F. Marandi et al. / Journal of Molecular Structure 1006 (2011) 136–141
141
adjacent Ag-bpy single chains are linked into a double chain by
[8] C.-Y. Su, C.-L. Chen, J.-Y. Zhang, B.-S. Kang, Silver(I) coordination polymers, in:
M.-C. Hong, L. Chen (Eds.), Design and Construction of Coordination Polymers,
John Wiley & Sons, Inc., Hoboken, NJ, USA, 2009 (Chapter 5).
weak AgꢀꢀꢀO and AgꢀꢀꢀAg interactions.
Intermolecular, intramolecular and
p–p stacking interactions
[
9] S. Bureekaew, S. Horike, M. Higuchi, M. Mizuno, T. Kawamura, D. Tanaka, N.
Yanai, S. Kitagawa, Nat. Mater. 8 (2009) 831.
are observed in 1 and 2. They seem to be responsible for the pack-
ing of the complexes. An inspection of the data of 1 and 2 for weak
directional intermolecular interactions using the programs PLA-
TON and MERCURY, which were used for calculating the supramo-
lecular interactions, has shown that there are OꢀꢀꢀHAC and CAHꢀꢀꢀF
interactions [44,45] (Table 3). Fig. 4 shows the packing of the mol-
ecules of 1 in the crystal highlighting of some of the weak intermo-
lecular interactions. The HꢀꢀꢀO and HꢀꢀꢀF separations range from
[
[
[
[
10] B. Wang, A.P. Côté, H. Furukawa, M. O’Keeffe, O.M. Yaghi, Nature 453 (2008)
07.
2
11] D. Sun, G.G. Luo, N. Zhang, J.H. Chen, R.B. Huang, L.R. Lin, L.S. Zheng,
Polyhedron 28 (2009) 2983.
12] A.N. Khlobystov, A.J. Blake, N.R. Champness, D.A. Lemenovskii, A.G. Majouga,
N.V. Zyk, M. Schröder, Coord. Chem. Rev. 222 (2001) 155.
13] G. Meyer, A. Berners, I. Pantenburg, Z. Anorg. Allg. Chem. 632 (2006) 34.
[14] J.W. Steed, D.R. Turner, K.J. Wallace, Core Concepts in Supramolecular
Chemistry and Nanochemistry, John Wiley and Sons Ltd., 2007 (Chapter 1).
15] J. Zhang, Y.-C. Shen, Y.-Y. Qin, Z.-J. Li, Y.-G. Yao, CrystEngComm 9 (2007) 636.
16] Y.-Q. Yu, W. Zhan, T.E. Albrecht-Schmitt, Inorg. Chem. 46 (2007) 10214.
[17] L. Cunha-Silva, R. Ahmad, M.J. Carr, A. Franken, J.D. Kennedy, M.J. Hardie, Cryst.
Growth Des. 7 (2007) 658.
18] Z.-X. Lian, J.-W. Cai, C.-H. Chen, Polyhedron 26 (2007) 2647.
19] S.E.-D.H. Etaiw, M.M. El-Bendary, J. Coord. Chem. 63 (2010) 1038.
[20] B.H. Ye, M.L. Tong, X.M. Chen, Coord. Chem. Rev. 249 (2005) 545.
[
[
2
.516 to 2.674 Å, which indicates moderate-to-strong hydrogen
bonds [46]. The packing of the molecules of 1 and 2 in the solid
state exhibits interesting self-assembled structure topologies
[
[
through different
p–p stacking modes with interlayer distances
of 3.347, 3.489 Å in 1 and 3.467 Å in 2 (see also Ref. [47]). The cen-
troid-to-centroid separations between neighboring aromatic rings
are exhibiting typical slipped p–p stacking interactions in an offset
fashion. Thus, a three-dimensional hydrogen-bonded and layer-
[21] C.N.R. Rao, S. Natarajan, R. Vaidhyanathan, Angew. Chem., Int. Ed. Engl. 43
(
2004) 1466.
[
22] B.R. Manzano, F.A. Jalon, M.L. Soriano, M.C. Carrion, M.P. Carranza, K. Mereiter,
A.M. Rodrıguez, A. De la Hoz, A. Sanchez-Migallon, Inorg. Chem. 47 (2008)
8957.
[23] A. Decken, C. Knapp, G.B. Nikiforov, J. Passmore, J.M. Rautiainen, X.-P. Wang,
X.-Q. Zeng, Chem. Eur. J. 15 (2009) 6504.
24] C.-L. Chen, C.-Y. Su, Y.-P. Cai, H.-X. Zhang, A.-W. Xu, B.-S. Kang, H.C. zur Loye,
Inorg. Chem. 42 (2003) 3738.
25] M.J. Hannon, C.L. Painting, E.A. Plummer, L.J. Childs, N.W. Alcock, Chem. Eur. J.
packed network is constructed, as is illustrated for 1 and 2 Figs. 4
0
and 5. The two aryl ring planes of ‘‘4,4 -bpy’’ form an angle of
1
7.89° for 1 and 38.94° for 2. It seems reasonable to assume that
[
[
[
0
the differences in the distorted aryl ring planes of ‘‘4,4 -bpy’’
around the silver atoms between 1 and 2 result from the network
of directed intermolecular interactions detected in the reported
structure. The formation of 3D networks is governed by the
above-mentioned directed intermolecular interactions.
8
(2002) 2226.
26] J.R. Price, Y.-H. Lan, G.B. Jameson, S. Brooker, Dalton Trans. (2006) 1491.
[27] A.M. Stadler, N. Kyritsakas, G. Vaughan, J.M. Lehn, Chem. Eur. J. 13 (2007) 59.
28] P.A. Vigato, V. Peruzzo, S. Tamburini, Coord. Chem. Rev. 253 (2009) 1099.
29] S.C. Ngo, K.K. Banger, P.J. Toscano, J.T. Welch, Polyhedron 21 (2002) 1289.
30] K.-M. Chi, K.-H. Chen, H.-C. Lin, K.-J. Lin, Polyhedron 16 (1997) 2147.
31] (a) K. Akhbari, A. Morsali, Cryst. Growth Des. 7 (2007) 2024;
[
[
[
[
Acknowledgments
(
3
b) F. Pointillart, P. Herson, K. Boubekeur, C. Train, Inorg. Chim. Acta 361 (2008)
73;
The authors acknowledge financial support by the Iran National
Science Foundation, INSF, Payame Noor University and the Univer-
sitat zu Köln.
(c) L. Zanotto, F. Benetollo, M. Natali, G. Rossetto, P. Zanella, S. Kaciulis, A.
Mezzi, Chem. Vap. Deposition 10 (2004) 207.
32] X-Shape 1.06, Crystal Optimisation for Numerical Absorption Correction (C),
STOE & Cie GmbH Darmstadt, 1999.
[
[
[
33] X-Area 1.16, Stoe & Cie GmbH Darmstadt, 2003.
34] X-RED 1.22, Stoe Data Reduction Program (C), Stoe & Cie GmbH Darmstadt,
Appendix A. Supplementary data
2001.
[
[
[
35] L.J. Farrugia, J. Appl. Crystallogr. 32 (1999) 837.
36] A. Altomare, G. Cascarano, C. Giacovazzo, J. Appl. Crystallogr. 26 (1993) 343.
37] G.M. Sheldrick, SHELXL-97; Programs for Crystal Structure Analysis, University
of Göttingen, 1997.
Full cif depositions, excluding structure factor amplitudes, re-
side with the Cambridge Crystallography Data center, CCDC-
8
26097 for 1, CCDC-826096 for 2. Copies of the data can be ob-
[38] J.B. Yu, L. Zhou, H.J. Zhang, Y.X. Zheng, H.R. Li, R.P. Deng, Z.P. Peng, Z.F. Li, Inorg.
Chem. 44 (2005) 1611.
[
tained, free of charge, on application from CCDC, 12 Union Road,
Cambridge CB2 1EZ, UK (fax: +44 1223 336033 or e-mail: depos-
39] I.M. Kolthoff, E.B. Sandel, E.J. Meehan, S. Brukenestein, Quantitative Chemical
Analysis, fourth ed., Macmillan, London, 1971.
[40] L. Yang, D.R. Powell, R.P. Houser, J. Chem. Soc., Dalton Trans. (2007) 955.
[41] X.-F. Zheng, L.-G. Zhu, Inorg. Chim. Acta 365 (2011) 419.
[
42] D. Sun, G.-G. Luo, N. Zhang, Q.-J. Xu, R.-B. Huang, L.-S. Zheng, Polyhedron 29
2010) 1243.
(
[
[
43] A. Bondi, J. Phys. Chem. 68 (1964) 441.
44] A.C. Moro, F.W. Watanabe, S.R. Ananias, A.E. Mauro, A.V.G. Netto, A.P.R. Lima,
J.G. Ferreira, R.H.A. Santos, Inorg. Chem. Commun. 9 (2006) 493.
45] J.W. Steed, J.L. Atwood, Supramolecular Chemistry, J. Wiley, Chichester, 2000.
46] (a) L.A. Barrios, G. Aromi, A. Frontera, D. Quinonero, P.M. Deya, P. Gamez, O.
Roubeau, E.J. Shotton, S.J. Teat, Inorg. Chem. 47 (2008) 5873;
References
[
[
[
[
[
[
[
1] G. Férey, Chem. Soc. Rev. 37 (2008) 191.
2] L.J. Murray, M. Dinca, J.R. Long, Chem. Soc. Rev. 38 (2009) 1294.
3] K. Koh, A.G. Wong-Foy, A.J. Matzger, Angew. Chem., Int. Ed. 47 (2008) 677.
4] Z. Wang, S.M. Cohen, Chem. Soc. Rev. 38 (2009) 1315.
(
b) C.A. Hollis, L.R. Hanton, J.C. Morris, C.J. Sumby, Cryst. Growth Des. 9 (2009)
911.
47] (a) T. Dorn, C. Janiak, K. Abu-Shandi, CrystEngComm 7 (2005) 633;
b) S. Banerjee, A. Ghosh, B. Wu, P.-G. Lassahn, C. Janiak, Polyhedron 24 (2005)
93;
2
5] J.L.C. Rowsell, E.C. Spencer, J. Eckert, J.A.K. Howard, O.M. Yaghi, Science 309
[
(
2005) 1350.
(
5
[
[
6] O. Shekhah, H. Wang, M. Paradinas, C. Ocal, B. Schupbach, A. Terfort, D. Zacher,
R.A. Fischer, C. Woll, Nat. Mater. 8 (2009) 481.
7] M.D. Allendorf, C.A. Bauer, R.K. Bhakta, R.J.T. Houk, Chem. Soc. Rev. 38 (2009)
(
(
c) S. Banerjee, B. Wu, P.-G. Lassahn, C. Janiak, A. Ghosh, Inorg. Chim. Acta 358
2005) 535.
1
330.