A pair of 2D chiral Ag() enantiomers with dual chiral elements: syntheses, structures, and photoluminescent and chiroptical properties

In this work, two new enantiopure bis-monodentate N -donor chiral ligands, namely (−)/(+)-2-(4′-pyridyl)-4,5-pinene-pyridine (L R /L S ), have been designed and synthesized. Using L R and L S as bridging ligands to react with AgClO 4 , a pair of novel 2D chiral Ag( i ) enantiomers formulated as [Ag 2 (L R ) 2 (ClO 4 ) 2 ] n ( R -1 ) and [Ag 2 (L S ) 2 (ClO 4 ) 2 ] n ( S -1 ) were isolated and characterized. In R -1 and S -1 , each Ag( i ) ion is bonded by two N atoms from two different chiral L R or L S ligands, leading to the formation of 1D right- or left-handed -L-Ag( i )-L- helical chains. Moreover, two adjacent helical chains are further doubly linked by two monodentate ClO 4 − anions through weak Ag-O contacts to form 2D network structures, in which dual chiral elements, i.e. , center chirality and helical chirality coexist. Interestingly, each free ligand L R /L S and R -1 / S -1 enantiomers show very different ECD spectra in the solid state and in solution, which are correlated to the intermolecular interactions and molecular structures in each state, respectively. Notably, as a representative, R -1 exhibits intense room temperature photoluminescence both in the solid state and in solution with different emission features and mechanisms, while it also shows more intense emission than that of free ligand L R . In particular, R -1 and S -1 represent the first examples of 2D Ag( i ) chiral coordination polymers (CCPs) supported by ClO 4 − anions, possessing dual chiral elements. 2D chiral Ag( i ) enantiomeric pair display intense emissions both in the solid state and in solution with very different emission features and mechanisms.