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Issue 47, 2017
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Influence of mole-ratio on the coordination behaviour of a ditopic N2O2S2-macrocycle: endo/exocyclic silver(I) coordination polymer exhibiting desolvation-induced SCSC transformation

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Abstract

Mole-ratio dependent formations of the macrocyclic silver(I) complexes with different coordination modes and topologies are reported. When one equivalent of AgPF6 was reacted with an N2O2S2-macrocycle (L), a typical endocyclic monomer complex [Ag(L)]PF6 (1) was isolated. Moreover, the use of three equivalents or above amount of AgPF6 afforded a one-dimensional (1-D) coordination polymer {[Ag4(L)2](PF6)4·2CH2Cl2}n (2a), in which the endocyclic monomer complex units are linked by different silver(I) atoms outside the macrocyclic cavity to form a unique endo/exocyclic infinite chain via the –endoAg–S–exoAg–S– bond linkages. Upon removal of the dichloromethane molecules in the crystal lattice of 2a in ambient conditions, conversion of the coordination geometry of the exocyclic Ag atom from linear (2a) to trigonal plane (2b, desolvated product) as well as sliding of the 1-D chains were observed in a single-crystal-to-single-crystal manner.

Graphical abstract: Influence of mole-ratio on the coordination behaviour of a ditopic N2O2S2-macrocycle: endo/exocyclic silver(i) coordination polymer exhibiting desolvation-induced SCSC transformation

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Publication details

The article was received on 24 Aug 2017, accepted on 09 Nov 2017 and first published on 10 Nov 2017


Article type: Paper
DOI: 10.1039/C7CE01540B
Citation: CrystEngComm, 2017,19, 7185-7190
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    Influence of mole-ratio on the coordination behaviour of a ditopic N2O2S2-macrocycle: endo/exocyclic silver(I) coordination polymer exhibiting desolvation-induced SCSC transformation

    S. Seo, E. Lee, H. Ju, S. Kim, I. Park, J. H. Jung and S. S. Lee, CrystEngComm, 2017, 19, 7185
    DOI: 10.1039/C7CE01540B

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