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首页> 外文期刊>Inorganica Chimica Acta >COMPLEXES OF P-TERT-BUTYLCALIX[4]ARENE WITH MONO- AND DIPOSITIVE CATIONS IN THE GAS PHASE
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COMPLEXES OF P-TERT-BUTYLCALIX[4]ARENE WITH MONO- AND DIPOSITIVE CATIONS IN THE GAS PHASE

机译:气相中对叔叔丁基杯[4]芳烃与单和正阳离子的络合物

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The host-guest chemistry of p-tert-butyl-calix[4]arene in the gas phase was studied using Fourier transform ion cyclotron resonance mass spectrometry. Gas phase complexes with laser-desorbed alkali metal cations (Na+, K+, Rb+ and Cs+) were generated. The calixarene was observed to complex with up to two metal cations at the same time with the accompanying loss of a proton, to yield species with a net charge of +1. Complexes with Sr2+, and Ba2+, with accompanying loss of a proton to maintain a net charge of +1, were also observed. Relative rate constants and reaction efficiencies for the formation of the 1:1 calixarene/alkali metal complexes vary inversely with cation size, probably reflecting differences in the polarizing capabilities of the cations. Reaction of the alkali metal and alkaline earth complexes with 15-crown-5 results in adduction of the crown in cases where the metals are large, suggesting the larger cations bind in exposed positions on the calixarene. Finally, complexes of the calixarene with benzylammonium cation were observed. Equilibrium measurements indicate Delta G degrees(350) for transfer of benzylammonium from the calixarene to 15-crown-5 is -9.1 +/- 0.4 kJ mol(-1). [References: 45]
机译:使用傅里叶变换离子回旋共振质谱法研究了气相中对叔丁基杯[4]芳烃的客体化学性质。生成了具有激光解吸的碱金属阳离子(Na +,K +,Rb +和Cs +)的气相络合物。观察到杯芳烃同时​​与多达两个金属阳离子络合,伴随着质子的损失,产生净电荷为+1的物质。还观察到具有Sr2 +和Ba2 +的配合物,伴随着质子的损失,以保持+1的净电荷。形成1:1杯芳烃/碱金属配合物的相对速率常数和反应效率与阳离子大小成反比,这可能反映了阳离子极化能力的差异。碱金属和碱土金属配合物与15-crown-5的反应在金属较大的情况下导致冠的加成,表明较大的阳离子结合在杯芳烃的暴露位置。最后,观察到杯芳烃与苄基铵阳离子的配合物。平衡测量表明,苄基铵从杯芳烃到15-crown-5的转移的Delta G度(350)为-9.1 +/- 0.4 kJ mol(-1)。 [参考:45]

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