Two Supramolecular Complexes with Hydrogen-bonds of N-H ··· O and C-H ··· O between Dicarboxylic Acids and Bis-imidazoles

• Autorzy: Jin S. W. , Wang D. Q. , Jin Z. J. , Wang L. Q.
• Języki publikacji: EN

Abstrakty

EN

Two imidazole derived supra molecular complexes (N,N'-butylenebis(imidazole) : (tere - phthalic acid)2 (1), and N,N'-butylenebis(imidazole) : sebacic acid (2)) were synthesized and structurally characterized by X-ray crystallography. Compounds 1 and 2 both crystallize in the triclinic P-1 space group. In compound 1, one-dimensional grid structure is formed through imidazolium moieties hydrogen bonded to mono-ion carboxylate groups of two par al lel terephthalate chains. Ad ja cent grids packed along the b axis through C-H ··· O hydrogen bonds form 3D network. For compound 2, with strong O-H ···N hydrogen bonds, the bis(imidazole) and the sebacic acid are arranged alternatively to form 1D in finite chain, which is further stacked into a 3D net work structure through additional C-H ··· O hydrogen bonds.

Słowa kluczowe

EN

crystal structure; 3D framework; hydrogen bonds

• Wydawca: Polskie Towarzystwo Chemiczne
• Czasopismo: Polish Journal of Chemistry
• Rocznik: 2009
• Tom: Vol. 83, nr 11
• Strony: 1937--1944
• Opis fizyczny: Bibliogr. 35 poz., rys.

Twórcy

autor

Jin S. W.

autor

Wang D. Q.

autor

Jin Z. J.

autor

Wang L. Q.

• Department of Chemistry, Faculty of Science, ZheJiang Forestry University, Lin’An Hangzhou 311300, P. R. China Tel & fax: [phone],

Bibliografia

• 1.            Jeffrey G. A. and Saenger W., Hydrogen Bonding in Biological Structures; Springer-Verlag, Berlin (1991).
• 2.            Burrows A.D., Struct. Bonding, 108, 55 (2004).
• 3.            Etter M.C., Acc. Chem. Res., 23, 120 (1990).
• 4.            Holman K.T., Pivovar A.M., Swift J.A. and Ward M.D., Acc. Chem. Res., 34, 107 (2001).
• 5.            Shan N., Bond A.D. and Jones W., Cryst. Eng., 5, 9 (2002).
• 6.            Bhogala B.R., Basavoju S. and Nangia A., CrystEngComm., 1, 551 (2005).
• 7.            Weber E., Design of Organic Solids. Topics in Current Chemistry; Springer, Berlin, Vol. 198 (1998).
• 8.            Bhogala B.R., Cryst. GrowthDes., 3, 547 (2003).
• 9.            Du M., Zhang Z.H. and Zhao X.J., Cryst. Growth Des., 5, 1199 (2005).
• 10.          Shattock T.R., Vishweshwar P., Wang Z.Q. and Zaworotko M.J., Cryst. Growth Des., 5, 2046 (2005).
• 11.          Sarkar M. and Biradha K., Cryst. Growth Des., 6, 202 (2006).
• 12.          Ballabh A., Trivedi D.R. and Dastidar P., Cryst. Growth Des., 5, 1545 (2005).
• 13.          Trivedi D.R. and Dastidar P., Cryst. Growth Des., 6, 1022 (2006).
• 14.          Aakeroy C.B., Beatty A.M. and Helfrich B.A., Angew. Chem. Int. Ed., 40, 3240 (2001).
• 15.          Melaiye A., Sun Z.H., Hindi K., Milsted A., Ely D., Reneker D.H., Tessier C.A. and Youngs W.J., J. Am. Chem. Soc, 127, 2285 (2005).
• 16.          DobrzanskaL.,LloydG.O., RaubenheimerH.G. and Barbour LJ.,J. Am. Chem. Soc, 127,13134(2005).
• 17.          Dobrzanska L., Lloyd G.O., Raubenheimer H.G. and Barbour L.J., J. Am. Chem. Soc, 128,698 (2006).
• 18.          Huang X.C., Lin YY, Zhang J.P. and Chen X.M., Angew. Chem. Int. Ed., 45, 1557 (2006).
• 19.          Lu W.G., Su C.Y, Lu T.B., Jiang L. and Chen J.M., J. Am. Chem. Soc, 128, 34 (2006).
• 20.          Zou R., Sakurai H. and Xu Q., Angew. Chem. Int. Ed., 45, 2542 (2006).
• 21.          MacDonald J.C., Dorrestein P.C. and Pilley M.M., Cryst. Growth Des., 1, 29 (2001).
• 22.          Trivedi D.R., Ballabh A. and Dastidar P., CrystEngComm., 5, 358 (2003).
• 23.          Akhriff Y, ServerCarrio J., Garcia-Lozano J., Folgado J.V., Sancho A., EscrivaE., VitoriaP. and Soto L., Cryst. Growth Des., 6, 1124 (2006).
• 24.          Aakeroy C.B., Salmon D.J., Leonard B. and Urbina J.F., Cryst. Growth Des., 5, 865 (2005).
• 25.          Aakeroy C.B., Salmon D.J., Smith M.M. and Desper J., Cryst. Growth Des., 6, 1033 (2006).
• 26.          Cheruzel L.E., Mashuta M.S. and Buchanan R.M., Chem. Commun., 2223 (2005).
• 27.          Roey P. V, Bullion K. A., Osawa Y, Bowman R.M. and Braun D.G., Acta Crystallogr., C47,1015(1991).
• 28.          Ma B.Q. and Coppens P., Cryst. Growth Des., 4, 1377 (2004).
• 29.          Jin S.W. and Chen W.Z., Polyhedron, 26, 3074 (2007).
• 30.          Jin S.W. and Chen W.Z., Inorg. Chim. Acta, 360, 3756 (2007).
• 31.          Schutze V.W. and Schubert H, J. Prakt. Chem., 8, 307 (1959).
• 32.          Blessing R.H., Acta Crystallogr., A51, 33 (1995).
• 33.          Sheldrick G.M., SADABS "Siemens Area Detector Absorption Correction"; University of Göttingen: Göttingen, Germany (1996).
• 34.          SHELXTL-PC, version 5.03; Siemens Analytical Instruments: Madison, WI.
• 35.          Aakeroy C.B., Desper J. and Fasulo M.E., CrystEngComm., 8, 586 (2006).