2,7-Bis(1<i>H</i>-pyrrol-2-yl)ethynyl-1,8naphthyridine:  An Ultrasensitive Fluorescent Probe for Glucopyranoside LiaoJen-Hai ChenChao-Tsen ChouHe-Chun ChengChung-Chih ChouPi-Tai FangJim-Min SlaninaZdenek ChowTashin J. 2002 A push−pull conjugated molecule, 2,7-bis(1<i>H</i>-pyrrol-2-yl)ethynyl-1,8-naphthyridine (BPN), has been designed to bind selectively with octyl glucopyranoside (OGU). The BPN/OGU quadruple hydrogen-bonding complex adopts a rigid BPN conformation in which the <i>proton donor (d) and acceptor (a)</i> relays (<i>daad</i>) are resonantly conjugated through the ethynyl bridge, inducing π-electron delocalization, i.e., a charge transfer effect. The excellent photophysical properties make BPN a highly sensitive probe for monitoring glucopyranoside to a detection limit of ∼100 pM.