• Korean Journal of Crystallography
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• v.4 no.1
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• pp.25-35
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• 1993

Tetra-tert-butyl-tetrapropionycalix (4) arena (C56H7208) is Triclinic, space group Pl, with a=13.664(5), b=17.585(5), c=12.863(2)A, a=109.33(2), B=111.97(2), γ=76.45(3) ˚, Z=2, V=2684.08A3, D, =1.152g/cm3, Dm=1.15g/cm3. The intensity data were collected on an Enraf-Nonius CAD-4 Diffractometer with a graphite monochromated Mo-Ka radiation. The structure was solved by direct methods and refined by leastsquares methods. The final R factor was 0.084 for 2561 observed reflections. The configuration of the molecule from the X-ray crystallographic investigation has the partial cone conformation, three tort-butylphenyls are down and a tort-butylphenyl is up. Three propionyloxy groups direct toward the exterior of the macrocycle cavity.

• Journal of the Korean Chemical Society
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• v.62 no.6
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• pp.427-432
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• 2018

The reaction of [$[Ni(L)]Cl_2{\cdot}2H_2O$ (L = 3,14-dimethyl-2,6,13,17-tetraazatricyclo[$14,4,0^{1.18},0^{7.12}$]docosane) with 1,1-cyclohexanediacetic acid ($H_2cda$) yields mononuclear nickel(II) complex, [$Ni(L)(Hcda^-)_2$] (1). This complex has been characterized by X-ray crystallography, electronic absorption, cyclic voltammetry and thermogravimetric analyzer. The crystal structure of 1 exhibits a distorted octahedral geometry with four nitrogen atoms of the macrocycle and two 1,1-cyclohexanediacetate ligands. It crystallizes in the triclinic system P-1 with a = 11.3918(7), b = 12.6196(8), $c=12.8700(8){\AA}$, $V=1579.9(2){\AA}^3$, Z = 2. Electronic spectrum of 1 also reveals a high-spin octahedral environment. Cyclic voltammetry of 1 undergoes one wave of a one-electron transfer corresponding to $Ni^{II}/Ni^{III}$ process. TGA curve for 1 shows three-step weight loss. The electronic spectra, electrochemical and TGA behavior of the complex are significantly affected by the nature of the axial $Hcda^-$ ligand.

• Bulletin of the Korean Chemical Society
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• v.25 no.1
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• pp.85-89
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• 2004

Geometrical structures of [Pd(L)$Cl_2$] with oxathia macrocycles have been calculated using ab initio secondorder Moller-Plesset (MP2) and Density Functional Theory (DFT) methods with triple zeta plus polarization (TZP) basis set level. In optimized Pd(L)$Cl_2$ complexes, Pd(II) locates at the center surrounded by a square planar array of two sulfurs on an oxathia macrocycle and two chlorides. The endo-Pd(II) complexes with an axial (Pd${\cdots}$O) interaction are more stable than the exo-Pd(II) complexes without the interaction. In the endo-Pd(II) complexes, the atomic charge of the oxygen atom moves to Pd(II) via the axial ($Pd{\cdots}$O) interaction and then, the charge transfer from Pd(II) to the S-atoms occurs stepwise via ${\pi}$-acceptors of the empty d-orbitals.

• Bulletin of the Korean Chemical Society
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• v.32 no.5
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• pp.1761-1764
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• 2011

• Rapid Communication in Photoscience
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• v.2 no.2
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• pp.39-41
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• 2013

It is interesting to introduce viologen moiety into photoactive compounds such as porphyrin and anthracene in the study of supramolecular system such as pseudorotaxanes. For the construction of photoactive pseudorotaxane based on porphyrin-viologen-anthracene triad or its zinc derivative threaded with bis-p-phenylene-34-crown-10 macrocycle, porphyrin-viologen-anthracene triad 1 and its zinc derivative zinc porphyrin-viologen-anthracene triad 2 were prepared and their absorption and fluorescence spectral properties were measured.

• Bulletin of the Korean Chemical Society
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• v.28 no.3
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• pp.489-492
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• 2007

• Bulletin of the Korean Chemical Society
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• v.32 no.1
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• pp.325-328
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• 2011

• Bulletin of the Korean Chemical Society
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• v.25 no.10
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• pp.1581-1584
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• 2004

• Bulletin of the Korean Chemical Society
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• v.28 no.2
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• pp.303-306
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• 2007

• Bulletin of the Korean Chemical Society
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• v.33 no.12
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• pp.4251-4254
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• 2012