Two new chromogenic and fluorescent probes for anions have been designed, synthesized, and characterized. These probes contain multiple hydrogen bonding donors including hydrazine, hydrazone, and hydroxyl functional groups for potential anion interacting sites. Despite the possible flexible structural framework due to the presence of sp3 carbon linkage, X-ray structure analysis of probe 2 displayed an essentially planar conformation in the solid state owing to strong crystal packing interactions comprising a combination of favorable pi-pi stacking effect and hydrogen bonding to cocrystallized CH3OH molecules. Both probes 1 and 2 display orange color in DMSO solution and show fairly weak fluorescence at room temperature. Binding studies revealed that both probes 1 and 2 show noticeable colorimetric and fluorescent responses only to F-, OAc-, and H2PO4- among the nine anions tested (F-, Cl-, Br-, I-, OAc-, H2PO4-, HSO4-, ClO4-, and NO3-). The general trend of the sensitivity to anions follows the order of F- > OAc- > H2PO4- > Cl- > Br- approximately I- approximately HSO4- approximately ClO4- approximately NO3-. A 1:2 (probe to anion) binding stoichiometry was found for probe 1 with OAc- and H2PO4- and probe 2 with F-, OAc-, and H2PO4-. The binding isotherm of probe 1 to F- was found to be complicated with apparent multiple equilibria occurring in solution. The formation of an aggregated supramolecular complex upon addition of fluoride is proposed to rationalize the observed optical responses and is supported by ESI mass spectrometry and pulsed-field gradient NMR spectroscopy. Data analysis suggests that the binding of probe 1 to F- shows positive homotropic cooperativity.

The reaction of (η4-MeC5H5)Fe(CO)2(η1-dppm), 1, with M(CO)3L3 produced (η5-MeC5H4)Fe(CO)(μ-η1:η1-dppm)(μ-H)M(CO)4, 3 (L3 = (C2H5CN)3, (THF)3, C7H8; M = W, Mo). The novel hydrido-bridged Fe(II)−M(0) compound was likely formed via the following steps:  coordination of the monodentate dppm to M and then CO migration from Fe to M with a sequential or concerted oxidative addition of the endo-C−H bond of the η4-MeC5H5 ligand to give the (η5-MeC5H4)FeH complex, followed by a trapping of the Fe−H bond by M, forming a six-membered heterocyclic ring in 3.