Reyheller Carsten, Kubik Stefan
Fachbereich Chemie-Organische Chemie, Technische Universität Kaiserslautern, Erwin-Schrödinger-Strasse, D-67663 Kaiserslautern, Germany.
Org Lett. 2007 Dec 6;9(25):5271-4. doi: 10.1021/ol702386e. Epub 2007 Nov 15.
Fluorescence of a bis(cyclopeptide) in which two cyclohexapeptide moieties with alternating L-proline and 6-aminopicolinic acid subunits are attached to a 4,4'-bis(dimethylamino)biphenyl linker is quenched in 1:1 (v/v) water/methanol in the presence of sulfate. Of eight other anions tested, none produced a similar effect. This bis(cyclopeptide) allows the qualitative and quantitative detection of sulfate even in the presence of an excess of chloride anions. Calculations provided insight into the causes of fluorescence quenching and anion selectivity.
一种双(环肽)的荧光被淬灭,该双(环肽)中两个具有交替的L-脯氨酸和6-氨基吡啶甲酸亚基的环己肽部分连接到一个4,4'-双(二甲氨基)联苯连接基上,在1:1(v/v)水/甲醇中,在硫酸根存在的情况下会发生这种情况。在测试的其他八种阴离子中,没有一种产生类似的效果。这种双(环肽)即使在存在过量氯离子的情况下也能对硫酸根进行定性和定量检测。计算结果有助于深入了解荧光淬灭和阴离子选择性的原因。