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Synthesis and crystal structure of a wheel-shaped supramolecular coordination complex

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Abstract

Supramolecular coordination complex (SCC) possessing spatially arranged three anthraquinone dimers in a slipped-cofacial orientation was achieved by the treatment of Re2(CO)10, 2-hydroxymethylanthraquinone and tritopic N-donor via fac-Re(CO)3-directed one pot approach. The off-set π-stacking and C≡O···H bonding interactions stabilize the ring structure.

Supramolecular coordination complex (SCC) possessing spatially arranged three anthraquinone dimers in a slipped-cofacial orientation was achieved by the treatment of Re2(CO)10, 2-hydroxymethylanthraquinone and tritopic N-donor via fac-Re(CO)3-directed one pot approach. The offset π-stacking and C≡O···H bonding interactions stabilize the ring structure.

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References

  1. (a) Lehn J M 1995 In Supramolecular Chemistry, Concepts and Perspectives (Weinheim: VCH); (b) Janiak C 2000 J. Chem. Soc., Dalton Trans. 3885; (c) Chakrabarty R, Mukherjee P S and Stang P J 2011 Chem. Rev. 111 6810; (d) Fujita M, Umemoto K, Yoshizawa M, Fujita N, Kusukawa T and Biradha K 2001 Chem. Commun. 509; (e) Gianneschi N C, Masar III M S and Mirkin C A 2005 Acc. Chem. Res. 38 825; (f) Han Y F, Jia W G and Jin G X 2009 Chem. Soc. Rev. 38 3419; (g) Nohra B, Graule S, Lescop C and Reau R 2006 J. Am. Chem. Soc. 128 3520

  2. (a) Amouri H, Desmarets C and Moussa J 2012 Chem. Rev. 112 2015; (b) Liao R T, Yang W C, Thanasekaran P, Tsai C C, Sathiyendiran M, Liu Y H, Rajendran T, Lin H M, Tseng T W and Lu K L 2008 Chem. Commun. 3175; (c) Shankar B, Elumalai P, Hussain F and Sathiyendiran M 2013 J. Organomet. Chem. 732 130; (d) Pardo E, Faus J, Lloret F, Munoz M C, Cano J, Ottenwaelder X, Journaux Y, Carrasco R, Blay G, Fernandez I and Ruiz-García R 2003 J. Am. Chem. Soc. 125 10770; (e) Shankar B, Sahu S, Deibel, N, Schweinfurth D, Sarkar B, Elumalai P, Gupta D, Hussain F, Krishnamoorthy G and Sathiyendiran M 2014 Inorg. Chem. 53 922; (f) Shankar B, Elumalai P, Shanmugam R, Singh V, Masram D T and Sathiyendiran M 2013 Inorg. Chem. 52 10217; (g) Rajakannu P, Elumalai P, Shankar B, Hussain F and Sathiyendiran M 2013 Dalton Trans. 42 11359; (h) Gupta D, Shankar B, Elumalai P, Shanmugam R, Mobin S M, Weisser F, Sarkar B and Sathiyendiran M 2014 J. Organomet. Chem. 754 59; (i) Shankar B, Rajakannu P, Kumar S, Gupta D, Kannan T and Sathiyendiran M 2011 Inorg. Chem. Commun. 14 374; (j) Rajakannu P, Elumalai P, Hussain F andSathiyendiran M 2013 J. Organomet. Chem. 725 1; (k) Shankar B, Elumalai P, Shanmugam R and Sathiyendiran M 2014 J. Organomet. Chem. 749 224; (l) Rajakannu P, Shankar B, Yadav A, Shanmugam R, Gupta D, Hussain F, Chang C H, Sathiyendiran M and Lu K L 2011 Organometallics 30 3168

  3. (a) Yang J, Yoon M C, Yoo H, Kim P and Kim D 2012 Chem. Soc. Rev. 41 4808; (b) Ahrens M J, Sinks L E, Rybtchinski B, Liu W, Jones B A, Giaimo J M, Gusev A V, Goshe A J, Tiede D M and Wasielewski M R 2004 J. Am. Chem. Soc. 126 8284; (c) Satake A and Kobuke Y 2007 Org. Biomol. Chem. 5 1679; (d) McDermott G, Prince S M, Freer A A, Hawthornthwaite-Lawless A M, Papiz M Z, Cogdell R J and Isaacs N W 1995 Nature 374 517; (e) Bhosale S, Sisson A L, Talukdar P, Fürstenberg A, Banerji N, Vauthey E, Bollot G, Mareda J, Röger C, Würthner F, Sakai N and Matile S 2006 Science 84 313

  4. (a) Benkstein K D and Hupp J T 2000 Mol. Cryst. Liq. Cryst. 342 151; (b) Sun S S and Lees A J 2001 Chem. Commun. 103; (c) Manimaran B, Rajendran T, Lu Y L, Lee G H, Peng S M and Lu K L 2001 Eur. J. Inorg. Chem. 633; (d) Gupta D, Rajakannu P, Shankar B, Shanmugam R, Hussain F, Sarkar B and Sathiyendiran M 2011 Dalton Trans. 40 5433; (e) Wu T, Weng L H and Jin G X 2012 Chem. Commun. 48 4435; (f) Mirtschin S, Slabon-Turski A, Scopelliti R, Velders A H and Severin K 2010 J. Am. Chem. Soc. 132 14004; (g) Therrien B 2009 Eur. J. Inorg. Chem. 2445; (h) Wu J Y, Chang C H, Thanasekaran P, Tsai C C, Tseng T W, Lee G H, Peng S M and Lu K L 2008 Dalton Trans. 6110

  5. Song Z, Zhan H and Zhou Y 2009 Chem. Commun. 448

  6. (a) Desiraju G R 2005 Chem. Commun. 2995; (b) Rajadurai C, Fuhr O, Enkelmann V and Baumgarten M 2006 J. Phys. Org. Chem. 19 257

  7. Bailar Jr. J C 1958 J. Inorg. Nucl. Chem. 8 165

  8. (a) Govindaswamy P, Linder D, Lacour J, Süss-Fink G and Therrien B 2006 Chem. Commun. 4691; (b) Caskey D C, Yamamoto T, Addicott C, Shoemaker R K, Vacek J, Hawkridge A M, Muddiman D C, Kottas G S, Michl J and Stang P J 2008 J. Am. Chem. Soc. 130 7620

  9. (a) Pawin G, Solanki U, Kwon K Y, Wong K L, Lin X, Jiao T and Bartels L 2007 J. Am. Chem. Soc. 129 12056; (b) Pawin G, Wong K L, Kwon K Y and Bartels L 2006 Science 313 961

  10. (a) CrysAlis Pro software system, Version 171.32; Oxford Diffraction Ltd., Oxford, U.K., 2007; (b) Sheldrick G M 2008 Acta. Crystallogr. A 64 112

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Acknowledgements

We thank Prof. R. Murugavel, IIT-Bombay for scientific support and the University Grants Commission (UGC) (F. No. 41-218/2012 (SR)), India for financial support. DG and BS thank the Council of Scientific and Industrial Research (CSIR) for Senior Research Fellowship. We are grateful to Perkin-Elmer for ESI-Mass analysis.

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Correspondence to MALAICHAMY SATHIYENDIRAN.

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GUPTA, D., RAJAKANNU, P., SHANKAR, B. et al. Synthesis and crystal structure of a wheel-shaped supramolecular coordination complex. J Chem Sci 126, 1501–1506 (2014). https://doi.org/10.1007/s12039-014-0655-3

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