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首页> 外文期刊>Journal of the American Chemical Society >KINETICS AND MECHANISM OF THE SODIUM CATION COMPLEXATION BY 5,11,17,21-TETRA-P-TERT-BUTYL-25,26,27,28-TETRAMETHOXY-CALIX[4]ARENE IN SOLUTION
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KINETICS AND MECHANISM OF THE SODIUM CATION COMPLEXATION BY 5,11,17,21-TETRA-P-TERT-BUTYL-25,26,27,28-TETRAMETHOXY-CALIX[4]ARENE IN SOLUTION

机译:5,11,17,21-四-对-叔丁基-25,26,27,28-四甲基-杯[4]芳烃溶液中钠阳离子络合的动力学和机理

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The kinetics and the mechanism of complexation of the sodium cation by the title compound (1) were studied in a 1:1 (v/v) mixture of chloroform and acetonitrile using Na-23 and 2D-EXSY H-1 NMR. The results show the formation of a 1:1 complex where the calixarene is fixed in the cone conformation, (Na,c)(+), with an equilibrium constant of formation of (9.3 +/- 0.7) x 10(2) at 320 K with Delta H = -22 +/- 2 kJ mol(-1) and Delta S = -7 +/- 5 J mol(-1) K-1. The exchange of the sodium cation between the solvated and the complexed sites follows a dissociation/recombination mechanism, with a dissociation rate constant of 37.3 +/- 0.4 s(-1) at 300 K. The kinetic parameters for the dissociation are Delta H double dagger = 47 +/- 2 kJ mol(-1) and Delta S double dagger = -61 +/- 6 J mol(-1) K-1. Calixarene 1 shows an intermediate behavior between crown ethers and cryptands for the complexation processes of the sodium cation in solution, dissociating with rates in the typical orders of magnitude found for crown ethers, but with rates of formation in the range of those typically found for cryptands. [References: 44]
机译:使用Na-23和2D-EXSY H-1 NMR在氯仿和乙腈的1:1(v / v)混合物中研究了标题化合物(1)引起的钠阳离子络合的动力学和机理。结果表明形成了1:1络合物,其中杯芳烃固定在视锥构象(Na,c)(+)中,在形成时的平衡常数为(9.3 +/- 0.7)x 10(2) 320 K,Delta H = -22 +/- 2 kJ mol(-1)和Delta S = -7 +/- 5 J mol(-1)K-1。溶剂化位点和络合位点之间的钠阳离子交换遵循解离/重组机制,在300 K时解离速率常数为37.3 +/- 0.4 s(-1)。解离的动力学参数为Delta H double匕首= 47 +/- 2 kJ mol(-1)和Delta S双匕首= -61 +/- 6 J mol(-1)K-1。在溶液中钠阳离子的络合过程中,杯芳烃1显示冠醚和穴状配体之间的中间行为,与冠状醚发现的典型量级速率发生解离,但形成速率在穴状配体通常发现的范围内。 [参考:44]

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