Pyridinocrownophanes (3a-e) were efficiently prepared by intramolecular [2+ 2] photocycloaddition of vinylpyridine derivatives under irradiation using a 400-W high- pressure mercury lamp through a Pyrex filter. They were of cis-configuration with respect to the cyclobutane ring, which was proven by the specific methine proton NMR resonances at δ 3.98-4.08. From ESI-MS analysis 3a-e were found to form 1: 1 complexes with Ag+ cation. ...