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- W4200557002 abstract "One-dimensional cationic coordination polymers have been a promising platform for designing solid-state physical properties through diverse coordination geometries. In particular, the folding mode of the coordination polymers that form a helical structure directly determines the metal-centered coordination environment. Herein, we report N-heterocyclic carbene (NHC) Cu(I) cationic coordination polymers with pyrazine as the linker, which construct a 4-fold or 3-fold helical column in luminescent crystals using octahedral anions (SbF6- and PF6-) or a tetrahedral anion (BF4-), respectively. Single-crystal XRD studies revealed that the folding modes depend on the structural shape of the counteranions, which form H-F interactions between ligands and anions. Indeed, the folding mode change from 4-fold to 3-fold by including a different shape of the counteranions, resulting in red-shifted emission from approximately 580 to 687 nm, which is difficult to modulate in the solid state." @default.
- W4200557002 created "2021-12-31" @default.
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- W4200557002 date "2021-12-16" @default.
- W4200557002 modified "2023-10-17" @default.
- W4200557002 title "Distinct Fold-Mode Formation of Crystalline Cu(I) Helical Coordination Polymers with Alternation of the Solid-State Emission Using Shape of the Counter Anions" @default.
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- W4200557002 doi "https://doi.org/10.1021/acs.inorgchem.1c02725" @default.
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