Synthesis, characterization and selective Cu²⁺ recognition of novel E– and Z–stilbenophanes

References

• Davis, F.; Higson, S. Macrocycles: Construction, Chemistry and Nanotechnology Applications; Wiley: Chennai, India, 2011.
   Google Scholar
• Brnjas-Kraljevi, J.; Pifat-Mrzljak, G. Supramolecular Structure and Function 10; Springer: Dordrecht, 2011.
   Google Scholar
• Dodziuk, H.;. Introduction to Supramolecular Chemistry; Kluwer Academic Publishers: Dordrecht, 2010.
   Google Scholar
• Steed, J.W.; Atwood, J.L. Supramolecular Chemistry; Wiley: Chichester, 2006.
   Google Scholar
• Ariga, K.; Kunitake, T. Supramolecular Chemistry: Fundamentals and Applications; Springer-Verlag: Berlin, Heidelberg, 2006.
   Google Scholar
• Tirado-Rives, J.; Gandour, R.D.; Fronczek, F.R. Tetrahedron Lett. 1982, 23, 1639–1642. doi:10.1016/S0040-4039(00)87178-6
   Web of Science ®Google Scholar
• Furstner, A.; Seidel, G.; Kopiske, C.; Kruger, C.; Mynott, R. Liebigs Ann. Chem. 1996, 1996, 655–662.
   Google Scholar
• Futterer, T.; Merz, A.; Lex, J. Angew. Chem., Int. Ed. Engl. 1997, 36, 611–613. doi:10.1002/anie.199706111
   Web of Science ®Google Scholar
• Tirado-Rives, J.; Oliver, M.A.; Fronczek, F.R.; Gandour, R.D. J. Org. Chem. 1984, 49, 1627–1634. doi:10.1021/jo00183a026
   Web of Science ®Google Scholar
• Ben, I.; Castedo, L.; Saa, J.M.; Seijas, J.A.; Suau, R.; Tojo, G. J. Org. Chem. 1985, 50, 2236–2240. doi:10.1021/jo00213a008
   Web of Science ®Google Scholar
• Álvarez, R.; López, V.; Mateo, C.; Medarde, M.; Peláez, R. Chem. Eur. J. 2011, 17, 3406–3419. doi:10.1002/chem.201002869
   PubMed Web of Science ®Google Scholar
• Mateo, C.; Pe´rez-Melero, C.; Peláez, R.; Medarde, M.J. Org. Chem. 2005, 70, 6544–6547. doi:10.1021/jo0508393
   PubMed Web of Science ®Google Scholar
• Mirza-Aghayan, M.; Darabi, H.R.; Ali-Saraie, L.; Ghassemzadeh, M.; Bolourtchian, M.; Jalali-Heravi, M.; Neumüller, B. Z. Anorg. Allg. Chem. 2002, 628, 681–684. doi:10.1002/1521-3749(200203)628:3<681::AID-ZAAC681>3.0.CO;2-T
   Web of Science ®Google Scholar
• Darabi, H.R.; Mirza-Aghayan, M.; Ali-Saraie, L.; Bolourtchian, M.; Neumueller, B.; Ghassemzadeh, M. Supramol. Chem. 2003, 15, 55–58. doi:10.1080/1061027021000003403
   Web of Science ®Google Scholar
• Darabi, H.R.; A. Mohebbi, R.; Bolourtchian, M. Supramol. Chem. 2003, 15, 465–468. doi:10.1080/10610270310001599195
   Web of Science ®Google Scholar
• Darabi, H.R.; Jadidi, K.; Mohebbi, A.R.; Faraji, L.; Aghapoor, K.; Shahbazian, S.; Azimzadeh Arani, M.; Nasseri, S.M. Supramol. Chem. 2008, 20, 327–333. doi:10.1080/10610270701258642
   Web of Science ®Google Scholar
• Darabi, H.R.; Azimzadeh Arani, M.; Motamedi, A.; Firouzi, R.; Herges, R.; Mohebbi, A.R.; Nasseri, S.; Naether, C. Supramol. Chem. 2009, 21, 632–637. doi:10.1080/10610270802657650
   Web of Science ®Google Scholar
• Darabi, H.R.; Darestani Farahani, A.; Hashemi Karouei, M.; Aghapoor, K.; Firouzi, R.; Herges, R.; Mohebbi, A.R.; Naether, C. Supramol. Chem. 2012, 24, 653–657. doi:10.1080/10610278.2012.678359
   Web of Science ®Google Scholar
• Darabi, H.R.; Mirzakhani, M.; Aghapoor, K.; Jadidi, K.; Faraji, L.; Sakhaee, N. J. Organometal. Chem. 2013, 740, 131–134. doi:10.1016/j.jorganchem.2013.05.008
   Web of Science ®Google Scholar
• Darabi, H.R.; Mirzakhani, M.; Aghapoor, K. J. Organomet. Chem. 2015, 786, 10–13. doi:10.1016/j.jorganchem.2015.02.047
   Web of Science ®Google Scholar
• Izatt, R.M.; Pawlak, K.; Bradshaw, J.S.; Bruening, R.L. Chem. Rev. 1991, 91, 1721–2085. doi:10.1021/cr00008a003
   Web of Science ®Google Scholar
• Taylor, I.F.; Amma, E.L. Acta Crystallogr. B. 1975, 31, 598–600. doi:10.1107/S0567740875003330
   Google Scholar
• McMurry, J.E.; Haley, G.J.; Matz, J.R.; Clardy, J.C.; Mitchell, J. J. Am. Chem. Soc. 1986, 108, 515–516. doi:10.1021/ja00263a032
   PubMed Web of Science ®Google Scholar
• Novotney, J.L.; Dichtel, W.R. ACS Macro Lett. 2013, 2, 423–426. doi:10.1021/mz4000249
   Web of Science ®Google Scholar
• Bunz, U.H.F.;. Macromol. Rapid Commun. 2009, 30, 772–805. doi:10.1002/marc.200800775
   PubMed Web of Science ®Google Scholar
• Tyler McQuade, D.; Pullen, A.E.; Swager, T.M. Chem. Rev. 2000, 100, 2537–2574.
   PubMed Web of Science ®Google Scholar
• X-ray data for Z1d: C₂₉H₂₂Br₂O₄, M = 594.27, monoclinic system, space group P2₁/c, a = 13.179(3) A, b = 8.5689(17), c = 21.900(4) Å; β = 98.70(3)º V = 2444.7(9) ų, Z = 4, D_calcd = 1.615 g cm⁻³, μ(Mo-Kα)= 3.350 mm⁻¹, crystal dimension of 0.50 × 0.50×0.40 mm. The X-ray diffraction measurement was made on a STOE IPDS 2T diffractometer with graphite monochromated Mo-Kα radiation. The structure was solved by using SHELXS. The Data reduction and structure refinement was carried out with SHELXL using the X-STEP32 crystallographic software package [X-STEP32 Version 1.07b, Crystallographic Package; Stoe & Cie GmbH: Darmstadt, Germany, 2000]. The non-hydrogen atoms were refined anisotropically by full matrix least-squares on F² values to final R₁ = 0.0640, wR₂ = 0.1633 and S = 0.805 with 316 parameters using 4292 independent reflection (θ range = 2.26-25º). Hydrogen atoms were added in idealized positions. The crystallographic information file has been deposited with the Cambridge Data Centre, CCDC 1556553.
   Google Scholar
• Since the detection limit using the S/B ratio is regarded as the most reliable and accurate, the detection limit for Cu²⁺ ions using the S/B ratio was determined on the basis of a plot of the ratio of the intensity versus the concentration of Cu²⁺.
   Google Scholar
• Guidelines for Drinking Water Quality. WHO Guidelines Values for Chemicals that are of Health Significance in Drinking Water, 3rd.; WHO press: Geneva, 2008.
   Google Scholar
• Ditchfield, R.;. Mol. Phys. 1974, 27, 789–807. doi:10.1080/00268977400100711
   Web of Science ®Google Scholar
• Klamt, A.; Schurmann, G. J. Chem. Soc. Perkin Trans. 1993, 2, 799–805. doi:10.1039/P29930000799
   Google Scholar
• Neese, F.;. WIREs Comput. Mol. Sci. 2012, 2, 73–78. doi:10.1002/wcms.81
   Web of Science ®Google Scholar