6533b7dafe1ef96bd126e2ed

RESEARCH PRODUCT

Copper(I) Halides (X = Br, I) Coordinated to Bis(arylthio)methane Ligands: Aryl Substitution and Halide Effects on the Dimensionality, Cluster Size and Luminescence Properties of the Coordination Polymers

Pierre D. HarveyAhmed Dini AleoDaniel FortinAnass El YaagoubiAbderrahim KhatyrAntony LapprandAntony LapprandMarek M. KubickiCarsten StrohmannMichael KnorrShawkat M. AlyYoann Rousselin

subject

Steric effectsArylGeneral ChemistryCrystal structureCondensed Matter PhysicsPhotochemistryMethanechemistry.chemical_compoundCrystallographychemistryCubaneRibbon[CHIM]Chemical SciencesGeneral Materials ScienceIsostructuralComputingMilieux_MISCELLANEOUSMonoclinic crystal system

description

Bis(phenylthio)methane (L1) reacts with CuI to yield the 1D-coordination polymer [{Cu4(μ3-I)4}(μ-L1)2]n (1) bearing cubane Cu4I4 clusters as connecting nodes. The crystal structures at 115, 155, 195, and 235 K provided evidence for a phase transition changing from the monoclinic space group C2/c to P21/c. The self-assembly process of CuI with bis(p-tolylthio)methane (L2), bis(4-methoxyphenylthio)methane (L3), and bis(4-bromo-phenylthio)methane (L4) affords the 1D-coordination polymers [{Cu4(μ3-I)4}(μ-Lx)2]n (x = 2, 3, or 4). Compounds 2 and 4 are isostructural with C2/c low temperature polymorph of 1, whereas the inversion centers and 2-fold axes are lost in 3 (space group Cc). The use of bis(m-tolylthio)methane (L5) has no impact on the composition and overall topology of the resulting 1D ribbon of [{Cu4(μ3-I)4}(μ-L5)2]n (5). Even the coordination of the sterically crowded dithioether bis(5-tert-butyl-2-methylphenylthio)methane (L8) does not alter the network topology generating the 1D polymer [{Cu4(μ3-I...

10.1021/cg500905zhttps://hal.archives-ouvertes.fr/hal-01275374