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Volume 66 
Part 3 
Pages m55-m57  
March 2010  

Received 6 January 2010
Accepted 14 January 2010
Online 3 February 2010

Two polymorphs of chlorido(cyclohexyldiphenylphosphine)gold(I)

aDepartment of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, WI 53706, USA, and bCenter for Integrated Nanotechnologies, Los Alamos National Laboratory, Los Alamos, NM 87545, USA
Correspondence e-mail: iguzei@chem.wisc.edu

The title compound, [AuCl(C18H21P)], a monomeric two-coordinate gold(I) complex, has been characterized at 100 K as two distinct monoclinic polymorphs, one from a single crystal, (Is), and one from a pseudo-merohedrally twinned crystal, (It). The molecular structures in the two monoclinic [P21/n for (Is) and P21/c for (It)] polymorphs are similar; however, the packing arrangements in the two lattices differ considerably. The structure of (It) is pseudo-merohedrally twinned by a twofold rotation about the a* axis.

Comment

Recently, there has been a significant increase in the amount of research focused on the synthesis, characterization and theoretical analysis of gold clusters and nanoparticles, as their potential applications encompass ever-increasing areas of modern technology and scientific advances, ranging from biological luminophores to the components of plasmonic devices and catalysis. Their ability to guide, enhance, emit and modify optical fields puts them on the center stage for such applications as photonic crystals, biosensors and optical materials (Pyykkö, 2004[Pyykkö, P. (2004). Angew. Chem. Int. Ed. Engl. 43, 4412-4456.], 2005[Pyykkö, P. (2005). Inorg. Chim. Acta, 358, 4113-4130.]; Andres et al., 1996[Andres, R. P., Bein, T., Dorogi, M., Feng, S., Henderson, J. I., Kubiak, C. P., Mahoney, W., Osifchin, R. G. & Reifenberger, R. (1996). Science, 272, 1323-1325.]).

[Scheme 1]

In our attempt to synthesize small luminescent gold clusters, we treated a preformed gold-phosphine cluster, [Au6(PPh2Cy)6](NO3)2 (Cy is cyclohexyl; Briant et al., 1986[Briant, C. E., Hall, K. P., Mingos, D. M. P. & Wheeler, A. C. (1986). J. Chem. Soc. Dalton Trans. pp. 687-692.]), with either n-butylamine or i-propylamine in various ratios in acetonitrile. The process yielded an unstable luminescent gold-containing product, the crystallization of which from its CH2Cl2 solution by layering with pentane resulted in the reaction of this luminescent gold species with CH2Cl2, yielding the title compound, (I), in high yield.

Compound (I) has been characterized at 100 K as two distinct monoclinic polymorphs, one from a single crystal, (Is)[link], and one from a pseudo-merohedrally twinned crystal, (It)[link]. The structures of (Is)[link] and (It)[link] are shown in Figs. 1[link] and 2[link], and their overlap is shown in Fig. 3[link].

The space groups are P21/n and P21/c for (Is)[link] and (It)[link], respectively; both contain one molecule in the asymmetric unit. The nonconventional setting for (Is)[link] was chosen based on the proximity of the [beta]-angle value to 90°. A Cambridge Structural Database (CSD, September 2009 release; Allen, 2002[Allen, F. H. (2002). Acta Cryst. B58, 380-388.]) search revealed four other P21/c-P21/c (or P21/n) monoclinic polymorphic pairs for phosphine-gold complexes: chloro(trimesitylphosphine)gold(I) in P21/c (Alyea et al., 1993[Alyea, E. C., Ferguson, G., Gallagher, J. F. & Malito, J. (1993). Acta Cryst. C49, 1473-1476.]) and P21/c (Bott et al., 2000[Bott, R. C., Bowmaker, G. A., Buckley, R. W., Healy, P. C. & Senake Perera, M. C. (2000). Aust. J. Chem. 53, 175-181.]), both at room temperature (RT); [OPh2PC(PPh2AuPPh2)2CPPh2(O)]·4CH2Cl2 in P21/c and P21/n, both at 173 K (Fernandez et al., 1993[Fernandez, E. J., Gimeno, M. C., Jones, P. G., Laguna, A., Laguna, M. & Lopez-de-Luzuriaga, J. M. (1993). J. Chem. Soc. Dalton Trans. pp. 3401-3406.]); [tris(2-cyanoethyl)phosphine]gold(I) in P21/c and P21/c, both at RT (Fackler et al., 1994[Fackler, J. P., Staples, R. J., Khan, M. N. I. & Winpenny, R. E. P. (1994). Acta Cryst. C50, 1020-1023.]); (tricyclohexylphosphine)gold(I) 2-mercaptobenzoate, with form I in P[\overline{1}] at RT (Cookson & Tiekink, 1992[Cookson, P. D. & Tiekink, E. R. T. (1992). J. Coord. Chem. 26, 313-320.]), form II in P21/n at 173 K, form III in P21/n at 173 K, and form IV in P[\overline{1}] at 173 K, all by Smyth et al. (2001[Smyth, D. R., Vincent, B. R. & Tiekink, E. R. T. (2001). Cryst. Growth Des. 1, 113-117.]).

There are no aurophilic interactions in either structure of (I). The overall packing is based on a ball motif, because the smallest box circumscribing the molecule is approximately isometric, measuring 10.51 × 11.03 × 10.98 Å for (Is)[link], and 10.56 × 10.96 × 11.86 Å for (It)[link]. Interestingly, the volumes of these boxes, viz. 1272.0 Å3 for (Is)[link] and 1373.6 Å3 for (It)[link], differ by over 100 Å. Crystal packing in the two lattices is dissimilar (Fig. 4[link]). The packing patterns were examined with a matching routine of the program Mercury (Bruno et al., 2002[Bruno, I. J., Cole, J. C., Edgington, P. R., Kessler, M., Macrae, C. F., McCabe, P., Pearson, J. & Taylor, R. (2002). Acta Cryst. B58, 389-397.]), which was able to superimpose five molecules out of 20 from the two structures with an r.m.s. deviation of 0.843 Å. The theoretically computed powder patterns have a similarity value of 0.921. Thus, the two polymorphs are indeed distinct.

Unfortunately, it was not possible to establish which polymorph is more stable based on the crystals' density or melting-point measurements. The polymorph densities differ by only 0.005 Mg m-3, and crystals of (Is)[link] and (It)[link] melted within 0.5 K of each other between 485 and 486 K. The unavailability of crystals of (It)[link] did not allow for additional, possibly more conclusive, melting-point measurements. We did compare the theoretically computed energies corresponding to the observed molecular conformations in (Is)[link] and (It)[link]. The geometries of the complexes were optimized with GAUSSIAN03 (Frisch et al., 2004[Frisch, M. J., et al. (2004). GAUSSIAN03. Revision C.02. Gaussian Inc., Wallingford, CT, USA.]) using the hybrid DFT PBE1PBE functional of TZVP triple-[zeta] quality with a polarization basis set on all nonmetallic atoms and the SDD basis set with a relativistically corrected Effective Core potential on gold. Our preliminary results suggest that (Is)[link] is the more stable conformer, probably due to stronger Au...H agostic interactions.

The molecular geometries of (Is)[link] and (It)[link] are typical, with bond distances and angles falling in the usual ranges. The P atom is in an equatorial position relative to the cyclohexyl ring. The two structures can be overlaid (Fig. 3[link]), with an r.m.s. deviation of 0.323 Å computed based on all non-H atoms. Herein we compare the selected molecular parameters for (Is)[link], (It)[link], the molecular geometry of (I) optimized with GAUSSIAN03, (Ig), and the average parameters (based on 201 complexes in 154 crystal structures) for high-quality crystal structures of phosphine-gold complexes containing a Cl-Au-PC3 unit as reported to the CSD, (II). The Au-Cl and Au-P bond distances and Cl-Au-P angle are 2.2885 (5), 2.2403 (5) Å and 177.668 (19)° in (Is)[link], 2.2915 (14), 2.2335 (13) Å and 176.41 (5)° in (It)[link], 2.2994, 2.2730 Å and 179.44° in (Ig), and 2.288 (11), 2.231 (10) Å and 176 (2)° for (II). The overall geometry of (Ig) compares well with that of (Is)[link] and (It)[link]; however, the bond distances about the Au atom in (Ig) are slightly longer than in the experimentally established geometries. The results of the CSD search did not reveal any mutual dependence between the Au-Cl and Au-P bonds. Thus, the data probably indicate that the two polymorphs are `conformational', and their existence is due to packing differences induced by different torsion angles, rather than by any change in covalent distances and angles.

The structure of (It)[link] was pseudo-merohedrally twinned, likely due to the proximity of the [beta] angle to 120° and similarity of the a and c axial lengths. We have recently reported a case of a nonmerohedrally twinned crystal of nonactin (Guzei et al., 2009[Guzei, I. A., Wang, C., Zhan, Y., Dolomanov, O. V. & Cheng, Y.-Q. (2009). Acta Cryst. C65, o521-o524.]) and treated the twinning in (It)[link] according to the procedure described therein. In the case of (It)[link] the twin law (101 0[\bar 1]0 00[\bar 1]) corresponded to a 180° rotation about the a* axis in reciprocal space. The contribution of the minor twin component was calculated to be 17.14 (9)%.

In summary, we have discovered and structurally characterized two polymorphs of a monomeric two-coordinate gold(I) complex Au(PPh2Cy)Cl, one of which is pseudo-merohedrally twinned.

[Figure 1]
Figure 1
The molecular structure of (Is)[link]. Displacement ellipsoids are shown at the 50% probability level.
[Figure 2]
Figure 2
The molecular structure of (It)[link]. Displacement ellipsoids are shown at the 50% probability level.
[Figure 3]
Figure 3
An overlay of structure (Is)[link] (green in the electronic version of the paper) and (It)[link].
[Figure 4]
Figure 4
A partial overlay of the lattices of (Is)[link] (black molecules) and (It)[link] (lighter molecules; orange in the electronic version of the paper), viewed along the c axis of (Is)[link]. An attempt to overlay 15 molecules resulted in a more or less successful overlay of five molecules (best seen near the origin). The diagram contains more than 15 molecules to emphasize the differences in packing.

Experimental

n-Butylamine (99.5%) were purchased from Aldrich. Ethanol, methanol, tetrahydrofuran, dichloromethane and pentane were purchased from Acros. Cyclohexyldiphenylphosphine (98%, PCyPPh2) was purchased from Strem chemicals. NaBH4 (98%) was purchased from Alfa Aesar. All the chemicals were used as received without further purification. The [Au6(PCyPh2)6](NO3)2 cluster was prepared by reduction of Au(PCyPh2)NO3 with NaBH4 in ethanol, as described by Briant et al. (1986[Briant, C. E., Hall, K. P., Mingos, D. M. P. & Wheeler, A. C. (1986). J. Chem. Soc. Dalton Trans. pp. 687-692.]). [Au6(PCyPh2)6](NO3)2 (0.0175 g) was dispersed in dichloromethane (10 ml) to form a transparent yellow-brown solution. n-Butylamine (0.05 ml) was added to the above solution and stirred at room temperature for 5-7 d. Over time, the yellow-brown color of the original [Au6(PCyPh2)6](NO3)2 cluster gradually disappeared producing a luminescent pale-yellow solution. The resulting solution was centrifuged and the supernatant was isolated in a flask and the solvent removed under vacuum to yield a light-yellow-brown precipitate. The precipitate was washed with hexane (twice) to remove excess amine and was then crystallized from dichloromethane by slow diffusion of pentane into the solution. One crystallization batch produced (Is), whereas a repetition of the reaction and crystallization produced (It).

Compound (Is)[link]

Crystal data
  • [AuCl(C18H21P)]

  • Mr = 500.73

  • Monoclinic, P 21 /n

  • a = 9.0059 (4) Å

  • b = 17.2762 (7) Å

  • c = 11.0719 (4) Å

  • [beta] = 91.610 (2)°

  • V = 1721.97 (12) Å3

  • Z = 4

  • Mo K[alpha] radiation

  • [mu] = 8.78 mm-1

  • T = 100 K

  • 0.39 × 0.36 × 0.34 mm

Data collection
  • Bruker SMART APEXII area-detector diffractometer

  • Absorption correction: analytical (SADABS; Bruker, 2009[Bruker (2009). APEX2 (Version 2.1-4), SADABS (Version 2008/1) and SAINT (Version 7.24a). Bruker AXS Inc., Madison, Wisconsin, USA.]) Tmin = 0.131, Tmax = 0.154

  • 28496 measured reflections

  • 5263 independent reflections

  • 4832 reflections with I > 2[sigma](I)

  • Rint = 0.032

Refinement
  • R[F2 > 2[sigma](F2)] = 0.017

  • wR(F2) = 0.037

  • S = 1.06

  • 5263 reflections

  • 190 parameters

  • H-atom parameters constrained

  • [Delta][rho]max = 1.13 e Å-3

  • [Delta][rho]min = -1.01 e Å-3

Compound (It)[link]

Crystal data
  • [AuCl(C18H21P)]

  • Mr = 500.73

  • Monoclinic, P 21 /c

  • a = 13.1440 (9) Å

  • b = 11.4900 (8) Å

  • c = 13.1056 (9) Å

  • [beta] = 119.786 (2)°

  • V = 1717.8 (2) Å3

  • Z = 4

  • Mo K[alpha] radiation

  • [mu] = 8.80 mm-1

  • T = 100 K

  • 0.33 × 0.32 × 0.27 mm

Data collection
  • Bruker SMART APEXII area-detector diffractometer

  • Absorption correction: analytical (SADABS; Bruker, 2009[Bruker (2009). APEX2 (Version 2.1-4), SADABS (Version 2008/1) and SAINT (Version 7.24a). Bruker AXS Inc., Madison, Wisconsin, USA.]) Tmin = 0.161, Tmax = 0.197

  • 32548 measured reflections

  • 4184 independent reflections

  • 4157 reflections with I > 2[sigma](I)

  • Rint = 0.053

Refinement
  • R[F2 > 2[sigma](F2)] = 0.031

  • wR(F2) = 0.088

  • S = 1.09

  • 4184 reflections

  • 191 parameters

  • H-atom parameters constrained

  • [Delta][rho]max = 2.20 e Å-3

  • [Delta][rho]min = -1.96 e Å-3

All H atoms were placed in idealized locations, with C-H distances of 0.95 Å for aromatic C atoms, 0.99 Å for secondary C atoms and 1.00 Å for the tertiary C atom, and refined as riding with Uiso(H) values set at 1.2Ueq(C).

The outlier reflections were omitted based on the statistics test described in Prince & Nicholson (1983[Prince, E. & Nicholson, W. L. (1983). Acta Cryst. A39, 407-410.]) and Rollett (1988[Rollett, J. S. (1988). Crystallographic Computing, Vol. 4, pp. 149-166. Oxford University Press.]), and implemented in the program FCF_filter (Guzei, 2007[Guzei, I. A. (2007). In-house crystallographic programs: FCF_filter, INSerter and modiCIFer. Molecular Structure Laboratory, University of Wisconsin-Madison, Madison, Wisconsin, USA.]). The number of omitted outliers was 4 for (Is)[link] and 47 for (It)[link].

For both compounds, data collection: APEX2 (Bruker, 2009[Bruker (2009). APEX2 (Version 2.1-4), SADABS (Version 2008/1) and SAINT (Version 7.24a). Bruker AXS Inc., Madison, Wisconsin, USA.]); cell refinement: SAINT (Bruker, 2009[Bruker (2009). APEX2 (Version 2.1-4), SADABS (Version 2008/1) and SAINT (Version 7.24a). Bruker AXS Inc., Madison, Wisconsin, USA.]); data reduction: SAINT; program(s) used to solve structure: SHELXTL (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); program(s) used to refine structure: SHELXTL and OLEX2 (Dolomanov et al., 2009[Dolomanov, O. V., Bourhis, L. J., Gildea, R. J., Howard, J. A. K. & Puschmann, H. (2009). J. Appl. Cryst. 42, 339-341.]); molecular graphics: SHELXTL; software used to prepare material for publication: SHELXTL.


Supplementary data for this paper are available from the IUCr electronic archives (Reference: SQ3235 ). Services for accessing these data are described at the back of the journal.


Acknowledgements

This research was supported by Los Alamos National Laboratory Directed Research and Development. This work was performed at the Center for Integrated Nanotechnologies, a US Department of Energy, Office of Basic Energy Sciences user facility. The manuscript was prepared with the beta test version 1.0.2 of the programs publCIF (Westrip, 2010[Westrip, S. P. (2010). publCIF. In preparation.]) and modiCIFer (Guzei, 2007[Guzei, I. A. (2007). In-house crystallographic programs: FCF_filter, INSerter and modiCIFer. Molecular Structure Laboratory, University of Wisconsin-Madison, Madison, Wisconsin, USA.]).

References

Allen, F. H. (2002). Acta Cryst. B58, 380-388.  [ISI] [CrossRef] [details]
Alyea, E. C., Ferguson, G., Gallagher, J. F. & Malito, J. (1993). Acta Cryst. C49, 1473-1476.  [CrossRef] [details]
Andres, R. P., Bein, T., Dorogi, M., Feng, S., Henderson, J. I., Kubiak, C. P., Mahoney, W., Osifchin, R. G. & Reifenberger, R. (1996). Science, 272, 1323-1325.  [CrossRef] [ChemPort] [PubMed] [ISI]
Bott, R. C., Bowmaker, G. A., Buckley, R. W., Healy, P. C. & Senake Perera, M. C. (2000). Aust. J. Chem. 53, 175-181.  [ISI] [CrossRef] [ChemPort]
Briant, C. E., Hall, K. P., Mingos, D. M. P. & Wheeler, A. C. (1986). J. Chem. Soc. Dalton Trans. pp. 687-692.  [CrossRef]
Bruker (2009). APEX2 (Version 2.1-4), SADABS (Version 2008/1) and SAINT (Version 7.24a). Bruker AXS Inc., Madison, Wisconsin, USA.
Bruno, I. J., Cole, J. C., Edgington, P. R., Kessler, M., Macrae, C. F., McCabe, P., Pearson, J. & Taylor, R. (2002). Acta Cryst. B58, 389-397.  [ISI] [CrossRef] [details]
Cookson, P. D. & Tiekink, E. R. T. (1992). J. Coord. Chem. 26, 313-320.  [CrossRef] [ChemPort] [ISI]
Dolomanov, O. V., Bourhis, L. J., Gildea, R. J., Howard, J. A. K. & Puschmann, H. (2009). J. Appl. Cryst. 42, 339-341.  [ISI] [CrossRef] [ChemPort] [details]
Fackler, J. P., Staples, R. J., Khan, M. N. I. & Winpenny, R. E. P. (1994). Acta Cryst. C50, 1020-1023.  [CrossRef] [details]
Fernandez, E. J., Gimeno, M. C., Jones, P. G., Laguna, A., Laguna, M. & Lopez-de-Luzuriaga, J. M. (1993). J. Chem. Soc. Dalton Trans. pp. 3401-3406.  [CrossRef]
Frisch, M. J., et al. (2004). GAUSSIAN03. Revision C.02. Gaussian Inc., Wallingford, CT, USA.
Guzei, I. A. (2007). In-house crystallographic programs: FCF_filter, INSerter and modiCIFer. Molecular Structure Laboratory, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Guzei, I. A., Wang, C., Zhan, Y., Dolomanov, O. V. & Cheng, Y.-Q. (2009). Acta Cryst. C65, o521-o524.  [CSD] [CrossRef] [details]
Prince, E. & Nicholson, W. L. (1983). Acta Cryst. A39, 407-410.  [CrossRef] [details]
Pyykkö, P. (2004). Angew. Chem. Int. Ed. Engl. 43, 4412-4456.  [ISI] [PubMed]
Pyykkö, P. (2005). Inorg. Chim. Acta, 358, 4113-4130.
Rollett, J. S. (1988). Crystallographic Computing, Vol. 4, pp. 149-166. Oxford University Press.
Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.  [CrossRef] [details]
Smyth, D. R., Vincent, B. R. & Tiekink, E. R. T. (2001). Cryst. Growth Des. 1, 113-117.  [CSD] [CrossRef] [ChemPort]
Westrip, S. P. (2010). publCIF. In preparation.


Acta Cryst (2010). C66, m55-m57   [ doi:10.1107/S0108270110001861 ]