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Effects of Solvent Composition and Temperature on K+–18-Crown-6 Complexation in Acetonitrile–Water Mixed Solvents

机译:溶剂组成和温度对乙腈-水混合溶剂中K + –18-Crown-6络合的影响

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摘要

Complexation of K+ by 18-crown-6 ether (18C6) in pure water and in acetonitrile–water mixed solvents containing 0.1 mol-dm− 3 (C2H5)4NCl has been systematically studied by isothermal titration calorimetry (ITC) at 293, 298, and 303 K. The formation constant K of the 1:1 [K(18C6)]+ complex and the complexation enthalpy Δ rH were simultaneously determined from the titration data. The logK and Δ rH(kJ-mol− 1) values at 298 K are 2.04, −26.2 in pure water and 2.23, −25.0; 2.61, −24.2; 2.95, −23.8; 3.48, −21.0; 3.85, −19.4; 4.36, −18.7; and 5.73, −17.0 in the mixed solvents at x AN (mole fraction of acetonitrile) of 0.043, 0.135, 0.258, 0.448, 0.578, 0.759, and 1.0, respectively. The change in heat capacity for the complex formation, Δ C p °, was also determined by the temperature dependence of Δ rH. Whereas the Δ C p ° is (57 ± 11) and (63 ± 20) J-mol− 1-K− 1 in pure water and in the solvent mixture at x AN = 0.043, respectively, it decreases with increasing x AN. The Δ C p ° values are −(48 ± 11), −(110 ± 25), −(354 ± 40), −(359 ± 24), and −(304 ± 30) J-mol− 1-K− 1 at x AN = 0.135, 0.258, 0.448, 0.578, and 0.759, respectively. The changes in complexation thermodynamics (Δ Δ rG, Δ ΔrH, and Δ Δ r S) are discussed in terms of the corresponding transfer thermodynamics of K+, 18-crown-6, and [K(18C6)]+ upon transferring from water to acetonitrile–water mixed solvents. It was found that hydrophobic solvation of the complex [K(18C6)]+ plays an important role in complex formation occurring in water and in the water-rich mixed solvent. Moreover, changes in solvent structure significantly affect the transfer enthalpy and entropy of each species, i.e., K+, 18-crown-6, and [K(18C6)]+. The observed monotonous changes in the complexation Gibbs energy, enthalpy, and entropy with solvent composition are due to the effective compensation of the Δ trG, Δ trH, and Δ tr S for K+ with those for 18-crown-6 and [K(18C6)]+.
机译:18冠-6醚(18C6)在纯水和含0.1 mol-dm−3 (C2 H5 )的乙腈-水混合溶剂中络合K + 通过等温滴定热法(ITC)在293、298和303 K上系统地研究了4 NCl。1:1 [K(18C6)] + 配合物的形成常数K和配合物从滴定数据同时确定焓ΔrH。 298 K的logK和Δr H(kJ-mol-1 )值在纯水中分别为2.04,-26.2和2.23,-25.0; 2.61,-24.2; 2.95,-23.8; 3.48,-21.0; 3.85,-19.4; 4.36,-18.7;在混合溶剂中,x AN(乙腈的摩尔分数)分别为0.043、0.135、0.258、0.448、0.578、0.759和1.0时的5.73,-17.0。配合物形成的热容量变化ΔC p ,也取决于Δr H的温度依赖性。在纯净水和xAN上的溶剂混合物中,ΔC p °为(57±11)和(63±20)J-mol− 1 -K−1 = 0.043,它随x AN的增加而减小。 ΔC p °值为-(48±11),-(110±25),-(354±40),-(359±24)和-(304±30)J-mol-在x AN 分别为1 -K-1 = 0.135、0.258、0.448、0.578和0.759。根据相应的K + 传递热力学,讨论了络合热力学的变化(ΔΔr G,ΔΔr H和ΔΔr S)。 -crown-6和[K(18C6)] + 从水转移到乙腈-水混合溶剂中。研究发现,复合物[K(18C6)] + 的疏水溶剂化作用在水和富水混合溶剂中形成的复合物中起着重要的作用。此外,溶剂结构的变化显着影响每种物质,即K + ,18-crown-6和[K(18C6)] + 的转移焓和熵。观察到的吉布斯能量,焓和熵与溶剂组成的单调变化是由于有效地补偿了Δtr,Δtr H和Δtr S K + 以及18-crown-6和[K(18C6)] + 的那些。

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