Advanced
Isostructural Heteronuclear (K<sup>+</sup>/M<sup>2+</sup>: M
Isostructural Heteronuclear (K+/M2+: M
Bulletin of the Korean Chemical Society. 2014. Jan, 35(1): 289-292
Copyright © 2014, Korea Chemical Society
  • Received : October 08, 2013
  • Accepted : October 15, 2013
  • Published : January 20, 2014
Download
PDF
e-PUB
PubReader
PPT
Export by style
Article
Author
Metrics
Cited by
TagCloud
About the Authors
Ja-Yeon Kim
Kihwan Kim
Ki-Min Park
Shim Sung Lee

Abstract
Keywords
PPT Slide
Lager Image
Results and Discussion
The crystalline products 1-3 , {[K 2 @( TCTC )(𝜇 2 -M)(H 2 O) 4 -(CH 3 OH) 2 ]·3H 2 O} n {M = Ni ( 1 , green), Co ( 2 , pink), and Zn ( 3 , colorless)} were synthesized from the respective reactions of K 4 TCTC in water and corresponding metal perchlorate except nickel(II) nitrate in methanol. The absence of characteristic bands at 1680-1715 cm −1 in the IR spectra for these products indicates that no protonation of the carboxylates of TCTC 4− has been occurred in each complex. The crystal structures of 1-3 were obtained by single-crystal X-ray diffraction analysis ( Table 1 ). The X-ray crystal structures of 1-3 with an isostructural form are shown in Figure 1 and their selected geometric parameters presented in Table 2 . Commonly, the products 1 , 2 , and 3 crystallize in a monoclinic system with space group P 2 1 / c adopting a 1D zigzag chain as neutral species without the anions in the coordination sphere and the lattice. Here, the structure of 1 is described as a representative example. Because the structure in Figure 1 is generated through an inversion symmetry, the asymmetric unit of 1 in its coordination sphere contains one TCTC 4− , two K atoms, one Ni atom, four water molecules, and two methanol molecules.
In 1 , the coordination environment of K1 and K2 atoms accommodated inside the 1,3-alternate calix unit shows no significant difference ( Figure 2(a) ). Each K atom is in a distorted pentagonal planar array of two monodentate carboxylate oxygens and two phenolic oxygens from two different 1,3-alternate pendant groups. The coordination environment of the K atom is completed by one monodentate water molecule. The bite angles around the K1 atom vary considerably, ranging from 62.0(8)° (O4-K1-O5) to 113.5(2)° (O4-K1-O10), presumably due to the steric strains of the metallacycles formed upon complexation. The K1-O(carboxylate) distances [K1-O5 2.696(7), K1-O11 2.641(6) Å] are found to be appreciably shorter than the K1-O(ether) [K1-O4 2.914(6), K1-O10 2.941(6) Å] and the K1-O(water) [K1-O3W 3.045(10) Å], suggesting that the negatively charged oxygens are bonded more tightly to the potassium center. The K1···K2 separation is 5.702 Å and each K atom is also stabilized by 𝜂 3 -type cation···π interactions with the aromatic rings (dashed lines in Figure 2(a) , K1···C 3.19- 3.45 Å, see Table 3 ). 8 Overall, the K 2 @ TCTC unit in 1 shows the synergic contribution of the three types of oxygen donors (ether, carboxylate, and water) and the aromatic rings to stabilize the dipotassium complexation.
Crystal data and structural refinement for1-3
PPT Slide
Lager Image
Crystal data and structural refinement for 1-3
PPT Slide
Lager Image
Isostructural zigzag-type 1D polymeric structure of 1-3, {[K2@(TCTC)(𝜇2-M)(H2O)4(CH3OH)2]·3H2O}n, (1: M = Ni, 2: M = Co, and 3: M = Zn).
Notably, the K 2 @ TCTC units are linearly linked by a 𝜇 2 -Ni atom to form an infinite 1D zigzag chain structure through Ni-O(carboxylate) bonds [Ni1-O3 2.015(5), Ni2-O9 2.014(6) Å] ( Figures 1 and 2(b) ). The Ni(II) center is sixcoordinate, being bound to two carboxylate oxygens from different K 2 @ TCTA units in a monodentate manner and two water molecules ( Figure 2(a) ). The distorted octahedral coordination sphere is completed by two additional methanol molecules.
Conclusion
Assembly of 1,3-alternate thiacalix[4]arene potassium tetraacetate with three transition metal salts afforded an isostructural metal-mediated heteronuclear coordination polymers. The present results illustrate how the appropriate modification of the 1,3-alternate thiacalix[4]arene derivative works as an approach in preparing desired metallosupramolecular networks. Further exploration of the synthesis and physical properties of novel metallosupramolecular network species based on the modification of the thiacalix[4]arene derivatives is underway.
Experimental
General. All chemicals were of reagent grade and used without further purification. FT-IR spectra were measured with a ThermoFisher Scientific Nicolet i S 10 FT-IR spectrometer using KBr pellet in the range 4000-400 cm −1 . The ligand K 4 TCTC was prepared as reported in the literature. 3a
Synthesis of [K2@(TCTC)(𝜇2-Ni)(H2O)4(CH3OH)2]·3H2O}n (1). K 4 TCTC (20.0 mg, 0.023 mmol) dissolved in water was added to a solution of Ni(NO 3 ) 2 ·6H 2 O (16 mg, 0.055 mmol) in methanol. Green single crystals suitable for X-ray analysis were obtained by slow evaporation of the resulting solution. mp 321-322 ℃ (decomp.). IR (KBr pellet): 3401, 1598, 1436, 1413, 1330, 1220, 1070, 1018, 846, 802, 761 cm −1 .
Selected bond lengths (Å) and bond angles (°) for1-3a
PPT Slide
Lager Image
aSymmetry operations: (A) − x, − y+2, − z; (B) − x+1, − y+1, − z.
PPT Slide
Lager Image
Crystal structure of 1-3: (a) core coordination unit and (b) a-axis packing structure. Hydrogen atoms and uncoordinated solvent molecules are omitted.
Distances of K+···π interactions (Å) in1-3
PPT Slide
Lager Image
Distances of K+···π interactions (Å) in 1 -3
Synthesis of [K2@(TCTC)(𝜇2-Co)(H2O)4(CH3OH)2]·3H2O}n (2). Synthetic procedures of 2 as pink single crystals are same as for 1 except the use of Co(ClO 4 ) 2 ·6H 2 O (16 mg, 0.044 mmol). mp 318-319 ℃ (decomp.). IR (KBr pellet): 3399, 1604, 1436, 1415, 1330, 1220, 1103, 1072, 1016, 846, 802, 761 cm −1 .
Synthesis of [K2@(TCTC)(𝜇2-Zn)(H2O)4(CH3OH)2]·3H2O}n (3). Synthetic procedures of 3 as colorless single crystals are same as for 1 except the use of Zn(ClO 4 ) 2 ·6H 2 O (16 mg, 0.043 mmol). mp 334-335 ℃ (decomp.). IR (KBr pellet): 3419, 1648, 1434, 1415, 1313, 1220, 1072, 1016, 943, 848, 798, 761 cm −1 .
X - ray Crystallography. Crystal data were collected on a Bruker SMART APEX II ULTRA diffractometer equipped with graphite monochromated Mo Kα radiation (λ = 0.71073 Å) generated by a rotating anode. The cell parameters for the compounds were obtained from a least-squares refinement of the spot (from 36 collected frames). Data collection, data reduction, and semi-empirical absorption correction were carried out using the software package of APEX2. 9 All of the calculations for the structure determination were carried out using the SHELXTL package. 10 In all cases, all nonhydrogen atoms were refined anisotropically and all hydrogen atoms except coordinated and lattice water molecules were placed in idealized positions and refined isotropically in a riding manner along with the their respective parent atoms. In the cases of coordinated water molecules, the initial positions of the hydrogen atoms were obtained from difference electron density maps and refined with riding constraints. The H atoms in the lattice water molecules did not involve in structure analysis because they could not be found from difference electron density maps. In all cases, the methyl group (C34) in the methanol molecule coordinated to M2 ion (M = Ni, Co, or Zn) was disordered over two sites (C34, C34') with equal site occupancy factors of 0.5. Also, the O7W and O7W' atoms in one lattice water molecule have two positions with the site occupancy factors of 0.5, respectively. The crystallographic data for 1-3 are summarized in Table 1 .
Acknowledgements
This work was supported by NRF (2012R1A4A1027750).Supplementary Materials.Crystallographic data for the structures reported here have been deposited with CCDC (Deposition No. CCDC 963943 (1), 963944 (2), and 963945 (3)). These data can be obtained free of charge from The Cambridge Crystallographic Data Centerviawww.ccdc.cam.ac.uk/data_request/cif.
References
Kostin G. A. , Borodin A. O. , Torgov V. G. , Kuratieva N. V. , Naumov D. Y. , Miroshnichenko S. I. , Kalchenko V. I. 2007 J. Inclusion Phenom. Macrocyclic Chem. 59 45 -    DOI : 10.1007/s10847-007-9293-4
Kim K. , Park S. , Park K.-M. , Lee S. S. 2011 Cryst. Growth Des. 11 4059 -    DOI : 10.1021/cg2006315
2000 SMART (ver. 5.625) and SAINT-plus (ver. 6.22): Area Detector Control and Integration Software Bruker AXS Inc. Madison, Wisconsin
2000 SHELXTL (ver. 6.10): Program for Solution and Refinement of Crystal Structures Bruker AXS Inc. Madison, Wisconsin