Structural chemistry of "defect" cyanometalate boxes: (Cs subset [CpCo(CN)3]4[Cp*Ru]3) and (M subset [Cp*Rh(CN)3]4[Cp*Ru]3) (M = NH4, Cs) |
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Authors: | Kuhlman Matthew L Rauchfuss Thomas B |
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Affiliation: | Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA. |
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Abstract: | A series of heptametallic cyanide cages are described; they represent soluble analogues of defect-containing cyanometalate solid-state polymers. Reaction of 0.75 equiv of [Cp*Ru(NCMe)3]PF6, Et(4)N[Cp*Rh(CN)3], and 0.25 equiv of CsOTf in MeCN solution produced (Cs subset [CpCo(CN)3]4[Cp*Ru]3)(Cs subset Rh4Ru3). 1H and 133Cs NMR measurements show that Cs subset Rh4Ru3 exists as a single Cs isomer. In contrast, (Cs subset [CpCo(CN)3]4[Cp*Ru]3) (Cs subset Co4Ru3), previously lacking crystallographic characterization, adopts both Cs isomers in solution. In situ ESI-MS studies on the synthesis of Cs subset Rh4Ru3 revealed two Cs-containing intermediates, Cs subset Rh2Ru2+ (1239 m/z) and Cs subset Rh3Ru3+ (1791 m/z), which underscore the participation of Cs+ in the mechanism of cage formation. 133Cs NMR shifts for the cages correlated with the number of CN groups bound to Cs+: Cs subset Co4Ru4+ (delta 1 vs delta 34 for CsOTf), Cs subset Rh4Ru3 where Cs+ is surrounded by ten CN ligands (delta 91), Cs subset Co4Ru3, which consists of isomers with 11 and 10 pi-bonded CNs (delta 42 and delta 89, respectively). Although (K subset [Cp*Rh(CN)3]4[Cp*Ru]3) could not be prepared, (NH4 subset [Cp*Rh(CN)3]4[Cp*Ru]3) (NH4 subset Rh4Ru3) forms readily by NH4+-template cage assembly. IR and NMR measurements indicate that NH4+ binding is weak and that the site symmetry is low. CsOTf quantitatively and rapidly converts NH4 subset Rh4Ru3 into Cs subset Rh4Ru3, demonstrating the kinetic advantages of the M7 cages as ion receptors. Crystallographic characterization of CsCo4Ru3 revealed that it crystallizes in the Cs-(exo)1(endo)2 isomer. In addition to the nine mu-CN ligands, two CN(t) ligands are pi-bonded to Cs+. M subset Rh4Ru3 (M = NH4, Cs) crystallizes as the second Cs isomer, that is, (exo)2(endo)1, wherein only one CN(t) ligand interacts with the included cation. The distorted framework of NH4 subset Rh4Ru3 reflects the smaller ionic radius of NH4+. The protons of NH4+ were located crystallographically, allowing precise determination of the novel NH4...CN interaction. A competition experiment between calix[4]arene-bis(benzocrown-6) and NH4 subset Rh4Ru3 reveals NH4 subset Rh4Ru3 has a higher affinity for cesium. |
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