• Bulletin of the Korean Chemical Society
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• v.26 no.3
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• pp.470-472
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• 2005

• Bulletin of the Korean Chemical Society
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• v.24 no.2
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• pp.165-166
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• 2003

• Bulletin of the Korean Chemical Society
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• v.24 no.5
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• pp.681-683
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• 2003

• Proceedings of the Membrane Society of Korea Conference
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• 1998.10a
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• pp.31-36
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• 1998

1. 서론 : 산업이 고도로 발달함에 따라 야기되는 환경오염의 심각성이 날로 더해가고 있다. 특히 원자력 관련시설중 핵연료 재활용 공정에서 발생되는 방사성 폐기물의 처리기술에 대한 개발이 무엇보다도 시급한 실정이다. 핵연료 재활용 조작은 고준위 및 중준위 방사능 액체 폐기물을 발생시키며 이러한 방사능 액체 폐기물의 주요핵종은 긴 반감기를 갖는 것들이다. 이러한 방사능 액체 폐기물의 무해한 저장을 위해서 세계적으로 노력해 왔으며 고준위 폐기물은 유리화한후 심층매립을 하는 것이 가장 안전한 방법으로 고려되고 있다.(생략)

• Bulletin of the Korean Chemical Society
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• v.17 no.6
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• pp.525-528
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• 1996

Seven cali[4]arenes, having two different substituents in AAAB or AABB pattern at the upper rim of calix were synthesized by fragmentation condensation reaction of p-substituted phenol trimer (AAA) with 2,6-bishydroxymethylated 4-substituted phenol (B) or that of dimer (AA) with 2,2'-bishydroxymethylated dimer (BB). An equimolar mixture of the coupling components (trimer and monomer or dimer and dimer) was refluxed in dioxane in the presence of TiCl4to afford calix[4]arene 6 and 7 in 15-38% yield. The structure of calix[4]arenes was confirmed by elemental analysis and the 1H/13C NMR spectroscopy.

• Bulletin of the Korean Chemical Society
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• v.25 no.1
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• pp.55-58
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• 2004

In this study we have performed ab initio computer simulations to investigate the conformational characteristics of the tetramethoxycalix[4]arenes (1 and 2). The structures of four types (cone, partial cone, 1,2-alternate, and 1,3-alternate) of conformers for each compound have been optimized using ab initio RHF/6-31G and 6-31$G^{**}$ methods. General trends in relative stabilities of tetramethyl ether derivatives of calix[4]arene 1 and p-tert-butylcalix[4]arene 2 are similar and decrease in following order: partial cone (most stable) > cone > 1,3-alternate > 1,2-alternate. The calculated results of the most stable conformation of partial cone structure agree with the reported NMR experimental observations.

• Bulletin of the Korean Chemical Society
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• v.25 no.2
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• pp.177-181
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• 2004

A PVC membrane electrode for silver ion based on a new cone shaped calix[4]arene (CASCA) as membrane carrier was prepared. The electrode exhibits a Nernstian response for $Ag^+$ over a wide concentration range ($1.0{\times}10^{-1}-8.0{\times}10^{-6}$M) with a slope of 58.2 {\pm}$ 0.5 mV per decade. The limit of detection of the sensor is $5.0{\times}10^{-6}$M. The sensor has a very fast response time (~5 s) in the concentration range of ${\leq}=1.0{\times}10^{-3}$ M, and a useful working pH range of 4.0-9.5. The proposed sensor displays excellent discriminating ability toward $Ag^+$ ion with respect to common alkali, alkaline earth, transition and heavy metal ions. It was used as an indicator electrode in potentiometric titration of $Ag^+$ with EDTA and in direct determination of silver ion in wastewater of silver electroplating.

• Korean Journal of Crystallography
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• v.12 no.2
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• pp.92-96
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• 2001

The configuration of the title compound, $C_{52}H_{70}Cl_2O_6$, synthesized from a mixture of p-tert-calix[4]arene, tosylate of 2-(2-chloroethoxy)ethanol, $K_2CO_3$ and acetonitrile has a distorted cone conformation and the molecule is stabilized by two intramolecular hydrogen bonds between oxy-gen atoms of hydroxy groups and dichloride tails.

• Bulletin of the Korean Chemical Society
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• v.18 no.1
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• pp.86-91
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• 1997

Complexation of primary alkylammonium ions by 1, 3-distal calix[4]arene diesters was studied by NMR spectroscopy. The guest alkylammonium ions are found to bind mainly to the two ester moieties and are oriented outward with respect to the cone cavity of the host, forming exo-type complexes unlike the case of alkylammonium-calix[6]arene systems. Measurement of T1 also revealed that the primary binding site is the two ester moities and phenolic OH groups. The temperature dependence of the chemical shifts of phenolic OH protons in these diesters correlates with the basicity of the solvent moderately well and the temperature coefficients of their chemical shifts are found to significantly decrease upon complexation with propylammonium ion.

• Bulletin of the Korean Chemical Society
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• v.23 no.4
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• pp.640-642
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• 2002