RESUMO
Impedance spectroscopy can be used to determine the influence of several membrane parameters on the membrane resistance of anion selective CHEMFETs. The concentration of the ammonium sites in the membrane, the anion-receptor complex stoichiometry, and the polarity of the membrane matrix are of particular importance. In general the resistance of polysiloxane membranes is higher than that of PVC membranes. However, in polysiloxane membranes the membrane polarity can be influenced by the type or concentration of polar substituents on the polysiloxane chain. Polysiloxane ion-exchange membranes with 25 mol% of polar sulfone substituents exhibit the same conductance as NPOE plasticized PVC membranes. Remarkably, the membrane resistance of cation-selective polysiloxane membranes is much lower and is much less dependent on the substituents.
Assuntos
Ânions/química , Membranas Artificiais , Algoritmos , Impedância Elétrica , Análise EspectralRESUMO
Herein we describe our results on the characterization of a wide variety of different hydrogen-bonded assemblies by means of a novel matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) technique with Ag+ labeling. The labeling technique with Ag+ ions is extremely mild and provides a nondestructive way to generate charged assemblies that can be detected by mass spectrometry. Up to now more than 25 different single (1(3).2(3)), double (3(3).2(6)), and tetrarosettes (4(3).2(12)) have been successfully characterized by the use of this method. The success of the method entirely depends on the presence of a suitable binding site for the Ag+ ion. A variety of functionalities has been identified that provide strong binding sites for Ag+, either acting in a cooperative way (pi-arene and pi-alkene donor functionalities) or individually (cyano and crown ether functionalities). The method works well for assemblies with molecular weights between 2,000 and 8,000 Da, and most likely far beyond this limit.
