Interfaces, Traitements, Organisation et Dynamique des Systèmes, Université Paris 7-CNRS UMR 7086, Bât. Lavoisier, 15 rue Jean Antoine de Baïf, 75205 Paris Cedex 13, France.
J Phys Chem B. 2010 Oct 7;114(39):12655-65. doi: 10.1021/jp1060232.
Norbadione A (NbA) is a mushroom pigment, which is assumed to be involved in (137)Cs accumulation all over Europe during the Chernobyl nuclear accident. NbA bears seven acid-base functional groups, among which are two enolic and two carboxylic acid moieties. This work deals with complex formation of Cs(+) and NbA in ethanol, ethanol/water (9:1) (M1), and water with, when required, the support of two Cs(+) ionophore probes, calix[4]arene-bis(crown-6-ether)dioxycoumarine (A1) and its tetrasuslfonated form (A2). In ethanol, two Cs(+) complexes are formed, with the affinity constants K(1EtOH) = (1.1 ± 0.25) × 10(5) and K(2EtOH) = (2.1 ± 0.4) × 10(3). In M1, a single Cs(+) complex occurs when only the enols are deprotonated, whereas a bicomplex is formed when both enols and carboxylic acids are deprotonated: K(1M1) = (1.5 ± 0.3) × 10(5) and K(2M1) = (4 ± 2) × 10(3). These data are confirmed by stopped-flow and T-jump kinetics. In ethanol, a fast Cs(+) exchange occurs between NbA and A1: direct rate constant, k(1) = (3.1 ± 0.1) × 10(7) M(-1) s(-1); reverse rate constant k(-1) = (2.8 ± 1) × 10(5) M(-1) s(-1); and Cs(+) exchange constant, K(1Exchange) = (9 ± 4) × 10(-3). In M1, the quenching of A2 fluorescence by NbA is used to determine the kinetics of complex formation with Cs(+): k(2) = (1.8 ± 0.4) × 10(9) M(-1) s(-1); k(-2) = (1.80 ± 0.15) × 10(4) s(-1); and K(1M1) = (1.5 ± 0.5) × 10(5). The affinity of NbA for Cs(+) is probably the result of the particular structure in which the two pulvinic acid arms adopt a conformation that forms two complexation sites composed of the two enolates and/or the two carboxylates. This renders the efficiency in Cs(+) uptake comparable to that of some calixarenes or crown ethers.
北美鞣花酸(NbA)是一种蘑菇色素,据推测它在切尔诺贝利核事故期间参与了欧洲各地(137)Cs 的积累。NbA 具有七个酸碱官能团,其中包括两个烯醇和两个羧酸部分。这项工作涉及到 Cs(+)与 NbA 在乙醇、乙醇/水(9:1)(M1)中的配合物形成,以及在需要时使用两种 Cs(+)离子载体探针,杯[4]芳烃-双(冠醚-6-醚)氧杂蒽(A1)及其四磺酸形式(A2)的支持。在乙醇中,形成了两种 Cs(+)配合物,亲和常数 K(1EtOH) = (1.1 ± 0.25) × 10(5) 和 K(2EtOH) = (2.1 ± 0.4) × 10(3)。在 M1 中,当只有烯醇被去质子化时,会形成单个 Cs(+)配合物,而当两个烯醇和羧酸都被去质子化时,会形成双配合物:K(1M1) = (1.5 ± 0.3) × 10(5) 和 K(2M1) = (4 ± 2) × 10(3)。这些数据通过停流和 T-跳跃动力学得到证实。在乙醇中,NbA 和 A1 之间发生快速 Cs(+)交换:直接速率常数 k(1) = (3.1 ± 0.1) × 10(7) M(-1) s(-1);反向速率常数 k(-1) = (2.8 ± 1) × 10(5) M(-1) s(-1);和 Cs(+)交换常数 K(1Exchange) = (9 ± 4) × 10(-3)。在 M1 中,用 NbA 猝灭 A2 荧光来测定与 Cs(+)形成配合物的动力学:k(2) = (1.8 ± 0.4) × 10(9) M(-1) s(-1);k(-2) = (1.80 ± 0.15) × 10(4) s(-1);和 K(1M1) = (1.5 ± 0.5) × 10(5)。NbA 对 Cs(+)的亲和力可能是由于其特殊的结构所致,其中两个 Pulvinic 酸臂采用一种构象,形成由两个烯醇盐和/或两个羧酸盐组成的两个配位位点。这使得 Cs(+)摄取的效率可与某些杯芳烃或冠醚相媲美。