2014
DOI: 10.1002/ejic.201402345
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AgI‐Directed Triple‐Stranded Helicates with meta‐Ethynylpyridine Ligands

Abstract: A series of triple‐stranded complexes, [1a3Ag]BF4, [1b3Ag]BF4, [2a3Ag2](BF4)2, [2b3Ag2](BF4)2, and [33Ag3](BF4)3, have been obtained through the self‐assembly of AgI ions with p‐phenylene ethynylpyridine ligands. X‐ray crystallographic studies unambiguously demonstrated a AgI‐directed monodentate triple‐stranded helical structure in the solid state for 1b and 2b. A combination of NMR spectroscopy, HRMS (ESI), and isothermal titration microcalorimetry studies further confirmed that strands 1, 2, and 3 are also … Show more

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Cited by 7 publications
(2 citation statements)
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“…We envisaged a self-assembly strategy based on noncovalent forces that would provide an efficient solution for some of these problems. Metal coordinative binding, one of the noncovalent forces, displays promise for constructing functional molecular devices, as exemplified by numerous elegant supramolecular systems on silver-mediated molecular rotary systems, helicates, and cages . In this contribution, we describe our self-assembly strategy for constructing novel molecular turnstiles and for regulating their bistability between an open and a closed form with metal ions as our continuous effort on functional molecular devices …”
Section: Introductionmentioning
confidence: 99%
“…We envisaged a self-assembly strategy based on noncovalent forces that would provide an efficient solution for some of these problems. Metal coordinative binding, one of the noncovalent forces, displays promise for constructing functional molecular devices, as exemplified by numerous elegant supramolecular systems on silver-mediated molecular rotary systems, helicates, and cages . In this contribution, we describe our self-assembly strategy for constructing novel molecular turnstiles and for regulating their bistability between an open and a closed form with metal ions as our continuous effort on functional molecular devices …”
Section: Introductionmentioning
confidence: 99%
“…Helical structures have been commonly recognized as a highly valuable shape and are ubiquitous in nature ranging from macroscopic phenomena to biomolecular systems. Motivated via aesthetical structures and biomimetic functions, an increasing contribution has been made by crystal engineers to design and synthesize molecular architectures that have capability to mimic biomacromolecules structurally and functionally. In general, helical structures usually are formations of multidentate organic strands with the assistance of a coordinate effect of the metal center. However, an overwhelming majority of helical chains in biomacromolecules are mainly constructed through the cooperative interaction of abundant and complex noncovalent interactions instead of metal coordination .…”
Section: Introductionmentioning
confidence: 99%