The new ligand 2-pyridinyl-3-pyridinylmethanone (L) proves to be an excellent building block for the construction of single-strand helical architectures. A series of helical complexes have been synthesized by the reaction of L with various metal salts, in which L exhibits three kinds of coordination modes involving two kinds of bridging conformations, resulting in four types of single-strand helical chains. The counter anions in the series of 2(1) helical silver( I) complexes {[Ag(L)]X}(infinity) (X = NO3, 1; PF6, 2; BF4, 3; ClO4, 4; CF3CO2, 5; CF3SO3, 6) are fully or partially embedded inside the cylindrical helix, and the pitch length corresponds not only to the size of the anion but also to its manner of docking into the groove of the helix. Formation of the helical structure in {[Cu(L)(CH3CN)(H2O)(ClO4)]ClO4}(infinity) (7) is driven by Ow-H center dot center dot center dot O (perchlorate) hydrogen bonding that leads to a stable triangular motif which rigidly fixes the configuration of the helix. In {[Co(L)(H2O)(3)](ClO4)(2)center dot 2H(2)O}(infinity) (8) and {[Zn(L)(H2O)(3)](CF3SO3)(2)center dot H2O}(infinity) (9), similar helical chains without anion embedment suggest that the pitch length can be tuned by the size of metal cations. Notably, complex {[Ag(L)] CF3SO3}(infinity) (10), a conformational polymorph of 6, has a 41 helix induced by argentophilic interaction.
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