Synthesis and Conformational Studies on [ 3 . 3 . 3 ] Metacyclophane Oligoketone Derivatives , and Their Metal Ion Recognition

Chemical reactions were used to synthesize 2,11,20-tris(ethanedithia)-9,18,27-trimethoxy-6,15, 24-tri-tert-butyl[3.3.3]metacyclophane 2 and 2,11-bis(ethanedithia)-9,18,27-trimethoxy-6,15,24tri-tert-butyl[3.3.3]metacyclophane 4 from 6,15,24-tri-tert-butyl-9,18,27-trimethoxy[3.3.3]metacyclophane-2,11,20-trione 1 and -2,11-dione 3. The yields of 2 and 4 were 70% and 81% respectively. The conformations of the synthesized compounds 2 and 4 were studied using mainly solution Proton Nuclear Magnetic Resonance (1H NMR) spectroscopic methods. Compounds 2 and 4 were found to have a partial-cone conformation. Detailed variable temperature Proton Nuclear Magnetic Resonance studies further confirmed the partial-cone conformation for the two products, 2, 4. During the variable temperature nuclear magnetic resonance spectroscopic studies, compound 2 was found to have a coalescence temperature of about 0 ̊C. Extraction of silver ions with compound 2 gave an extractability of 82% while the parent compound 1 showed zero (0) silver affinity. A 1:1 mol/mol mixture of compound 2 and silver ions studied by solution 1H NMR revealed a novel “Molecular Roulette” type of motion.


Introduction
For several decades various research groups have been attracted to the chemistry and spectral properties of the metacyclophanes [1] [2].Some of the studies bother on synthesis and conformational studies of the macrocyclic compounds in which researchers try to convert the flexible conformations of the synthesized macrocyclic compounds into rigid structures to serve as suitable platforms for various complexation experiments.Notable among the methods employed in constructing the rigid structures are those that deal with the introduction of various functional groups into the upper and lower rims, Figure 1, of the cyclic structures [3].This method of preparing very stable units for host-guest studies places the functional groups on the aromatic units within the cyclic structure [4]- [7].Other ways of freezing the various conformers include the introduction of the functional groups into the aliphatic units linking the various aromatic groups.This approach has been employed in studies involving cyclophanes with aromatic rings linked through -CH 2 COCH 2 -bridges [8] [9].These bridges are of special interest because of the ease with which carbonyl groups can be converted into other functional groups.For example, the conversion of the carbonyl groups into dithio groups yields hosts with sulfur atoms which can serve as further binding units for molecular recognition studies.The sulfur atoms together with the benzene rings tend to serve as sources of electrons needed to bind guests in the form of metal ions.
Cyclophane compounds bearing sulfur atoms [8] [9] have been known as intermediates in the preparation of various cyclophanes, particularly the paracyclophanes [10].However, the use of sulfur atoms as binding units within cyclophane units is limited.The few examples include those compounds known to bind strongly to gold surfaces thus making it possible for several self-assembled monolayers of adsorbates with a surface-active sulfur group, an alkyl chain and a terminal functional group [11] [12].Reinhoudt and his coworkers also reported the synthesis of various resorcin [4] arene adsorbates with four dialkyl sulfide chains underneath, a receptor, which they used in detecting a specific gas [13]- [17].In this study sulfur units were employed to freeze the conformation of some cyclophanes in order to use them for metal ion recognition studies.

3.3]metacyclophane 2 Using the Mole Ratio Method [19]
A freshly prepared stock solution of the host, cyclic thioketal 2 [40 × 10 −5 M] using THF (UV grade) was se-rially diluted to obtain 10 ml each of various concentrations.5 ml of each of these solutions was mixed with 5 ml of 5.0 × 10 −5 M solution of silver picrate (also in THF).These mixtures were shaken at 26˚C for 3 h after which the absorbance of each was measured on a UV spectrophotometer in the wavelength range 500 -200 nm.Absorbances at 220 nm were plotted against the mole ratio of host to guest which were whole numbers of 1, 2, 3, 4, 5, and 6.The point of inflexion on the mole ratio axis (x-axis) gave the number of silver ions complexed as 3.

Results and Discussion
The starting materials 6,15,24-tri-tert-butyl-9,18,27-trimethoxy [3.This could be interpreted to mean the inversion of one of the benzene rings, precisely the signal up-field.A further confirmation of this arrangement of the benzene rings could also be deduced from the intensities of the two sets of aromatic signals.The two broad signals have been integrated and show 4 protons at 7.6 ppm and 2 protons at 7.2 ppm which can be interpreted as one of the three benzene rings undergoing inversion.
The coalescence temperature (Tc) for the benzylic protons was found to be 0˚C and the free energy of activation for the ring inversion was estimated to be 13.2 kcal/mol.The rate of inversion at the coalescence temperature was calculated from the expression; Kcoalescence = π(∆ν 2 + 6J 2 ) 1/2 /2 1/2 where Δν is the difference in chemical shift between the centres of the two doublets arising from the benzylic protons, and J is the coupling constant.Substituting this value into the Eyring rate equation 35 gives the expression; ΔG ≠ = RTln(6.62× 10 12 / Kcoalescence) which was used for the estimation of the free energy of activation for ring inversion.
Titration of the cyclic thioketal 2 with CF 3 SO 3 Ag in acetone-d 6 /CDCl 3 (3:1 v/v), monitored by 1 H NMR, Figure 3, clearly demonstrates that a 1:3 complex with "partial-cone" conformation is formed which is quite stable on the NMR time scale.
This ratio of complexation for the cyclic thioketal 2 with Ag + was experimentally confirmed by the mole ratio method, Figure 4.A two-phase solvent extraction experiment indicated that the cyclic thioketal 2 shows a strong affinity for the Ag + making it possible for a high Ag + selectivity to be observed, Figure 5.The lone pairs of electrons on the sulfur atoms and the π-electrons of the benzene rings might be responsible for the binding of the silver ions.Thus these two groups arrange themselves in a manner forming pockets into which the silver ions enter, Figure 6.
On the contrary, the parent triketone 1 shows a rather poor metal affinity,      [4] arene, a motion that they named "Metal Tunnelling" [36].Extraction conditions: Aqueous phase (5 ml) contains AgNO Interestingly, an intramolecular Ag + rolling phenomenon in which the Ag + rolls from one binding site to the other in a circular motion like a "Molecular Roulette" was observed for the first time by 1 H NMR spectroscopy in the 1:1 complex between the cyclic thioketal 2 and Ag + above room temperature, Figure 7 and Figure 8.A mole ratio of 1:1 of the cyclic thioketal 2 and Ag + seems to portray a picture in which the Ag + undergoes an in-

Figure 8 .
Figure 8. Intramolecular Ag + rolling phenomenon like a "Molecular Roulette".termolecularmotion between the uncomplexed cyclic thioketal 2 and the complexed, Figure9.One cannot rule out the possibility of the intramolecular motion, like that of the "Molecular Roulette", also occurring in this sys-

Figure 9 .
Figure 9.The inter-and intramolecular motion between uncomplexed and complexed cyclic thioketal 2. tem.Similar studies involving the cyclic thioketal 4 are currently going on.