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Synthesis of Diazacrown Ethers Containing Phenolic Side Arms and Their Complex with Divalent Metal Ions

机译:含酚侧臂的二氮杂皇冠醚及其与二价金属离子配合物的合成

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The aminomethylation of phenols with para-substituents by the Mannich reaction has successfully been accomplished to produce the Mannich bases 2-6. The compounds 7-8 have also been synthesized in order to identify the effect of the side arms and the macrocycle in the complex formation. Protonation constants and stability constants of the double armed diaza-18-crown-6 ethers 2-7 with metal ions have been determined by potentiometric method at 25 ∩ in 95 % methanol solution. Under a basic condition (pH > 8.0), the double-armed crown ethers 2-6 revealed stronger interaction with divalent metal ions than the simple diazacrown ether 1. The stability constants with these metal ions were Co 2+ < Ni2+ < Cu2+ > Zn 2+ in increasing order, which are in accordance with the order of the Williams-Irving series. The stability constants with alkali earth metal ions were Ca 2+ < Sr 2+ < Ba 2+ in increasing order, which may be explained by the concept of size effect. It is noteworthy that the hosts 2-6, which have phenolic side arms and a macrocycle, bind stronger with metal ions than the hosts 1 and 7. On the other hand, the host 8, which has phenolic side arms with a pyperazine ring,provided comparable stability constants to those with the host 3. These facts demonstrate that phenolic side arms play a more important role than the azacrown ether ring in the process of making a complex with metal ions especially in a basic condition. In particular, the log KML values for complexation of divalent metal ions with the hosts 2-6 had the sequence, i.e., 2 (R=OCH3) < 3 (R=CH3) < 4 (R=H) < 5 (R=Cl) < 6 (R=CF3). The stability constants of the hosts 5 and 6 containing an electron-withdrawing group are larger than those of the hosts 2 and 3 containing an electron-donating group. This substituent effect is attributed to the solvent effect in which the aryl oxide with an electron-donating group has a tendency to be tied strongly with protic solvents.
机译:通过曼尼希反应成功地完成了具有对位取代基的苯酚的氨甲基化反应,以制备曼尼希碱2-6。为了鉴定侧臂和大环在复合物形成中的作用,还合成了化合物7-8。通过电势法在25∩和95%甲醇溶液中,测定了带有金属离子的双分子二氮杂18-18-皇冠-6醚2-7的质子化常数和稳定性常数。在碱性条件下(pH> 8.0),双臂冠醚2-6显示出与二价金属离子的相互作用强于简单的二氮杂冠醚1。这些金属离子的稳定性常数为Co 2 + 递增,与威廉姆斯-欧文的顺序一致系列。碱土金属离子的稳定常数按递增顺序依次为Ca 2 + 大小效应的概念。值得注意的是,具有酚侧链和大环的主体2-6与金属离子的结合要强于主体1和7。另一方面,具有酚侧链和吡嗪环的主体8,提供了与主机3相当的稳定性常数。这些事实表明,在与金属离子形成络合物的过程中,尤其是在碱性条件下,酚侧臂比氮杂冠醚环起着更重要的作用。特别地,用于二价金属离子与主体2-6络合的log KML值具有以下序列,即2(R = OCH 3 )<3(R = CH 3 < / sub>)<4(R = H)<5(R = Cl)<6(R = CF 3 )。包含吸电子基团的主体5和6的稳定性常数大于包含供电子基团的主体2和3的稳定性常数。该取代作用归因于溶剂作用,其中具有给电子基团的芳基氧化物具有与质子溶剂牢固结合的趋势。

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