Di-tert-butyl N,N'-{[13,15,28,30,31,33-hexa-ethyl-3,10,18,25,32,34-hexa-aza-penta-cyclo-[25.3.1.1(5,8).1(12,16).1(20,23)]tetra-triaconta-1(31),3,5,7,9,12(33),13,15,18,20,22,24,27,29-tetra-deca-ene-14,29-di-yl]bis-(methyl-ene)}dicarbamate methanol disolvate, C(52)H(72)N(8)O(4)·2CH(3)OH, was found to crystallize in the space group P2(1)/c with one half of the macrocycle (host) and one mol-ecule of solvent (guest) in the asymmetric unit of the cell, i.e. the host mol-ecule is located on a crystallographic symmetry center. Within the 1:2 host-guest complex, the solvent mol-ecules are accommodated in the host cavity and held in their positions by O-Hâ¯N and N-Hâ¯O bonds, thus forming ring synthons of graph set R (2) (2)(7). The connection of the 1:2 host-guest complexes is accomplished by C-Hâ¯O, C-Hâ¯N and C-Hâ¯Ï inter-actions, which create a three-dimensional supra-molecular network.
Crystal structure of a methanol solvate of a macrocycle bearing two flexible side-arms.
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作者:Amrhein Felix, Schwarzer Anke, Mazik Monika
| 期刊: | Acta Crystallographica Section E: Crystallographic Communications | 影响因子: | 0.500 |
| 时间: | 2021 | 起止号: | 2021 Feb 5; 77(Pt 3):233-236 |
| doi: | 10.1107/S2056989021001067 | ||
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