Syddansk Universitet Oxygen Chemisorption / Desorption in a Reversible Single-Crystal-To-Single-Crystal Transformation

Crystalline salts of a series of cationic multimetallic cobalt complexes reversibly, selectively and stoichiometrically chemisorb dioxygen in a process involving the two electron oxidation of dimetallic sites with concurrent reduction of two equivalents of sorbed O2 to form μ-η1,η2-peroxide ligands. The coordinating ability of counteranions, ClO4−, PF6−, BF4−, CF3SO3− and NO3− determine the O2 affinity of the deoxygenated forms, and the nitrate and triflate salts sorb dioxygen at a significantly slower rate compared to the PF6− and BF4− salts (hours versus sub-seconds at ambient temperature and pressure). Single crystal X-ray structural determination for a nitrate salt of the 2-aminoterephthalato-linked deoxy system, [{(bpbp)Co2II(NO3)}2(NH2bdc)](NO3)2·2H2O (bpbp− = 2,6-bis(N,N-bis(2-pyridylmethyl)aminomethyl)-4-tert-butylphenolato, NH2bdc2− = 2-amino-1,4-benzenedicarboxylato) shows that nitrate ions are coordinated as bridging ligands. These crystals undergo reversible single-crystal-to-single-crystal (SC-to-SC) transformations on the stoichiometric uptake of O2. During this process O2 replaces the two nitrate ligands. Thus the Co ions are six coordinated in both the oxy and deoxy states. This SC-to-SC process involves the concerted fast migration of neutral dioxygen through the crystal lattice and the translational movement by 4–6 A of at least two of nitrate anions. Rapid hydration/dehydration processes involving several molecules of co-crystallized water per unit cell accompany the reaction. Besides large atom movements involving O2, NO3− and H2O, these impressive examples of consecutive SC-to-SC-to-SC transformations involve the cleavage of four bonds, and the creation of four new bonds, in one single molecule. The solid state structural rearrangements observed provide an explanation for the slower rates of dioxygen uptake for the complexes isolated as nitrate salts, and by inference, the triflate salts, compared to the salts of more weakly coordinating counteranions, ClO4−, PF6− and BF4−.


Introduction
Reactions of dioxygen are essential in a wide range of biological and chemical processes: the reversible binding of dioxygen, its activation in order to prime it for the oxidation of substrates, and its release aer formation. The presence of paramagnetic states of iron, copper, nickel and manganese in enzymes like hemoglobin, hemerythrin, hemocyanin, cytochrome P450s, superoxide dismustases and the Oxygen Evolving Center in photosynthesis is essential. The risk of formation of reactive oxygen species, and possible consequent non-specic chain reactions, mean that the metal-based redox reactions must be very nely adjusted to prevent one electron transfers and possible release of cytotoxic superoxide. O 2 binding by metalloenzymes can be regarded as a highly selective "chemisorptive process", i.e., bond formation occurs between the O 2 and the metal co-factors. The separation of O 2 from other gases by reversible sorption is similarly essential for many industrial processes. However, efficiency and selectivity equal to biological processes has not yet been achieved. While O 2 concentration by sorptive materials is potentially less energy intensive compared with cryogenic distillation, currently this method can be used only in applications where it is not required in higher purity. These processes, based on zeolite materials, 1 are physisorptive in contrast to the aforementioned biological reactions. 2 Solid state metal-organic compounds offer a chemical middle ground between dynamic and exible enzymes and rigid inorganic zeolites for the design of materials capable of performing reversible O 2 binding. An obvious place to start in the design of these materials is by exploiting coordination complexes which are known to perform this task in the solution state. Co and Ir complexes, e.g. Co(salen) 3 and Vaska's 4 complex, have been long recognised as capable of oxidative addition and reductive elimination of O 2 in solution as they cycle between M(I) and M(III) oxidation states. 5 Thus it is not surprising that the immobilisation of these types of complexes in membranes 6 and polymers, 7 with the intention that practical materials and devices for O 2 separation processes might be constructed, has been pursued. However, none of these systems has achieved the O 2 binding active site concentration, nor the reversibility of [{(bpbp)Co 2 III (O 2 )} 2 (bdc)](PF 6 ) 4 (bpbp À ¼ 2,6-bis(N,N-bis (2-pyridylmethyl)aminomethyl)-4-tert-butylphenolato, bdc 2À ¼ 1,4benzenedicarboxylato). The cation in this compound is shown in Scheme 1, structure 2a. The deoxy form, 2a deoxy (PF 6 ) 4 reversibly binds O 2 from air in the solid state with affinities equalling that of myoglobin. 8 The O 2 sorption/desorption process of this compound can be cycled many times without any loss of activity. Solid 2a(PF 6 ) 4 $3H 2 O concentrates O 2 by a factor of 32 times the density of O 2 gas at 1 atm, or 160 times that in air. Apart from a higher capacity than the zeolites currently used on industrial scale for a far less efficient O 2 concentration, what is very interesting is the extreme affinity that this material shows for O 2 . At room temperature an excess of the material will reversibly remove more than 99% of oxygen from the air with a 38 fold selectivity factor for O 2 over N 2 . Compared to recently discovered systems showing selectivity for O 2 uptake, this is almost double that of the dichromium(II)tetracarboxylate paddlewheel based metal-organic framework, 9 and almost four times higher than the coordination network Fe 2 (dobdc) (dobdc 4À ¼ 2,5-dioxido-1,4-benzenedicarboxylate) (MOF-74). 10 Despite not being polymeric, 2a(PF 6 ) 4 $3H 2 O also shows greater stability towards irreversible redox processes. While the oxy 2a(PF 6 ) 4 $3H 2 O has been structurally characterized, the deoxy and by its nature, air sensitive form, 2a deoxy (PF 6 ) 4 , has not.
In solution, the O 2 affinity of a series of parent dinuclear complexes, Scheme 1, structures 1a-e, is tuned by the substitutions on the basic framework using electron donating or withdrawing groups on the carboxylate co-ligand. 11 Thus for every chloro group introduced onto the acetato bridge the O 2 affinity is reduced. The O 2 affinities for 1a-e ranged from similar to myoglobin through to haemoglobin respectively. Conversely, when a dicobalt complex was anchored to gold surfaces using 1f, the O 2 affinity was increased so much that the system is no longer an effective reversible O 2 binder. 12 With a view to practical applications the motivation for the work described in this report was carried out to ascertain whether or not this considerable range of solution state tunability could be translated into the solid state. With readily tuneable solid state materials on hand it is possible to imagine the construction of systems, capable not only of O 2 storage, but through layering, also of the vectorial transport of this biologically and industrially important molecule.

Synthesis
The cationic oxy complexes depicted in Scheme 1 (1a-e and 2a) were previously isolated for the most part as perchlorate salts. The safety issues associated with the need for heating solid samples for the present study forced the preparation of alternative formulations. We have now synthesized 2a as two new salts along with relatives which are functionalized on the bdc 2À linker (2b-d) as hexauorophosphate, tetrauoroborate, triate and nitrate salts. Typically the dinucleating pro-ligand, bpbpH, the appropriate carboxylic acid and base were mixed in stoichiometric amounts in mixtures of methanol, acetone and H 2 O under aerobic conditions. This reaction results in dark solutions from which the near black Co(III) oxy forms (as depicted in Scheme 1) crystallize over hours to days. The production of crystalline materials was crucial for the observation of consistent sorption/desorption properties, suggesting that solid phase structure plays an important role in the chemisorptive properties of these materials. Rapid precipitation formed light brown amorphous powders, which were inactive or only minimally active towards reversible O 2 binding. Apart from an apparent need for crystalline materials, and therewith highly regular 3D structures, a possible explanation for the colour and low O 2 uptake is contamination by "met" (Co(II) 2 to Co(III) 2 -based oxidation only-no O 2 binding and reduction) forms in which the carboxylato ligands are replaced by hydroxido. 13 On heating, the crystalline materials change to a pink colour due to the loss of O 2 and the generation of "deoxy" materials containing the counterpart Co(II) 4 -containing 1a-e deoxy and 2a-d deoxy (not shown in Scheme 1). On cooling back to room temperature the dark colour re-emerges as the materials chemisorb O 2 from the air to form the Co(III) 4 oxy materials 1a-e and 2a-d. This process was mostly accompanied by loss of crystal integrity, apart from one case, vide infra.

Thermogravimetry
The tetracobalt series 2, varied systematically with respect to counteranions and substitution on the benzene unit of the bdc 2À co-ligand, show slight variation in the temperatures at which the samples of crystalline compounds release O 2 . Thermogravimetric plots of O 2 release are shown in Fig. 1 complicates the interpretation of measurements, however, O 2 desorption appears to be complete for all samples. As seen in Fig. 1 the samples of the triate and the hexauorophosphate salts used for the experiments do not appear to contain any cocrystallized solvent. A more obvious two-stage process of guest removal is evidenced by inections in the TGA curves for the BF 4 À and NO 3 À salts, which may correspond to successive removal of water and oxygen with weight losses corresponding to two and four water molecules respectively. At approximately 100 C the nitrate salt has lost both O 2 molecules, whereas the PF 6 À salt is completely deoxygenated rst at 160 C. Perhaps consistently, dioxygen resorption is signicantly faster for the PF 6 À and BF 4 À salts where it is immediate upon exposure to air. This can be associated with loss of co-crystallized solvent. The formulation of one sample ts best to 2a(BF 4 ) 4 $5H 2 O$MeOH according to elemental analysis, so this is reasonable. Over the next 9 cycles we see only a marginal decrease in reversibility in O 2 uptake for each cycle. The weight loss and gain on the nal cycle amounts to a 92.9% yield if assuming that the sample is fully desolvated and deoxygenated, i.e., near stoichiometric. Resorption of O 2 is signicantly slower for the triate and nitrate salts for which colour change from pink back to dark brown occurs over hours to days. The enthalpy of O 2 binding to the structurally equivalent Co(II) 2 sites should be almost identical for each complex, so the difference relates to inaccessibility of O 2 binding sites, as reected by slow kinetics. Clearly the counteranions inuence the O 2 sorption/ desorption properties. Thus in our next experiments we kept the counteranion constant, choosing nitrate for which the slowest re-sorption of O 2 was observed. We then chemically tweaked the supporting ligand system by varying substituents on the bridging di-carboxylato linkers, 2a-d. Our prediction, based on the solution chemistry of 1a-e was that by introducing electron withdrawing groups onto the supporting scaffold, we would lower the O 2 affinity, further than that already achieved by using nitrate as a counteranion, potentially by orders of magnitude. We therefore expected that the nitrate salt of tetrauoride substituted bdc 2À -bridged complex, 2d, would show the lowest O 2 affinity of the series. For reference, the isolation of 1e required À20 C and an O 2 atmosphere. 11 The intention was to increase the chances for structural characterization of a deoxy form of these materials. Fig. 3 shows that the difference in O 2 release temperatures of the series of nitrate salts of 2a-d is, however, marginal. So this attempt at the rational design of the active molecular component of a functional solid state material did not meet our expectations and conrmed that aspects of    2a), NH 2 bdc 2À (blue, 2b) and F 4 bdc 2À (grey, 2d) showing temperature difference in deoxygenation and dehydration. crystal phase play a major role. The weight losses correspond to a minimum of stoichiometric loss of two O 2 molecules per tetracobalt unit, however, the concurrent release of unknown amounts of solvent makes direct analysis difficult. Inexion points in the weight loss curves for the materials containing 2a, 2b and 2c would suggest the loss of two chemically different species consistent with water and O 2 . These losses occur just under 100 C and distinguishing the order of loss has not been possible.

Crystal structure of a deoxy complex
The affinity of the PF 6 À salt of the complex 2a deoxy towards O 2 is approximately 10 times greater in the solid state compared to its O 2 affinity in solution. In the absence of a crystal structure of the deoxy form of any member of this series, we attributed this effect to the formation of more reactive coordinatively unsaturated ve-coordinated Co(II) sites on deoxygenation. Accordingly we assumed that the relative stabilization of the deoxy form in solution is due to solvent (acetonitrile, acetone or methanol) coordination to the Co(II) sites, which would then remain six coordinated. The solvent ligands would inhibit O 2 binding in both dissociative and associative mechanisms. DFT calculations supported this hypothesis. 10 Although we have precipitated solid compounds for several members of series 1 and 2 and related hexacobalt systems under dioxygen-free atmospheres, 14 none of these air-sensitive materials have formed single crystals suitable for X-ray diffraction analysis. The increased stability of the nitrate and triate salts of these deoxy complexes prompted further effort in this direction. We were, however, unable to grow single crystals of the compounds under anaerobic conditions using either ab initio preparations, or crystallizations from deoxygenated solutions. Fortunately, upon careful heating to approximately 100 C, single crystals of [{(bpbp)Co 2 (O 2 )} 2 (NH 2 bdc)](NO 3 ) 4 $xH 2 O (2b(NO 3 ) 4 $xH 2 O) change colour from near black to reddish pink, with many of them remaining intact (Fig. 4). Cracking was observed in some crystals, especially larger specimens. This must be due to large strain caused by thermal stress and the molecular movement requisite for desolvation and deoxygenation. When cooled to room temperature and le exposed to oxygen, the crystals slowly reabsorb O 2 over a period between 24 and 48 h depending on size. Even during the resorption of oxygen many of the single crystals did not lose integrity. Through successive X-ray diffraction data collections on one single crystal as its oxy, then deoxy, then oxy form again, we can now not only report the rst structure of a deoxy form of this type of complex, [{(bpbp)Co 2 (NO 3 )} 2 (NH 2 bdc)](NO 3 ) 2 $2H 2 O, 2b deoxy (NO 3 ) 2 $2H 2 O, but also that this material has formed by a remarkable single-crystal-to-single-crystal (SC-to-SC) transformation. It can then undergo a second equally remarkable SCto-SC to reform the oxy complex. Crystal structures were recorded in all three steps on one crystal, amounting to 1.5 desorption/sorption cycles and 2b deoxy (NO 3 ) 2 $2H 2 O is the middle phase of a SC-to-SC-to-SC transformation (Table 1). Diffraction quality decreased over successive cycles, although visual inspection with a light microscope suggests that good crystals can repeat this process consecutively through at least 5 cycles. They will typically lose integrity, but not crystallinity, aer a few cycles, making X-ray diffraction analysis using our machine impossible. Functionality is not lost since the resultant crystalline powders can still reversibly bind O 2 .
Crystals of 2b(NO 3 ) 4 $xH 2 O are weakly diffracting, leading to low quality intensity data, and considerable disorder in both cocrystallized solvent molecules and nitrate counteranions is observed. Aer heating and the structure of the resultant pink deoxy form had been determined, this same crystal was carefully placed in a drop of Fomblin® Y oil on a microscope slide and le for 48 h whereupon it converted back to the dark colour. Another data set was collected and the re-formation of the 2b(NO 3 ) 4 $7H 2 O veried. The structures of the cations in 2b(NO 3 ) 4 $7H 2 O and 2b deoxy (NO 3 ) 2 $2H 2 O are shown in Fig. 5a and b respectively. Important distances and angles are given in Table 2.
The peroxide ligand is, as expected, absent in the deoxy form. The surprise to us was that the Co(II) ions are still six coordinated. Two of the formally counter anionic nitrate ions are now coordinated in a bridging mode. The coordinated nitrates and peroxo ligands of the deoxy and oxy forms respectively are located on opposite sides of the plane formed by the Co 4 (NH 2 bdc) unit. Although impossible to decipher which two of the four nitrate anions move and become coordinated in the deoxy form, it is reasonable to assume that it is those in closest proximity to the binding sites at each end of the molecule. A comparison of the oxy and deoxy structures suggest that the translational movement needed for the pertinent O atoms of the closest nitrate ions to each end of the molecule are between 4-6Å. These closest nitrate oxygen atoms (those associated with N14 and N15) to each dinuclear site are located on the opposite side of the molecule from each other (as dened by the plane of the linking aminobenzene ring). The O NO 3 /Co distances are O14/Co1, 5.597Å O16/Co2, 4.648Å, O11/Co4, 5.56Å and O12/Co3, 4.201Å, ESI Fig. S1. † Thus a scenario for the deoxygenation reaction mechanism of a SN 2 type reaction at each Co ion where the nitrates push the O 2 release can be envisaged. This scenario involves some donor atom slipping and movement of the supporting ligands. An impression of the movement of the atoms of the dinucleating ligand can be seen in the overlay of 2b and 2b deoxy in ESI Fig. S2. † Relative to the movement of O 2 , nitrate and water, this must be a minor rattling for the crystals. It does not, however, lessen the impressiveness of the SC-to-SC transformations observed. The distance between the nitrate coordinated oxygen atoms are on average 2.185(7)Å, whereas the O-O bond distance is av. 1.423(9)Å. The Co(II)-Co(II) distance in 2b deoxy averages 3.448 (2) A, and this is shortened to a Co(III)-Co(III) distance of av. 3.171(2)Å in the oxygenated form, 2b. This difference is due to   the bite of the syn-m 2 -nitrate 2À vs. that of syn-m 2 -O 2 2À , the respective metal ion radii, and the more powerful geometric preference for the Co(III) system to show a regular octahedral geometry. Chemically, each end of 2b and 2b deoxy is different due to the single amine group ortho to one of the carboxylato groups in the linker 2-aminoterephthalato ligand. In both of the structures this amine group is disordered approximately equally over the two positions para to each other (both positions depicted in Fig. 5). There is H-bonding between the NH 2 bdc 2À amine group and the adjacent coordinated carboxylato oxygen Inspection of unit cell sizes reveals that the crystal lattice expands by around 2% when it expels O 2 . This is surprising given that the material is being converted from a tetracation to a dianion with correspondingly four and two counter nitrates respectively, and a lower water content in the deoxy from. The calculated void space in fully desolvated models of 2b(NO 3 ) 4 $7H 2 O and 2b deoxy (NO 3 ) 2 $2H 2 O using a probe radius of 1.2Å are 4.8% and 7.0% respectively. Another possible contributing factor for the relatively slow uptake of O 2 by the nitrate salt is that the voids do not form channels in 2b deoxy -(NO 3 ) 2 $2H 2 O. By contrast they do in 2b(NO 3 ) 4 $7H 2 O. This might facilitate the desorption process. If the probe radius is expanded to 1.6Å for 2b(NO 3 ) 4 $7H 2 O and 1.9Å for 2b deoxy -(NO 3 ) 2 $2H 2 O the void space effectively becomes 0% in both structures (calculated within the Mercury CSD 3.1.1 suite from CCDC 15,16 ). The kinetic diameter of O 2 is 3.46Å. 17 See ESI Fig. S6-S9 † for impressions of voids/pseudo voids. These facts suggest an active transport mechanism for the O 2 where conduit voids are not actually essential for sorption/desorption. We have shown that signicant atomic movement is possible in the crystals and we conclude that the O 2 hops between the chemisorptive binding sites. The pronounced structural exibility observed here upon guest desorption is reminiscent of that seen in a range of other discrete supramolecular host materials, 18,19 in which retention of monocrystallinity occurs despite the rather extreme requirements that guest molecule migration and structural transformation place on the host crystal. Host materials have been shown to undergo phase transitions from non-porous to porous on uptake of CO 2 . 19 Of particular note here is that the system retains crystallinity with the migration and subsequent binding of nitrate anions on the dinuclear Co(II) sites (see ESI Fig. S2(b) † for molecular overlays showing the resulting distortion of the discrete tetranuclear host).
The hydrogen bonding interaction of the amine group with the coordinated carboxylate at one end of the molecule might be expected to modulate the O 2 binding affinity of this end such that the semioxy intermediate, [(bpbp)Co 2 (NO 3 )(NH 2 bdc)(bpbp)-Co 2 (O 2 )](NO 3 ) 3 , is thermally stable at intermediate temperatures. We have, however, not found conditions by which we can detect this putative species during attempts to follow the single crystal structure of a sorbing crystal. We note that the temperature dependent cycling of reversible O 2 binding by 2b(BF 4 ) 4 (Fig. S10 †) shows yields decrease marginally more on each successive cycle compared to 2a(NO 3 ) 4 (Fig. 2). It seems obvious to speculate that the BF 4 À ions do not interact with the Co(II) 2 sites as intimately as NO 3 À . Thus on O 2 desorption lattice water coordinates to the resultant Co(II) ions. If the aquo ligands of these putative {Co(II)(OH 2 )} 2 motifs cannot be substituted by O 2 during its oxidative sorption, "met" Co 2 III sites containing aquo and hydoxo ligands will result through an outersphere oxidation process. We have observed previously that reduction of complexes with this H-bonded Co III (HOHOH)Co III motif is not favorable, 13 thus the active sites will be poisoned.

Vibrational spectroscopy
The solid state transformations between 2b(NO 3 ) 4 $7H 2 O and 2b deoxy (NO 3 ) 2 $2H 2 O can be observed using resonance Raman and IR spectroscopies ( Fig. 6 and 7, respectively). Specically, the band at 840 cm À1 , assigned to the O-O stretch, is much reduced in the resonance Raman spectra when 2b(NO 3 ) 4 $7H 2 O is heated. During this process new bands associated with the coordinated bridging nitrate at 570, 710 and 1700 cm À1 grow in. IR spectra show that water is lost in the rst heating of 2b(NO 3 ) 4 $7H 2 O as the broad band between 3000 and 3500 cm À1 reduces signicantly, see SI Fig. S3. † Otherwise the most signicant changes occur between 800 and 1000 cm À1 and these can predominantly be associated with changes in the N-O bond strength within the nitrate ions, especially those moving from coordinated to non-coordinated positions. The two coordinated  nitrates can be expected to be chemically different due to the presence of the amine adjacent to one of these and this will smear the spectra further. A small difference in the n as (ca. 1570 cm À1 ) and n s (ca. 1440 cm À1 ) due to the bridging carboxylato bands of the NH 2 bdc 2À unit can be seen in the IR spectra of the oxy and deoxy forms. This is rationalized mainly by the observed changes in the C-O bond distances in the Co(II) and Co(III) complexes.

Conclusions
With the cleavage of four bonds, and the creation of four bonds in one molecule/cation, the complete evacuation and selective uptake of a diatomic gas, atom movements by up to 7Å of anions, hydration changes and donor atom sliding, the successive SC-to-SC-to-SC transformations we have followed by single crystal Xray diffraction are remarkable. Although several impressive examples of SC-to-SC transformations are known, 18-20 to our knowledge none undergo such extensive atom movements, bond cleavage and formation and reversibility with gas sorption and desorption.
Previously we had speculated that the active site of 2a deoxy (PF 6 ) 4 in the solid state was coordinatively unsaturated and that this accounted for a higher affinity, by an order of magnitude, for O 2 compared to when 2a deoxy is dissolved and hence having solvent molecules occupying the sixth position. 8 The present work shows this assumption may not be entirely correct: The respective degrees of association of the counteranions of the series with the Co(II) atoms of the deoxy forms play a major role in determining reaction rates of sorption and desorption processes. Nitrate is the strongest donor of the counteranions selected in this study, thus it will form the strongest interaction (formally coordination) with the metal ions. The uorinated anions, typically regarded as non-coordinating or very weakly coordinating, 21 are presumably more weakly associated with the metal centers in the deoxy forms, if they move at all during the sorption/desorption processes.
In the solid state this series of compounds show O 2 binding affinities and reversibility which rival that of myoglobin. We have found, however, that crystal structure plays a far greater role in tuning these properties compared with the electronic tuning possible through the introduction of substituents on the linker dicarboxylate unit. BET measurements of 2a deoxy (PF 6 ) 4 had indicated that this material was non-porous. 8 This result, along with the calculated insufficient void space in 2b deoxy (NO 3 ) 2 $2H 2 O for physisorbing O 2 implies that the O 2 molecules are actively transported through the crystalline phases of these materials: a biomimetic chemisorptive hopping mechanism of the O 2 molecules from Co 2 site to Co 2 site can be imagined. This will require considerable molecular exibility, molecule and nitrate ion movement, yet crystallinity is retained.

Experimental
ESI-MS spectra were recorded on a Bruker microTOF-QII. Thermogravimetric analysis was performed on a PerkinElmer TGA 4000. Samples were heated from 30 C to 140 C at 5 C min À1 under a stream of N 2 (20.0 mL min À1 ). Cooling was done at same rate under a stream of O 2 (20.0 mL min À1 ). VT-IR measurements were collected from 25 C up to 240 C (ramping and then holding at each temperature) and then back down again to RT using a Bruker FT-IR spectrometer with ATR attachment. VT-Raman was performed between À20 C and 120 C using a Renishaw Raman in Via Reex spectrometer (514 nm laser). Elemental microanalyses were performed at the Department of Chemistry, University of Copenhagen, Denmark. Single crystal data were collected with a Bruker-Nonius X8 Kappa Apex II at 150 K using Mo Ka radiation (l ¼ 0.71073Å). Semi-empirical absorption corrections were applied using SADABS. 22 Initial models were obtained with SHELXS-2013 using Direct Methods and further rened with SHELXL-2013. 23 Hydrogen atoms on C atoms were placed at calculated positions and allowed to ride during renement with U iso (H) ¼ 1.5U eq when connected to methyl groups and U iso (H) ¼ 1.2U eq for others. Hydrogen atoms connected to heteroatoms were not located in different Fourier maps and were excluded in the renement. [{Co 2 (bpbp)(O 2 )} 2 (bdc)](PF 6 ) 4 $3H 2 O (2a(PF 6 ) 4 $3H 2 O) and bpbpH were prepared as previously reported. 8,24 Synthesis [{Co 2 (bpbp)(O 2 )} 2 (bdc)](BF 4 ) 4 $5H 2 O$MeOH (2a(BF 4 ) 4 $ 5H 2 O$MeOH). A solution of sodium 1,4-benzenedicarboxylate (Na 2 bdc; 55.0 mg, 0.26 mmol) was dissolved in H 2 O (10 mL) and added dropwise to a solution of Co(BF 4 ) 2 $6H 2 O (356.7 mg, 1.05 mmol) and bpbpH (299.8 mg, 0.52 mmol) in acetone-MeOH (1 : 1, 50 mL). Slow evaporation of the resulting dark brown solution yielded black needle-like crystals which were collected by ltration, washed with ice cold H 2 O (3 Â 5 mL) and air-dried (289.7 mg, 0.15 mmol, 57.0%). Anal. calcd (found)