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A series of M[Au(CN)2]2(analyte)x coordination polymers (M = Co, Ni; analyte = dimethylsulfoxide (DMSO), N,N-dimethylformamide (DMF), pyridine; x = 2 or 4) was prepared and characterized. Addition of analyte vapours to solid M(μ-OH2)[Au(CN)2]2 yielded visible vapochromic responses for M = Co but not M = Ni; the IR νCN spectral region changed in every case. A single crystal structure of Zn[Au(CN)2]2(DMSO)2 revealed a corrugated 2-D layer structure with cis-DMSO units. Reacting a Ni(II) salt and K[Au(CN)2] in DMSO yielded the isostructural Ni[Au(CN)2]2(DMSO)2 product. Co[Au(CN)2]2(DMSO)2 and M[Au(CN)2]2(DMF)2 (M = Co, Ni) complexes have flat 2-D square-grid layer structures with trans-bound DMSO or DMF units; they are formed via vapour absorption by solid M(μ-OH2)[Au(CN)2]2 and from DMSO or DMF solution synthesis. Co[Au(CN)2]2(pyridine)4 is generated via vapour absorption by Co(μ-OH2)[Au(CN)2]2; the analogous Ni complex is synthesized by immersion of Ni(μ-OH2)[Au(CN)2]2 in 4% aqueous pyridine. Similar immersion of Co(μ-OH2)[Au(CN)2]2 yielded Co[Au(CN)2]2(pyridine)2, which has a flat 2-D square-grid structure with trans-pyridine units. Absorption of pyridine vapour by solid Ni(μ-OH2)[Au(CN)2]2 was incomplete, generating a mixture of pyridine-bound complexes. Analyte-free Co[Au(CN)2]2 was prepared by dehydration of Co(μ-OH2)[Au(CN)2]2 at 145 °C; it has a 3-D diamondoid-type structure and absorbs DMSO, DMF and pyridine to give the same materials as by vapour absorption from the hydrate.
Vapochromic materials, which display colour (optical absorption) or luminescence changes upon exposure to vapours of volatile organic compounds (VOCs), are of great interest due to their potential applications for chemical vapour detection [1–16]. Such sensors are commercially important as environmental monitoring devices, as safety systems in industrial settings and for defence and security applications [17]. As an example of a vapochromic material, the polymeric Prussian Blue-type Co2+/[Re6Q8(CN)6]4− (Q = S, Se) material yields dramatic changes in the visible spectrum when exposed to specific VOCs; the colour changes are linked to the sensed solvent impacting the geometry and hydration around the Co(II) centres [12]. A range of compounds based on Au(I), Pd(II) and Pt(II) coordination polymers have also been extensively investigated for their vapochromic responses [1–12,14]. The vapochromism in these systems is based on changes in both the visible absorption and emission spectra. In the linear {Tl[Au(C6Cl5)2]}n polymer, weak interactions between the Tl atoms and the absorbed VOC molecules modify the emission spectra [8]. On the other hand, emission changes in [Pt(CN-R)4][M(CN)4] (R= iso-C3H7 or C6H4-CnH2n+1; n=6, 10, 12, 14 and M = Pt, Pd) occur when metal-metal distances are modified due to the presence of VOC molecules in lattice voids [9,10,18]. A related mode of action is operative for supramolecular columns of Au3(MeN=COMe)3 molecules, in which VOCs intercalate or otherwise impact the stacking of one polymorph, thereby altering the emission properties [1–3,19,20]; similarly, crystalline, luminescent {Au3(p-MeC6H4N=COEt)3}2 becomes non-emissive upon exposure to hexafluorobenzene [7].
Among coordination polymers, cyanometallate building blocks have been particularly heavily utilized to form extended networks [21–25]. Despite this, [Au(CN)2]− has been relatively neglected as a building block in coordination polymers despite its unusual features: it is linear, forms gold-gold intermolecular interactions, and is luminescent [26–34]. We have reported the new vapochromic Cu(μ-OH2)2[Au(CN)2]2 and Zn[Au(CN)2]2 coordination polymer materials [35–38]. The Cu(μ-OH2)2 [Au(CN)2]2 system reacts reversibly with certain VOCs containing nitrogen- or oxygen-donors (or irreversibly with NH3) in the solid-state, generating significant analyte-specific colour changes, as well as distinct changes to the number and position of the νCN IR bands. An examination of the crystal structures of the dimethylsulfoxide (DMSO), N,N-dimethylformamide (DMF) and pyridine adducts allowed a postulation of the mechanism of reversible vapochromism: the Cu[Au(CN)2]2 superstructure flexibly distorts to accommodate analyte binding to Cu(II); this binding changes the ligand field, thereby impacting the colour. Changes in the cyanometallate superstructure can also be transmitted via the νCN pattern [35,36].
Substitution of copper(II) for zinc(II) yields four polymorphs of Zn[Au(CN)2]2 [37,38], which are highly emissive upon UV-excitation and, more importantly, are extremely sensitive to ammonia vapour; exposure causes a large emission shift [37]. As in the Cu(II) system, ammonia binds to the Zn(II) centre, which triggers the flexible Zn[Au(CN)2]2 superstructure framework to dynamically adapt to accommodate the analyte. This changes the gold-gold distances in the structure and, since these aurophilic interactions are the source of the emission [30–32], any change in their geometry or topology impacts the emission energy. Both the Cu(II) and Zn(II) coordination polymers are oxygen-stable and thermally robust.
It is clear from the mode of action that the ligand coordination preferences of the metal cation (Cu or Zn) are a key feature influencing which analytes are ultimately sensed, and which are more favoured from a sensitivity perspective [39]. Thus, examining other metal cations as the binding site is worthwhile both as a comparison to the copper(II) and zinc(II) systems and in the possibility of preparing improved sensor materials or a sensor for new analytes that would not be significantly detected by the vapochromic Cu(II) or luminescent Zn(II) cyanoaurate systems.
Towards this end, we recently reported the isostructural M(μ-OH2)2[Au(CN)2]2 series, where M = Mn, Fe, Co, Ni and Cu [40,41]. The Cu(II) analogue shows strong, sensitive vapochromic responses to a series of analytes, as described above [35,36]. This manuscript examines the vapochromic response of the isomorphous Co(II) and Ni(II) analogues to a series of analytes—DMF, DMSO and pyridine—which were studied in detail for the Cu(II) system and which showed moderate sensitivity, thereby allowing for a direct comparison of vapochromic efficacy and superstructural flexibility as a function of metal cation. A qualitative report on the vapochromic response of Co[Au(CN)2]2 with a series of analytes and their IR shifts was very recently reported, but was lacking in any structural or other characterization data on the Co-analyte system or the parent compound [42,43].
Experimental SectionGeneral Procedures
All manipulations were performed in air unless otherwise noted. All reagents were purchased from commercial sources and used as received, except for M(μ-OH2)[Au(CN)2]2 (M = Co, Ni), which were prepared as previously described [40,41].
CAUTION: Although we have experienced no difficulties, perchlorate salts are potentially explosive and should be used in small quantities and handled with care.
Infrared spectra were recorded on a Thermo Nicolet Nexus 670 FT-IR spectrometer with samples prepared as KBr pressed pellets or analyzed with a Pike Miracol ATR attachment (Table 1). The resolution of the instrument was set at 1 cm−1 and the spectra were collected between 400 (KBr) or 700 (ATR) and 4,000 cm−1. Microanalyses (carbon, hydrogen and nitrogen) were performed at Simon Fraser University using a computer-controlled Carlo Erba (Model 1110) CHN analyzer. Thermogravimetric analyses (TGA) of all complexes were performed in an air atmosphere on a Shimadzu TGA-50 instrument at a rate of 5 °C per minute. Solid-state UV-Vis-NIR absorption spectra were measured by reflectance using an Ocean Optics SD2000 spectrophotometer equipped with tungsten halogen and deuterium lamps. Prior to analysis, the samples were ground into fine powders and placed on a glass plate. Magnesium oxide powder, prepared in the same fashion, was used as a reference. Powder X-ray diffractograms were collected on a Rigaku RAXIS-Rapid Auto diffractometer equipped with a Cu Kα source (λ = 1.54056 Å). Samples were mounted on a glass fiber using grease and were exposed, as the phi axis was spinning (10° s−1), for a period of 20 to 60 minutes (with the chi axis fixed at 0 and omega fixed at 90°).
Synthesis of Zn[Au(CN)<sub>2</sub>]<sub>2</sub>(DMSO)<sub>2</sub>
To a DMSO solution (0.5 mL) of Zn(ClO4)2 (32 mg, 0.086 mmol), a DMSO solution (0.5 mL) of K[Au(CN)2] (50 mg, 0.17 mmol) was added dropwise. The solution was allowed to evaporate slowly. Crystals of Zn[Au(CN)2]2(DMSO)2 were formed over several days of slow evaporation. Yield: 0.030 g, 42%. Anal. Calcd. for C8H12N4Au2O2Zn: C, 13.35%; H, 7.79%; N, 1.68%. Found: C, 13.50%; H, 8.04%; N, 1.72%. IR (KBr): 3,009 (w), 2,919 (w), 2,186 (m, νCN), 2,175 (m, νCN), 1,314 (w), 1,299(w), 1,030 (m), 1,013 (s, νS=O), 1,005 (s, νS=O), 957 (m) cm−1.
Synthesis of Co[Au(CN)<sub>2</sub>]<sub>2</sub>(DMSO)<sub>2</sub>
Co(μ-OH2)2[Au(CN)2]2 (0.125 g, 0.211 mmol) was mixed with DMSO (1 mL) and left to sit for 72 hours, covered. The resulting pink fine powder was then isolated by decantation and left to dry in ambient air. The composition was found to be Co[Au(CN)2]2(DMSO)2. Yield: 0.121 g, 80.4%. Anal. Calcd for C8H12N4Au2CoO2S2: C, 13.47%; H, 1.70%; N, 7.86%. Found: C, 13.51%; H, 1.73%; N, 7.69%. IR (KBr): 3,021(w), 3,009(w), 2,920(w), 2,177(s, νCN), 1,421(w), 1,408(w), 1,316(w), 1,298(w), 1,031(m), 997(s), 957(m), 938(m), 905(w), 717(w), 467(w), 441(w) cm−1. The same product can also be obtained by vapour absorption of DMSO by Co(μ-OH2)2[Au(CN)2]2 or Co[Au(CN)2]2.
Synthesis of Ni[Au(CN)<sub>2</sub>]<sub>2</sub>(DMSO)<sub>2</sub>
A DMSO solution (0.75 mL) of Ni(NO3)2·6H2O (0.057 g, 0.20 mmol) was added to a DMSO solution (1.75 mL) of K[Au(CN)2] (0.123 g, 0.427 mmol). A turquoise blue powder started to precipitate after approximately one hour. It was collected by filtration 24 hours later and air-dried. The composition of the final product was determined to be Ni[Au(CN)2]2(DMSO)2. Yield: 0.101 g, 70.8%. Anal. Calcd. For C8H12N4Au2NiO2S2: C, 13.48%; H, 1.70%; N, 7.86%. Found: C, 13.70%; H, 1.81%; N, 8.10%. IR (KBr): 3,434(m), 3,010(w), 2,919(w), 2,189(s, νCN), 2,180(s, νCN), 1,629(w), 1,409(w), 1,314(w), 1,299(w), 1,032(m), 1,008(s), 1,001(s), 956(m), 713(w), 480(w), 430(w) cm−1.
Synthesis of Ni[Au(CN)<sub>2</sub>]<sub>2</sub>(DMF)<sub>2</sub>
Ni(μ-OH2)2[Au(CN)2]2 (0.115 g, 0.194 mmol) was mixed with DMF (1 mL) and left to sit for 24 hours, covered. The resulting blue powder was then isolated by filtration and the composition of the final product was found to be Ni[Au(CN)2]2(DMF)2. Yield: 0.092 g, 69%. Anal. Calcd for C10H14N6Au2NiO2: C 17.09%, H 2.01%, N 11.96%. Found: C 16.95%, H 2.08%, N 12.24%. IR (KBr): 3,429(m), 2,994(w), 2,964(w), 2933(m), 2,892(w), 2,809(w), 2,189(s, νCN), 1,658(s), 1,498(w), 1,434(m), 1,418(w), 1,384(m), 1,252(m), 1,109(s), 1,061(m), 689(s), 488(w) cm−1.
Synthesis of Co[Au(CN)<sub>2</sub>]<sub>2</sub>(Pyridine)<sub>2</sub>
Co(μ-OH2)2[Au(CN)2]2 (0.052 g, 0.088 mmol) was mixed with water/pyridine (2.5 mL, 95:5) and let to sit for 24 hours, covered. The powder became more orange, was isolated by filtration and dried in ambient air. The composition was found to be Co[Au(CN)2]2(pyridine)2. Yield: 0.049 g, 78%. Anal. Calcd for C14H10N6Au2Co: C 23.51%, H 1.41%, N 11.75%. Found: C 23.67%, H 1.55%, N 11.68%. IR (KBr): 3,086(w), 3,068(w), 3,053(w), 3,024(w), 2,168(s, νCN), 1,605(s), 1,574(s), 1,486(m), 1,447(s), 1,242(w), 1,216(m), 1,157(w), 1,073(m), 1,041(m), 1,016(w), 946(w), 882(w), 759(m), 698(s), 633(m), 460(w), 431(m) cm−1.
Synthesis of Ni[Au(CN)<sub>2</sub>]<sub>2</sub>(Pyridine)<sub>4</sub>
A 96:4 water/pyridine solution (1.5 mL) of K[Au(CN)2] (0.059 g, 0.21 mmol) was prepared. This solution was added to a 96:4 water/pyridine solution (1 mL) of Ni(NO3)2·6H2O (0.030 g, 0.10 mmol). A purple powder was obtained immediately, which was filtered and air-dried. The product was determined to be Ni[Au(CN)2]2(pyridine)4. Yield: 0.070 g, 78%. Anal. Calcd for C24H20N8Au2Ni: C 33.02%, H 2.31%, N 12.83%. Found: C 32.64%, H 2.25%, N 12.55%. IR (KBr): 3,095(w), 3,070(w), 3,041(w), 3,023(w), 2,993(w), 2,924(w), 2,855(w), 2,171(s, νCN), 2,143(s, νCN), 1,602(s), 1,574(m), 1,488(m), 1,449(s), 1,443(s), 1,237(w), 1,216(m), 1,151(w), 1,068(m), 1,042(m), 1,011(w), 769(m), 756(m), 699(s), 631(m), 469(w), 435(m) cm−1.
Synthesis of Co[Au(CN)<sub>2</sub>]<sub>2</sub>
Co(μ-OH2)2[Au(CN)2]2 was heated to 145 °C in an oven for 2 hours to afford cobalt-blue coloured Co[Au(CN)2]2 quantitatively. The product is stable in air for approximately two days, and was stored under an inert atmosphere to prevent rehydration. Anal. calcd. for C4N4Au2Co: C, 8.63%; H, 0%; N, 10.06%. Found: C, 8.51%; H, trace%; N, 9.67%. IR (ATR): 2,177 (s, νCN), 2,140 cm−1 (vw, 13νCN).
Single Crystal X-Ray Structure of Zn[Au(CN)<sub>2</sub>]<sub>2</sub>(DMSO)<sub>2</sub>
A 0.42 × 0.22 × 0.14 mm3 crystal of Zn[Au(CN)2]2(DMSO)2 was mounted on a glass fiber using epoxy adhesive. The data were collected at room temperature on an Enraf Nonius Delft CAD-4 diffractometer with a PMT point detector using the control program DIFRAC [44]. A Mo Kα normal-focus sealed tube operated at 0.736 kW power (46 kV, 16 mA) was utilized for data collection over the range 4° < 2θ < 60°. The data was corrected by integration for the effects of absorption using a semi-empirical psi-scan method with a 0.073–0.262 transmission range. Data reduction included corrections for Lorentz and polarization effects using the NRCVAX software suite [45]. Final unit-cell dimensions were determined based on 43 well-centred reflections with a range of 47° < 2θ < 51°. The structure of Zn[Au(CN)2]2(DMSO)2 was solved in CRYSTALS [46] using direct methods (SIR92) and expanded using Fourier techniques. Diagrams were prepared using ORTEP-3 [47] and POV-Ray [48].
The coordinates and anisotropic temperature factors for all non-hydrogen atoms were refined. The final refinement using observed data (Io ≥ 2.50 σ(Io)) included an extinction parameter, and statistical weights with 177 parameters for 2,953 unique reflections. Hydrogen atoms were placed in calculated positions (dC-H 0.95 Å) and initially refined with soft restraints on the bond lengths and angles to regularise their geometry; afterwards their coordinate shifts were linked with those of the respective carbon atoms during refinement. Isotropic thermal parameters for the hydrogen atoms were initially assigned proportionately to the equivalent isotropic thermal parameters of their respective carbon atoms. Subsequently the isotropic thermal parameters for the H atoms on the DMSO were constrained to have identical shifts during refinement. Crystallographic data for Zn[Au(CN)2]2(DMSO)2 are tabulated in Table 2. Selected bond lengths and angles are given in Table 3.
Powder X-Ray Data Indexing/Structure Determination of M[Au(CN)<sub>2</sub>]<sub>2</sub>(analyte)<sub>x</sub> (M = Co and Ni)
The structures of Ni[Au(CN)2]2(DMF)2 and Co[Au(CN)2]2(pyridine)2 were solved and refined using the DASH software package [49]. After indexing the experimental diffractogram, an automatic background fitting and subtraction was performed, followed by peak fitting to extract the intensity of each peak. To solve the crystal structure, a predefined building block was used. The asymmetric units of Co[Au(CN)2]2(DMF)2 [50] and Cu[Au(CN)2]2(pyridine)2 [35] were chosen as the building blocks used to solve the structure of Ni[Au(CN)2]2(DMF)2 and Co[Au(CN)2]2(pyridine)2 respectively. Optimization of the position and orientation of this building block was performed using a simulated annealing algorithm to maximize the agreement with the experimental diffractogram (relative intensity and peak position). The coordinates of each atom in the building blocks were further optimized once a structural model was obtained. The orientation of the pyridine molecules in Co[Au(CN)2]2(pyridine)2 was not refined as the diffractogram is mainly affected by the atomic position of the heavy atoms and slight changes in the position of the pyridine molecules do not cause noticeable changes in the diffractogram. The atomic coordinates for Ni[Au(CN)2]2(DMF)2 and Co[Au(CN)2]2(pyridine)2 are reported in Tables S1 and S2, respectively. Due to the poor quality of the powder diffractogram, the structure of Ni[Au(CN)2]2(DMSO)2 could not be determined using DASH. The diffractogram could, however, be indexed using WinPLOTR [51] to a unit cell very similar to that of the analogous Zn-containing polymer. The powder diffractogram for Co[Au(CN)2]2(DMSO)2 was also poor and was therefore only indexed with WinPLOTR but not utilized to generate an atomic resolution structure.
Results and Discussion
The vapochromic behaviour of the M(μ-OH2)2[Au(CN)2]2 (M = Co, Ni) coordination polymers was investigated by exposing them to vapours of DMSO, DMF and pyridine for several hours/days in a sealed container, after which the FT-IR and UV-vis-NIR spectra and the powder X-ray diffractogram of the product were collected. The νCN bands for each product are reported in Table 1 and compared with those of the product made from solution (see below); visible colour changes were more noticeable for the Co(II) system (Figure 1) than for the Ni(II) analogue. Details for each metal/VOC vapour combination are outlined below.
DMSO-Containing Complexes
Upon exposure to DMSO, the pink Co(μ-OH2)2[Au(CN)2]2 coordination polymer (λmax ≥ 1110, 525 nm) was converted over a three day period to a lighter, brighter pink coloured product (Figure 1; λmax = 1,040, 500, 470 nm) with a νCN band at 2,176 cm−1 (Table 1). This material was stable for months after exposure to ambient atmospheric conditions, indicating that replacement of DMSO molecules for water molecules does not occur at room temperature, which contrasts with the two previously reported Cu[Au(CN)2]2(DMSO)2 polymorphs that readily undergo conversion when exposed to ambient moisture [35]. On the other hand, when Ni(μ-OH2)2[Au(CN)2]2 was exposed to DMSO vapour for one week, νCN bands attributable to the starting material were still present, as well as new bands at 2,181/2,164 cm−1. No visible colour change occurred.
Since VOC absorption by M(μ-OH2)2[Au(CN)2]2 powders does not lead to single crystals suitable for structural analysis, in order to assist in deciphering the identity and structure of these M[Au(CN)2]2(DMSO)x products, the preparation of the analogous materials via solution methods was targeted. Thus, the reaction of Co(II), Ni(II) and Zn(II) salts with K[Au(CN)2] in DMSO was conducted; the Zn(II) analogue is included since it is the only one which forms single crystals from DMSO. The Ni and Zn reactions afforded the formation of a blue/turquoise precipitate (Ni) or colourless crystals (Zn) of M[Au(CN)2]2(DMSO)2, determined by elemental analysis. The FT-IR spectra show two strong bands in the cyanide stretching region (νCN = 2,189/2,180 and 2,186/2,175 cm−1 for the Ni and Zn systems, respectively) as well as bands attributable to the sulfoxide (S=O) moiety (1,032–956 cm−1) [52]. The slight shift in νCN between the Ni and Zn materials can be attributed to the different transition metal bound to the nitrogen atom of each cyanide group [53].
The Zn[Au(CN)2]2(DMSO)2 structure (Figure 2, Tables 2 and 3) contains a single octahedral Zn(II) centre, with two cis-coordinated oxygen-bound DMSO molecules (Figure 2(a), Zn-O = 2.120(6) and 2.075(6) Å). The remaining four sites around the Zn(II) are coordinated with [Au(CN)2]− units with an average Zn-N bond length of 2.144(8) Å, longer than the <2.0 Å Zn-N bond lengths in the tetrahedrally coordinated polymorphs of Zn[Au(CN)2]2 [37,38]. A 2-D corrugated structure, with DMSO molecules protruding from the apex of the corrugation, is formed by the bridging [Au(CN)2]− units (Figure 2(c)). The closest contact between sheets is a Au-Au interaction of 3.4943(6) Å. A similar crystal structure was observed for the Cu(II) system [35].
Although no single crystal of Ni[Au(CN)2]2(DMSO)2 suitable for X-ray crystallography could be obtained, its powder X-ray diffractogram showed similar features to the diffractograms of the Zn[Au(CN)2]2(DMSO)2 and Cu[Au(CN)2]2(DMSO)2 (blue polymorph) coordination polymers (Figure 3) [35]. The diffractogram of Ni[Au(CN)2]2(DMSO)2 could be indexed to a monoclinic unit cell, with parameters very similar to those of the Zn analogue (Table 4). Thus, the structure of Ni[Au(CN)2]2(DMSO)2 likely consists of octahedral Ni(II) ions coordinated by two DMSO molecules in a cis fashion and connected to four other Ni(II) centres via [Au(CN)2]− units, generating corrugated 2-D sheets; due to the poor quality of the diffractogram, no effort was made to structurally model the data any further. Note that the νCN data and powder X-ray diffractograms for Ni[Au(CN)2]2(DMSO)2 do not perfectly match those obtained via vapour absorption of DMSO by Ni(μ-OH2)2[Au(CN)2]2, indicating that a related, but different structure is likely accessed by vapour absorption.
Although the analogous reaction between a Co(II) salt and K[Au(CN)2] in neat DMSO yielded an inseparable mixture of products, when pink Co(μ-OH2)2[Au(CN)2]2 was immersed in DMSO for three days, a slight colour change occurred. The resulting light pink powder was isolated and the chemical composition was determined to be Co[Au(CN)2]2(DMSO)2. The FT-IR spectrum of this product contains only one νCN band (2,176 cm−1), analogous to that observed by vapour absorption (Table 1).
This reaction did not yield single crystals suitable for X-ray analysis, only microcrystalline powder. The powder diffractogram (Figure 4) was indexed and the unit cell parameters obtained are reported in Table 4. The diffractogram and the unit cell parameters do not match that of the Zn, Cu or Ni-containing M[Au(CN)2]2(DMSO)2 polymers (Figure 3 and Table 4), which suggests that a different structural arrangement is adopted. Due to the poor quality of the diffractogram, no structure refinement could be performed, but a structural model is proposed based on comparisons with other known complexes.
The presence of only one νCN band, shifted from free [Au(CN)2]−, suggests that all the cyanide groups are in a similar environment and N-bound to Co(II). This could be the case if the structure of Co[Au(CN)2]2(DMSO)2 contained square-grid arrays of Co[Au(CN)2]2 with DMSO molecules bound to Co(II) ions in a trans fashion, on each side of the grid. This type of structure has been observed for the previously reported Co[Au(CN)2]2(DMF)2 [50] and Mn[Au(CN)2]2(H2O)2 [54] coordination polymers. Although the νCN band observed for Co[Au(CN)2]2(DMSO)2 (2,176 cm−1) is similar to that for the DMF analogue (2,179 cm−1) [35], the powder diffractograms are a poor match.
The main features in the diffractograms of Co[Au(CN)2]2(DMSO)2 and Mn[Au(CN)2]2(H2O)2 [54] are similar (Figure 4). The packing in Co[Au(CN)2]2(DMF)2 differs from Mn[Au(CN)2]2(H2O)2 since the Co[Au(CN)2]2 layers stack in discrete pairs whereas the Mn[Au(CN)2]2 layers are equally spaced and do not form pairs of layers. It is hence suggested that, analogous to the Mn[Au(CN)2]2(H2O)2 superstructure, the Co[Au(CN)2]2(DMSO)2 polymer contains flat and equally spaced square-grid arrays, with DMSO molecules bound in a trans fashion.
With this information in hand, it is clear that vapour absorption of DMSO by Co(μ-OH2)2[Au(CN)2]2 gives Co[Au(CN)2]2(DMSO)2 cleanly; the solution method yields a product with comparable UV-vis, powder X-ray and IR data. However, the Ni(II) system does not run to completion, even after a week of vapour exposure, and the products from vapour and solution methods, although related, do not appear to be identical.
DMF-Containing Complexes
When Co(μ-OH2)2[Au(CN)2]2 was exposed to DMF vapour, faint colour changes to a light, bright pink (λmax = 1035, 490, 468 nm) were observed after several hours (Figure 1), and the IR spectrum indicated a clean conversion; a single νCN peak at 2,182 cm−1 was generated (Table 1). The analogous solution-based synthetic product has a comparable FTIR spectrum and powder X-ray diffractogram to that obtained by vapour absorption, both of which are indistinguishable from that of the previously published Co[Au(CN)2]2(DMF)2 system (Figure 5) [50]; this is therefore the product that is obtained. For the Ni(II) analogue, after one week of being exposed to DMF vapour, the FT-IR spectrum of the product showed the presence of the starting Ni(μ-OH2)2[Au(CN)2]2 compound as well as an additional band at 2,184 cm−1; no significant colour change was observed.
For comparison, when Ni(μ-OH2)2[Au(CN)2]2 was immersed in DMF for one day, a colour change from light green to blue was observed, similar to Co[Au(CN)2]2(DMF)2. The FT-IR spectrum of the isolated product showed only one νCN band at 2,189 cm−1. The chemical composition was determined to be Ni[Au(CN)2]2(DMF)2 from elemental analysis, comparable to the previously reported Co[Au(CN)2]2(DMF)2 coordination polymer [50] but different from that of the Cu(II)-containing analogue, in which only one DMF molecule was incorporated. The unit cell obtained from indexing the powder X-ray diffractogram of Ni[Au(CN)2]2(DMF)2 (Figure 5-Ni) is also similar to that of Co[Au(CN)2]2(DMF)2 (Table 5) [50].
Using the atomic coordinates of the published Co(II) analogue as a starting point, the structure of Ni[Au(CN)2]2(DMF)2 was determined from the observed powder X-ray diffractogram (the atomic coordinates are reported in Table S1). Figure 6 shows the proposed model for Ni[Au(CN)2]2(DMF)2.
As with Co[Au(CN)2]2(DMF)2, the structure contains 2-D square grids of Ni[Au(CN)2]2 (Figure 6(A)). The DMF molecules are O-bound to the Ni(II) centres on each side of the grids, which stack in an offset manner to accommodate the DMF molecules. The [Au(CN)2]− units are slightly bent and sit above and below the plane containing the Ni(II) centres (Figure 6(B,C)). As observed in the Co[Au(CN)2]2(DMF)2 structure, the layers stack in discrete pairs with aurophilic interactions of ca. 3.3 Å forming the pair, whereas Au-Au distances of ca. 5.4 Å separate each pair of layers.
Thus, both Co(II) and Ni(II) analogues of M(μ-OH2)2[Au(CN)2]2 sense DMF as an analyte, although the Co(II) system reacts more cleanly and quickly. Both form similar 2-D layer structures of M[Au(CN)2]2(DMF)2, with the same product being generated from solution or vapour absorption. However, the Ni(II) analogue only partially converts to product in the vapour absorption experiment, and as a result the expected visible vapochromism (green to blue by solution methods) was not observed; this putative vapochromic response was likely attenuated by the residual absorption bands of the unreacted starting material.
Pyridine-Containing Complexes
When Co(μ-OH2)2[Au(CN)2]2 was exposed to pyridine vapour, conversion to a light pink product (λmax = 1,000, 525, 485 nm, Figure 1) having νCN bands at 2,168/2,144 cm−1 occurred (Table 1). Upon exposure to pyridine vapour, Ni(μ-OH2)2[Au(CN)2]2 undergoes a colour change, from light green to blue over several days. The FT-IR spectrum shows νCN bands of the starting material and additional bands at 2,170/2,162/2,141 cm−1; this complexity likely indicates the formation of a mixture of analyte-containing products.
On the solution synthesis side, when a powdered sample of Co(μ-OH2)2[Au(CN)2]2 was immersed for one day in a mixture of water and pyridine (96:4), a slight colour change was observed. The FT-IR spectrum of the isolated powder showed only one strong νCN band at 2,168 cm−1 (Table 1), reminiscent of that of the Co[Au(CN)2]2(DMF)2 system. Thus, a different product is obtained in solution. Pyridine-based bands could also be observed.
The powder X-ray diffractogram of the solution-based product, which analyzes as Co[Au(CN)2]2(pyridine)2, is shown in Figure 7 and is different than the material obtained by vapour diffusion; it also shows similar features to the diffractogram of Co[Au(CN)2]2(DMF)2 (Figure 5) and Cu[Au(CN)2]2(pyridine)2. The diffractogram was indexed and the optimized unit cell parameters are reported in Table 5. They are comparable with those of the Ni and Co-containing M[Au(CN)2]2(DMF)2 complexes (Figure 6).
Using a combination of the Cu[Au(CN)2]2(pyridine)2 and Co[Au(CN)2]2(DMF)2 structures as a starting point, a structural model is proposed for Co[Au(CN)2]2(pyridine)2 (the corresponding atomic coordinates are reported in Table S2). The structure consists of 2-D square grids of Co[Au(CN)2]2 with pyridine molecules N-bound to the Co(II) centres on both sides of the layer (Figure 8(A)). The structure differs from the Cu(II) analogue as all the cyanide groups are equidistant from the Co(II) centres and no Jahn-Teller distortion is observed. Also, the Co[Au(CN)2]2 layers are not completely flat as in the Cu[Au(CN)2]2 system, but the [Au(CN)2]− units are buckled in an alternate way on each side of the layer (Figure 8(B)), as is observed in the related Co[Au(CN)2]2(DMF)2 polymer [50]. This arrangement allows π–π interactions between the pyridine rings, but no aurophilic interactions are present as the closest contact between two Au atoms is approx. 3.7 Å. The powder diffractogram predicted by this model is compared to the experimental diffractogram of Co[Au(CN)2]2(pyridine)2 in Figure 7.
The addition of Ni(NO3)2·6H2O to KAu(CN)2 in a mixture of water and pyridine (96:4) generated purple Ni[Au(CN)2]2(pyridine)4, confirmed by elemental analysis. The FT-IR spectrum of this product shows two νCN bands (2,171 and 2,143 cm−1), consistent with two of the three bands observed by vapour diffusion. Depending on the reaction conditions, variable amounts of an uncharacterized material could also be generated (as indicated by IR: 2182, 2153 cm−1) but a pure sample could not be isolated.
Clearly, pyridine as an analyte yields the most complex, least clean conversions for both Co(II) and Ni(II) analogues. Thus, for Co(II), a bis-pyridine adduct forms from aqueous pyridine solution, while vapour absorption methods generated a different product. A Ni[Au(CN)2]2(pyridine)4 complex was isolated via solution methods, confirmed by elemental analysis. The powder X-ray diffractograms of Ni[Au(CN)2]2(pyridine)4 and the Co vapochromic product are very similar, which suggests that the product of pyridine vapour with the Co(II) system is a tetrakis-pyridine adduct. Finally, pyridine vapour absorption by Ni(μ-OH2)2[Au(CN)2]2 is the least clean of all the reactions studied herein, generating Ni[Au(CN)2]2(pyridine)4, another unidentified product (perhaps a bis-pyridine adduct) as well as leaving residual starting material.
Analyte-Free M[Au(CN)<sub>2</sub>]<sub>2</sub> Systems
Analyte-free systems were investigated in order to see if the vapochromic response would be improved without the presence of an initial analyte molecule (H2O) in the structure. Co[Au(CN)2]2 was synthesized by heating Co(μ-OH2)2[Au(CN)2]2 to at least 110 °C for a minimum of one hour (ideally, 145 °C for two hours; heating at 180 °C for 10 minutes was very recently reported as an alternative synthesis [42]). The compound changes from a light pink colour (octahedral Co(II)) to an intense cobalt-blue colour (tetrahedral Co(II)). Co[Au(CN)2]2 is stable in ambient air for approximately two days, whereupon it rehydrates to a compound with a similar powder X-ray diffractogram and IR spectrum to Co(μ-OH2)2[Au(CN)2]2, but is a light purple colour; its identity is under investigation.
The structure of Co[Au(CN)2]2 was deduced by matching the powder X-ray diffractogram to that of the isostructural compound [37], γ-Zn[Au(CN)2]2 (Figure S1), indexing the data accordingly (spacegroup P-4b2, a = 6.7968(17) Å, c = 8.4651(3) Å) and refining atomic positions (Tables S3 and S4). The cobalt(II) centres are tetrahedrally coordinated through the nitrogen end of four [Au(CN)2]− units, creating a tetragonal diamond-type lattice (Figure 9). There are four interpenetrated networks that are linked together via aurophilic interactions (3.33 and 3.56 Å). Note that a previously reported synthesis of Co[Au(CN)2]2 (by a simple addition of salt [55]) generated a different polymorph (equivalent to quartz-type α-Zn[Au(CN)2]2) [37,38], while using another route, via solvent-free grinding of Co(OH2)2[Au(CN)2]2, the structure was not determined [42].
Vapochromic experiments were also performed on Co[Au(CN)2]2 with DMF, DMSO, and pyridine as analytes. Uptake occurred in all cases, yielding Co[Au(CN)2]2(analyte)x materials in similar shades of light pink; with DMF as the analyte, the complex showed the fastest conversion (about 1 day), whereas pyridine showed the slowest conversion (several days). Based on IR and powder X-ray diffraction data, the complexes that form using DMF and DMSO are identical to those produced from vapour absorption by Co(μ-OH2)2[Au(CN)2]2. The complex with pyridine shows two νCN bands at 2,170 and 2,142 cm−1 and a powder X-ray diffractogram matching the Co[Au(CN)2]2(pyridine)4 adduct identified via vapour absorption by Co(μ-OH2)2[Au(CN)2]2, rather than the bis-pyridine adduct obtained by solution methods. These IR spectroscopic results broadly match those very recently reported for the addition of a range of donor solvents (including pyridine, DMSO and DMF, as reported here) to Co[Au(CN)2]2 [42].
The synthesis of Ni[Au(CN)2]2 was attempted by several methods but the desired product could not be obtained. Since the dehydration temperature for Ni(μ-OH2)2[Au(CN)2]2 is between 215–260 °C, it is necessary to heat above 260 °C for extended periods of time to dehydrate it, but doing so resulted in decomposition. Attempts to effect chemical dehydration by stirring Ni(μ-OH2)2[Au(CN)2]2 in glacial acetic acid or refluxing in trimethylsilylchloride resulted in no change. The addition of [nBu4N][Au(CN)2] [56] to anhydrous NiCl2·DME in dry organic solvents under an inert, dry atmosphere yielded other products which are under investigation [57], but did not generate Ni[Au(CN)2]2. It therefore appears that Ni(μ-OH2)2[Au(CN)2]2 is exceptionally stable, which is in agreement with the vapour absorption results, which indicate only partial conversion in every case.
Comparison of M[Au(CN)<sub>2</sub>]<sub>2</sub>-Based Vapochromic Materials (M = Co, Ni, Cu)
The M[Au(CN)2]2(analyte)x polymers show visible vapochromism since each analyte molecule that is incorporated binds to the M(II) centre and modifies differently its crystal field splitting. As a consequence, the colours of the vapochromic compounds change as the d–d absorbance bands shift [35,36]. Table 6 shows the solid-state UV-vis-NIR absorbance maxima for the analyte-containing compounds prepared from solution (vs. direct analyte absorption by the solid).
The data in Table 6 and Figure 1 suggests that identification of the different M[Au(CN)2]2(analyte)2 polymers (M = Co, Ni) purely on the basis of colour cannot be accomplished as easily as for the Cu(II)-based analogues [35,36]. The M(II) coordination sphere in the M[Au(CN)2]2(analyte)2 polymers is very similar: an octahedral geometry with four cyanide groups occupying the same plane. The only difference lies in the two donor analytes that are trans to each other (M(NC)4(O-ligand)2vs. M(NC)4(N-ligand)2). As a result, the crystal field splitting of the M(II) centres in each M[Au(CN)2]2(analyte)2 is very similar and, hence, so is their colour, particularly for DMSO and DMF analytes; some differentiation for pyridine is possible. The spectra of the M(μ-OH2)2[Au(CN)2]2 polymers containing M(NC)2(O-ligand)4 centres is, however, shifted to slightly lower energy. The analyte-free Co[Au(CN)2]2 system is also markedly different from all Co(II)-analyte adducts, consistent with tetrahedral vs. octahedral Co(II) centres.
Upon comparing the reactivity of the M[Au(CN)2]2-based systems, analyte exchange is quickest for M = Cu(II) and Zn(II) [35–38], followed by the Co(II) system and least so in the Ni(II) system, for which analyte exchange was found to be only partial, with a mixture of products obtained; this is likely due to the relative kinetic inertness of Ni(II) complexes. Thus, the Ni(II)-systems are not likely to be very useful vapochromic materials for VOC sensing. Indeed, the most easily visible vapochromic system reported here is the analyte-free Co[Au(CN)2]2, for which drastic colour changes upon analyte-binding occurs, but differentiation of the products obtained with different analytes is more difficult. Note that other factors, such as particle size/surface area and analyte vapour pressure, also influence the overall kinetic response of the material.
From a structural perspective, it is known that a system does not need to be porous in order to undergo guest uptake [58]. For example, a flexible metal-ligand superstructure can dynamically adapt in order to accommodate a variety of potential guests, as is the case here [58–64]. Despite the range of analyte molecules utilized, the basic structural motif of the M[Au(CN)2]2(analyte)x coordination polymers remained the same in most cases: a 2-D square-grid M[Au(CN)2]2 network was the basic structural feature, which is flexible and can adapt to accommodate the requisite structural changes, depending on the metal ion and analyte type. Scheme 1 summarizes the different types of structural distortions observed for the M[Au(CN)2]2-based systems (M = Co, Ni, Cu).
The major mode of flexibility [62–64] lies in the fact that the 2-D square-grid can be entirely flat, as in the M[Au(CN)2]2(DMF)2 or M[Au(CN)2]2(pyridine)2 complexes, or it can buckle to generate a corrugated 2-D array, as observed in several M[Au(CN)2]2(DMSO)2 (M = Zn, Ni or Cu (blue polymorph)) polymers. In addition, in a flat square-grid, the [Au(CN)2]− units can lie completely co-planar with the M(II) centres as in Cu[Au(CN)2]2(pyridine)2 or bent out of the M(II)-containing plane, as in M[Au(CN)2]2(DMF)2. For a given analyte, similar structures are usually observed despite the change in metal centre. DMSO is the only type of guest utilized that forces corrugation of the layers, whereas DMF and pyridine favour flat square-grid arrays to be obtained.
Due to Jahn-Teller distortions, the structures of the polymers containing Cu(II) ions are more axially elongated than that of the Ni(II) and Co(II)-containing polymers. This form of structural flexibility is particularly important since substantially different FT-IR signatures in the cyanide vibration region for the Cu(II)-analogues are generated depending on the axial/equatorial cyanide bonding arrangement in the system; this detection methodology is less striking for the Co/Ni analogues, which don’t have the same geometric flexibility as Cu(II) [35]. In the Cu[Au(CN)2]2(analyte)2 system, the differences in cyanide vibration frequency between certain analyte adducts vary by up to 70 cm−1. However, the differentiation between DMF, DMSO, and pyridine analytes in the Co(II) analogue is poorer due to similar colour and νCN frequencies. The FT-IR signatures in the cyanide vibration region for the Ni[Au(CN)2]2(analyte)x polymers, on the other hand, are different from each other, allowing for analyte identification if analyte exchange actually occurs.
Conclusions
In summary, the Co[Au(CN)2]2-based systems react when exposed to different analytes, but detection and identification of the analyte by FT-IR and UV-vis spectroscopies are more difficult than in the analogous Cu(II) system, except for the analyte-free Co[Au(CN)2]2, which undergoes large structural and visible colour changes upon analyte-binding, albeit slowly. The Ni(II)-based system is relatively inert and does not undergo analyte exchange easily, at least with the analytes tested in this study, although the identity of the analyte present is more easily discerned than for the analogous Co(II) system. Nevertheless, it is clear that a flexible non-porous M[Au(CN)2]2-superstructure can readily adapt to integrate selected analytes, the efficacy and spectroscopic signatures of which depend on the metal cation in question. An examination of new M[Au(CN)2]-based systems with respect to detecting potential VOC analytes with different donor characteristics is worthwhile and efforts are underway towards this end.
Supplementary Information
Unit cell parameters and powder X-ray diffractogram for Co[Au(CN)2]2, atomic coordinates for the powder X-ray diffraction models for Ni[Au(CN)2]2(DMF)2, Co[Au(CN)2]2(pyridine)2, and Co[Au(CN)2]2, and X-ray crystallographic data in cif format (CCDC Deposition #745836) for Zn[Au(CN)2]2(DMSO)2.
We are grateful to NSERC of Canada, the World Gold Council GROW program and Simon Fraser University for financial support of this project. JL, JLK and MJK are grateful to NSERC for CGS-D, CGS-M and PGS-D Fellowships respectively.
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Powders of Co[Au(CN)2]2 (top left), Co(μ-OH2)2[Au(CN)2]2 (top middle), Co[Au(CN)2]2(pyridine)4 (top right), Co[Au(CN)2]2(DMF)2 (bottom left) and Co[Au(CN)2]2(DMSO)2 (bottom right). The latter three were synthesized by vapour absorption by solid Co[Au(CN)2]2.
Extended 2-D structure of Zn[Au(CN)2]2(DMSO)2. (a) Local geometry of Zn, showing thermal ellipsoids; (b) A single 2-D sheet, viewed down the face of the sheet; (c) A pair of 2-D sheets, viewed perpendicular to the sheet face, long Au(1)-Au(2*) interactions 3.4943(6) Å represents the closest contact between sheets (DMSO molecules excluded for clarity).
Comparison between the powder X-ray diffractograms predicted for Zn[Au(CN)2]2(DMSO)2 (Zn, green) and the blue Cu[Au(CN)2]2(DMSO)2 polymorph (Cu, blue), with the diffractogram obtained experimentally for Ni[Au(CN)2]2(DMSO)2 (Ni, orange), prepared via solution methods.
Comparison between the powder X-ray diffractogram determined experimentally for the Co[Au(CN)2]2(DMSO)2 (Co, purple) and the diffractogram predicted for Mn[Au(CN)2]2(H2O)2 from the single crystal structure (Mn, blue) [54].
Comparison between the powder X-ray diffractogram (generated from single-crystal data) for Co[Au(CN)2]2(DMF)2 (Co, purple) [50], the experimental diffractogram for Ni[Au(CN)2]2(DMF)2 (Ni, orange) and the diffractogram predicted by the proposed structural model (Ni*, black).
Structural model proposed for Ni[Au(CN)2]2(DMF)2: (A). A 2-D square grid array with DMF molecules coordinated on both sides of the Ni[Au(CN)2]2 layer; (B) and (C). Side-view of a layer showing the relative position of the [Au(CN)2]− units with respect to the Ni(II) centres.
Comparison between the powder X-ray diffractogram (generated from single-crystal data) for Cu[Au(CN)2]2(pyridine)2 (Cu, orange) [35], the experimental diffractogram of Co[Au(CN)2]2(pyridine)2 (Co, purple), and the diffractogram predicted by its structural model (Co*, black).
Structural model proposed for Co[Au(CN)2]2(pyridine)2: (A) 2-D square-grid array with pyridine molecules on both sides of the grid; (B) Side-view of a 2-D layer, showing the position of the [Au(CN)2]− units with respect to the Co(II) centres.
Extended 3-D structure of Co[Au(CN)2]2, looking down the c axis. Dashed lines represent Au-Au interactions.
Different structural models observed for the M[Au(CN)2]2(analyte)x polymers, all resulting from the structural flexibility of the basic M[Au(CN)2]2 square-grid array.
Cyanide vibration frequencies (νCN, cm−1) for different M[Au(CN)2]2(analyte)x (M = Co, Ni) complexes synthesized from solution and from vapour absorption.
From Solution
From Absorption a
Complex
νCN (cm−1)
Vapour
νCN (cm−1)
Co(μ-OH2)2[Au(CN)2]2
2,204(s), 2,168(s)
Co[Au(CN)2]2(DMSO)2
2,177(s)
DMSO
2,176(s)
Co[Au(CN)2]2(DMF)2
2,182(s)
DMF
2,182(s)
Co[Au(CN)2]2(pyridine)xb
2,168(s)
pyridine
2,168(s), 2,144(s)
Ni(μ-OH2)2[Au(CN)2]2
2,214(s), 2,204(sh), 2,170(s)
Ni[Au(CN)2]2(DMSO)2
2,189(s), 2,180(s)
DMSO
2,214(m), 2,203(w), 2,181(s), 2,170(s), 2,164(s)
Ni[Au(CN)2]2(DMF)2
2,189(s)
DMF
2,215(m), 2,189(s), 2,171(m)
Ni[Au(CN)2]2(pyridine)4
2,171(s), 2,143(s)
Pyridine
2,213(s), 2,202(m), 2,170(s), 2,162(s), 2,141(s)
Solvent adducts were prepared from Co(μ-OH2)2[Au(CN)2]2 and from Ni(μ-OH2)2[Au(CN)2]2.
x = 2 from solution and 4 from absorption methods.
Crystallographic data for Zn[Au(CN)2]2(DMSO)2.
Formula
C8H12N4Au2O2S2Zn
Formula weight, Mr
719.66
Colour
colourless
Shape
chunk
Dimensions, mm3
0.14 × 0.22 × 0.42
Crystal system
monoclinic
Space group
P21/c
Z
4
T, K
293
a, Å
7.8403(11)
b, Å
12.8395(12)
c, Å
16.4572(17)
β, deg
98.891(10)
Volume, Å3
1636.8(3)
Dcalcd, g/cm3
2.920
λ, nm (Mo Kα)
0.71073
2θ range, deg
4–60
μ, mm−1
19.592
Reflns, total
5010
Reflns, unique
4801
Reflns, Io ≥ 2.50 σ(Io)
2953
Extinction coefficient
16.0(15)
R (Fo)
0.0342
wR (Fo)
0.0396
Selected bond lengths (Å) and angles (deg) for Zn[Au(CN)2]2(DMSO)2a.
Zn(1)–N(1)
2.163(7)
Zn(1)–N(2′)
2.167(8)
Zn(1)–N(3)
2.140(8)
Zn(1)–N(4″)
2.104(8)
Zn(1)–O(1)
2.120(6)
Zn(1)–O(2)
2.075(6)
Au(1)–Au(2*)
3.4943(6)
N(2′)–Zn(1)–N(4″)
91.3(3)
N(2′)–Zn(1)–O(1)
88.8(3)
N(4″)–Zn(1)–O(1)
175.7(3)
N(2′)–Zn(1)–O(2)
88.3(3)
N(4″)–Zn(1)–O(2)
91.2(3)
O(1)–Zn(1)–O(2)
93.2(3)
N(2′)–Zn(1)–N(1)
172.5(3)
N(4″)–Zn(1)–N(1)
93.0(3)
O(1)–Zn(1)–N(1)
87.4(3)
O(2)–Zn(1)–N(1)
85.4(3)
N(2′)–Zn(1)–N(3)
94.1(3)
N(4″)–Zn(1)–N(3)
87.9(3)
O(1)–Zn(1)–N(3)
87.8(3)
O(2)–Zn(1)–N(3)
177.4(3)
N(1)–Zn(1)–N(3)
92.3(3)
Zn(1)–O(1)–S(1)
126.3(4)
Zn(1)–O(2)–S(2)
126.0(4)
Zn(1)–N(1)–C(1)
172.8(8)
Zn(1′)–N(2′)–C(2′)
169.4(8)
Zn(1)–N(3)–C(3)
172.8(10)
Zn(1)–N(4″)–C(4″)
167.3(8)
Au(2*)–Au(1)–C(1)
105.3(3)
Symmetry operations: ′ = x − 1, −y + 3/2, z − ½; ″ = −x + 4, y − 1/2, −z + 1/2;
* = −x + 4, −y + 2, −z + 1.
Unit cell parameters determined for the M[Au(CN)2]2(DMSO)2 coordination polymers (M = Zn, Cu (blue polymorph), Ni and Co), by either single crystal or powder X-ray diffraction.
Zn
Cu (Blue)
Ni
Co
Sample
Crystal
Crystal
Powder
Powder
crystal system
monoclinic
triclinic
monoclinic
monoclinic
space group
P21/c
P-1
P21/c
C2/m
a, Å
7.8403(11)
7.874(7)
7.63
6.35
b, Å
12.8395(12)
12.761(11)
12.84
14.80
c, Å
16.4572(17)
16.207(13)
16.30
7.35
α, deg
90.0
89.61(7)
90.0
90.0
β, deg
98.891(10)
82.29(7)
98.89
100.77
γ, deg
90.0
88.57(7)
90.0
90.0
Volume, Å3
1,636.77
1,613.2(24)
1,577.65
677.52
Unit cell parameters determined for the M[Au(CN)2]2(DMF)2 (M = Co, Ni) and Co[Au(CN)2]2(pyridine)2 coordination polymers by either single crystal or powder X-ray diffraction.
Co[Au(CN)2]2(DMF)2
Ni[Au(CN)2]2(DMF)2
Co[Au(CN)2]2(pyridine)2
Sample
Crystal32
Powder
Powder
crystal system
monoclinic
monoclinic
monoclinic
space group
P21/c
P21/c
P21/c
a, Å
8.375(2)
8.5659
8.9334
b, Å
14.054(5)
14.1445
14.0712
c, Å
15.077(4)
14.7907
15.0425
α, deg
90.0
90.0
90.0
β, deg
92.75(2)
95.011
99.2538
γ, deg
90.0
90.0
90.0
Volume, Å3
1,772.6(9)
1785.2
1,866.3
Absorbance maxima (λmax abs, nm) observed in the solid-state UV-Vis-NIR absorbance spectra of the M[Au(CN)2]2(analyte)x (M = Co, Ni) coordination polymers prepared from solution.